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 | 2306 | 2007 |
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 | 564 | 2010 |
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 | 427 | 2016 |
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 | 372 | 2011 |
HapCUT: an efficient and accurate algorithm for the haplotype assembly problem V Bansal, V Bafna Bioinformatics 24 (16), i153-i159, 2008 | 348 | 2008 |
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 | 339 | 2013 |
HapCUT2: robust and accurate haplotype assembly for diverse sequencing technologies P Edge, V Bafna, V Bansal Genome research 27 (5), 801-812, 2017 | 334 | 2017 |
A statistical method for the detection of variants from next-generation resequencing of DNA pools V Bansal Bioinformatics 26 (12), i318-i324, 2010 | 227 | 2010 |
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 | 174 | 2008 |
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 | 130 | 2010 |
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 | 115 | 2010 |
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 | 103 | 2017 |
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 | 99 | 2007 |
A fundamental decomposition theory for phylogenetic networks and incompatible characters D Gusfield, V Bansal Research in Computational Molecular Biology: 9th Annual International …, 2005 | 90 | 2005 |
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 | 83 | 2017 |
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 | 81 | 2014 |
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 | 81 | 2011 |
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 | 54 | 2017 |
Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations V Bansal, O Libiger BMC bioinformatics 16, 1-11, 2015 | 54 | 2015 |
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 | 53 | 2007 |