Found: 4

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  • Validation and assessment of variant calling pipelines for next-generation sequencing.

    Published in:
    Human Genomics, 2014, v. 8, n. 1, p. 14, doi. 10.1186/1479-7364-8-14
    By:
    • Pirooznia, Mehdi Pirooznia;
    • Kramer, Melissa;
    • Parla, Jennifer;
    • Goes, Fernando S;
    • Potash, James B;
    • McCombie, W Richard;
    • Zandi, Peter P
    Publication type:
    Article

  • Exome Sequencing of Familial Bipolar Disorder.

    Published in:
    2016
    By:
    • Goes, Fernando S.;
    • Pirooznia, Mehdi;
    • Parla, Jennifer S.;
    • Kramer, Melissa;
    • Ghiban, Elena;
    • Mavruk, Senem;
    • Yun-Ching Chen;
    • Monson, Eric T.;
    • Willour, Virginia L.;
    • Karchin, Rachel;
    • Flickinger, Matthew;
    • Locke, Adam E.;
    • Levy, Shawn E.;
    • Scott, Laura J.;
    • Boehnke, Michael;
    • Stahl, Eli;
    • Moran, Jennifer L.;
    • Hultman, Christina M.;
    • Landén, Mikael;
    • Purcell, Shaun M.
    Publication type:
    journal article

  • A comparative analysis of exome capture.

    Published in:
    Genome Biology, 2011, v. 12, n. 9, p. 1, doi. 10.1186/gb-2011-12-9-r97
    By:
    • Parla, Jennifer S.;
    • Iossifov, Ivan;
    • Grabill, Ian;
    • Spector, Mona S.;
    • Kramer, Melissa;
    • Richard McCombie, W.
    Publication type:
    Article

  • A Hybrid Likelihood Model for Sequence-Based Disease Association Studies.

    Published in:
    PLoS Genetics, 2013, v. 9, n. 1, p. 1, doi. 10.1371/journal.pgen.1003224
    By:
    • Yun-Ching Chen;
    • Carter, Hannah;
    • Parla, Jennifer;
    • Kramer, Melissa;
    • Goes, Fernando S.;
    • Pirooznia, Mehdi;
    • Zandi, Peter P.;
    • McCombie, W. Richard;
    • Potash, James B.;
    • Karchin, Rachel
    Publication type:
    Article