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Gabor T Marth
Gabor T Marth
Professor of Human Genetics, University of Utah
Verified email at genetics.utah.edu - Homepage
Title
Cited by
Cited by
Year
The sequence alignment/map format and SAMtools
H Li, B Handsaker, A Wysoker, T Fennell, J Ruan, N Homer, G Marth, ...
bioinformatics 25 (16), 2078-2079, 2009
550782009
A global reference for human genetic variation
AGR 1000 Genomes Project Consortium, Auton A, Brooks LD, Durbin RM, Garrison ...
Nature 526 (7571), 68-74, 2015
14858*2015
The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
128182011
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
87932010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82872012
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
International SNP Map Working Group Cold Spring Harbor Laboratories ...
Nature 409 (6822), 928-933, 2001
44322001
Haplotype-based variant detection from short-read sequencing
E Garrison, G Marth
arXiv preprint arXiv:1207.3907, 2012
41402012
An integrated map of structural variation in 2,504 human genomes
PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ...
Nature 526 (7571), 75-81, 2015
23822015
ART: a next-generation sequencing read simulator
W Huang, L Li, JR Myers, GT Marth
Bioinformatics 28 (4), 593-594, 2012
14902012
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65, 2011
12822011
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
9182011
Multi-platform discovery of haplotype-resolved structural variation in human genomes
MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ...
Nature communications 10 (1), 1784, 2019
7642019
Haplotype-based variant detection from short-read sequencing. arXiv
E Garrison, G Marth
arXiv preprint arXiv:1207.3907 9, 2012
7162012
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
7092011
A general approach to single-nucleotide polymorphism discovery
GT Marth, I Korf, MD Yandell, RT Yeh, Z Gu, H Zakeri, NO Stitziel, ...
Nature genetics 23 (4), 452-456, 1999
7051999
1000 Genomes Project Analysis Group. 2011
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
The variant call format and VCFtools. Bioinformatics 27 (15), 2156-2158, 2011
6612011
Subgroup 1000 Genome Project Data Processing. 2009. The Sequence Alignment/Map format and SAMtools
H Li, B Handsaker, A Wysoker, T Fennell, J Ruan, N Homer, G Marth, ...
Bioinformatics 25 (16), 2078-2079, 2009
5922009
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
5862008
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
5302015
Human diallelic insertion/deletion polymorphisms
JL Weber, D David, J Heil, Y Fan, C Zhao, G Marth
The American Journal of Human Genetics 71 (4), 854-862, 2002
4562002
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