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ORCIDVikas Bansal 0001
Person information
- affiliation: University of California, San Diego, Department of Pediatrics, School of Medicine, La Jolla, CA, USA
- affiliation: Scripps Translational Science Institute, Department of Molecular and Experimental Medicine, Scripps Genomic Medicine, La Jolla, CA, USA
- affiliation (PhD 2008): University of California, San Diego, Department of Computer Science and Engineering, CA, USA
Other persons with the same name
- Vikas Bansal — disambiguation page
- Vikas Bansal 0002 — FU Berlin, Germany
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2020 – today
- 2023
[j13]Timofey Prodanov
, Vikas Bansal:
A multilocus approach for accurate variant calling in low-copy repeats using whole-genome sequencing. Bioinform. 39(Supplement-1): 279-287 (2023)
2010 – 2019
- 2019
- [j12]Vikas Bansal:
Integrating read-based and population-based phasing for dense and accurate haplotyping of individual genomes. Bioinform. 35(14): i242-i248 (2019) - 2018
- [j11]Vikas Bansal:
An accurate algorithm for the detection of DNA fragments from dilution pool sequencing experiments. Bioinform. 34(1): 155-162 (2018) - [c6]Mehrdad Bakhtiari, Sharona Shleizer-Burko, Melissa Gymrek, Vikas Bansal, Vineet Bafna:
Targeted Genotyping of Variable Number Tandem Repeats with AdVNTR. RECOMB 2018: 243-244 - 2017
- [j10]Vikas Bansal:
A computational method for estimating the PCR duplication rate in DNA and RNA-seq experiments. BMC Bioinform. 18(S-3): 113-123 (2017) - 2016
- [j9]Vikas Bansal, Ondrej Libiger:
A statistical method for the detection of variants from next-generation resequencing of DNA poolsA probabilistic method for the detection and genotyping of small indels from population-scale sequence data. Bioinform. 32(20): 3213 (2016) - 2015
- [j8]Vikas Bansal, Ondrej Libiger:
Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations. BMC Bioinform. 16: 4:1-4:11 (2015) - 2011
- [j7]Vikas Bansal, Ondrej Libiger:
A probabilistic method for the detection and genotyping of small indels from population-scale sequence data. Bioinform. 27(15): 2047-2053 (2011) - [j6]Christine Lo, Ali Bashir, Vikas Bansal, Vineet Bafna:
Strobe sequence design for haplotype assembly. BMC Bioinform. 12(S-1): S24 (2011) - [c5]Vikas Bansal, Ondrej Libiger, Ali Torkamani, Nicholas J. Schork:
An Application and Empirical Comparison of Statistical Analysis Methods for Associating Rare Variants to a Complex Phenotype. Pacific Symposium on Biocomputing 2011: 76-87 - 2010
- [j5]Vikas Bansal:
A statistical method for the detection of variants from next-generation resequencing of DNA pools. Bioinform. 26(12): 318-324 (2010) - [j4]Gaurav Bhatia, Vikas Bansal, Olivier Harismendy, Nicholas J. Schork, Eric J. Topol, Kelly A. Frazer, Vineet Bafna:
A Covering Method for Detecting Genetic Associations between Rare Variants and Common Phenotypes. PLoS Comput. Biol. 6(10) (2010)
2000 – 2009
- 2008
- [b1]Vikas Bansal:
Computational methods for analyzing human genetic variation. University of California, San Diego, USA, 2008 - [c4]Vikas Bansal, Vineet Bafna:
HapCUT: an efficient and accurate algorithm for the haplotype assembly problem. ECCB 2008: 153-159 - 2007
- [j3]Dan Gusfield, Vikas Bansal, Vineet Bafna, Yun S. Song:
A Decomposition Theory for Phylogenetic Networks and Incompatible Characters. J. Comput. Biol. 14(10): 1247-1272 (2007) - 2006
- [j2]Vineet Bafna, Vikas Bansal:
Inference about Recombination from Haplotype Data: Lower Bounds and Recombination Hotspots. J. Comput. Biol. 13(2): 501-521 (2006) - 2005
- [c3]Dan Gusfield, Vikas Bansal:
A Fundamental Decomposition Theory for Phylogenetic Networks and Incompatible Characters. RECOMB 2005: 217-232 - [c2]Vineet Bafna, Vikas Bansal:
Improved Recombination Lower Bounds for Haplotype Data. RECOMB 2005: 569-584 - 2004
- [j1]Vineet Bafna, Vikas Bansal:
The Number of Recombination Events in a Sample History: Conflict Graph and Lower Bounds. IEEE ACM Trans. Comput. Biol. Bioinform. 1(2): 78-90 (2004) - [c1]Vikas Bansal, Friedhelm Meyer auf der Heide, Christian Sohler:
Labeling Smart Dust. ESA 2004: 77-88
Coauthor Index
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