Labeling Smart Dust. - Vikas Bansal 001; Friedhelm Meyer auf der Heide; Christian Sohler (ESA, 2004)

The Number of Recombination Events in a Sample History: Conflict Graph and Lower Bounds. - Vineet Bafna; Vikas Bansal 001 (IEEE ACM Trans. Comput. Biol. Bioinform., 2004)

Improved Recombination Lower Bounds for Haplotype Data. - Vineet Bafna; Vikas Bansal 001 (RECOMB, 2005)

A Fundamental Decomposition Theory for Phylogenetic Networks and Incompatible Characters. - Dan Gusfield; Vikas Bansal 001 (RECOMB, 2005)

Inference about Recombination from Haplotype Data: Lower Bounds and Recombination Hotspots. - Vineet Bafna; Vikas Bansal 001 (J. Comput. Biol., 2006)

A Decomposition Theory for Phylogenetic Networks and Incompatible Characters. - Dan Gusfield; Vikas Bansal 001; Vineet Bafna; Yun S. Song (J. Comput. Biol., 2007)

HapCUT: an efficient and accurate algorithm for the haplotype assembly problem. - Vikas Bansal 001; Vineet Bafna (ECCB, 2008)

Computational methods for analyzing human genetic variation. - Vikas Bansal 001 (2008)

A statistical method for the detection of variants from next-generation resequencing of DNA pools. - Vikas Bansal 001 (Bioinform., 2010)

A Covering Method for Detecting Genetic Associations between Rare Variants and Common Phenotypes. - Gaurav Bhatia; Vikas Bansal 001; Olivier Harismendy; Nicholas J. Schork; Eric J. Topol; Kelly A. Frazer; Vineet Bafna (PLoS Comput. Biol., 2010)

An Application and Empirical Comparison of Statistical Analysis Methods for Associating Rare Variants to a Complex Phenotype. - Vikas Bansal 001; Ondrej Libiger; Ali Torkamani; Nicholas J. Schork (Pacific Symposium on Biocomputing, 2011)

A probabilistic method for the detection and genotyping of small indels from population-scale sequence data. - Vikas Bansal 001; Ondrej Libiger (Bioinform., 2011)

Strobe sequence design for haplotype assembly. - Christine Lo; Ali Bashir; Vikas Bansal 001; Vineet Bafna (BMC Bioinform., 2011)

Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations. - Vikas Bansal 001; Ondrej Libiger (BMC Bioinform., 2015)

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. - Vikas Bansal 001; Ondrej Libiger (Bioinform., 2016)

A computational method for estimating the PCR duplication rate in DNA and RNA-seq experiments. - Vikas Bansal 001 (BMC Bioinform., 2017)

Targeted Genotyping of Variable Number Tandem Repeats with AdVNTR. - Mehrdad Bakhtiari; Sharona Shleizer-Burko; Melissa Gymrek; Vikas Bansal 001; Vineet Bafna (RECOMB, 2018)

An accurate algorithm for the detection of DNA fragments from dilution pool sequencing experiments. - Vikas Bansal 001 (Bioinform., 2018)

Integrating read-based and population-based phasing for dense and accurate haplotyping of individual genomes. - Vikas Bansal 001 (Bioinform., 2019)

A multilocus approach for accurate variant calling in low-copy repeats using whole-genome sequencing. - Timofey Prodanov; Vikas Bansal 001 (Bioinform., 2023)

Analysis of targeted and whole genome sequencing of PacBio HiFi reads for a comprehensive genotyping of gene-proximal and phenotype-associated Variable Number Tandem Repeats. - Sara Javadzadeh; Aaron Adamson; Jonghun Park; Se-Young Jo; Yuan-Chun Ding; Mehrdad Bakhtiari; Vikas Bansal 001; Susan L. Neuhausen; Vineet Bafna (PLoS Comput. Biol., 2025)