View on Amazon.com
Results of Medical Text Analysis with Natural Language Processing (NLP): Latest in Genomics Methodologies for Therapeutics: Gene Editing, NGS
https://www.amazon.com/dp/B0BRD8JXTL
Results of Medical Text Analysis with Natural Language Processing (NLP): Latest in Genomics Methodologies for Therapeutics: Gene Editing, NGS & BioInformatics, … de la investigación genómica Book 3) Kindle Edition
by Madison Davis (Author), Aviva Lev-Ari (Editor), Stephen J. Williams (Editor), Marcus W. Feldman (Editor) Format: Kindle Edition
Serie B: Fronteras de la investigación genómica
(3 book series) Kindle Edition
by Larry H. Bernstein (Author) , Stephen J. Williams (Author) , Sudipta Saha (Author) , Ritu Saxena (Author) , Tilda Barliya (Author) , Anamika Sarkar (Author) , Marcus W. Feldman (Author) , Demet Sag (Author) , Prabodh kandala (Author) , Larry H. Bernstein (Author) , Aviva Lev-Ari (Author) , Madison Davis (Author)
https://www.amazon.com/dp/B0BQGZYZVT?binding=kindle_edition&ref=dbs_dp_rwt_sb_pc_tukn
- NEW GENRE Volume Three: Results of Medical Text Analysis with Natural Language Processing (NLP). It is known in 2022, as Genomics Volume Three in NEW GENRE Series B: Frontiers in Genomics Research
NEW GENRE Series B, Genomics Volume Three:
Results of Medical Text Analysis with
Natural Language Processing (NLP)
by
Madison Davis
NLP Results Interpretation
by
Prof. Stephen J. Williams, Prof. Marcus W. Feldman and
Dr. Aviva Lev-Ari, PhD, RN
Leaders in Pharmaceutical Business Intelligence (LPBI) Group, Boston
Editor-in-Chief, BioMed E-Series and
NEW GENRE Audio English-Spanish BioMed e-Series
UC, Berkeley, PhD’83
avivalev-ari@alum.berkeley.edu
NEW GENRE Series B, Genomics Volume Three: was known as PART B in NEW GENRE Series B, Volume Two]. Now, it is Volume Three in the NEW GENRE BioMed e-Series, Series B.
The Original Text: Genomics VOLUME TWO
Latest in Genomics Methodologies for Therapeutics: Gene Editing, NGS & BioInformatics, Simulations and the Genome Ontology
Available on Amazon.com since 12/28/2019
https://www.amazon.com/dp/B08385KF87
In 2022, this original Book https://www.amazon.com/dp/B08385KF87
has two additional versions:
· New Genre Volume Two: Latest in Genomics Methodologies for Therapeutics: Gene Editing, NGS and BioInformatics, Simulations and the Genome Ontology
· PART A (Spanish Audio, Bilingual Text) & PART C (English Audio)
· NEW GENRE Volume Three: Results of Medical Text Analysis with Natural Language Processing (NLP). It is known in 2022, as Genomics Volume Three in NEW GENRE Series B: Frontiers in Genomics Research. PART B in NEW GENRE Series B, Volume 3
· PART B (Graphics, English Text)
Serie B: Fronteras de la investigación genómica
Asesor de contenidos de la serie:
Larry H. Bernstein, MD, FCAP, Emeritus CSO, LPBI Group
2012 – 2017
Asesor de contenidos del volumen:
Prof. Marcus W. Feldman
2012 – Actualidad
https://www.youtube.com/watch?v=aT-Jb0lKVT8
BURNET C. Y MILDRED FINLEY WOHLFORD, PROFESORA EN LA SCHOOL OF HUMANITIES AND SCIENCES
Universidad de Stanford, codirectora del Center for Computational Evolutionary and Human Genetics
SEGUNDO VOLUMEN
Traducción a español
Lo último en metodologías genómicas para agentes terapéuticos:
edición génica, SMP y bioinformática,
simulaciones y la ontología del genoma
Prof. Marcus W. Feldman, PhD, Editor
Stephen J Williams, PhD, Editor
y
Aviva Lev-Ari, PhD, RN, Editor
Disponible en Amazon.com desde el 28/12/2019
https://www.amazon.com/dp/B08385KF87
Series B: Frontiers in Genomics Research
Series Content Consultant:
Larry H. Bernstein, MD, FCAP, Emeritus CSO, LPBI Group
2012 – 2017
Volume Content Consultant:
Prof. Marcus W. Feldman
2012 – Present
https://www.youtube.com/watch?v=aT-Jb0lKVT8
BURNET C. AND MILDRED FINLEY WOHLFORD PROFESSOR IN THE SCHOOL OF HUMANITIES AND SCIENCES
Stanford University, Co-Director, Center for Computational, Evolutionary and Human Genetics
VOLUME TWO
Latest in Genomics Methodologies for Therapeutics:
Gene Editing, NGS & BioInformatics,
Simulations and the Genome Ontology
Prof. Marcus W. Feldman, PhD, Editor
Stephen J Williams, PhD, Editor
and
Aviva Lev-Ari, PhD, RN, Editor
Available on Amazon.com since 12/28/2019
https://www.amazon.com/dp/B08385KF87
ENLACE a otros libros electrónicos sobre genómica en Amazon.com de nuestro equipo
Orientaciones genómicas para la medicina personalizada
PRIMER VOLUMEN
Traducción a español
LINK to other e-Books on Genomics on Amazon.com by Our Team
Genomics Orientations for Personalized Medicine
VOLUME ONE
En Amazon.com desde el 23/11/2015
http://www.amazon.com/dp/B018DHBUO6
UC, Berkeley, PhD’83
Redactor jefe de la serie de libros electrónicos BioMed
Leaders in Pharmaceutical Business Intelligence (LPBI) Group,
Boston
avivalev-ari@alum.berkeley.edu
LPBI Group’s New Genre of Scientific Books
Genomics Volume 2, PART A:
Part A.1: electronic Table of Contents (eTOCs) in Spanish Audio
Part A.2: electronic Table of Contents (eTOCs) in Bilingual Spanish & English Test
This volume covers
only
Genomics Volume 3 was known as Volume 2, PART B
Results of Medical Text Analysis with
Natural Language Processing (NLP)
by
Madison Davis
NLP Results Interpretation
by
Prof. Stephen J. Williams, Prof. Marcus W. Feldman and
Dr. Aviva Lev-Ari, PhD, RN
Genomics Volume 2, PART C:
Selective Editorials of the original text – English Audio
Genomics Volume 3:
Results of Medical Text Analysis with
Natural Language Processing (NLP)
by
Madison Davis
NLP Results Interpretation
by
Prof. SJ Williams, Prof. MW Feldman and
Dr. Aviva Lev-Ari, PhD, RN
Leaders in Pharmaceutical Business Intelligence (LPBI) Group, Boston
Editor-in-Chief, BioMed E-Series and
NEW GENRE Audio English-Spanish BioMed e-Series
UC, Berkeley, PhD’83
avivalev-ari@alum.berkeley.edu
NLP Software
WOLFRAM FUNCTION REPOSITORY
Instant-use add-on functions for the Wolfram Language
- HypergraphPlot – Plot a hypergraph defined by a list of hyperedges
https://resources.wolframcloud.com/FunctionRepository/resources/HypergraphPlot/
and
- TreePlot – Plot a tree diagram specified by edge rules
https://reference.wolfram.com/language/ref/TreePlot.html
Text Analysis with NLP of Original
Genomics Volume 2, Part 1:
Next Generation Sequencing (NGS)
1.1 The NGS Science
1.1.1 BioIT Aspect
|
Hypergraph Plot #1 and Tree Diagram #1 for 1.1.1 based on 16 articles & on 12 keywords protein, cancer, dna, genes, rna, survival, immune, tumor, patients, human, genome, expression |


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List of articles included in 1.1.1
1.1.1.1 International Award for Human Genome Project
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
https://pharmaceuticalintelligence.com/2018/02/09/international-award-for-human-genome-project/
1.1.1.2 Cracking the Genome – Inside the Race to Unlock Human DNA – quotes in newspapers
Reporter: Aviva Lev-Ari, PhD, RN
1.1.1.3 mRNA Data Survival Analysis
Curators: Larry H. Bernstein, MD, FCAP and Aviva Lev-Ari, PhD, RN
https://pharmaceuticalintelligence.com/2016/06/18/mrna-data-survival-analysis/
1.1.1.4 Novel Discoveries in Molecular Biology and Biomedical Science
Curator: Larry H. Bernstein, MD, FCAP
1.1.1.5 Switching on genes
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/05/19/switching-on-genes/
1.1.1.6 The Role of Big Data in Medicine
Author: Gail S. Thornton, M.A.
https://pharmaceuticalintelligence.com/2016/05/16/the-role-of-big-data-in-medicine/
1.1.1.7 Disease related changes in proteomics, protein folding, protein-protein interaction
Curator: Larry H. Bernstein, MD, FCAP
1.1.1.8 Bio-IT World 2016 – Reception with Dr. Howard Jacob – Aviva Lev-Ari, PhD, RN will attend
Reporter: Aviva Lev-Ari, PhD, RN
1.1.1.9 How do we address medical diagnostic errors?
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/03/26/how-do-we-address-medical-diagnostic-errors/
1.1.1.10 DNA and Origami
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/03/17/dna-and-origami/
1.1.1.11 Phenotypic Screening must evolve to ensure successful Drug Development
Reporter: Aviva Lev-Ari, PhD, RN
1.1.1.12 3-D visualization of cancer cells
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/02/28/3-d-visualization-of-cancer-cells/
1.1.1.13 Leadership in Genomics: VarElect – Variants in Disease and UCSC Genome Technology Center
Reporter: Aviva Lev-Ari, PhD, RN
1.1.1.14 Signaling of Immune Response in Colon Cancer
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/01/09/signaling-of-immune-response-in-colon-cancer/
1.1.1.15 Periodic table of protein complexes
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/01/09/periodic-table-of-protein-complexes/
1.1.1.16 AGENDA for Oligonucleotide Therapeutics and Delivery, April 4-5, 2016, HYATT Hotel, Cambridge, MA
Reporter: Aviva Lev-Ari, PhD, RN
1.1.2 BioInformatics-NGS
| Hypergraph Plot #2 and Tree Diagram #2
for 1.1.2 based on 17 articles & on 10 keywords
cancer, mutations, patients, disease, genetic, mutation, clinical, tumor, genes, protein |


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List of articles included in 1.1.2
1.1.2.1 Extracellular RNA and their carriers in disease diagnosis and therapy
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
1.1.2.2 Gender affects the prevalence of the cancer type
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
https://pharmaceuticalintelligence.com/2019/04/02/gender-affects-the-prevalence-of-the-cancer-type/
1.1.2.3 Pancreatic cancer survival is determined by ratio of two enzymes
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
1.1.2.4 Immuno-editing can be a constant defense in the cancer landscape
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
1.1.2.5 Immunotherapy may help in glioblastoma survival
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
https://pharmaceuticalintelligence.com/2019/03/16/immunotherapy-may-help-in-glioblastoma-survival/
1.1.2.6 Knowing the genetic vulnerability of bladder cancer for therapeutic intervention
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
1.1.2.7 SNP-based Study on high BMI exposure confirms CVD and DM Risks – no associations with Stroke
Reporter: Aviva Lev-Ari, PhD, RN
1.1.2.8 Sperm Analysis by Smart Phone
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
https://pharmaceuticalintelligence.com/2017/03/29/sperm-analysis-by-smart-phone/
1.1.2.9 Dr. Doudna: RNA synthesis capabilities of Synthego’s team represent a significant leap forward for Synthetic Biology
Reporter: Aviva Lev-Ari, PhD, RN
1.1.2.10 Etiologies of Cardiovascular Diseases: Epigenetics, Genetics and Genomics: Request for Book Review Writing on Amazon.com
Editors: Larry H. Bernstein and Aviva Lev-Ari, PhD, RN
https://pharmaceuticalintelligence.com/2016/09/11/request-for-book-review-writing-on-amazon-com/
1.1.2.11 Cancer detection and therapeutics
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/05/02/cancer-detection-and-therapeutics/
1.1.2.12 Pull at Cancer’s Levers
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/04/02/pull-at-cancers-levers/
1.1.2.13 The world’s most innovative intersection
Reported by: Irina Robu
https://pharmaceuticalintelligence.com/2016/01/02/the-worlds-most-innovative-intersection/
1.1.2.14 Complex Cancer Genetics Testing
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/10/complex-cancer-genetics-testing/
1.1.2.15 The Need for an Informatics Solution in Translational Medicine
Curator: Larry H. Bernstein, MD, FCAP
1.1.2.16 Human Genetics and Childhood Diseases
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/03/human-genetics-and-childhood-diseases/
1.1.2.17 GEN Tech Focus: Rethinking Gene Expression Analysis
Curator: Larry H. Bernstein, MD, FCAP
1.1.3 Computation Biology
| Hypergraph Plot #3 and Tree Diagram #3
for 1.1.3 based on 21 articles & on 8 keywords
protein, dna, cancer, cells, gene, sequence, chemical, complexes |

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List of articles included in 1.1.3
1.1.3.1 BioInformatic Resources at the Environmental Protection Agency: Tools and Webinars on Toxicity Prediction
Curator: Stephen J. Williams Ph.D.
1.1.3.2 Live Conference Coverage @MedCity news Converge 2018 Philadelphia: Early Diagnosis Through Predictive Biomarkers, NonInvasive Testing
Reporter: Stephen J. Williams, Ph.D.
1.1.3.3 DISCUSSION – Genomics-driven personalized medicine for Pancreatic Cancer
Reporter: Aviva Lev-Ari, PhD, RN
1.1.3.4 CancerBase.org – The Global HUB for Diagnoses, Genomes, Pathology Images: A Real-time Diagnosis and Therapy Mapping Service for Cancer Patients – Anonymized Medical Records accessible to anyone on Earth
Reporter: Aviva Lev-Ari, PhD, RN
1.1.3.5 Innovative Gene Families for exploring patterns of Genetic Families applied by Craig Venter’s Team in Deeply Sequencing 10,500 Genomes: an average of 8,579 novel variants found per person –Intolerant sites, might be essential for life or health.
Reporter: Aviva Lev-Ari, PhD, RN
1.1.3.6 First challenge to make use of the new NCI Cloud Pilots – Somatic Mutation Challenge – RNA: Best algorithms for detecting all of the abnormal RNA molecules in a cancer cell
Reporter: Aviva Lev-Ari, PhD, RN
1.1.3.7 Somatic Mutation Theory – Why it’s Wrong for Most Cancers
Reporter: Aviva Lev-Ari, PhD, RN
1.1.3.8 Genomics and epigenetics link to DNA structure
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/04/11/genomics-and-epigenetics-link-to-dna-structure
1.1.3.9 3-D molecular structures
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/02/28/3-d-molecular-structures/
1.1.3.10 Correspondence on Leadership in Genomics and other Gene Curations: Dr. Williams with Dr. Lev-Ari
Authors: Stephen J Williams, PhD and Aviva Lev-Ari, PhD, RN
1.1.3.11 Leadership in Genomics: VarElect – Variants in Disease and UCSC Genome Technology Center
Reporter: Aviva Lev-Ari, PhD, RN
1.1.3.12 Gene Editing for Exon 51: Why CRISPR Snipping might be better than Exon Skipping for DMD
Reporter: Aviva Lev-Ari, PhD, RN
1.1.3.13 Periodic Table of Protein Complexes
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/01/09/periodic-table-of-protein-complexes/
1.1.3.14 Genomics’ Proprietary Statistical Analysis Tools and Integrated Multi-Phenotype Database to be used to Support Research and Development at Vertex Pharmaceuticals
Reporter: Aviva Lev-Ari, PhD, RN
1.1.3.15 N3xt generation carbon nanotubes
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/12/14/n3xt-generation-carbon-nanotubes/
1.1.3.16 Biochemistry and Dysmetabolism of Aging and Serious Illness
Curator: Larry H. Bernstein, MD, FCAP
1.1.3.17 Identifying Cancers and Resistance
Curator: Larry H/ Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/18/identifying-cancers-and-resistance/
1.1.3.18 Complexity of Protein-Protein Interactions
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/12/protein-protein-interactions/
1.1.3.19 Variability of Gene Expression and Drug Resistance
Curator: Larry H. Bernstein, MD, FCAP
1.1.3.20 Sequence the Human Genome
Curator: Larry H Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/11/sequence-the-human-genome/
1.1.3.21 Single Nucleotide Repair and Tunable DNA-directed Assembly of Nanomaterials
Curator: Larry H. Bernstein, MD, FCAP
1.1.4 NGS – Discoveries in Medicine Derived from Advanced Sequencing
| Hypergraph Plot #4 and Tree Diagram #4
for 1.1.4 based on 2 articles & on 11 keywords
sequencing, medicine, genes, women, genome, medical, genetics, disorder, bipolar, autism, variations
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List of articles included in 1.1.4
1.1.4.1 Genomic relationship between autism and bipolar disorder
Curator: Larry H. Bernstein, MD, FCAP
1.1.4.2 Sequencing yourself! and Learn more on Genome Sequencing on Tuesday, November 17, 2015 from 8am-5pm in the Joseph B. Martin Conference Center of the Harvard New Research Building at Harvard Medical School
Reporter: Aviva Lev-Ari, PhD, RN
1.2 Technologies and Methodologies
1.2.1 BioIT
| Hypergraph Plot #5 and Tree Diagram #5
for 1.2.1 based on 18 articles & on 9 keywords
cancer, cells, signature, genome, variants, gene, genomic, human, features |
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List of articles included in 1.2.1
1.2.1.1 A Nonlinear Methodology to Explain Complexity of the Genome and Bioinformatic Information
Reporter: Stephen J. Williams, Ph.D.
1.2.1.2 18th Annual 2019 BioIT, Conference & Expo, April 16-18, 2019, Boston, Seaport World Trade Center, Track 5 Next-Gen Sequencing Informatics – Advances in Large-Scale Computing
Real Time Coverage with Social Media: Aviva Lev-Ari, PhD, RN
1.2.1.3 2019 Koch Institute Symposium – Machine Learning and Cancer, June 14, 2019, 8:00 AM-5:00 PM ET MIT Kresge Auditorium, 48 Massachusetts Ave, Cambridge, MA
Real Time Coverage with Social Media: Aviva Lev-Ari, PhD, RN
1.2.1.4 Can Blockchain Technology and Artificial Intelligence Cure What Ails Biomedical Research and Healthcare
Curator: Stephen J. Williams, Ph.D.
1.2.1.5 Bioinformatics Tool Review: Genome Variant Analysis Tools
Curator: Stephen J. Williams, Ph.D.
1.2.1.6 2018 CHI’s BioIT World conference THURSDAY, MAY 17 | 8:00 – 9:45 AM – Awards and Keynote
Real Time Coverage with Social Media: Aviva Lev-Ari, PhD, RN
1.2.1.7 Vyasa Analytics Demos Deep Learning Software for Life Sciences at Bio-IT World 2018 – Vyasa’s booth (#632)
Reporter: Aviva Lev-Ari, PhD, RN
1.2.1.8 Synopsis Track 7: NGS in Real Time @pharma_BI 2018 CHI’s BioIT World conference & Expo, May 15 – 17, 2018, Boston, MA – Seaport World Trade Center
Reporter: Aviva Lev-Ari, PhD, RN
1.2.1.9 2017 Agenda – BioInformatics: Track 6: BioIT World Conference & Expo ’17, May 23-35, 2017, Seaport World Trade Center, Boston, MA
Reporter: Aviva Lev-Ari, PhD, RN
1.2.1.10 The 16th annual EmTech MIT – A Place of Inspiration, October 18-20, 2016, Cambridge, MA
Real Time coverage with Social Media: Aviva Lev-Ari, PhD, RN
1.2.1.11 10 Most Successful Big Data Technologies
Guest Author: Gil Press
https://pharmaceuticalintelligence.com/2016/04/25/10-most-successful-big-data-technologies/
1.2.1.12 Big Data Self-Delusion
Guest Author: Gil Press
https://pharmaceuticalintelligence.com/2016/04/02/big-data-self-delusion/
1.2.1.13 Top 100 Big Data Experts to Follow
Reporter: Aviva Lev-Ari, PhD, RN
https://pharmaceuticalintelligence.com/2016/01/20/top-100-big-data-experts-to-follow/
1.2.1.14 Crystal Resolution in Raman Spetctoscopy for Pharmaceutical Analysis
Curator: Larry H. Bernstein, MD, FCAP
1.2.1.15 Imaging of Cancer Cells
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/04/20/imaging-of-cancer-cells/
1.2.1.16 Bioinformatic Tools for Cancer Mutational Analysis: COSMIC and Beyond
Curator: Stephen J. Williams, Ph.D.
1.2.1.17 Laboratory Automation Today
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/23/laboratory-automation-today/
1.2.1.18 Bioinformatics Tool Review: Genome Variant Analysis Tools
Curator: Stephen J. Williams, Ph.D.
1.2.2 BioInformatics – NGS
| Hypergraph Plot #6 and Tree Diagram #6
for 1.2.2 based on 18 articles & on 11 keywords
cancer, cells, drug, protein, human, bioinformatics, genes, clinical, medicine, dna, genomics
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List of articles included in 1.2.2
1.2.2.1 A Nonlinear Methodology to Explain Complexity of the Genome and Bioinformatic Information
Reporter: Stephen J. Williams, Ph.D.
1.2.2.2 18th Annual 2019 BioIT, Conference & Expo, April 16-18, 2019, Boston, Seaport World Trade Center, Track 5 Next-Gen Sequencing Informatics – Advances in Large-Scale Computing
Reporter: Aviva Lev-Ari, PhD, RN
1.2.2.3 Thriving at the Survival Calls during Careers in the Digital Age – An AGE like no Other, also known as, DIGITAL
Author and Curator: Aviva Lev-Ari, PhD, RN
1.2.2.4 Synopsis Track 7: NGS in Real Time @pharma_BI 2018 CHI’s BioIT World conference & Expo, May 15 – 17, 2018, Boston, MA – Seaport World Trade Center
Real Time Reporter: Aviva Lev-Ari, PhD, RN
1.2.2.5 The BioPharma Industry’s Unrealized Wealth of Data, by Ben Szekely, Vice President, Cambridge Semantics
Reporter: Aviva Lev-Ari, PhD, RN
1.2.2.6 2017 Agenda – BioInformatics: Track 6: BioIT World Conference & Expo ’17, May 23-35, 2017, Seaport World Trade Center, Boston, MA
Reporter: Aviva Lev-Ari, PhD, RN
1.2.2.7 A novel 5-gene pancreatic adenocarcinoma classifier: Meta-analysis of transcriptome data – Clinical Genomics Research @BIDMC
Curator: Tilda Barliya, PhD
1.2.2.8 Recap of Bio-IT World 2016 by Sanjay Joshi CTO, Healthcare & Life Sciences, EMC Emerging Technologies Division
Reporter: Aviva Lev-Ari, PhD, RN
1.2.2.9 Genome Analysis Toolkit (GATK) the Industry Standard will govern the New Tools in Biomedical Research by the Collaboration of Broad Institute and Intel
Curator: Aviva Lev-Ari, PhD, RN
1.2.2.10 Curbing Cancer Cell Growth & Metastasis-on-a-Chip’ Models Cancer’s Spread
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/03/19/curbing-cancer-cell-growth/
1.2.2.11 Simulation of DNA Sequencing through Graphene Nanopore
Reporter: Danut Dragoi, PhD
1.2.2.12 2016 BioIT World: Track 5 – April 5 – 7, 2016 Bioinformatics Computational Resources and Tools to Turn Big Data into Smart Data
Reporter: Aviva Lev-Ari, PhD, RN
1.2.2.13 Biomarker Development
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/16/biomarker-development/
1.2.2.14 Genetically Engineered Algae
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/15/genetically-engineered-algae/
1.2.2.15 Sequence the Human Genome
Curator: Larry H Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/11/sequence-the-human-genome/
1.2.2.16 Atul Butte TALK on YouTube on Big Data, Open Data and Clinical Trials
Reporter: Aviva Lev-Ari, PhD
1.2.2.17 How to identify Genes associated with Genetic Diseases and Cancer: A Phylogenetic Profiling Evolutionary Approach @ HUJI
Reporter: Aviva Lev-Ari, PhD, RN
1.2.2.18 Tweets by @pharma_BI at 2015 BioIT, Boston, 4/21/2015- 4/23/2015
Live Press Coverage: Aviva Lev-Ari, PhD, RN
1.2.3 Computation Biology
| Hypergraph Plot #7 and Tree Diagram #7
for 1.2.3 based on 11 articles & on 11 keywords
dna, cancer, protein, gene, search, amino, health, medicine, cells, genome, editing
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List of articles included in 1.2.3
1.2.3.1 A New Computational Method illuminates the Heterogeneity and Evolutionary Histories of cells within a Tumor
Reporter: Aviva Lev-Ari, PhD, RN
1.2.3.2 Through Data Science: Stanford Medicine and Google will transform Patient Care and Medical Research
Reporter: Aviva Lev-Ari, PhD, RN
1.2.3.3 A New Potential Target for Pancreatic Cancer Treatment: Rapid Screening Technique finds Gene Defending Tumors from DNA Damage @M. D. Anderson Cancer Center
Reporter: Aviva Lev-Ari, PhD, RN
1.2.3.4 Deep Learning for In-silico Drug Discovery and Drug Repurposing: Artificial Intelligence to search for molecules boosting response rates in Cancer Immunotherapy: Insilico Medicine @John Hopkins University
Reporter: Aviva Lev-Ari, PhD, RN
1.2.3.5 Gene Editing: The Role of Oligonucleotide Chips
Curators: Larry H Bernstein, MD, FCAP and Aviva Lev-Ari, PhD, RN
https://pharmaceuticalintelligence.com/2016/01/07/gene-editing-the-role-of-oligonucleotide-chips/
1.2.3.6 How Will FDA’s new precision FDA Science 2.0 Collaboration Platform Protect Data?
Reporter: Stephen J. Williams, Ph.D.
1.2.3.7 Computer Aided Design
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/17/computer-aided-design/
1.2.3.8 Genomic Pathogen Typing
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/16/genomic-pathogen-typing/
1.2.3.9 Best Big Data?
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/16/best-big-data/
1.2.3.10 Better Bioinformatics
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/09/better-bioinformatics/
1.2.3.11 Healthcare conglomeration to access Big Data and lower costs
Curator: Larry H. Bernstein, MD, FCAP
1.2.4 NGS – Discoveries Driven by Advanced Sequencing
| Hypergraph Plot #8 and Tree Diagram #8
for 1.2.4 based on 5 articles & on 10 keywords
genetic, sequencing, gene, clinical, genome, reproductive, disease, diagnostics, medicine, ngs
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List of articles included in 1.2.4
1.2.4.1 Crowdsourcing Genetic Data Yields Discovery of DNA loci associated with Major Depressive Disorder (MDD) in European Descendants
Reporter: Kelly Perlman, Life Sciences Student and Research Assistant, McGill University
1.2.4.2 Using Online Mendelian Inheritance in Man (OMIM) database and the Human Genome Mutation Database (HGMD) Pro 2015.2 for Quantification of the growth in gene-disease and variant-disease associations
Reporter: Aviva Lev-Ari, PhD, RN
1.2.4.3 Roche is developing a high-throughput low cost sequencer for NGS, How NGS Will Revolutionize Reproductive Diagnostics: November Meeting, Boston MA
Reporter: Stephen J. Williams, PhD
1.2.4.4 How NGS Will Revolutionize Reproductive Diagnostics: November Meeting, Boston MA
Reporter: Stephen J. Williams, PhD
1.2.4.5 LIVE Plenary Session 2015 BioIT, April 21, 2015, 4:00 – 5:00PM – Cambridge HealthTech Institute’s 14th Annual Meeting BioIT World – Conference & Expo ’15, April 21 – 23, 2015 @Seaport World Trade Center, Boston, MA
Real Time Reporter: Dr. Aviva Lev-Ari will be in attendance on April 21, 22, 23
1.3 NGS – Clinical Aspects
| Hypergraph Plot #9 and Tree Diagram #9
for 1.3 based on 11 articles & on 14 keywords
cells, medicine, cancer, clinical, gene, medical, patients, sequencing, health, therapy, pharma, drug, genetic, genome
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1.3.1 BioInformatics – NGS
List of articles included in 1.3.1
1.3.1.1 Translation of whole human genome sequencing to clinical practice: The Joint Initiative for Metrology in Biology (JIMB) is a collaboration between the National Institute of Standards & Technology (NIST) and Stanford University.
Reporter: Aviva Lev-Ari, PhD, RN
1.3.1.2 Transparency in Clinical Trials
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/09/transparency-in-clinical-trials/
1.3.2 Computation Biology & NGS
List of articles included in 1.3.2
1.3.2.1 Topical Solution for Combination Oncology Drug Therapy: Patch that delivers Drug, Gene, and Light-based Therapy to Tumor
Reporter: Aviva Lev-Ari, PhD, RN
1.3.3 NGS – Clinical Aspects
List of articles included in 1.3.3
1.3.3.1 New NGS Guidances for Laboratory Developed Tests (LDT): FDA’s Liz Mansfield on Audio Podcast
Reporter: Aviva Lev-Ari, PhD, RN
1.3.3.2 Next Generation Sequencing in Clinical Laboratory
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/03/22/next-generation-sequencing-in-clinical-laboratory/
1.3.3.3 First Cost-Effectiveness Study of Multi-Gene Panel Sequencing in Advanced Non-Small Cell Lung Cancer Shows Moderate Cost-Effectiveness, Exposes Crucial Practice Gap
Guest Author: Press Release by Personalized Medicine Coalition
1.3.3.4 2019 Warren Alpert Foundation Award goes to Four Scientists for Seminal Discoveries in OptoGenetics – Illuminating the Human Brain
Reporter: Aviva Lev-Ari, PhD, RN
1.3.3.5 Broad@15 – In 2004, the Broad Institute of MIT and Harvard launched with a mission to improve human health
Reporter: Aviva Lev-Ari, PhD, RN
1.3.3.6 New Mutant KRAS Inhibitors Are Showing Promise in Cancer Clinical Trials: Hope For the Once ‘Undruggable’ Target
Curator: Stephen J. Williams, Ph.D.
1.3.3.7 eProceedings 15th Annual Personalized Medicine Conference at Harvard Medical School – THE PARADIGM EVOLVES, November 13 – 14, 2019 • Harvard Medical School, Boston, MA
Real Time Press Coverage: Aviva Lev-Ari, PhD, RN
1.3.3.8 Tweets and Retweets by @AVIVA1950 and by @pharma_BI for 15th Annual Personalized Medicine Conference at Harvard Medical School – THE PARADIGM EVOLVES, November 13 – 14, 2019 • Harvard Medical School, Boston, MA
Real Time Press Coverage: Aviva Lev-Ari, PhD, RN
1.3.3.9 Complex rearrangements and oncogene amplification revealed by long-read DNA and RNA sequencing of a breast cancer cell line
Reporter: Stephen J. Williams, PhD
1.3.3.10 eProceedings – Day 1: Charles River Laboratories – 3rd World Congress, Delivering Therapies to the Clinic Faster, September 23 – 24, 2019, 25 Edwin H. Land Boulevard, Cambridge, MA
Reporter: Aviva Lev-Ari, PhD, RN
1.3.3.11 Genetic Testing in CVD and Precision Medicine
Reporter: Aviva Lev-Ari, PhD, RN
https://pharmaceuticalintelligence.com/2019/12/16/genetic-testing-in-cvd-and-precision-medicine/
1.4 Business and Legal
| Hypergraph Plot #10 and Tree Diagram #10
for 1.4 based on 18 articles & on 10 keywords
oncology, healthcare, cancer, data, cells, sequencing, health, life, gene, AI |

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1.4.1 BioIT
List of articles included in 1.4.1
1.4.1.1 Japan’s National Cancer Center Adopts Qiagen Bioinformatics Platform for Precision Med Program
1.4.1.2 37th Annual J.P. Morgan HEALTHCARE CONFERENCE: #JPM2019 for Jan. 8, 2019; Opening Videos, Novartis expands Cell Therapies, January 7 – 10, 2019, Westin St. Francis Hotel | San Francisco, California
Reporter: Stephen J. Williams, PhD
1.4.1.3 Healthcare conglomeration to access Big Data and lower costs
Curator: Larry H. Bernstein, MD, FCAP
1.4.1.4 Future of Big Data for Societal Transformation
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/12/14/future-of-big-data-for-societal-transformation/
1.4.1.5 Avvinity will have exclusive rights in oncology to use Alphamer therapeutic platform, invented by a Nobel Laureate and developed by Centauri: A Case of a Joint Venture Model
Reporter: Aviva Lev-Ari, PhD, RN
1.4.2 Bioinformatics – NGS
List of articles included in 1.4.2
1.4.2.1 Role of Informatics in Precision Medicine: Notes from Boston Healthcare Webinar: Can It Drive the Next Cost Efficiencies in Oncology Care?
Reporter: Stephen J. Williams, Ph.D.
1.4.2.2 TSUNAMI in HealthCare under the New Name Verily.com
Curator: Aviva Lev-Ari, PhD, RN
1.4.3 Computation Biology
List of articles included in 1.4.3
1.4.3.1 Convergence of Biology, Medicine, and Computing: Biomedical Informatics Entrepreneurs Salon (BIES), HMS, 2/7/19, 4:30 – 6:30PM
Real Time Reporter: Aviva Lev-Ari, PhD, RN
1.4.3.2 On its way for an IPO: mRNA platform, Moderna, Immune Oncology is recruiting 100 new Life Scientists in Cambridge, MA
Curator: Aviva Lev-Ari, PhD, RN
1.4.3.3 #JPM19 Conference: Lilly Announces Agreement To Acquire Loxo Oncology
Reporter: Gail S. Thornton
1.4.3.4 JP Morgan Healthcare Day Two: Thermo Fisher; Qiagen; Danaher; Counsyl; Human Longevity; Adaptive Bio, 10X Genomics and Pacific Biosciences
Reporter: Aviva Lev-Ari, PhD, RN
1.4.3.5 Day One at #JPM16: Breakout sessions of 23andMe, Myriad Genetics, Genomic Health, and Alere
Reporter: Aviva Lev-Ari, PhD, RN
1.4.3.6 #JPM16: Illumina’s CEO on new genotyping array called Infinium XT and Bio-Rad Partnership for single-cell sequencing workflow
Reporter: Aviva Lev-Ari, PhD, RN
1.4.3.7 Juno Acquires AbVitro for $125M: high-throughput and single-cell sequencing capabilities for Immune-Oncology Drug Discovery
Reporter: Aviva Lev-Ari, PhD, RN
1.4.3.8 #JPM16: Illumina’s CEO on new genotyping array called Infinium XT and Bio-Rad Partnership for single-cell sequencing workflow
Reporter: Aviva Lev-Ari, PhD, RN
1.4.4 NGS
List of articles included in 1.4.4
1.4.4.1 QIAGEN – International Leader in NGS and RNA Sequencing
Reporter: Aviva Lev-Ari, PhD, RN
1.4.4.2 Four patents and one patent application on Nanopore Sequencing and methods of trapping a molecule in a nanopore assigned to Genia, is been claimed in a Law Suit by The Regents of the University of California, should be assigned to UCSC
Reporter: Aviva Lev-Ari, PhD, RN
1.4.4.3 Invivoscribe, Thermo Fisher Ink Cancer Dx Development Deal
Reporter: Stephen J. Williams, PhD
Text Analysis with NLP of the Original
Genomics Volume 2, Part 2:
CRISPR for Gene Editing and DNA Repair
2.1 CRISPR – Aspects of the Science
2.1.1 Basic Biochemical Issues
| Hypergraph Plot #11 and Tree Diagram #11
for 2.1.1 based on 22 articles & on 14 keywords
cells, crispr, cas, gene, beta, dna, protein, editing, genome, cancer, target, ripk, rna, expression |

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List of articles included in 2.1.1
2.1.1.1 Breakthrough in Gene Editing CRISPR–Cas systems: First example of a fully programmable, RNA-guided integrase and lays the foundation for genomic manipulations that obviate the requirements for double-strand breaks and homology-directed repair.
Reporter: Aviva Lev-Ari, PhD, RN
2.1.1.2 Alternative to CRISPR/Cas9 – CAST (CRISPR-associated transposase) – A New Gene-editing Approach for Insertion of Large DNA Sequences into a Genome developed @BroadInstitute @MIT @Harvard
Reporter: Aviva Lev-Ari, PhD, RN
2.1.1.3 Innovations on the CRISPR System for Gene Editing: (1) Cryo-electron microscopy-based visualization of Cas3 Enzyme Cleavage (2) New tool testing an entire genome against a CRISPR molecule to predict potential errors and interactions
Curator and Reporter: Aviva Lev-Ari, PhD, RN
2.1.1.4 Researchers at Dana-Farber/Boston Children’s: Differences in wiring of “exhausted” and effective T cells indicate possible gene-editing targets
Reporter: Aviva Lev-Ari, PhD, RN
2.1.1.5 “CRISPR-Cas9, bring me a gene”, Encoding for a specific protein: Three words: CRISPR. A Capella
Reporter: Aviva Lev-Ari, PhD, RN
2.1.1.6 Novel Discoveries in Molecular Biology and Biomedical Science
Curator: Larry H. Bernstein, MD, FCAP
2.1.1.7 A Genetic Switch to Control Female Sexual Behavior
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
2.1.1.8 Preliminary Agenda Available and Exclusive Discount to attend Understanding CRISPR: Mechanisms to Applications Symposium in Boston (September 19, 2016)
Reporter: Aviva Lev-Ari, PhD, RN
2.1.1.9 Gene Editing with CRISPR gets Crisper
Curators: Larry H. Bernstein, MD, FCAP and Aviva Lev-Ari, PhD, RN
https://pharmaceuticalintelligence.com/2016/05/03/gene-editing-with-crispr-gets-crisper/
2.1.1.10 CRISPR-Cas9 Screening by Horizon Discovery, Cambridge, UK – HDx™ Reference Standards
Reporters: David Orchard-Webb, PhD and Aviva Lev-Ari, PhD, RN
2.1.1.11 Recent Progress in Gene Editing Error Reduction
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/04/21/recent-progress-in-gene-editing-error-reduction/
2.1.1.12 CRISPR/Cas9 and HIV1
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/04/16/crisprcas9-and-hiv1/
2.1.1.13 Rice University researches develop new CRISPR-CAS9 strategy to reduce off-target gene editing effects
Reporter: Stephen J. Williams
2.1.1.14 @MIT: New delivery method boosts efficiency of CRISPR genome-editing system
Reporters: Aviva Lev-Ari, PhD, RN and Stephen J Williams, PhD
2.1.1.15 Alternative CRISPR discovered @MIT
Reporter: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/02/15/alternative-crispr-discovered/
2.1.1.16 Shortened Time for Cell Renewal
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/12/15/shortened-time-for-cell-renewal/
2.1.1.17 Turning CRISPR/Cas9 On or Off
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/21/turning-crisprcas9-on-or-off/
2.1.1.18 Cell Death Pathway Insights
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/09/cell-death-pathway-insights/
2.1.1.19 Gene Silencing
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/05/gene-silencing/
2.1.1.20 New CRISPR-non Cas9 proteins
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/10/27/new-crispr-non-cas9-proteins/
2.1.1.21 Regulatory DNA Engineered
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/02/11/regulatory-dna-engineered/
2.1.1.22 At Technical University of Munich (TUM) Successful Genetical modification of a patient’s own immune cells, T cell receptors, using CRISPR-Cas9 gene editing tool. The engineered T cells are very similar to the physiological immune cells.
Reporter: Aviva Lev-Ari, PhD, RN
2.1.2 Drug Discovery
| Hypergraph Plot #12 and Tree Diagram #12
for 2.1.2 based on 8 articles & on 14 keywords
crispr, cas, cells, genome, dna, genes, rna, protein, genetic, editing, disease, target, human, technology |


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List of articles included in 2.1.2
2.1.2.1 CRISPR/Cas9 Finds Its Way As an Important Tool For Drug Discovery & Development
Curator: Stephen J. Williams, Ph.D.
2.1.2.2 Delineating a Role for CRISPR-Cas9 in Pharmaceutical Targeting
Author & Curator: Larry H. Bernstein, MD, FCAP, Chief Scientific Officer, Leaders in Pharmaceutical Intelligence (LPBI) Group, Boston, MA
2.1.2.3 Where is the most promising avenue to success in Pharmaceuticals with CRISPR-Cas9?
Author: Larry H. Bernstein, MD, FCAP
2.1.2.4 Use of CRISPR & RNAi for Drug Discovery, CHI’s World PreClinical Congress – Europe, November 14-15, 2016, Lisbon, Portugal
Reporter: Aviva Lev-Ari, PhD, RN
2.1.2.5 2nd Annual Translational Gene Editing: Exploiting CRISPR/Cas9 for Building Tools for Drug Discovery & Development: June 16, 2016, Boston, MA
Reporter: Aviva Lev-Ari, PhD, RN
2.1.2.6 Intestinal Inflammatory Pharmaceutics
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/02/11/intestinal-inflammatory-pharmaceutics/
2.1.2.7 Disease Disablers
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/23/disease-disablers/
2.1.2.8 Gene-Silencing and Gene-Disabling in Pharmaceutical Development
Curator: Larry H. Bernstein, MD, FCAP
2.1.3 CRISPR as a Therapeutics Modality
| Hypergraph Plot #13 and Tree Diagram #13
for 2.1.3 based on 15 articles & on 14 keywords
crispr, cas, protein, cells, genome, editing, dna, rna, disease, genes, cancer, human, target, technology
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List of articles included in 2.1.3
2.1.3.1 UPDATED – Medical Interpretation of the Genomics Frontier – CRISPR – Cas9: Gene Editing Technology for New Therapeutics
Authors and Curators: Larry H Bernstein, MD, FCAP and Stephen J Williams, PhD and Curator: Aviva Lev-Ari, PhD, RN
2.1.3.2 Advances in Gene Editing Technology: New Gene Therapy Options in Personalized Medicine
Curators: Stephen J Williams, PhD and Aviva Lev-Ari, PhD, RN
Recent Advances in Gene Editing Technology Adds New Therapeutic Potential for the Genomic Era
Author and Curator: Stephen J Williams, PhD
2.1.3.3 People with two copies of the Δ32 mutation died at rates 21 percent higher than those with one or no copies – application of CRISPR @Berkeley
Reporter: Aviva Lev-Ari, PhD, RN
2.1.3.4 TWEETS by @pharma_BI and @AVIVA1950 at #IESYMPOSIUM – @kochinstitute 2019 #Immune #Engineering #Symposium, 1/28/2019 – 1/29/2019
Real Time Press Coverage: Aviva Lev-Ari, PhD, RN
2.1.3.5 Jennifer Doudna and NPR science correspondent Joe Palca, several interviews
Reporter: Aviva Lev-Ari, PhD, RN
2.1.3.6 Original Tweets Re-Tweets and Likes by @pharma_BI and @AVIVA1950 at #kisymposium for 17th annual Summer Symposium: Breakthrough Cancer Nanotechnologies: Koch Institute, MIT Kresge Auditorium, June 15, 2018, 9AM-4PM
Real Time Press Coverage: Aviva Lev-Ari, PhD, RN
2.1.3.7 Lysyl Oxidase (LOX) gene missense mutation causes Thoracic Aortic Aneurysm and Dissection (TAAD) in Humans because of inadequate cross-linking of collagen and elastin in the aortic wall – Mutation carriers may be predisposed to vascular diseases because of weakened vessel walls under stress conditions.
Reporter: Aviva Lev-Ari, PhD, RN
2.1.3.8 AACR2016 – Cancer immunotherapy
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/05/19/aacr2016-cancer-immunotherapy/
2.1.3.9 CRISPR/Cas9, Familial Amyloid Polyneuropathy (FAP) and Neurodegenerative Disease
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/04/17/crisprcas9-fap-and-neurodegenerative-disease/
2.1.3.10 Can CRISPR/Cas9 Target Multiple Targets?
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/22/can-crisprcas9-target-multiple-targets/
2.1.3.11 Genomic Pathogen Typing
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/16/genomic-pathogen-typing/
2.1.3.12 Breaking News about Genomic Engineering, T2DM and Cancer Treatments – 9/28/2015
Curator: Larry H Bernstein, MD, FCAP
2.1.3.13 Disease related changes in proteomics, protein folding, protein-protein interaction
Curator: Larry H. Bernstein, MD, FCAP
2.1.3.14 @BroadInstitute a shift from Permanently editing DNA to Temporarily revising RNA – An approach with promise for addressing the risk of developing Alzheimer’s by deactivating APOE4 – RESCUE: RNA Editing for Specific C to U Exchange, the platform builds on REPAIR: RNA Editing for Programmable A to I
Reporter: Aviva Lev-Ari, PhD, RN
2.1.3.15 At Technical University of Munich (TUM) Successful Genetical modification of a patient’s own immune cells, T cell receptors, using CRISPR-Cas9 gene editing tool. The engineered T cells are very similar to the physiological immune cells.
Reporter: Aviva Lev-Ari, PhD, RN
2.1.4 Ethics Issues related to CRISPR Technology
| Hypergraph Plot #14 and Tree Diagram #14
for 2.1.4 based on 6 articles & on 15 keywords
gene, crispr, human, editing, cas, genome, technology, cells, genetic, embryos, genes, dna, cancer, nature, germline
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List of articles included in 2.1.4
2.1.4.1 Level of Comfort with Making Changes to the DNA of an Organism
Curator: Aviva Lev-Ari, PhD, RN
2.1.4.2 Opportunities and Ethics of Editing Genomes: A CRISPR-Inspired Conversation, Prof. Jennifer Doudna’s Lecture at Stanford University, JANUARY 24, 2019 – 7:00PM TO 8:30PM, CEMEX AUDITORIUM, GRADUATE SCHOOL OF BUSINESS
Reporter: Aviva Lev-Ari, PhD, RN
2.1.4.3 Gene-editing Second International Summit in Hong Kong: George Church, “Let’s be quantitative before we start being accusatory”
Reporter: Aviva Lev-Ari, PhD, RN
2.1.4.4 GENE EDITING: Promises and Challenges: HSPH and NBC News Digital, Friday, May 19, 2017 Live webcast: 12:30-1:30pm ET
Reporter: Aviva Lev-Ari, PhD, RN
2.1.4.5 CRISPR and Human Embryo
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/04/18/crispr-and-human-embryo/
2.1.4.6 Unchecked Spread of Engineered Genes
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/18/unchecked-spread-of-engineered-genes/
2.1.5 Other topics related to the advent of CRISPR as a Gene Editing Method
| Hypergraph Plot #15 and Tree Diagram #15
for 2.1.5 based on 28 articles & on 11 keywords
crispr, cells, cas, editing, dna, genome, technology, rna, genes, human, genetic
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List of articles included in 2.1.5
2.1.5.1 A. Richard Newton Distinguished Innovator Lecture Series – Dr. Jennifer Doudna, April 23, 2019, UC, Berkeley
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.2 Top 10 CRISPR Podcasts Every Scientist (& Non-Scientist) by Synthego.com
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.3 National Academy of Sciences for work in chemical sciences: Jennifer Doudna, University of California, Berkeley
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.4 CRISPR Based Research Awarded NHGRI Grants, The University of California, Berkeley’s Doudna will receive $2.1 million and The Broad Institute’s Zhang will receive $1.1 million
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.5 Promising research for a male birth control pill
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
https://pharmaceuticalintelligence.com/2017/03/23/promising-research-for-a-male-birth-control-pill/
2.1.5.6 Top 50 Women in CRISPR : Women in CRISPR, Legal Status of Inventions and Declaration of the Heroes in CRISPR
Curator: Aviva Lev-Ari, PhD, RN
2.1.5.7 We Celebrate 5,000 Scientific Articles @pharmaceuticalintelligence.com – 2016 was a GREAT Year – Record Articles on CRISPR !!!!!
Curator and Open Access Journal Editor-in-Chief: Aviva Lev-Ari, PhD, RN
2.1.5.8 LIVE – Day 1, OCTOBER 18 @The 16th annual EmTech MIT – A Place of Inspiration, October 18-20, 2016, Cambridge, MA
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.9 More Awards to Jennifer Doudna: 2016 Warren Alpert Foundation Prize and The 2015 Pfizer Lecture
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.10 Federation of European Biochemical Societies FEBS Journal Special Issue on CRISPR/Cas9 Gene Editing by news.wiley.com – State of CRISPR/Cas9 Science on 9/2016
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.11 Real Time Coverage and eProceedings of Presentations on 9/19-9/21 @CHI’s 14th Discovery On Target, 9/19 – 9/22/2016, Westin Boston Waterfront, Boston
Curator: Aviva Lev-Ari, PhD, RN
2.1.5.12 Genomics Orientations for Personalized Medicine: Request for Book Review Writing on Amazon.com
http://www.amazon.com/dp/B018DHBUO6
2.1.5.13 The Roles of Graduate Students and Postdocs in the Emergence of Gene Editing: CRISPR Science and Technology
Curator: Aviva Lev-Ari, PhD, RN
2.1.5.14 A Conversation with Jennifer Doudna, Interviewer: Jan Witkowski, Executive Director, Banbury Center at Cold Spring Harbor Laboratory
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.15 Women Leaders in Cell and Gene Therapy
Reporter: Aviva Lev-Ari, PhD, RN
https://pharmaceuticalintelligence.com/2016/07/11/women-leaders-in-cell-and-gene-therapy/
2.1.5.16 John Holdren tells Nature about the Highs and Lows of nearly eight years in the White House, Holdren is the longest-serving presidential Science Adviser in US history.
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.17 Glassman Lecture “From Bacterial Adaptive Immunity to the Future of Genome Engineering” Jennifer A. Doudna, University of California, Berkeley; Howard Hughes Medical Institute
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.18 Genome Engineering: The CRISPR-Cas Revolution, August 17 – 20, 2016, Cold Spring Harbor Laboratory
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.19 The 16th annual EmTech MIT – A Place of Inspiration, October 18-20, 2016, Cambridge, MA
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.20 CRISPR: Genome Editing and Cancer was ranked 7th on the List of Disruptive Dozen Technologies @2016 World Medical Innovation Forum
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.21 Best in Precision Medicine: RNA May Surpass DNA in Precision Medicine
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/03/23/best-in-precision-medicine/
2.1.5.22 Jennifer Doudna, Woman of Science Award
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/03/18/jennifer-doudna-woman-of-science-award/
2.1.5.23 CRISPR: A Podcast from Nature.com on Gene Editing
Reporter: Aviva Lev-Ari, PhD, RN
https://pharmaceuticalintelligence.com/2016/03/17/crispr-a-podcast-from-nature-com-on-gene-editing/
2.1.5.24 Lab Management: About The Doudna Lab, RNA Biology at UC Berkeley, HHMI
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.25 International Summit on Human Gene Editing: A Global Discussion, National Academy of Sciences, WashDC, December 1-3, 2015
Reporter: Aviva Lev-Ari, PhD, RN
2.1.5.26 Cambridge Healthtech Institute’s Second Annual New Frontiers in Gene Editing, SF, 3/10-3/11, 2016
Reporter: Stephen J. Williams, PhD
2.1.5.27 CRISPR/Cas-mediated Genome Engineering
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/09/08/crisprcas-mediated-genome-engineering/
2.1.5.28 Advances in Gene Editing and Gene Silencing | September 20-21, 2016 | Boston, MA
Author and Curator: Stephen J Williams, PhD
2.2 Technologies and Methodologies
| Hypergraph Plot #16 and Tree Diagram #16
for 2.2 based on 27 articles & on 13 keywords
cas, crispr, dna, protein, expression, stem, rna, target, genome, editing, genes, cancer, human
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List of articles included in 2.2
2.2.1 Alter the Code of Life – Technologies for Gene Editing from MammothBiosciences, San Francisco, CA
Reporter: Aviva Lev-Ari, PhD, RN
2.2.2 CRISPR on TED Ideas worth spreading – Ellen Jorgensen
Reporter: Aviva Lev-Ari, PhD, RN
2.2.3 CRISPR snips a strand of DNA – Visualization of the Process
Reporter: Aviva Lev-Ari, PhD, RN
2.2.4 Pancreatic Cancer Modeling using Retrograde Viral Vector Delivery and IN-Vivo CRISPR/Cas9-mediated Somatic Genome Editing
Curators: Larry H. Benstein, MD, FCAP and Aviva Lev-Ari, PhD, RN
2.2.5 Bacterial immune system may be utilized as a tool harboring an impressive recording capacity
Curator: Larry H. Bernstein, MD, FCAP
2.2.6 CHI’s Inaugural Oligonucleotide Therapeutics & Delivery | April 4-5, 2016 | Hyatt Regency | Cambridge, Massachusetts
Reporter: Aviva Lev-Ari, PhD, RN
2.2.7 Innovative Genomics Initiative (IGI) 2016 CRISPR WORKSHOP: PRACTICAL ASPECTS OF PRECISION BIOLOGY, UC, Berkeley, July 11-15, 2016
Reporter: Aviva Lev-Ari, PhD, RN
2.2.8 RNA-Based Drugs Turn CRISPR/Cas9 On and Off
Reporter: Stephen J. Williams
https://pharmaceuticalintelligence.com/2016/02/17/rna-based-drugs-turn-crisprcas9-on-and-off/
2.2.9 Reengineering Therapeutics
Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/02/06/reengineering-therapeutics/
2.2.10 Deciphering the Epigenome
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/01/28/deciphering-the-epigenome/
2.2.11 Gene Editing for Exon 51: Why CRISPR Snipping might be better than Exon Skipping for DMD
Reporter: Aviva Lev-Ari, PhD, RN
2.2.12 Genome Engineering: Genome Editing with CRISPR-Cas9
Reporter: Aviva Lev-Ari, PhD, RN
2.2.13 Enhanced Cas9 for more precise editing
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/12/11/enhanced-cas9-for-more-precise-editing/
2.2.14 Genetically Engineered Algae
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/15/genetically-engineered-algae/
2.2.15 Cas9 Proofreads
Curator: Larry H Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/13/cas9-proofreads/
2.2.16 RNAi, CRISPR and Gene Expression
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/02/rnai-crispr-and-gene-expression/
2.2.17 Obesity Variant Circuitry
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/10/31/obesity-variant-circuitry/
2.2.18 CRISPR-Cas9 and Regenerative Medicine
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/10/31/crispr-cas9-crispr-cas9-and-regenerative-medicine/
2.2.19 Gene Editing by Creation of a Complement without Transcription Error
Curator: Larry H. Bernstein, MD, FCAP
2.2.20 Principles of Gene Editing
Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/10/30/principles-of-gene-editing/
2.2.21 Top 10 Medical Innovations for 2016 by Cleveland Clinic
Reporter: Aviva Lev-Ari, PhD, RN
2.2.22 NIH to Award Up to $12M to Fund DNA, RNA Sequencing Research: single-cell genomics, sample preparation, transcriptomics and epigenomics, and genome-wide functional analysis.
Reporter: Aviva Lev-Ari, PhD, RN
2.2.23 CRISPR/Cas9 genome editing tool for Staphylococcus aureus Cas9 complex (SaCas9) @ MIT’s Broad Institute
Reporter: Aviva Lev-Ari, PhD, RN
2.2.24 RNAi, CRISPR, and Gene Editing: Discussions on How To’s and Best Practices @14th Annual World Preclinical Congress June 10-12, 2015 | Westin Boston Waterfront | Boston, MA
Reporter: Aviva Lev-Ari, PhD, RN
2.2.25 CRISPR/Cas9: Contributions on Endoribonuclease Structure and Function, Role in Immunity and Applications in Genome Engineering
Writer and Curator:Larry H Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/03/27/crisprcas9/
2.2.26 GUIDE-seq: First genome-wide method of detecting off-target DNA breaks induced by CRISPR-Cas nucleases
Reporter: Aviva Lev-Ari, PhD, RN
2.2.27 2nd Annual Translational Gene Editing: Exploiting CRISPR/Cas9 for Building Tools for Drug Discovery & Development: June 16, 2016 @Boston, MA
Reporter: Stephen J. Williams, PhD
2.3 CRISPR – The Clinical Aspects
| Hypergraph Plot #17 and Tree Diagram #17
for 2.3 based on 9 articles & on 15 keywords
crispr, cas, editing, cells, disease, genome, dna, human, genetic, target, therapy, ttr, protein, genes, amyloid
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2.3.1 Sickle Cell and Beta Thalassemia chosen for first human trial of the gene editing technology, CRISPR by sponsoring companies CRISPR Therapeutics and Vertex Pharmaceuticals, trial at a single site in Germany
Reporter: Aviva Lev-Ari, PhD, RN
2.3.2 Updated: First-in-Man: CRISPR, the Genome Editing Technology is Nearing Human Trials: Human T cells will soon be Modified using the CRISPR Technique in a Clinical Trial to attack Cancer Cells
Curator: Aviva Lev-Ari, PhD, RN
2.3.3 The Promise of Gene Editing for Slowing Progression of Disease: Translational Application toward Cure of Disease
Reporters: Gerard Loiseau, ESQ and Aviva Lev-Ari, PhD, RN
2.3.4 Translational Gene Editing – June 16-17, 2016 in Boston, MA by CHI, Westin Boston Waterfront, Boston, MA
Reporter: Aviva Lev-Ari, PhD, RN
2.3.5 FDA Cellular & Gene Therapy Guidances: Implications for CRSPR/Cas9 Trials
Reporter: Stephen J. Williams, PhD
2.3.6 CRISPR Gene Editing Trial
Curator: Larry H Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/10/crispr-gene-editing-trial/
2.3.7 UNESCO Calls for More Regulations on Genome Editing, DTC Genetic Testing
Reporter: Aviva Lev-Ari, PhD, RN
2.3.8 CRISPR/Cas9, Familial Amyloid Polyneuropathy (FAP) and Neurodegenerative Disease
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/04/17/crisprcas9-fap-and-neurodegenerative-disease/
2.3.9 CRISPR cuts turn gels into biological watchdogs
Reporter: Irina Robu, PhD
https://pharmaceuticalintelligence.com/2019/08/30/crispr-cuts-turn-gels-into-biological-watchdogs/
2.4 CRISPR – Business and Legal
| Hypergraph Plot #18 and Tree Diagram #18
for 2.4 based on 20 articles & on 10 keywords
crispr, cas, editing, patents, gene, therapeutics, cells, interference, genomics, biotech
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2.4.1 CRISPR – The Business and Legal Aspects of IP Development
Patent on Methods and compositions for RNA-directed target DNA modification and for RNA-directed modulation of transcription was awarded to UC, Berkeley on October 30, 2018
- site-specific modification of a target DNA and/or a polypeptide associated with the target DNA, a DNA-targeting RNA
- genetically modified cells that produce Cas9 and Cas9 transgenic non-human multicellular organisms.
Reporter: Aviva Lev-Ari, PhD, RN
2.4.2 Will the Supreme Court accept a UC Berkeley Appeal of the Sep. 10th, US Court of Appeals for the Federal Circuit decision to uphold the patent filed by the Broad Institute on CRISPR/Cas9 gene editing?
Reporter: Aviva Lev-Ari, PhD, RN
2.4.3 On June 12, 2018 – Berkeley was granted a patent on using CRISPR/Cas9 to edit single-stranded RNA. On June 19, 2018 – Berkeley was granted a second patent, covering the use of CRISPR-Cas9 gene editing with formats that will be particularly useful in developing human therapeutics and improvements in food security.
Reporter and Curator: Aviva Lev-Ari, PhD, RN
2.4.4 Developments in CRISPR Patent Dispute: EPO Revokes Broad’s CRISPR Patent
Curator: Aviva Lev-Ari, PhD, RN
2.4.5 Appellate Brief Seeking Reversal of U.S. Patent Board Decision on CRISPR/Cas9 Gene Editing
Reporter: Aviva Lev-Ari, PhD, RN
2.4.6 Doudna and Charpentier and their teams to receive wide-ranging patents in many countries: European Patent Office (EPO) and UK Intellectual Property Office – broad patent for CRISPR-Cas9 gene-editing technology to the University of California and the University of Vienna
Reporter: Aviva Lev-Ari, PhD, RN
2.4.7 UPDATED – Gene Editing Consortium of Biotech Companies: CRISPR Therapeutics $CRSP, Intellia Therapeutics $NTLA, Caribou Biosciences, ERS Genomics, UC, Berkeley (Doudna’s IP) and University of Vienna (Charpentier’s IP), is appealing the decision ruled that there was no interference between the two sides, to the U.S. Court of Appeals for the Federal Circuit, targeting patents from The Broad Institute.
Curator: Aviva Lev-Ari, PhD, RN
2.4.8 CRISPR Patent Battle Determined on 2/15/2017 – USPTO issues a verdict in legal tussle over rights to genome-editing technology
Curator: Aviva Lev-Ari, PhD, RN
2.4.9 Dr. Doudna: RNA synthesis capabilities of Synthego’s team represent a significant leap forward for Synthetic Biology
Reporter: Aviva Lev-Ari, PhD, RN
2.4.10 Dr. Jennifer Doudna (UC Berkeley): PMWC 2017 Luminary Award, January 22, 2017 @PMWC 2017, January 23-25, Silicon Valley
Reporter: Aviva Lev-Ari, PhD, RN
2.4.11 CRISPR Therapeutics raises a $56M IPO, but patent battles, potential stock drops loom
Reporter: Aviva Lev-Ari, PhD, RN
2.4.12 Licensing Agreements for CRISPR/Cas9 Genome Editing Technology Patent
Curator: Aviva Lev-Ari, PhD, RN
2.4.13 Licensing deal with Regeneron to accelerate CRISPR biotech Intellia (Jennifer Doudna’s Start Up) for an IPO
Reporter: Aviva Lev-Ari, PhD, RN
2.4.14 Nine Parties had come forward: Opposition Procedure to the Broad Institute’s first European CRISPR–Cas9 Patent
Curator: Aviva Lev-Ari, PhD, RN
2.4.15 Use of CRISPR/CAS9 to Edit Genome of Pigs: Recominetics announces $10M Funding Round
Reporter: Stephen J. Williams
2.4.16 UPDATED – Status “Interference — Initial memorandum” – CRISPR/Cas9 – The Biotech Patent Fight of the Century: UC, Berkeley and Broad Institute @MIT
Reporter: Aviva Lev-Ari, PhD, RN
2.4.17 Editas, CEO predicts 2017 to be the Year of Human Gene Editing
Reporter: Aviva Lev-Ari, PhD, RN
2.4.18 Anatomy of a $105M Deal for Joint R&D in Genomics: CRISPR Therapeutics & Vertex Pharmaceuticals
Reporter: Aviva Lev-Ari, PhD, RN
2.4.19 CRISPR companies calling for article retraction from Nature Methods – If the same or similar sequence of letters appears elsewhere in the genome, that can result in an unintentional or off-target edit – Concerns of Harm caused by Gene Editing using CRISPR-Cas9
Reporter: Aviva Lev-Ari, PhD, RN
2.4.20 Merck KGaA-owned Sigma-Aldrich has petitioned the US Patent and Trademark Office (USPTO) to open an interference proceeding between its own pending CRISPR-Cas9 patents and patents awarded to the University of California, Berkeley (UC Berkeley).
Reporter: Aviva Lev-Ari, PhD, RN
Text Analysis with NLP of the Original
Genomics Volume 2, Part 3:
Artificial Intelligence in Medicine
3.1 The Science
| Hypergraph Plot #19 and Tree Diagram #19
for 3.1 based on 8 articles & on 9 keywords
ai, data, health, medicine, clinical, healthcare, patient, radiology, innovation
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3.1.1 World Medical Innovation Forum, Partners Innovations, ARTIFICIAL INTELLIGENCE | APRIL 8–10, 2019 | Westin, BOSTON
Reporter: Aviva Lev-Ari, PhD, RN
https://worldmedicalinnovation.org/agenda/
3.1.2 LIVE Day Three – World Medical Innovation Forum ARTIFICIAL INTELLIGENCE, Boston, MA USA, Monday, April 10, 2019
Real Time Coverage: Curator: Aviva Lev-Ari, PhD, RN
3.1.3 LIVE Day Two – World Medical Innovation Forum ARTIFICIAL INTELLIGENCE, Boston, MA USA, Monday, April 9, 2019
Real Time Coverage: Curator: Aviva Lev-Ari, PhD, RN
3.1.4 LIVE Day One – World Medical Innovation Forum ARTIFICIAL INTELLIGENCE, Boston, MA USA, Monday, April 8, 2019
Real Time Coverage: Curator: Aviva Lev-Ari, PhD, RN
3.1.5 2018 Annual World Medical Innovation Forum Artificial Intelligence April 23–25, 2018 Boston, Massachusetts | Westin Copley Place https://worldmedicalinnovation.org/
Real Time Coverage: Curator: Aviva Lev-Ari, PhD, RN
3.1.6 Synopsis Days 1,2,3: 2018 Annual World Medical Innovation Forum Artificial Intelligence April 23–25, 2018 Boston, Massachusetts | Westin Copley Place
Real Time Coverage: Curator: Aviva Lev-Ari, PhD, RN
3.1.7 Interview with Systems Immunology Expert Prof. Shai Shen-Orr
Reporter: Aviva Lev-Ari, PhD, RN
Interview with Systems Immunology Expert Prof. Shai Shen-Orr
3.1.8 Unique immune-focused AI model creates largest library of inter-cellular communications at CytoReason. Used to predict 335 novel cell-cytokine interactions, new clues for drug development.
Reporter: Aviva Lev-Ari, PhD, RN
- CytoReason features in hashtag #DeepKnowledgeVentures‘s detailed Report on AIin hashtag #drugdevelopment report
- https://lnkd.in/dKV2BB6
https://www.eurekalert.org/pub_releases/2018-06/c-uia061818.php
3.2 Technologies and Methodologies
| Hypergraph Plot #20 and Tree Diagram #20
for 3.2 based on 9 articles & on 11 keywords
cells, cancer, gene, schizophrenia, protein, brain, frontal, imaging, patients, disease, dna
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List of articles included in 3.2
3.2.1 R&D for Artificial Intelligence Tools & Applications: Google’s Research Efforts in 2018
Reporter: Aviva Lev-Ari, PhD, RN
3.2.2 Can Blockchain Technology and Artificial Intelligence Cure What Ails Biomedical Research and Healthcare
Curator: Stephen J. Williams, Ph.D.
3.2.3 N3xt generation carbon nanotubes
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/12/14/n3xt-generation-carbon-nanotubes/
3.2.4 Mindful Discoveries
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/01/28/mindful-discoveries/
3.2.5 Novel Discoveries in Molecular Biology and Biomedical Science
Curator: Larry H. Bernstein, MD, FCAP
3.2.6 Imaging of Cancer Cells
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/04/20/imaging-of-cancer-cells/
3.2.7 Retrospect on HistoScanning: an AI routinely used in diagnostic imaging for over a decade
Author and Curator: Dror Nir, PhD
3.2.8 Prediction of Cardiovascular Risk by Machine Learning (ML) Algorithm: Best performing algorithm by predictive capacity had area under the ROC curve (AUC) scores: 1st, quadratic discriminant analysis; 2nd, NaiveBayes and 3rd, neural networks, far exceeding the conventional risk-scaling methods in Clinical Use
Reporter: Aviva Lev-Ari, PhD, RN
3.2.9 An Intelligent DNA Nanorobot to Fight Cancer by Targeting HER2 Expression
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
3.3 Clinical Aspects
| Hypergraph Plot #21 and Tree Diagram #21
for 3.3 based on 23 articles & on 12 keywords
data, cancer, patients, ai, clinical, exon, gene, splicing, health, cells, rna, imaging
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List of articles included in 3.3
3.3.1 9 AI-based initiatives catalyzing immunotherapy in 2018
By Tanima Bose
https://www.prescouter.com/2018/07/9-ai-based-initiatives-catalyzing-immunotherapy-in-2018/
3.3.2 mRNA Data Survival Analysis
Curators: Larry H. Bernstein, MD, FCAP and Aviva Lev-Ari, PhD, RN
https://pharmaceuticalintelligence.com/2016/06/18/mrna-data-survival-analysis/
3.3.3 Medcity Converge 2018 Philadelphia: Live Coverage @pharma_BI
Reporter: Stephen J. Williams
3.3.4 Live Coverage: MedCity Converge 2018 Philadelphia: AI in Cancer and Keynote Address
Reporter: Stephen J. Williams, PhD
3.3.5 VIDEOS: Artificial Intelligence Applications for Cardiology
Reporter: Aviva Lev-Ari, PhD, RN
3.3.6 Artificial Intelligence in Health Care and in Medicine: Diagnosis & Therapeutics
Reporter: Aviva Lev-Ari, PhD, RN
3.3.7 Digital Therapeutics: A Threat or Opportunity to Pharmaceuticals
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
3.3.8 The 3rd STATONC Annual Symposium, April 25-27, 2019, Hilton Hartford, CT, 315 Trumbull St., Hartford, CT 06103
Reporter: Stephen J. Williams, Ph.D.
3.3.9 2019 Biotechnology Sector and Artificial Intelligence in Healthcare
Reporter: Aviva Lev-Ari, PhD, RN
3.3.10 Artificial intelligence can be a useful tool to predict Alzheimer
Reporter: Irina Robu, PhD
3.3.11 Unlocking the Microbiome
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/02/07/unlocking-the-microbiome/
3.3.12 Biomarker Development
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/11/16/biomarker-development/
3.3.13 AI System Used to Detect Lung Cancer
Reporter: Irina Robu, PhD
https://pharmaceuticalintelligence.com/2019/06/28/ai-system-used-to-detect-lung-cancer/
3.3.14 AI App for People with Digestive Disorders
Reporter: Irina Robu, PhD
https://pharmaceuticalintelligence.com/2019/06/24/ai-app-for-people-with-digestive-disorders/
3.3.15 Sepsis Detection using an Algorithm More Efficient than Standard Methods
Reporter: Irina Robu, PhD
3.3.16 How Might Sleep Apnea Lead to Serious Health Concerns like Cardiac and Cancer?
Author: Larry H Bernstein, MD, FCAP
3.3.17 An Intelligent DNA Nanorobot to Fight Cancer by Targeting HER2 Expression
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
3.3.18 Artificial Intelligence and Cardiovascular Disease
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
3.3.19 Using A.I. to Detect Lung Cancer gets an A!
Reporter: Irina Robu, PhD
https://pharmaceuticalintelligence.com/2019/08/04/using-a-i-to-detect-lung-cancer-gets-an-a/
3.3.20 Complex rearrangements and oncogene amplification revealed by long-read DNA and RNA sequencing of a breast cancer cell line
Reporter: Stephen J. Williams, PhD
3.3.21 Multiple Barriers Identified Which May Hamper Use of Artificial Intelligence in the Clinical Setting
Reporter: Stephen J. Williams, PhD.
3.3.22 Deep Learning–Assisted Diagnosis of Cerebral Aneurysms
Author and Curator: Dror Nir, PhD
3.3.23 Artificial Intelligence Innovations in Cardiac Imaging
Reporter: Aviva Lev-Ari, PhD, RN
3.4 Business and Legal
| Hypergraph Plot #22 and Tree Diagram #22
for 3.4 based on 16 articles & on 8 keywords
ai ,data, healthcare, patients, medical, digital, clinical, access
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3.4.1 McKinsey Top Ten Articles on Artificial Intelligence: 2018’s most popular articles – An executive’s guide to AI
Reporter: Aviva Lev-Ari, PhD, RN
3.4.2 HOTTEST Artificial Intelligence Hub: Israel’s High Tech Industry – Why?
Reporter: Aviva Lev-Ari, PhD, RN
3.4.3 The Regulatory challenge in adopting AI
Author and Curator: Dror Nir, PhD
https://pharmaceuticalintelligence.com/2019/04/07/the-regulatory-challenge-in-adopting-ai/
3.4.4 HealthCare focused AI Startups from the 100 Companies Leading the Way in A.I. Globally
Reporter: Aviva Lev-Ari, PhD, RN
3.4.5 IBM’s Watson Health division – How will the Future look like?
Reporter: Aviva Lev-Ari, PhD, RN
3.4.6 HUBweek 2018, October 8-14, 2018, Greater Boston – “We The Future” – coming together, of breaking down barriers, of convening across disciplinary lines to shape our future
Reporter: Aviva Lev-Ari, PhD, RN
3.4.7 Role of Informatics in Precision Medicine: Notes from Boston Healthcare Webinar: Can It Drive the Next Cost Efficiencies in Oncology Care?
Reporter: Stephen J. Williams, Ph.D.
3.4.8 Healthcare conglomeration to access Big Data and lower costs
Curator: Larry H. Bernstein, MD, FCAP
3.4.9 Linguamatics announces the official launch of its AI self-service text-mining solution for researchers.
Reporter: Aviva Lev-Ari, PhD, RN
3.4.10 Future of Big Data for Societal Transformation
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2015/12/14/future-of-big-data-for-societal-transformation/
3.4.11 Deloitte Analysis 2019 Global Life Sciences Outlook
https://www.cioapplications.com/news/making-a-breakthrough-in-drug-discovery-with-ai-nid-3114.html
3.4.12 OpenAI: $1 Billion to Create Artificial Intelligence Without Profit Motive by Who is Who in the Silicon Valley
Reporter: Aviva Lev-Ari, PhD, RN
3.4.13 The Health Care Benefits of Combining Wearables and AI
Reporter: Gail S. Thornton, M.A.
3.4.14 These twelve artificial intelligence innovations are expected to start impacting clinical care by the end of the decade.
Reporter: Gail S. Thornton, M.A.
3.4.15 Forbes Opinion: 13 Industries Soon To Be Revolutionized By Artificial Intelligence
Reporter: Aviva Lev-Ari, PhD, RN
3.4.16 AI Acquisitions by Big Tech Firms Are Happening at a Blistering Pace: 2019 Recent Data by CBI Insights
Reporter: Stephen J. Williams, Ph.D.
3.5 Machine Learning (ML) Algorithms harnessed for Medical Diagnosis: Pattern Recognition & Prediction of Disease Onset
| Hypergraph Plot #23 and Tree Diagram #23
for 3.5 based on 9 articles & on 12 keywords
cancer, risk, brain, breast, mri, data, molecular, density, women, image, aging, tissue
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List of articles included in 3.5
3.5.1 Cases in Pathology
3.5.1.1 Deep Learning extracts Histopathological Patterns and accurately discriminates 28 Cancer and 14 Normal Tissue Types: Pan-cancer Computational Histopathology Analysis
Reporter: Aviva Lev-Ari, PhD, RN
3.5.2 Cases in Radiology
3.5.2.1 Cardiac MRI Imaging Breakthrough: The First AI-assisted Cardiac MRI Scan Solution, HeartVista Receives FDA 510(k) Clearance for One Click™ Cardiac MRI Package
Reporter: Aviva Lev-Ari, PhD, RN
3.5.2.2 Disentangling molecular alterations from water-content changes in the aging human brain using quantitative MRI
Reporter: Dror Nir, PhD
3.5.2.3 Showcase: How Deep Learning could help radiologists spend their time more efficiently
Reporter and Curator: Dror Nir, PhD
3.5.2.4 CancerBase.org – The Global HUB for Diagnoses, Genomes, Pathology Images: A Real-time Diagnosis and Therapy Mapping Service for Cancer Patients – Anonymized Medical Records accessible to anyone on Earth
Reporter: Aviva Lev-Ari, PhD, RN
3.5.2.5 Applying AI to Improve Interpretation of Medical Imaging
Author and Curator: Dror Nir, PhD
3.5.2.6 Imaging: seeing or imagining? (Part 2)
Author and Curator: Dror Nir, PhD
https://pharmaceuticalintelligence.com/2019/04/07/imaging-seeing-or-imagining-part-2-2/
3.5.3 Cases in Prediction Cancer Onset
3.5.3.1 A Deep Learning Mammography-based Model for Improved Breast Cancer Risk Prediction
Adam Yala
Constance Lehman
Tal Schuster
Tally Portnoi
Published Online: May 7 2019 RadiologyVol. 292, No. 1 https://doi.org/10.1148/radiol.2019182716
3.5.3.2 Comparison of a Deep Learning Risk Score and Standard Mammographic Density Score for Breast Cancer Risk Prediction
Karin Dembrower , Yue Liu, Hossein Azizpour, Martin Eklund, Kevin Smith, Peter Lindholm, Fredrik Strand
Published Online: Dec 17 2019 https://doi.org/10.1148/radiol.2019190872
Text Analysis with NLP of the Original
Genomics Volume 2, Part 4:
Single Cell Genomics
4.1 The Science
| Hypergraph Plot #24 and Tree Diagram #24
for 4.1 based on 9 articles & on 12 keywords
cells, human, atlas, genomics, cellular, cancer, sequencing, disease, map, immune, biology, body
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List of articles included in 4.1
4.1.1 Single-cell biology
Special | 05 July 2017
https://www.nature.com/collections/gbljnzchgg
4.1.2 The race to map the human body — one cell at a time, A host of detailed cell atlases could revolutionize understanding of cancer and other diseases
- by Heidi Ledford 20 February 2017
https://www.nature.com/news/the-race-to-map-the-human-body-one-cell-at-a-time-1.21508
4.1.3 Single-cell Genomics: Directions in Computational and Systems Biology – Contributions of Prof. Aviv Regev @Broad Institute of MIT and Harvard, Cochair, the Human Cell Atlas Organizing Committee with Sarah Teichmann of the Wellcome Trust Sanger Institute
Curator: Aviva Lev-Ari, PhD, RN
4.1.4 Cellular Genetics
https://www.sanger.ac.uk/science/programmes/cellular-genetics
4.1.5 Cellular Genomics
https://www.garvan.org.au/research/cellular-genomics
4.1.6 SINGLE CELL GENOMICS 2019 – sometimes the sum of the parts is greater than the whole, September 24-26, 2019, Djurönäset, Stockholm, Sweden http://www.weizmann.ac.il/conferences/SCG2019/single-cell-genomics-2019
Reporter: Aviva Lev-Ari, PhD, RN
4.1.7 Norwich Single-Cell Symposium 2019, Earlham Institute, single-cell genomics technologies and their application in microbial, plant, animal and human health and disease, October 16-17, 2019, 10AM-5PM
Reporter: Aviva Lev-Ari, PhD, RN
4.1.8 Newly Found Functions of B Cell
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
https://pharmaceuticalintelligence.com/2019/05/23/newly-found-functions-of-b-cell/
4.1.9 RESEARCH HIGHLIGHTS: HUMAN CELL ATLAS
https://www.broadinstitute.org/research-highlights-human-cell-atlas
4.2 Technologies and Methodologies
| Hypergraph Plot #25 and Tree Diagram #25
for 4.2 based on 6 articles & on 12 keywords
cells, ai, sequencing, molecular, expression, fluorescence, protein, rna, streptavidin, population, surface, magnetic
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List of articles included in 4.2
4.2.1 How to build a human cell atlas – Aviv Regev is a maven of hard-core biological analyses. Now she is part of an effort to map every cell in the human body.
Anna Nowogrodzki, 05 July 2017, Article tools
https://www.nature.com/news/how-to-build-a-human-cell-atlas-1.22239
4.2.2 Featuring Computational and Systems Biology Program at Memorial Sloan Kettering Cancer Center, Sloan Kettering Institute (SKI), The Dana Pe’er Lab
Reporter: Aviva Lev-Ari, PhD, RN
4.2.3 Genomic Diagnostics: Three Techniques to Perform Single Cell Gene Expression and Genome Sequencing Single Molecule DNA Sequencing
Curator: Aviva Lev-Ari, PhD, RN
4.2.4 Three Technology Leaders in Single Cell Sequencing: 10X Genomics, Illumina and MissionBio
Reporter: Aviva Lev-Ari, PhD, RN
4.2.5 scPopCorn: A New Computational Method for Subpopulation Detection and their Comparative Analysis Across Single-Cell Experiments
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
4.2.6 Nano-guided cell networks: new methods to detect intracellular signaling and implications
Curator: Stephen J. Williams, PhD
4.3 Clinical Aspects
| Hypergraph Plot #26 and Tree Diagram #26
for 4.3 based on 7 articles & on 10 keywords
cells, mutation, sequencing, data, cancer, heterogeneity, tumor, mutations, gene, immune
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List of articles included in 4.3
4.3.1 Using single cell sequencing data to model the evolutionary history of a tumor.
Kim KI, Simon R.
BMC Bioinformatics. 2014 Jan 24;15:27. doi: 10.1186/1471-2105-15-27.
4.3.2 eProceedings 2019 Koch Institute Symposium – 18th Annual Cancer Research Symposium – Machine Learning and Cancer, June 14, 2019, 8:00 AM-5:00 PM ET MIT Kresge Auditorium, 48 Massachusetts Ave, Cambridge, MA
Real Time Press Coverage: Aviva Lev-Ari, PhD, RN
4.3.3 The Impact of Heterogeneity on Single-Cell Sequencing
Samantha L. Goldman 1,2, Matthew MacKay 1,2, Ebrahim Afshinnekoo 1,2,3, Ari M. Melnick4, Shuxiu Wu5,6 and Christopher E. Mason 1,2,3,7*
https://www.frontiersin.org/articles/10.3389/fgene.2019.00008/full
4.3.4 Single-cell approaches to immune profiling
https://www.nature.com/articles/d41586-018-05214-w
4.3.5 Single-cell sequencing made simple. Data from thousands of single cells can be tricky to analyse, but software advances are making it easier.
https://www.nature.com/news/single-cell-sequencing-made-simple-1.22233
4.3.6 Single-cell RNA-seq helps in finding intra-tumoral heterogeneity in pancreatic cancer
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
4.3.7 Cancer Genomics: Multiomic Analysis of Single Cells and Tumor Heterogeneity
Curator: Stephen J. Williams, PhD
4.4 Business and Legal
| Hypergraph Plot #27 and Tree Diagram #27
for 4.4 based on 2 articles & on 10 keywords
cells, platform, sequencing, isolation, endotoxin, aging, lifespan, dna, clonal, cellplate
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| HYPERGRAPH INTERPRETATION
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| TREE PLOT DIAGRAM INTERPRETATION
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List of articles included in 4.4
4.4.1 iBioChips integrate diagnostic assays and cellular engineering into miniaturized chips that achieve cutting-edge sensitivity and high-throughput. We have resolved traditional biotech challenges with innovative biochip approaches
4.4.2 Targeted Single-Cell Solutions for High Impact Applications – Mission Bio’s Tapestri® Platform is the only technology that provides single-cell targeted DNA sequencing at single-base resolution.
Text Analysis with NLP of the Original
Genomics Volume 2, Part 5:
Evolution Biology Genomics Modeling
@Feldman Lab, Stanford University
One article is included in Part 5
5.1 Human Genomic Variation, Population Diversity, and Genome-Wide Associations
Author: Marcus W. Feldman, PhD
5.1 Human Genomic Variation, Population Diversity, Genome-Wide Applications
| Hypergraph Plot #28 and Tree Diagram #28
for 5.1 based on 2 articles & on 15 keywords
populations, genetic, evolution, variation, gwas, snps, association, heritability, ancestry, african, variants, traits, humans, genomic, genes
|
PART 5.1: HYPER-GRAPH and TREE PLOT DIAGRAM INTERPRETATION by Prof. Marcus Feldman
The hypergraph is in general not very informative concerning the content of the article. The following assessments also apply to the tree plot.
- The “humans” branch leading to homo and groups is partly satisfactory because the article did discuss Homo sapiens and genetic similarity and differences between human groups. It also mentioned migration among human populations.
- The “evolution” branch is less useful because it is obvious that evolution is a biological process. It can also be a cultural process. The process is descent with modification and includes mutation, natural selection, and migration. Just saying it is a process is rather useless.
- “Association”. The secondary links here are quite meaningless; memory and remembering should not be separated, and neither has to do with human genomic variation and/or evolution. Social activity might result in cultural evolution, but it is not a valid secondary link.
- “Ancestry” is the only node that makes sense in the context of the article. It is a result of inheritance, it does comprise a hereditary pattern, and it can be quantified by a family tree.
- “Variation”. This is the most useless of all the categories. There is no reason for “dance” to be a secondary link. Although variation among individuals and populations does imply that something has changed, making change a secondary to variation is not helpful. Activity is not at all informative as a secondary link.
The remarks above concerning the hypergraph apply equally well to the tree plot, which is, of course, equivalent to the hypergraph.
The Original Genomics Volume 2, Part 6:
Simulation Modeling in Genomics
Not included in Text Analysis with NLP,
Genomics, Volume 3
Text Analysis with NLP of the Original
Genomics Volume 2, Part 7:
Applications of Genomics:
Genotypes, Phenotypes and Complex Diseases
7.1 Genome-wide associations with complex diseases (GWAS)
| Hypergraph Plot #29 and Tree Diagram #29
for 7.1 based on 3 articles & on 13 keywords
disease, variants, genetic, risk, sequencing, genome, gene, loci, diabetes, depression, heart, genetics, variant
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| HYPERGRAPH INTERPRETATION
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| TREE PLOT DIAGRAM INTERPRETATION
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List of articles included in 7.1
7.1.1 Crowdsourcing Genetic Data Yields Discovery of DNA loci associated with Major Depressive Disorder (MDD) in European Descendants
Reporter: Kelly Perlman
7.1.2 Finding the Genetic Links in Common Disease: Caveats of Whole Genome Sequencing Studies
Writer and Reporter: Stephen J. Williams, Ph.D.
7.1.3 23andMe Genome-Wide Association Study on Human propensity to Get up early or Sleep in the Morning
Reporter: Aviva Lev-Ari, PhD, RN
7.2 Non-coding DNA and phenotypes—including diseases like cancer
| Hypergraph Plot #30 and Tree Diagram #30
for 7.2 based on 2 articles & on 12 keywords
cells, cancer, protein, dna, genes, tumor, immune, rna, humans, biology, genome, drug
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| HYPERGRAPH INTERPRETATION
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| TREE PLOT DIAGRAM INTERPRETATION
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List of articles included in 7.2
7.2.1 Novel Discoveries in Molecular Biology and Biomedical Science
Curator: Larry H. Bernstein, MD, FCAP
7.2.2 Genomic expression carried over from Neanderthal DNA
Larry H. Bernstein, MD, FCAP, Curator
7.2.3 Junk DNA and Breast Cancer
Larry H. Bernstein, MD, FCAP, Curator
https://pharmaceuticalintelligence.com/2016/02/02/junk-dna-and-breast-cancer/
7.3 Transcriptomic and ‘omic associations with phenotypes including cancer and rare variant diseases
| Hypergraph Plot #31 and Tree Diagram #31
for 7.3 based on 4 articles & on 11 keywords
cells, variants, cancer, genome, disease, sequencing, gene, dna, biomarkers, subpopulations, rna
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| HYPERGRAPH INTERPRETATION
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| TREE PLOT DIAGRAM INTERPRETATION
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List of articles included in 7.3
7.3.1 scPopCorn: A New Computational Method for Subpopulation Detection and their Comparative Analysis Across Single-Cell Experiments
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
7.3.2 Complex rearrangements and oncogene amplification revealed by long-read DNA and RNA sequencing of a breast cancer cell line
Reporter: Stephen J. Williams, PhD
7.3.3 Live Conference Coverage @Medcitynews Converge 2018 Philadelphia: Early Diagnosis Through Predictive Biomarkers, NonInvasive Testing
Curator: Stephen J. Williams, PhD
7.3.4 Millions of inherited DNA differences – which ones matter: NIH Grants in Genomics to research Disease Risk
Reporter: Aviva Lev-Ari, PhD, RN
7.4 Applications of Bioinformatic Analysis of ‘Omic Data
| Hypergraph Plot #32 and Tree Diagram #32
for 7.4 based on 3 articles & on 12 keywords
thickspace, variants, multifractal, fractal, genomic, genomes, dna, bioinformatics, variant, sequences, regions, genes
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| HYPERGRAPH INTERPRETATION
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| TREE PLOT DIAGRAM INTERPRETATION
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List of articles included in 7.4
7.4.1 A Nonlinear Methodology to Explain Complexity of the Genome and Bioinformatic Information
Reporter: Stephen J. Williams, Ph.D.
7.4.2 Bioinformatics Tool Review: Genome Variant Analysis Tools
Curator: Stephen J. Williams, Ph.D.
7.4.3 Bioinformatic Tools for RNA-Seq Analysis
Curator: Stephen J. Williams, Ph.D
https://pharmaceuticalintelligence.com/2019/12/18/bioinformatic-tools-for-rnaseq-a-curation/
7.5 Population-level genomics and the meaning of group differences
| Hypergraph Plot #33 and Tree Diagram #33
for 7.5 based on 5 articles & on 12 keywords
populations, mutation, variation, loci, diversity, chromosome, genome, inclusion, locus, genetic, differences, snps
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| HYPERGRAPH INTERPRETATION
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|
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| TREE PLOT DIAGRAM INTERPRETATION
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List of articles included in 7.5
7.5.1 Genomics and Evolution
Author: Marcus W. Feldman, PhD
https://pharmaceuticalintelligence.com/2013/02/14/genomics-and-evolution/
7.5.2 Tandem Repeats, with Application to Human Population-Divergence Time
Larry H. Bernstein, MD, FCAP, Curator
7.5.3 Gender affects the prevalence of the cancer type
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
https://pharmaceuticalintelligence.com/2019/04/02/gender-affects-the-prevalence-of-the-cancer-type/
7.5.4 Access to Precision Medicine: Genomics is failing on Diversity
Reporter: Aviva Lev- Ari, PhD, RN
7.5.5 Diversity and Health Disparity Issues Need to be Addressed for GWAS and Precision Medicine Studies
Curator: Stephen J. Williams, PhD
7.6 Targeting drugs for complex diseases
| Hypergraph Plot #34 and Tree Diagram #34
for 7.6 based on 2 articles & on 15 keywords
mrtx, kras, cells, krasgc, inhibition, tumor, signaling, combination, erk, treatment, dose, mutant, protein, antitumor, pathway
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| HYPERGRAPH INTERPRETATION
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| TREE DIAGRAM INTERPRETATION
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List of articles included in 7.6
7.6.1 Anti-tumor necrosis factor drugs (TNF inhibitors) is the treatment for otulipenia, a new inflammatory disease discovered by NIH researchers using NGS
Reporter: Aviva Lev-Ari, PhD, RN
7.6.2 New Mutant KRAS Inhibitors Are Showing Promise in Cancer Clinical Trials: Hope For the Once ‘Undruggable’ Target
Curator: Stephen J. Williams, Ph.D.
Text Analysis with NLP of Original
Genomics Volume 2, Part 8:
Epigenomics and Genomic Regulation
Introduction to Part 8: Epigenomics and Genomic Regulation – Voice of Professor Williams
See Below
https://pharmaceuticalintelligence.com/biomed-e-books/series-a-e-books-on-cardiovascular-diseases/volume-three-etiologies-of-cardiovascular-diseases-epigenetics-genetics-genomics/
8.1 Genomic Controls on Epigenomics
8.1.1 Series A: e-Books on Cardiovascular Diseases, Series A Content Consultant: Justin D Pearlman, MD, PhD, FACC
VOLUME THREE, Etiologies of Cardiovascular Diseases: Epigenetics, Genetics and Genomics, Larry H Bernstein, MD, FCAP, Senior Editor, Author and Curator and Aviva Lev-Ari, PhD, RN, Editor and Curator
http://www.amazon.com/dp/B018PNHJ84
8.2 The ENCODE project and gene regulation
| Hypergraph Plot #35 and Tree Diagram #35
for 8.2 based on 6 articles & on 18 keywords
signature, genome, encode, cancer, dna, types, cells, protein, genes, mutations, regions, regulatory, transcription, binding, elements, etiology, sites, functional
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| HYPERGRAPH INTERPRETATION |
| TREE PLOT DIAGRAM INTERPRETATION
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List of articles included in 8.2
8.2.1 Bioinformatic Tools for Cancer Mutational Analysis: COSMIC and Beyond
Curator: Stephen J. Williams, Ph.D.
8.2.2 ENCODE (Encyclopedia of DNA Elements) Program: ‘Tragic’ Sequestration Impact on NHGRI Programs
Reporter: Aviva Lev-Ari, PhD, RN
8.2.3 Reveals from ENCODE project will invite high synergistic collaborations to discover specific targets
Author and Reporter: Anamika Sarkar, Ph.D
8.2.4 ENCODE: the key to unlocking the secrets of complex genetic diseases
Author: Ritu Saxena, Ph.D.
8.2.5 Impact of evolutionary selection on functional regions: The imprint of evolutionary selection on ENCODE regulatory elements is manifested between species and within human populations
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
8.2.6 ENCODE Findings as Consortium
Reporter: Aviva Lev-Ari, PhD, RN
https://pharmaceuticalintelligence.com/2012/09/10/encode-findings-as-consortium/
8.3 Small interfering RNAs and gene expression
| Hypergraph Plot #36 and Tree Diagram #36
for 8.3 based on 5 articles & on 12 keywords
cancer, mrna, cells, rna, vaccines, protein, micrornas, immune, dna, therapeutic, tfna, polyneuropathy
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| HYPERGRAPH INTERPRETATION
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| TREE PLOT DIAGRAM INTERPRETATION
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List of articles included in 8.3
8.3.1 Moderna Therapeutics Deal with Merck: Are Personalized Vaccines here?
Curator & Reporter: Stephen J. Williams, Ph.D.
8.3.2 IsomicroRNA
Larry H. Bernstein, MD, FCAP, Curator
https://pharmaceuticalintelligence.com/2016/02/18/isomicrorna/
8.3.3 An Intelligent DNA Nanorobot to Fight Cancer by Targeting HER2 Expression
Reporter and Curator: Dr. Sudipta Saha, Ph.D.
8.3.4 Exosomes: Natural Carriers for siRNA Delivery using extracellular vesicles through endocytic pathway.
Reporter: Aviva Lev-Ari, PhD, RN
https://pharmaceuticalintelligence.com/2017/04/24/exosomes-natural-carriers-for-sirna-delivery/
8.3.5 Alnylam Announces First-Ever FDA Approval of an RNAi Therapeutic, ONPATTRO™ (patisiran) for the Treatment of the Polyneuropathy of Hereditary Transthyretin-Mediated Amyloidosis in Adults
Reporter: Aviva Lev-Ari, PhD, RN
8.4 Epigenomics in Cancer
| Hypergraph Plot #37 and Tree Diagram #37
for 8.4 based on 4 articles & on 15 keywords
cells, cancer, protein, methylation, dna, rna, expression, epigenetic, gene, pyruvate, glutamine, metabolism, molecules, stem, human
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| HYPERGRAPH INTERPRETATION
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| TREE PLOT DIAGRAM INTERPRETATION
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List of articles included in 8.4
8.4.1 Deciphering the Epigenome
Curator: Larry H. Bernstein, MD, FCAP
https://pharmaceuticalintelligence.com/2016/01/28/deciphering-the-epigenome/
8.4.2 Methylation and cancer epigenomics
Larry H. Bernstein, MD, FCAP, Curator
https://pharmaceuticalintelligence.com/2016/02/19/methylation-and-cancer-epigenomics/
8.4.3 A New Potential Target for Pancreatic Cancer Treatment: Rapid Screening Technique finds Gene Defending Tumors from DNA Damage @M. D. Anderson Cancer Center
Reporter: Aviva Lev-Ari, PhD, RN
8.4.4 Is the Warburg effect an effect of deregulated space occupancy of methylome?
Larry H. Bernstein and Radoslav Bozov, co-curation
8.5 Environmental Epigenomics
| Hypergraph Plot #38 and Tree Diagram #38
for 8.5 based on 4 articles & on 11 keywords
epa, chemical, toxrefdb, toxicity, toxicology, kes, gene, environmental, sperm, air, safety
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| HYPERGRAPH INTERPRETATION
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| TREE PLOT DIAGRAM INTERPRETATION
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List of articles included in 8.5
8.5.1 BioInformatic Resources at the Environmental Protection Agency: Tools and Webinars on Toxicity Prediction
Curator Stephen J. Williams Ph.D.
8.5.2 Live 2:30-4:30 PM Mediterranean Diet and Lifestyle: A Symposium on Diet and Human Health: October 19, 2018
Reporter: Stephen J. Williams, Ph.D.
8.5.3 Live 12:00 – 1:00 P.M Mediterranean Diet and Lifestyle: A Symposium on Diet and Human Health : October 19, 2018
Reporter: Stephen J. Williams, Ph.D.
8.5.4 Decline in Sperm Count – Epigenetics, Well-being and the Significance for Population Evolution and Demography
Contributors of Co-Curation
Dr. Marc Feldman, Expert Opinion on the significance of Sperm Count Decline on the Future of Population Evolution and Demography
Dr. Sudipta Saha, Effects of Sperm Quality and Quantity on Human Reproduction
Dr. Aviva Lev-Ari, Psycho-Social Effects of Poverty, Unemployment and Epigenetics on Male Well-being, Physiological Conditions affecting Sperm Quality and Quantity
In summary to this volume, five comments of note are repeated here from the Original Book and from the New Genre, Genomics Volume 2, PART A & PART C because of their significance:
Latest in Genomics Methodologies for Therapeutics: Gene Editing, NGS & BioInformatics, Simulations and the Genome Ontology
Comment #1:
- No other book covers the same topics in a single volume
Comment #2:
- No other book incorporates 74 e-Proceedings created in real time by the Book’s authors and editors at conferences on Genomics
Comment #3:
- No other book incorporates four collections of Tweets representing quotes from speakers at global leading conferences on Genomics
Comment #4:
- No other book has 13 locations of Videos and Audio Podcasts that serve to enrich the e-Reader’s experience
Comment #5:
- No other book has 326 articles on the topics covered and included in the title of this Book: Latest in Genomics Methodologies for Therapeutics: Gene Editing, NGS & BioInformatics, Simulations and the Genome Ontology
The e-Reader is encouraged to read the Preface, the Introduction and the Epilogue to Genomics Volume 2
- Original Volume Two:
On Amazon.com since 12/28/2019
https://www.amazon.com/dp/B08385KF87
AND
the e-Reader is encouraged to continue to Genomics Volume 1
Genomics Orientations for Personalized Medicine
VOLUME ONE
On Amazon.com since 23/11/2015
http://www.amazon.com/dp/B018DHBUO6
NEW GENRE Genomics, Volume Three:
Appendix to this volume
Appendix – Wolfram Code
for Hypergraph Plots & for Tree Diagram Plots
NLP Code writing for Parts 1,2,3,4,5,7,8
by
Madison Davis
Code used in production of Hyper-graph Plots at the Book Part Level
| Hypergraph Plot #1
for 1.1.1 based on 16 articles & on 14 keywords |
wordSheet ={
protein,cancer,dna,gene,genes,rna,survival,immune,tumor,research,patients,human, genome,expression }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #2
for 1.1.2 based on 17 articles & on 12 keywords |
wordSheet ={
cancer,mutations,patients,gene,disease,genetic,mutation,data,clinical,tumor,genes, protein }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #3
for 1.1.3 based on 21 articles & on 14 keywords |
wordSheet ={
protein,dna,cancer,cells,information,gene,hdx,mass,sequence,research,chemical, analysis,approach,complexes }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #4
for 1.1.4 based on 2 articles & on 18 keywords |
wordSheet ={
sequencing,medicine,hospital,genes,women,genome,harvard,genetic,conference, research,rare,medical,genetics,disorder,department,bipolar,autism,variations }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #5
for 1.2.1 based on 18 articles & on 16 keywords |
wordSheet ={
data,cancer,cells,signature,analysis,genome,information,variants,gene,research, genomic,learning,human,frequency,features,system }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #6
for 1.2.2 based on 18 articles & on 19 keywords |
wordSheet ={
cancer,cells,genome,analysis,research,drug,protein,human,information,gene, bioinformatics,genomic,genes,clinical,medicine,development,dna,genomics,world }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #7
for 1.2.3 based on 11 articles & on 12 keywords |
wordSheet ={
dna,cancer,protein,source,gene,search,amino,health,medicine,cells,genome,editing }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #8
for 1.2.4 based on 5 articles & on 14 keywords |
wordSheet ={
genetic,sequencing,research,gene,clinical,pacbio,genome,reproductive,disease, diagnostics,medicine,sinai,ngs,results }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #9
for 1.3 based on 11 articles & on 16 keywords |
wordSheet ={
cells,medicine,cancer,personalized,clinical,gene,medical,patients,research,sequencing, health,therapy,pharma,drug,genetic,genome }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #10
for 1.4 based on 18 articles & on 15 keywords |
wordSheet ={
oncology,healthcare,cancer,data,cells,verily,research,sequencing,conference,technology,horizon,health,life,gene,AI }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #11
for 2.1.1 based on 22 articles & on 17 keywords |
wordSheet ={
cells,crispr,cas,gene,beta,figure,dna,protein,editing,genome,cancer,target,ripk,rna, system,genes,expression }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #12
for 2.1.2 based on 8 articles & on 18 keywords |
wordSheet ={
crispr,cas,cells,gene,genome,dna,rnai,genes,rna,research,protein,genetic,editing, disease,system,target,human,technology }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #13
for 2.1.3 based on 15 articles & on 17 keywords |
wordSheet ={
crispr,cas,protein,cells,gene,genome,editing,dna,rna,disease,genes,doudna,cancer, human,target,mit,technology }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #14
for 2.1.4 based on 6 articles & on 19 keywords |
wordSheet ={
gene,crispr,human,editing,cas,genome,technology,cells,research,doudna,genetic, embryos,genes,science,engineering,dna,cancer,nature,germline }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #15
for 2.1.5 based on 28 articles & on 16 keywords |
wordSheet ={
crispr,cells,gene,cas,editing,dna,genome,technology,rna,research,genes,human,doudna,science,genetic,engineering }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #16
for 2.2 based on 27 articles & on 16 keywords |
wordSheet ={
cas,crispr,gene,dna,protein,expression,stem,rna,target,genome,editing,genes,cancer, system,research,human }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #17
for 2.3 based on 9 articles & on 19 keywords |
wordSheet ={
crispr,gene,cas,editing,cells,disease,genome,dna,human,genetic,target,therapy,ttr, protein,research,genes,system,amyloid,technology }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #18
for 2.4 based on 20 articles & on 16 keywords |
wordSheet ={
crispr,patent,cas,editing,institute,patents,gene,berkeley,therapeutics,technology,cells, interference,intellia,genomics,biotech,doudna }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #19
for 3.1 based on 8 articles & on 13 keywords |
wordSheet ={
ai,data,hms,health,mgh,medicine,care,clinical,healthcare,ballroom,patient,radiology, innovation }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #20
for 3.2 based on 9 articles & on 14 keywords |
wordSheet ={
cells,cancer,gene,schizophrenia,research,protein,brain,frontal,imaging,patients,disease,dna,researchers,system }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #21
for 3.3 based on 23 articles & on 16 keywords |
wordSheet ={
data,cancer,patients,ai,clinical,exon,patient,gene,learning,analysis,splicing,health,cells, rna,clinicians,imaging }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #22
for 3.4 based on 16 articles & on 12 keywords |
wordSheet ={
ai,data,healthcare,patients,technology,world,partners,medical,digital,clinical,access, research }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #23
for 3.5 based on 9 articles & on 16 keywords |
wordSheet ={
cancer,risk,brain,breast,model,mri,data,molecular,mtv,density,women,mdm,image, aging,analysis,tissue }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #24
for 4.1 based on 9 articles & on 17 keywords |
wordSheet ={
cells,human,single,atlas,genomics,cellular,science,institute,nature,cancer,sequencing, disease,map,immune,biology,body,researchers }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #25
for 4.2 based on 6 articles & on 16 keywords |
wordSheet ={
cells,single,ai,sequencing,molecular,information,expression,fluorescence,protein,rna, streptavidin,population,surface,output,magnetic,seq }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #26
for 4.3 based on 7 articles & on 12 keywords |
wordSheet ={
cells,single,mutation,sequencing,data,cancer,heterogeneity,tumor,analysis,mutations, gene,immune }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #27
for 4.4 based on 2 articles & on 17 keywords |
wordSheet ={
cells,single,platform,analysis,sequencing,products,rare,isolation,endotoxin,aging,view, tapestri,lifespan,dna,clonal,cellplate,mission }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #28
for 5.1 based on 1 article & on 17 keywords |
wordSheet ={
populations,genetic,human,population,variation,heritability,snps,gwas,traits,genome, african,genomic,ancestry,polygenic,feldman,diversity,data }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #29
for 7.1 based on 3 articles & on 18 keywords |
wordSheet ={
disease,variants,genetic,risk,sequencing,genome,gene,studies,rare,loci,genes,diseases,diabetes,depression,heart,genetics,variant,personalized }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #30
for 7.2 based on 2 articles & on 18 keywords |
wordSheet ={
cells,cancer,protein,dna,gene,fibonacci,genes,tumor,human,data,immune,research,rna, structure,humans,biology,genome,drug }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #31
for 7.3 based on 4 articles & on 14 keywords |
wordSheet ={
cells,variants,cancer,genome,disease,sequencing,gene,dna,biomarkers,subpopulations, rna,diseases,researchers,data }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #32
for 7.4 based on 3 articles & on 18 keywords |
wordSheet ={
thickspace,genome,variants,gene,information,tools,multifractal,fractal,genomic, genomes,dna,bioinformatics,variant,sequences,human,regions,data,genes }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #33
for 7.5 based on 5 articles & on 15 keywords |
wordSheet ={
populations,mutation,population,variation,loci,human,diversity,data,chromosome, genome,inclusion,locus,genetic,differences,snps }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #34
for 7.6 based on 2 articles & on 18 keywords |
wordSheet ={
mrtx,kras,cells,krasgc,inhibition,tumor,signaling,combination,erk,treatment,dose, mutant,demonstrated,protein,antitumor,activity,single,pathway }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #35
for 8.2 based on 6 articles & on 23 keywords |
wordSheet ={
signature,genome,encode,cancer,dna,human,types,gene,data,cells,mutational,protein, genes,mutations,regions,regulatory,transcription,binding,elements,associated,aetiology,sites,functional }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #36
for 8.3 based on 5 articles & on 17 keywords |
wordSheet ={
cancer,mrna,cells,rna,moderna,vaccines,protein,micrornas,vaccine,immune,treatment, dna,therapeutic,personalized,merck,tfna,polyneuropathy }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #37
for 8.4 based on 4 articles & on 16 keywords |
wordSheet ={
cells,cancer,protein,methylation,dna,rna,expression,epigenetic,gene,pyruvate, glutamine,metabolism,epigenetics,molecules,stem,human }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
| Hypergraph Plot #38
for 8.5 based on 4 articles & on 18 keywords |
wordSheet ={
data,epa,chemical,information,toxrefdb,toxicity,toxicology,chemicals,kes,gene, environmental,national,sperm,air,si,safety,mies,mesh }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; edgeList = Append[edgeList,Prepend[words1, “”]] ; For[i = 1, i <= Length[words1], i++, edgeList = Append[edgeList, Append[broadTerms[[i]], words1[[i]]]]]; ResourceFunction[“HypergraphPlot”][edgeList, VertexSize -> 0.01, VertexLabels -> Automatic, PlotTheme -> “Detailed”, SubsetEdge -> False, SubsetBoundaryScale -> 7, VertexStyle -> Red,”BaseLayout” -> “RadialEmbedding”,”SubsetEdgeStyle” -> ColorData[100, “ColorList”]] |
Code used in production of Tree Diagram Plots
| Tree Diagram Plot #1
for 1.1.1 based on 16 articles & on 14 keywords |
wordSheet ={
protein,cancer,dna,gene,genes,rna,survival,immune,tumor,research,patients,human, genome,expression }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 1.1.1” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #2
for 1.1.2 based on 17 articles & on 12 keywords |
wordSheet ={
cancer,mutations,patients,gene,disease,genetic,mutation,data,clinical,tumor,genes, protein }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 1.1.2” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #3
for 1.1.3 based on 21 articles & on 14 keywords |
wordSheet ={
protein,dna,cancer,cells,information,gene,hdx,mass,sequence,research,chemical, analysis,approach,complexes, }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 1.1.3” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #4
for 1.1.4 based on 2 articles & on 18 keywords |
wordSheet ={
sequencing,medicine,hospital,genes,women,genome,harvard,genetic,conference, research,rare,medical,genetics,disorder,department,bipolar,autism,variations }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 1.1.4” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #5
for 1.2.1 based on 18 articles & on 16 keywords |
wordSheet ={
data,cancer,cells,signature,analysis,genome,information,variants,gene,research, genomic,learning,human,frequency,features,system }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 1.2.1” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #6
for 1.2.2 based on 18 articles & on 19 keywords |
wordSheet ={
cancer,cells,genome,analysis,research,drug,protein,human,information,gene, bioinformatics,genomic,genes,clinical,medicine,development,dna,genomics,world }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 1.2.2” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #7
for 1.2.3 based on 11 articles & on 12 keywords |
wordSheet ={
dna,cancer,protein,source,gene,search,amino,health,medicine,cells,genome,editing }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 1.2.3” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Hypergraph Plot #8
for 1.2.4 based on 5 articles & on 14 keywords |
wordSheet ={
genetic,sequencing,research,gene,clinical,pacbio,genome,reproductive,disease, diagnostics,medicine,sinai,ngs,results }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 1.2.4” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #9
for 1.3 based on 11 articles & on 16 keywords |
wordSheet ={
cells,medicine,cancer,personalized,clinical,gene,medical,patients,research,sequencing, health,therapy,pharma,drug,genetic,genome }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 1.3” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #10
for 1.4 based on 18 articles & on 15 keywords |
wordSheet ={
oncology,healthcare,cancer,data,cells,verily,research,sequencing,conference,technology,horizon,health,life,gene,AI }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 1.4” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #11
for 2.1.1 based on 22 articles & on 17 keywords |
wordSheet ={
cells,crispr,cas,gene,beta,figure,dna,protein,editing,genome,cancer,target,ripk,rna, system,genes,expression }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 2.1.1” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #12
for 2.1.2 based on 8 articles & on 18 keywords |
wordSheet ={
crispr,cas,cells,gene,genome,dna,rnai,genes,rna,research,protein,genetic,editing, disease,system,target,human,technology }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 2.1.2” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #13
for 2.1.3 based on 15 articles & on 17 keywords |
wordSheet ={
crispr,cas,protein,cells,gene,genome,editing,dna,rna,disease,genes,doudna,cancer, human,target,mit,technology }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 2.1.3” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #14
for 2.1.4 based on 6 articles & on 19 keywords |
wordSheet ={
gene,crispr,human,editing,cas,genome,technology,cells,research,doudna,genetic, embryos,genes,science,engineering,dna,cancer,nature,germline }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 2.1.4” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #15
for 2.1.5 based on 28 articles & on 16 keywords |
wordSheet ={
crispr,cells,gene,cas,editing,dna,genome,technology,rna,research,genes,human,doudna,science,genetic,engineering }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 2.1.5” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #16
for 2.2 based on 27 articles & on 16 keywords |
wordSheet ={
cas,crispr,gene,dna,protein,expression,stem,rna,target,genome,editing,genes,cancer, system,research,human }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 2.2” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #17
for 2.3 based on 9 articles & on 19 keywords |
wordSheet ={
crispr,gene,cas,editing,cells,disease,genome,dna,human,genetic,target,therapy,ttr, protein,research,genes,system,amyloid,technology }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 2.3” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #18
for 2.4 based on 20 articles & on 16 keywords |
wordSheet ={
crispr,patent,cas,editing,institute,patents,gene,berkeley,therapeutics,technology,cells, interference,intellia,genomics,biotech,doudna }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 2.4” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #19
for 3.1 based on 8 articles & on 13 keywords |
wordSheet ={
ai,data,hms,health,mgh,medicine,care,clinical,healthcare,ballroom,patient,radiology, innovation }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 3.1” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #20
for 3.2 based on 9 articles & on 14 keywords |
wordSheet ={
cells,cancer,gene,schizophrenia,research,protein,brain,frontal,imaging,patients, disease,dna,researchers,system }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 3.2” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #21
for 3.3 based on 23 articles & on 16 keywords |
wordSheet ={
data,cancer,patients,ai,clinical,exon,patient,gene,learning,analysis,splicing,health,cells, rna,clinicians,imaging }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 3.3” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #22
for 3.4 based on 16 articles & on 12 keywords |
wordSheet ={
ai,data,healthcare,patients,technology,world,partners,medical,digital,clinical,access, research }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 3.4” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #23
for 3.5 based on 9 articles & on 16 keywords |
wordSheet ={
cancer,risk,brain,breast,model,mri,data,molecular,mtv,density,women,mdm,image, aging,analysis,tissue }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 3.5” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #24
for 4.1 based on 9 articles & on 17 keywords |
wordSheet ={
cells,human,single,atlas,genomics,cellular,science,institute,nature,cancer,sequencing, disease,map,immune,biology,body,researchers }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 4.1” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #25
for 4.2 based on 6 articles & on 16 keywords |
wordSheet ={
cells,single,ai,sequencing,molecular,information,expression,fluorescence,protein,rna, streptavidin,population,surface,output,magnetic,seq }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 4.2” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #26
for 4.3 based on 7 articles & on 12 keywords |
wordSheet ={
cells,single,mutation,sequencing,data,cancer,heterogeneity,tumor,analysis,mutations, gene,immune }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 4.3” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #27
for 4.4 based on 2 articles & on 17 keywords |
wordSheet ={
cells,single,platform,analysis,sequencing,products,rare,isolation,endotoxin,aging,view, tapestri,lifespan,dna,clonal,cellplate,mission }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 4.4” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #28
for 5.1 based on 1 article & on 17 keywords |
wordSheet ={
populations,genetic,human,population,variation,heritability,snps,gwas,traits,genome, african,genomic,ancestry,polygenic,feldman,diversity,data }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 5.1” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #29
for 7.1 based on 3 articles & on 18 keywords |
wordSheet ={
disease,variants,genetic,risk,sequencing,genome,gene,studies,rare,loci,genes,diseases,diabetes,depression,heart,genetics,variant,personalized }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 7.1” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #30
for 7.2 based on 2 articles & on 18 keywords |
wordSheet ={
cells,cancer,protein,dna,gene,fibonacci,genes,tumor,human,data,immune,research,rna, structure,humans,biology,genome,drug }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 7.2” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #31
for 7.3 based on 4 articles & on 14 keywords |
wordSheet ={
cells,variants,cancer,genome,disease,sequencing,gene,dna,biomarkers,subpopulations, rna,diseases,researchers,data }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 7.3” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #32
for 7.4 based on 3 articles & on 18 keywords |
wordSheet ={
thickspace,genome,variants,gene,information,tools,multifractal,fractal,genomic, genomes,dna,bioinformatics,variant,sequences,human,regions,data,genes }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 7.4” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #33
for 7.5 based on 5 articles & on 15 keywords |
wordSheet ={
populations,mutation,population,variation,loci,human,diversity,data,chromosome, genome,inclusion,locus,genetic,differences,snps }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 7.5” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #34
for 7.6 based on 2 articles & on 18 keywords |
wordSheet ={
mrtx,kras,cells,krasgc,inhibition,tumor,signaling,combination,erk,treatment,dose, mutant,demonstrated,protein,antitumor,activity,single,pathway }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 7.6” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #35
for 8.2 based on 6 articles & on 23 keywords |
wordSheet ={
signature,genome,encode,cancer,dna,human,types,gene,data,cells,mutational,protein, genes,mutations,regions,regulatory,transcription,binding,elements,associated,aetiology,sites,functional }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 8.2” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #36
for 8.3 based on 5 articles & on 17 keywords |
wordSheet ={
cancer,mrna,cells,rna,moderna,vaccines,protein,micrornas,vaccine,immune,treatment, dna,therapeutic,personalized,merck,tfna,polyneuropathy }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 8.3” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #37
for 8.4 based on 4 articles & on 16 keywords |
wordSheet ={
cells,cancer,protein,methylation,dna,rna,expression,epigenetic,gene,pyruvate, glutamine,metabolism,epigenetics,molecules,stem,human }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 8.4” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
| Tree Diagram Plot #38
for 8.5 based on 4 articles & on 18 keywords |
wordSheet ={
data,epa,chemical,information,toxrefdb,toxicity,toxicology,chemicals,kes,gene, environmental,national,sperm,air,si,safety,mies,mesh }; topN = Length[wordSheet]; words = {}; For[i = 1, i <= topN, i++, words = Append[words, ToString[wordSheet[[i]]]]]; Print[words]; maxN = 3; broadTerms = {}; words1 = {}; words2 = {}; For[i = 1, i <= topN, i++,If[Length[Position[WordData[], Extract[words, i]]] > 0, broadTerms = Append[broadTerms, Flatten[Values[WordData[Extract[words, i], “BroaderTerms”]]]]; words1 = Append[words1, Extract[words, i]], words2 = Append[words2, Extract[words, i]]]]; For[i = 1, i <= Length[broadTerms], i++, If[Length[broadTerms[[i]]] > maxN, broadTerms[[i]] = broadTerms[[i]][[1 ;; maxN]]]];
edgeList = {}; For[i = 1 , i <= Length[broadTerms], i++, edgeList = Append[edgeList, broadTerms[[i]]]]; For[i = 1 , i <= Length[broadTerms], i++, For[j = 1, j <= Length[edgeList[[i]]], j++, edgeList[[i]][[j]] = words1[[i]] -> edgeList[[i]][[j]]]]; For[i = 1 , i <= Length[words1], i++, edgeList = Append[edgeList, {“Chapter 8.5” -> words1[[i]]}]]; TreePlot[Flatten[edgeList], VertexSize -> 0.1, VertexLabels -> Automatic] |
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