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      SomaticSniper: identification of somatic point mutations in whole genome sequencing data.

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          Abstract

          The sequencing of tumors and their matched normals is frequently used to study the genetic composition of cancer. Despite this fact, there remains a dearth of available software tools designed to compare sequences in pairs of samples and identify sites that are likely to be unique to one sample.

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          Author and article information

          Journal
          Bioinformatics
          Bioinformatics (Oxford, England)
          Oxford University Press (OUP)
          1367-4811
          1367-4803
          Feb 01 2012
          : 28
          : 3
          Affiliations
          [1 ] The Genome Institute, Washington University, St Louis, MO 63108, USA. delarson@wustl.edu
          Article
          btr665
          10.1093/bioinformatics/btr665
          3268238
          22155872
          2a445630-bbae-4bca-b0ff-860c8afd14a2
          History

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