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
280122009
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
70802010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56-65, 2012
65502012
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
62302015
The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
52962011
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
R Sachidanandam, D Weissman, SC Schmidt, JM Kakol, LD Stein, ...
Nature 409 (6822), 928-934, 2001
38312001
Haplotype-based variant detection from short-read sequencing
E Garrison, G Marth
arXiv preprint arXiv:1207.3907, 2012
15332012
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
12272015
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
10232011
ART: a next-generation sequencing read simulator
W Huang, L Li, JR Myers, GT Marth
Bioinformatics 28 (4), 593-594, 2012
8542012
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
6151999
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
5182011
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
5182008
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
4302011
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
3472002
Integrative annotation of variants from 1092 humans: application to cancer genomics
E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ...
Science 342 (6154), 2013
3332013
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
3132008
The allele frequency spectrum in genome-wide human variation data reveals signals of differential demographic history in three large world populations
GT Marth, E Czabarka, J Murvai, ST Sherry
Genetics 166 (1), 351-372, 2004
3122004
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
2762009
MOSAIK: a hash-based algorithm for accurate next-generation sequencing short-read mapping
WP Lee, MP Stromberg, A Ward, C Stewart, EP Garrison, GT Marth
PloS one 9 (3), e90581, 2014
2632014
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Articles 1–20