Bansal V, Boehm BO, et al. Identification of a rare missense mutation in the WFS1 gene that causes a mild form of Wolfram syndrome. in preparation
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, Gassenhuber J, Phillips T, ..., Boehm BO. Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6,888 individuals. BMC Medicine, 2017 Commentary in BMC Medicine
Chu WK, Edge P, Lee HS, Bansal V, Bafna V, Huang X, Zhang K. Ultra-Accurate Genome Sequencing And Haplotyping Of Single Human Cells. published in PNAS, October 2017.
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.