Michael Ryan
Cell · with Wang · 2015–2018
A researcher in the Science corpus: 2 papers; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Papers from Michael Ryan's perspective
Ordered by how strongly the researchers Michael Ryan trusts endorse each paper. Same corpus, a different order for every researcher.
- NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins (Nucleic Acids Res.)
- Entrez: molecular biology database and retrieval system.
- ClinVar: public archive of relationships among sequence variation and human phenotype
- Analysis of protein-coding genetic variation in 60,706 humans
- Predicting the functional impact of protein mutations: application to cancer genomics
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.
- Generating samples under a Wright-Fisher neutral model of genetic variation (Bioinform.)
- A general framework for estimating the relative pathogenicity of human genetic variants
- Cancer-specific High-throughput Annotation of Somatic Mutations: computational prediction of driver missense mutations (Cancer Research)
- Detection of nonneutral substitution rates on mammalian phylogenies.
Their papers
- Assessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST‐Indel) (2015) — 138 citations
- Comprehensive Characterization of Cancer Driver Genes and Mutations (2018) — 2,007 citations