2011 - Fellow of the American Association for the Advancement of Science (AAAS)
Richard M. Myers spends much of his time researching Genetics, Computational biology, Gene, Human genome and Genome. His study in Genomics, DNA methylation, Peak calling, ChIP-exo and Chromatin is carried out as part of his studies in Genetics. The study incorporates disciplines such as Genetic traits, Gene expression profiling, Annotation, Transcription factor and ENCODE in addition to Computational biology.
He interconnects GENCODE and DNase-Seq in the investigation of issues within ENCODE. His Human genome research incorporates elements of Radiation Hybrids, Map Location and Gene map. Richard M. Myers combines subjects such as DNA sequencing theory, Personal genomics and Hybrid genome assembly, Contig with his study of Cancer genome sequencing.
The scientist’s investigation covers issues in Genetics, Gene, Computational biology, Genome and Internal medicine. Human genome, Single-nucleotide polymorphism, Genome-wide association study, Locus and Transcription factor are the primary areas of interest in his Genetics study. Gene is frequently linked to Molecular biology in his study.
The Computational biology study combines topics in areas such as Chromatin, ENCODE and Genomics. His Genome study frequently draws connections to adjacent fields such as DNA sequencing. His Internal medicine research includes elements of Endocrinology, Oncology and Cardiology.
Richard M. Myers mainly focuses on Gene, Computational biology, Genetics, Genome and Transcription factor. His biological study spans a wide range of topics, including Pancreatic cancer and Drug resistance. His work deals with themes such as Human genome, Chromatin immunoprecipitation, Enhancer, Chromatin and DNA sequencing, which intersect with Computational biology.
His Genetics study often links to related topics such as Bipolar disorder. His Genome study combines topics from a wide range of disciplines, such as Transcriptional regulation and DNA. Richard M. Myers works mostly in the field of Transcription factor, limiting it down to topics relating to Gene expression and, in certain cases, Triple-negative breast cancer, STAT3 and Breast cancer.
Richard M. Myers mostly deals with Gene, Computational biology, Genetics, Chromatin and Severe acute respiratory syndrome coronavirus 2. His study in the field of Human genome, Amplicon and Genotype also crosses realms of Stickleback and Azithromycin. He has researched Computational biology in several fields, including Genomic data, Chromatin immunoprecipitation, Uncertain significance and Sequencing data.
His study of Exome sequencing is a part of Genetics. His Chromatin research integrates issues from ENCODE, Genome, Enhancer, Transcription factor and Epigenomics. His Severe acute respiratory syndrome coronavirus 2 study incorporates themes from Genetic variants, Generation time and Genetic diversity.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Initial sequencing and analysis of the human genome.
Eric S. Lander;Lauren M. Linton;Bruce Birren;Chad Nusbaum.
Model-based analysis of ChIP-Seq (MACS).
Yong Zhang;Tao Liu;Clifford A Meyer;Jérôme Eeckhoute.
Genome Biology (2008)
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
Ewan Birney;John A. Stamatoyannopoulos;Anindya Dutta;Roderic Guigó.
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
Roger McLendon;Allan Friedman;Darrell Bigner;Erwin G. Van Meir.
Integrated genomic analyses of ovarian carcinoma
D. Bell;A. Berchuck;M. Birrer;J. Chien.
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
Robert L Strausberg;Elise A Feingold;Lynette H Grouse;Jeffery G Derge.
Proceedings of the National Academy of Sciences of the United States of America (2002)
Genome-Wide Mapping of in Vivo Protein-DNA Interactions
David S. Johnson;Ali Mortazavi;Richard M. Myers;Barbara Wold.
The ENCODE (ENCyclopedia of DNA elements) Project
E. A. Feingold;P. J. Good;M. S. Guyer;S. Kamholz.
An integrated encyclopedia of DNA elements in the human genome
Ian Dunham;Anshul Kundaje;Shelley F. Aldred;Patrick J. Collins.
Human Homolog of patched, a Candidate Gene for the Basal Cell Nevus Syndrome
Ronald L. Johnson;Alana L. Rothman;Jingwu Xie;Lisa V. Goodrich.
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