متابعة
Gabor T Marth
Gabor T Marth
Professor of Human Genetics, University of Utah
بريد إلكتروني تم التحقق منه على genetics.utah.edu - الصفحة الرئيسية
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
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
602482009
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
166192015
The variant call format and VCFtools‏
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...‏
Bioinformatics 27 (15), 2156-2158, 2011‏
146792011
A map of human genome variation from population scale sequencing‏
1000 Genomes Project Consortium‏
Nature 467 (7319), 1061, 2010‏
90662010
An integrated map of genetic variation from 1,092 human genomes‏
1000 Genomes Project Consortium‏
Nature 491 (7422), 56, 2012‏
86422012
Haplotype-based variant detection from short-read sequencing‏
E Garrison, G Marth‏
arXiv preprint arXiv:1207.3907, 2012‏
48732012
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
44812001
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
25782015
ART: a next-generation sequencing read simulator‏
W Huang, L Li, JR Myers, GT Marth‏
Bioinformatics 28 (4), 593-594, 2012‏
16392012
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
13332011
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
10562011
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
8502019
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
7472011
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
7402011
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
7191999
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
5862015
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
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel.‏
MJ Delaneau O, GP Consortium‏
Nat Commun. 5 (3934), 2014‏
4772014
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
4702002
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
4212013
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مقالات 1–20