Aaron R. Quinlan
Molecular Biology · 2008–2017
A researcher in the Science corpus: 12 papers; trusts 20 researchers and is trusted by 20 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 149 citations into it; #2,429 of 17,773 by trust here, #3,204 by citations
- Genetics — 135 citations into it; #3,065 of 6,854 by trust here, #1,101 by citations
- Plant Science — 25 citations into it
- Artificial Intelligence — 22 citations into it; #31,163 of 35,345 by trust here, #27,551 by citations
- Cancer Research — 21 citations into it
- Computational Biology & Bioinformatics — 15 citations into it
Whom Aaron R. Quinlan trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li
- James Y. Zou
- Kai Wang
- Peter N. Robinson
- Genome analysis
- ENCODEConsortium
- Hui Yang
- Gonçalo R. Abecasis
- Katherine S. Pollard
- Ivan A. Adzhubei
Who trusts Aaron R. Quinlan overall
- Jared T. Simpson
- Nicholas J. Loman
- Hengyun Lu
- Daniel C. Koboldt
- Valentina Galata
- Wouter De Coster
- Martin Hunt
- Davide Heller
- Joshua Quick
- Daniel Quang
Papers from Aaron R. Quinlan's perspective
Ordered by how strongly the researchers Aaron R. Quinlan trusts endorse each paper. Same corpus, a different order for every researcher.
- A method and server for predicting damaging missense mutations
- dbSNP: the NCBI database of genetic variation
- Exome sequencing as a tool for Mendelian disease gene discovery
- The human genome browser at UCSC.
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- A general framework for estimating the relative pathogenicity of human genetic variants
- Analysis of protein-coding genetic variation in 60,706 humans
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- ClinVar: public archive of interpretations of clinically relevant variants
- The Sequence Alignment/Map format and SAMtools (Bioinform.)
Their papers
- Nanopore sequencing and assembly of a human genome with ultra-long reads (2017) — 1,714 citations
- Mosdepth: quick coverage calculation for genomes and exomes (2017) — 1,045 citations
- LUMPY: a probabilistic framework for structural variant discovery (2012) — 1,443 citations
- Poretools: a toolkit for analyzing nanopore sequence data (2014) — 414 citations
- Whole-genome sequencing and variant discovery in C. elegans (2008) — 454 citations
- GEMINI: Integrative Exploration of Genetic Variation and Genome Annotations (2013) — 412 citations
- Pybedtools: a flexible Python library for manipulating genomic datasets and annotations (2011) — 497 citations
- BamTools: a C++ API and toolkit for analyzing and managing BAM files (2011) — 969 citations
- Settling the score: variant prioritization and Mendelian disease (2017) — 217 citations
- Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers (2015) — 661 citations
- SpeedSeq: Ultra-fast personal genome analysis and interpretation (2014) — 544 citations
- Copy number variation detection and genotyping from exome sequence data (2012) — 660 citations