Searching journal content for Vikas Bansal in author.

Displaying results 1-7 of 7
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  1. Erratum: Erratum: Ultralow-input single-tube linked-read library method enables short-read second-generation sequencing systems to routinely generate highly accurate and economical long-range sequencing information
    • Zhoutao Chen,
    • Long Pham,
    • Tsai-Chin Wu,
    • Guoya Mo,
    • Yu Xia,
    • Peter L. Chang,
    • Devin Porter,
    • Tan Phan,
    • Huu Che,
    • Hao Tran,
    • Vikas Bansal,
    • Justin Shaffer,
    • Pedro Belda-Ferre,
    • Greg Humphrey,
    • Rob Knight,
    • Pavel Pevzner,
    • Son Pham,
    • Yong Wang,
    • and Ming Lei
    Genome Res. May 2021 31: 934; doi:10.1101/gr.275614.121
    OPEN ACCESS ARTICLE
  2. Method: Ultralow-input single-tube linked-read library method enables short-read second-generation sequencing systems to routinely generate highly accurate and economical long-range sequencing information
    • Zhoutao Chen,
    • Long Pham,
    • Tsai-Chin Wu,
    • Guoya Mo,
    • Yu Xia,
    • Peter L. Chang,
    • Devin Porter,
    • Tan Phan,
    • Huu Che,
    • Hao Tran,
    • Vikas Bansal,
    • Justin Shaffer,
    • Pedro Belda-Ferre,
    • Greg Humphrey,
    • Rob Knight,
    • Pavel Pevzner,
    • Son Pham,
    • Yong Wang,
    • and Ming Lei
    Genome Res. June 2020 30: 898-909; Published in Advance June 15, 2020, doi:10.1101/gr.260380.119
  3. Method: Targeted genotyping of variable number tandem repeats with adVNTR
    • Mehrdad Bakhtiari,
    • Sharona Shleizer-Burko,
    • Melissa Gymrek,
    • Vikas Bansal,
    • and Vineet Bafna
    Genome Res. November 2018 28: 1709-1719; Published in Advance October 23, 2018, doi:10.1101/gr.235119.118
  4. Method: HapCUT2: robust and accurate haplotype assembly for diverse sequencing technologies
    • Peter Edge,
    • Vineet Bafna,
    • and Vikas Bansal
    Genome Res. May 2017 27: 801-812; Published in Advance December 9, 2016, doi:10.1101/gr.213462.116
  5. Resource: Accurate detection and genotyping of SNPs utilizing population sequencing data
    • Vikas Bansal,
    • Olivier Harismendy,
    • Ryan Tewhey,
    • Sarah S. Murray,
    • Nicholas J. Schork,
    • Eric J. Topol,
    • and Kelly A. Frazer
    Genome Res. April 2010 20: 537-545; Published in Advance February 11, 2010, doi:10.1101/gr.100040.109
  6. Methods: An MCMC algorithm for haplotype assembly from whole-genome sequence data
    • Vikas Bansal,
    • Aaron L. Halpern,
    • Nelson Axelrod,
    • and Vineet Bafna
    Genome Res. August 2008 18: 1336-1346; doi:10.1101/gr.077065.108
  7. Methods: Evidence for large inversion polymorphisms in the human genome from HapMap data
    • Vikas Bansal,
    • Ali Bashir,
    • and Vineet Bafna
    Genome Res. February 2007 17: 219-230; Published in Advance December 21, 2006, doi:10.1101/gr.5774507
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