• DocumentCode
    2039015
  • Title

    A comparative study of methods for detecting small somatic variants in disease-normal paired next generation sequencing data

  • Author

    Qingguo Wang ; Zhongming Zhao

  • Author_Institution
    Sch. of Med., Dept. of Biomed. Inf., Vanderbilt Univ., Nashville, TN, USA
  • fYear
    2012
  • fDate
    2-4 Dec. 2012
  • Firstpage
    38
  • Lastpage
    41
  • Abstract
    While high-throughput next generation sequencing technologies are rapidly approaching maturity, computational tools for variant calling have significant room for improvement. The recently emerged computational methods typically compare a disease sample directly with its matched control in order to improve the accuracy of variant calling and search disease specific mutations. In this paper, we performed a comparative study of five methods, JointSNVMix, SAMtools, SomaticSniper, Strelka and VarScan, for simultaneous detection of small somatic variants from disease-normal pairs. This paper evaluates the sensitivity and false discovery rate of these methods, aiming to provide guidelines for users and algorithm developers. The computational efficiency and other issues are also explored.
  • Keywords
    biology computing; diseases; genetics; genomics; macromolecules; molecular biophysics; molecular configurations; polymorphism; sensitivity; JointSNVMix; SAMtools; SomaticSniper; Strelka; VarScan; algorithm developers; computational methods; disease-normal paired next generation sequencing data; disease-normal pairs; false discovery rate; genomics; high-throughput next generation sequencing technology; matched control; search disease specific mutations; sensitivity; single-nucleotide polymorphism; small somatic variant detection; computational tool; deletion; insertion; next generation sequencing; single-nucleotide polymorphism; variant call;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Genomic Signal Processing and Statistics, (GENSIPS), 2012 IEEE International Workshop on
  • Conference_Location
    Washington, DC
  • ISSN
    2150-3001
  • Print_ISBN
    978-1-4673-5234-5
  • Type

    conf

  • DOI
    10.1109/GENSIPS.2012.6507721
  • Filename
    6507721