Gabor T Marth
Gabor T Marth
Professor of Human Genetics, University of Utah
Verified email at genetics.utah.edu - Homepage
TitleCited byYear
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
208282009
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
65232010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
58682012
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
43322015
The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
38792011
1000 Genome Project Data Processing Subgroup. 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
37892009
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
International SNP Map Working Group
Nature 409 (6822), 928, 2001
36392001
Haplotype-based variant detection from short-read sequencing
E Garrison, G Marth
arXiv preprint arXiv:1207.3907, 2012
11412012
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, 2011
9472011
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, 2015
9032015
ART: a next-generation sequencing read simulator
W Huang, L Li, JR Myers, GT Marth
Bioinformatics 28 (4), 593-594, 2011
6752011
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, 1999
5911999
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, 2008
5062008
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
4362011
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
3322011
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
3082002
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), 1235587, 2013
3012013
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
3002008
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
2952004
Pyrobayes: an improved base caller for SNP discovery in pyrosequences
AR Quinlan, DA Stewart, MP Strömberg, GT Marth
Nature methods 5 (2), 179, 2008
2402008
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