Richard A. Gibbs
Genetics · 2000–2019
A researcher in the Science corpus: 86 papers; trusts 1 researcher and is trusted by 4 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 695 citations into it; #4,707 of 6,854 by trust here, #7 by citations
Whom Richard A. Gibbs trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Richard A. Gibbs overall
Papers from Richard A. Gibbs's perspective
Ordered by how strongly the researchers Richard A. Gibbs trusts endorse each paper. Same corpus, a different order for every researcher.
- A method and server for predicting damaging missense mutations
- BLAT--the BLAST-like alignment tool. (Genome Research)
- Predicting the effects of amino acid substitutions on protein function.
- COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer
- A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. (Systematic Biology)
- Biological Sequence Analysis: Probabilistic Models of Proteins and Nucleic Acids
- [Structural variation in the human genome]. (Yi chuan = Hereditas)
- Transcriptional regulatory elements in the human genome. (Annual review of genomics and human genetics (Print))
- FAIRE (Formaldehyde-Assisted Isolation of Regulatory Elements) isolates active regulatory elements from human chromatin. (Genome Research)
- Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome (Nature Genetics)
Their papers
- The genome sequence of Drosophila melanogaster. (2000) — 6,282 citations
- Initial sequencing and analysis of the human genome (2001) — 24,262 citations
- Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes. (2005) — 4,049 citations
- Minimum information about a marker gene sequence (MIMARKS) and minimum information about any (x) sequence (MIxS) specifications (2011) — 745 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) — 5,374 citations
- A framework for human microbiome research (2012) — 2,418 citations
- Genome sequence of the Brown Norway rat yields insights into mammalian evolution (2004) — 2,140 citations
- Structure, Function and Diversity of the Healthy Human Microbiome (2012) — 10,771 citations
- PipMaker--a web server for aligning two genomic DNA sequences. (2000) — 1,263 citations
- The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (2004) — 602 citations
- A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
- Personalized Copy-Number and Segmental Duplication Maps using Next-Generation Sequencing (2009) — 789 citations
- A systematic survey of loss-of-function variants in human protein-coding genes (2012) — 1,227 citations
- Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate species (2013) — 725 citations
- Comparative genomics of the eukaryotes. (2000) — 1,017 citations
- Initial sequencing and comparative analysis of the mouse genome. (2002) — 4,291 citations
- Somatic mutations affect key pathways in lung adenocarcinoma (2008) — 2,751 citations
- A physical map of the human genome (2001) — 824 citations
- Comprehensive Molecular Characterization of Human Colon and Rectal Cancer (2012) — 7,754 citations