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Method

TITAN: inference of copy number architectures in clonal cell populations from tumor whole-genome sequence data

  • First Published July 24, 2014
Method

nFuse: Discovery of complex genomic rearrangements in cancer using high-throughput sequencing

  • First Published June 28, 2012
Resource

Simultaneous structural variation discovery among multiple paired-end sequenced genomes

  • First Published November 2, 2011
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