Aaron Quinlan
Aaron Quinlan
Professor of Human Genetics, U. of Utah;
Verified email at - Homepage
Cited by
Cited by
BEDTools: a flexible suite of utilities for comparing genomic features
AR Quinlan, IM Hall
Bioinformatics 26 (6), 841-842, 2010
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
BEDTools: the Swiss‐army tool for genome feature analysis
AR Quinlan
Current protocols in bioinformatics 47 (1), 11.12. 1-11.12. 34, 2014
Nanopore sequencing and assembly of a human genome with ultra-long reads
M Jain, S Koren, KH Miga, J Quick, AC Rand, TA Sasani, JR Tyson, ...
Nature biotechnology 36 (4), 338-345, 2018
LUMPY: a probabilistic framework for structural variant discovery
RM Layer, C Chiang, AR Quinlan, IM Hall
Genome biology 15, 1-19, 2014
BamTools: a C++ API and toolkit for analyzing and managing BAM files
DW Barnett, EK Garrison, AR Quinlan, MP Strömberg, GT Marth
Bioinformatics 27 (12), 1691-1692, 2011
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
Copy number variation detection and genotyping from exome sequence data
N Krumm, PH Sudmant, A Ko, BJ O'Roak, M Malig, BP Coe, AR Quinlan, ...
Genome research 22 (8), 1525-1532, 2012
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
S Onengut-Gumuscu, WM Chen, O Burren, NJ Cooper, AR Quinlan, ...
Nature genetics 47 (4), 381-386, 2015
Mosdepth: quick coverage calculation for genomes and exomes
BS Pedersen, AR Quinlan
Bioinformatics 34 (5), 867-868, 2018
Whole-genome sequencing and variant discovery in C. elegans
LDW Hillier, GT Marth, AR Quinlan, D Dooling, G Fewell, D Barnett, P Fox, ...
Nature methods 5 (2), 183-188, 2008
SpeedSeq: ultra-fast personal genome analysis and interpretation
C Chiang, RM Layer, GG Faust, MR Lindberg, DB Rose, EP Garrison, ...
Nature methods 12 (10), 966-968, 2015
GEMINI: integrative exploration of genetic variation and genome annotations
U Paila, BA Chapman, R Kirchner, AR Quinlan
PLoS computational biology 9 (7), e1003153, 2013
Poretools: a toolkit for analyzing nanopore sequence data
NJ Loman, AR Quinlan
Bioinformatics 30 (23), 3399-3401, 2014
Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus
W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ...
PLoS genetics 6 (2), e1000841, 2010
Pybedtools: a flexible Python library for manipulating genomic datasets and annotations
RK Dale, BS Pedersen, AR Quinlan
Bioinformatics 27 (24), 3423-3424, 2011
Rapid whole-genome mutational profiling using next-generation sequencing technologies
DR Smith, AR Quinlan, HE Peckham, K Makowsky, W Tao, B Woolf, ...
Genome research 18 (10), 1638-1642, 2008
Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome
AR Quinlan, RA Clark, S Sokolova, ML Leibowitz, Y Zhang, ME Hurles, ...
Genome research 20 (5), 623-635, 2010
Pyrobayes: an improved base caller for SNP discovery in pyrosequences
AR Quinlan, DA Stewart, MP Strömberg, GT Marth
Nature methods 5 (2), 179-181, 2008
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
JY An, K Lin, L Zhu, DM Werling, S Dong, H Brand, HZ Wang, X Zhao, ...
Science 362 (6420), eaat6576, 2018
The system can't perform the operation now. Try again later.
Articles 1–20