Search Results - "Stewart, Chip"

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    SvABA: genome-wide detection of structural variants and indels by local assembly by Wala, Jeremiah A, Bandopadhayay, Pratiti, Greenwald, Noah F, O'Rourke, Ryan, Sharpe, Ted, Stewart, Chip, Schumacher, Steve, Li, Yilong, Weischenfeldt, Joachim, Yao, Xiaotong, Nusbaum, Chad, Campbell, Peter, Getz, Gad, Meyerson, Matthew, Zhang, Cheng-Zhong, Imielinski, Marcin, Beroukhim, Rameen

    Published in Genome research (01-04-2018)
    “…Structural variants (SVs), including small insertion and deletion variants (indels), are challenging to detect through standard alignment-based variant calling…”
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    Journal Article
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    Somatic retrotransposition in human cancer revealed by whole-genome and exome sequencing by Helman, Elena, Lawrence, Michael S, Stewart, Chip, Sougnez, Carrie, Getz, Gad, Meyerson, Matthew

    Published in Genome research (01-07-2014)
    “…Retrotransposons constitute a major source of genetic variation, and somatic retrotransposon insertions have been reported in cancer. Here, we applied…”
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    Journal Article
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    MOSAIK: a hash-based algorithm for accurate next-generation sequencing short-read mapping by Lee, Wan-Ping, Stromberg, Michael P, Ward, Alistair, Stewart, Chip, Garrison, Erik P, Marth, Gabor T

    Published in PloS one (05-03-2014)
    “…MOSAIK is a stable, sensitive and open-source program for mapping second and third-generation sequencing reads to a reference genome. Uniquely among current…”
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    Journal Article
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    DeTiN: overcoming tumor-in-normal contamination by Taylor-Weiner, Amaro, Stewart, Chip, Giordano, Thomas, Miller, Mendy, Rosenberg, Mara, Macbeth, Alyssa, Lennon, Niall, Rheinbay, Esther, Landau, Dan-Avi, Wu, Catherine J., Getz, Gad

    Published in Nature methods (01-07-2018)
    “…Comparison of sequencing data from a tumor sample with data from a matched germline control is a key step for accurate detection of somatic mutations…”
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    Journal Article
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