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Vikas Bansal
Vikas Bansal
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Titel
Zitiert von
Zitiert von
Jahr
The diploid genome sequence of an individual human
S Levy, G Sutton, PC Ng, L Feuk, AL Halpern, BP Walenz, N Axelrod, ...
PLoS biology 5 (10), e254, 2007
23082007
Statistical analysis strategies for association studies involving rare variants
V Bansal, O Libiger, A Torkamani, NJ Schork
Nature Reviews Genetics 11 (11), 773-785, 2010
5642010
Dynamics of the human and viral m6A RNA methylomes during HIV-1 infection of T cells
G Lichinchi, S Gao, Y Saletore, GM Gonzalez, V Bansal, Y Wang, ...
Nature microbiology 1 (4), 1-9, 2016
4322016
The importance of phase information for human genomics
R Tewhey, V Bansal, A Torkamani, EJ Topol, NJ Schork
Nature Reviews Genetics 12 (3), 215-223, 2011
3722011
HapCUT: an efficient and accurate algorithm for the haplotype assembly problem
V Bansal, V Bafna
Bioinformatics 24 (16), i153-i159, 2008
3482008
Whole-genome haplotype reconstruction using proximity-ligation and shotgun sequencing
S Selvaraj, J R Dixon, V Bansal, B Ren
Nature biotechnology 31 (12), 1111-1118, 2013
3402013
HapCUT2: robust and accurate haplotype assembly for diverse sequencing technologies
P Edge, V Bafna, V Bansal
Genome research 27 (5), 801-812, 2017
3362017
A statistical method for the detection of variants from next-generation resequencing of DNA pools
V Bansal
Bioinformatics 26 (12), i318-i324, 2010
2272010
An MCMC algorithm for haplotype assembly from whole-genome sequence data
V Bansal, AL Halpern, N Axelrod, V Bafna
Genome research 18 (8), 1336-1346, 2008
1742008
Accurate detection and genotyping of SNPs utilizing population sequencing data
V Bansal, O Harismendy, R Tewhey, SS Murray, NJ Schork, EJ Topol, ...
Genome research 20 (4), 537-545, 2010
1302010
A covering method for detecting genetic associations between rare variants and common phenotypes
G Bhatia, V Bansal, O Harismendy, NJ Schork, EJ Topol, K Frazer, ...
PLoS computational biology 6 (10), e1000954, 2010
1152010
Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals
V Bansal, J Gassenhuber, T Phillips, G Oliveira, R Harbaugh, N Villarasa, ...
BMC medicine 15, 1-14, 2017
1032017
Evidence for large inversion polymorphisms in the human genome from HapMap data
V Bansal, A Bashir, V Bafna
Genome research 17 (2), 219-230, 2007
992007
A fundamental decomposition theory for phylogenetic networks and incompatible characters
D Gusfield, V Bansal
Research in Computational Molecular Biology: 9th Annual International …, 2005
902005
Zika virus infection reprograms global transcription of host cells to allow sustained infection
SK Tiwari, J Dang, Y Qin, G Lichinchi, V Bansal, TM Rana
Emerging microbes & infections 6 (1), 1-10, 2017
832017
Evidence for the role of EP HX2 gene variants in anorexia nervosa
SV Zeeland, CS Bloss, R Tewhey, V Bansal, A Torkamani, O Libiger, ...
Molecular psychiatry 19 (6), 724-732, 2014
822014
Efficient and cost effective population resequencing by pooling and in-solution hybridization
V Bansal, R Tewhey, EM LeProust, NJ Schork
PloS one 6 (3), e18353, 2011
822011
Ultraaccurate genome sequencing and haplotyping of single human cells
WK Chu, P Edge, HS Lee, V Bansal, V Bafna, X Huang, K Zhang
Proceedings of the National Academy of Sciences 114 (47), 12512-12517, 2017
542017
Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations
V Bansal, O Libiger
BMC bioinformatics 16, 1-11, 2015
542015
A decomposition theory for phylogenetic networks and incompatible characters
D Gusfield, V Bansal, V Bafna, YS Song
Journal of Computational Biology 14 (10), 1247-1272, 2007
532007
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