Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS.
Anne-Katrin EmdeMarcel H. SchulzDavid WeeseRuping SunMartin VingronVera M. KalscheuerStefan A. HaasKnut ReinertPublished in: Bioinform. (2012)
Keyphrases
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