Hasil Pencarian - Vincent Ferretti

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  1. 1
    Evaluation of alignment algorithms for discovery and identification of pathogens using RNA-Seq.

    Evaluation of alignment algorithms for discovery and identification of pathogens using RNA-Seq. oleh Ivan Borozan, Stuart N Watt, Vincent Ferretti

    Diterbitkan 2013-01-01
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  2. 2
    Fostering population-based cohort data discovery: The Maelstrom Research cataloguing toolkit.

    Fostering population-based cohort data discovery: The Maelstrom Research cataloguing toolkit. oleh Julie Bergeron, Dany Doiron, Yannick Marcon, Vincent Ferretti, Isabel Fortier

    Diterbitkan 2018-01-01
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  3. 3
    The Dockstore: enabling modular, community-focused sharing of Docker-based genomics tools and workflows [version 1; referees: 2 approved]

    The Dockstore: enabling modular, community-focused sharing of Docker-based genomics tools and workflows [version 1; referees: 2 approved] oleh Brian D. O'Connor, Denis Yuen, Vincent Chung, Andrew G. Duncan, Xiang Kun Liu, Janice Patricia, Benedict Paten, Lincoln Stein, Vincent Ferretti

    Diterbitkan 2017-01-01
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  4. 4
    P832: Discovering phenotype-gene correlations using Variant WorkBench

    P832: Discovering phenotype-gene correlations using Variant WorkBench oleh Yiran Guo, Qi Li, Jared Rozowsky, Jeremy Costanza, Michele Mattioni, Jean-Philippe Thibert, Miguel Brown, David Higgins, Yuankun Zhu, Allison Heath, Adam Resnick, Vincent Ferretti

    Diterbitkan 2024-01-01
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  5. 5
    Germline EPHB2 receptor variants in familial colorectal cancer.

    Germline EPHB2 receptor variants in familial colorectal cancer. oleh George Zogopoulos, Claus Jorgensen, Julinor Bacani, Alexandre Montpetit, Pierre Lepage, Vincent Ferretti, Lauren Chad, Subani Selvarajah, Brent Zanke, Thomas J Hudson, Tony Pawson, Steven Gallinger

    Diterbitkan 2008-08-01
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  6. 6
    P597: All for One Clinical Genomics Network: Linking Canadian diagnostic laboratories to share genome-wide sequencing data to support rare disease diagnosis

    P597: All for One Clinical Genomics Network: Linking Canadian diagnostic laboratories to share genome-wide sequencing data to support rare disease diagnosis oleh E. Magda Price, Meredith Gillespie, Caitlin Chisholm, Ruben Attali, Talia Silver, Anna Szuto, GSO Study Team, Jacques Michaud, Dennis Bulman, Jordan Lerner-Ellis, Ma'n Zawati, Vincent Ferretti, Francois Bernier, Christian Marshall, Kym Boycott

    Diterbitkan 2024-01-01
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  7. 7
    A user guide for the online exploration and visualization of PCAWG data

    A user guide for the online exploration and visualization of PCAWG data oleh Mary J. Goldman, Junjun Zhang, Nuno A. Fonseca, Isidro Cortés-Ciriano, Qian Xiang, Brian Craft, Elena Piñeiro-Yáñez, Brian D. O’Connor, Wojciech Bazant, Elisabet Barrera, Alfonso Muñoz-Pomer, Robert Petryszak, Anja Füllgrabe, Fatima Al-Shahrour, Maria Keays, David Haussler, John N. Weinstein, Wolfgang Huber, Alfonso Valencia, Peter J. Park, Irene Papatheodorou, Jingchun Zhu, Vincent Ferretti, Miguel Vazquez

    Diterbitkan 2020-07-01
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