Edge P, Bansal V. Integrated genotyping and phasing of SNVs from error-prone long read data. In preparation.
Bansal V, Boehm BO, Darvasi A. Identification of a rare missense mutation in the WFS1 gene that causes a mild form of Wolfram syndrome and is associated with risk of type 2 diabetes in Ashkenazi Jewish. accepted for publication in Diabetologica.
Bakhtiari M, Shleizer-Burko S, Gymrek M, Bansal V, Bafna V. Targeted Genotyping of Variable Number Tandem Repeats with
adVNTR. bioarxiv preprint accepted for presentation at RECOMB 2018
Bansal V. A computational method for estimating the PCR duplication rate in high-throughput DNA sequencing experiments. accepted for presentation at APBC 2017 and published in BMC Bioinformatics, March 2017. PDF[software link][SLIDES]
Levy S, Sutton G, Ng PC, Feuk L, Halpern AL, Walenz BP, Axelrod N, Huang J, Kirkness EF, Denisov G, Lin Y, MacDonald JR, Pang AW, Shago M, Stockwell TB, Tsiamouri A, Bafna V, Bansal V, Kravitz SA, Busam DA, Beeson KY, McIntosh TC, Remington KA, Abril JF, Gill J, Borman J, Rogers YH, Frazier ME, Scherer SW, Strausberg RL, Venter JC. The diploid genome sequence of an individual human. PLoS Biol. 2007 Sep 4;5(10):e254.