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Bob Handsaker
Bob Handsaker
Broad Institute / Harvard Medical School
Verified email at broadinstitute.org - 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
563832009
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
563832009
The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
144372011
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
114652009
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence
G Genovese, AK Kähler, RE Handsaker, J Lindberg, SA Rose, ...
New England Journal of Medicine 371 (26), 2477-2487, 2014
36202014
The GTEx Consortium atlas of genetic regulatory effects across human tissues
GTEx Consortium
Science 369 (6509), 1318-1330, 2020
32712020
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
R Saxena, BF Voight, V Lyssenko, NP Burtt, PIW de Bakker, H Chen, ...
Science 316 (5829), 1331-1336, 2007
30702007
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
25502015
Schizophrenia risk from complex variation of complement component 4
A Sekar, AR Bialas, H De Rivera, A Davis, TR Hammond, N Kamitaki, ...
Nature 530 (7589), 177-183, 2016
25052016
Genome sequence and analysis of the Irish potato famine pathogen Phytophthora infestans
BJ Haas, S Kamoun, MC Zody, RHY Jiang, RE Handsaker, LM Cano, ...
Nature 461 (7262), 393-398, 2009
17422009
SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
AD Johnson, RE Handsaker, SL Pulit, MM Nizzari, CJ O'Donnell, ...
Bioinformatics 24 (24), 2938-2939, 2008
15362008
A systematic survey of loss-of-function variants in human protein-coding genes
DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ...
Science 335 (6070), 823-828, 2012
14252012
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
13202011
Integrated detection and population-genetic analysis of SNPs and copy number variation
SA McCarroll, FG Kuruvilla, JM Korn, S Cawley, J Nemesh, A Wysoker, ...
Nature genetics 40 (10), 1166-1174, 2008
11662008
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), 1-16, 2019
8412019
Whole-genome sequence variation, population structure and demographic history of the Dutch population
LC Francioli, A Menelaou, SL Pulit, F Van Dijk, PF Palamara, CC Elbers, ...
Nature genetics 46 (8), 818-825, 2014
7392014
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
6962011
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth
M Fromer, JL Moran, K Chambert, E Banks, SE Bergen, DM Ruderfer, ...
The American Journal of Human Genetics 91 (4), 597-607, 2012
6692012
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
6282009
Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations
FT Merkle, S Ghosh, N Kamitaki, J Mitchell, Y Avior, C Mello, S Kashin, ...
Nature 545 (7653), 229-233, 2017
5432017
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