Vikas Bansal - RankMe

21 papers A 1B 3C 1Misc 1Journal 14

Year	Rank	Type	Title / Venue / Authors
2025	J	`jnl`	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. PLoS Comput. Biol. Sara Javadzadeh, Aaron Adamson, Jonghun Park, Se-Young Jo, Yuan-Chun Ding, Mehrdad Bakhtiari, Vikas Bansal, Susan L. Neuhausen, Vineet Bafna
2023	J	`jnl`	A multilocus approach for accurate variant calling in low-copy repeats using whole-genome sequencing. Bioinform. Timofey Prodanov, Vikas Bansal
2019	J	`jnl`	Integrating read-based and population-based phasing for dense and accurate haplotyping of individual genomes. Bioinform. Vikas Bansal
2018	J	`jnl`	An accurate algorithm for the detection of DNA fragments from dilution pool sequencing experiments. Bioinform. Vikas Bansal
2018	B	`conf`	Targeted Genotyping of Variable Number Tandem Repeats with AdVNTR. RECOMB Mehrdad Bakhtiari, Sharona Shleizer-Burko, Melissa Gymrek, Vikas Bansal, Vineet Bafna
2017	J	`jnl`	A computational method for estimating the PCR duplication rate in DNA and RNA-seq experiments. BMC Bioinform. Vikas Bansal
2016	J	`jnl`	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. Vikas Bansal, Ondrej Libiger
2015	J	`jnl`	Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations. BMC Bioinform. Vikas Bansal, Ondrej Libiger
2011	J	`jnl`	A probabilistic method for the detection and genotyping of small indels from population-scale sequence data. Bioinform. Vikas Bansal, Ondrej Libiger
2011	Misc	`conf`	An Application and Empirical Comparison of Statistical Analysis Methods for Associating Rare Variants to a Complex Phenotype. Pacific Symposium on Biocomputing Vikas Bansal, Ondrej Libiger, Ali Torkamani, Nicholas J. Schork
2011	J	`jnl`	Strobe sequence design for haplotype assembly. BMC Bioinform. Christine Lo, Ali Bashir, Vikas Bansal, Vineet Bafna
2010	J	`jnl`	A Covering Method for Detecting Genetic Associations between Rare Variants and Common Phenotypes. PLoS Comput. Biol. Gaurav Bhatia, Vikas Bansal, Olivier Harismendy, Nicholas J. Schork, Eric J. Topol, Kelly A. Frazer, Vineet Bafna
2010	J	`jnl`	A statistical method for the detection of variants from next-generation resequencing of DNA pools. Bioinform. Vikas Bansal
2008	—	`—`	Computational methods for analyzing human genetic variation. Vikas Bansal
2008	C	`conf`	HapCUT: an efficient and accurate algorithm for the haplotype assembly problem. ECCB Vikas Bansal, Vineet Bafna
2007	J	`jnl`	A Decomposition Theory for Phylogenetic Networks and Incompatible Characters. J. Comput. Biol. Dan Gusfield, Vikas Bansal, Vineet Bafna, Yun S. Song
2006	J	`jnl`	Inference about Recombination from Haplotype Data: Lower Bounds and Recombination Hotspots. J. Comput. Biol. Vineet Bafna, Vikas Bansal
2005	B	`conf`	A Fundamental Decomposition Theory for Phylogenetic Networks and Incompatible Characters. RECOMB Dan Gusfield, Vikas Bansal
2005	B	`conf`	Improved Recombination Lower Bounds for Haplotype Data. RECOMB Vineet Bafna, Vikas Bansal
2004	A	`conf`	Labeling Smart Dust. ESA Vikas Bansal, Friedhelm Meyer auf der Heide, Christian Sohler
2004	J	`jnl`	The Number of Recombination Events in a Sample History: Conflict Graph and Lower Bounds. IEEE ACM Trans. Comput. Biol. Bioinform. Vineet Bafna, Vikas Bansal