Rezultaty - Virginie Saillour

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  1. 1
    SNooPer: a machine learning-based method for somatic variant identification from low-pass next-generation sequencing

    SNooPer: a machine learning-based method for somatic variant identification from low-pass next-generation sequencing od Jean-François Spinella, Pamela Mehanna, Ramón Vidal, Virginie Saillour, Pauline Cassart, Chantal Richer, Manon Ouimet, Jasmine Healy, Daniel Sinnett

    Wydane 2016
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  2. 2
    Integration of High-Resolution Methylome and Transcriptome Analyses to Dissect Epigenomic Changes in Childhood Acute Lymphoblastic Leukemia

    Integration of High-Resolution Methylome and Transcriptome Analyses to Dissect Epigenomic Changes in Childhood Acute Lymphoblastic Leukemia od Stephan Busche, Bing Ge, Ramón Vidal, Jean-François Spinella, Virginie Saillour, Chantal Richer, Jasmine Healy, Shu‐Huang Chen, Arnaud Droit, Daniel Sinnett, Tomi Pastinen

    Wydane 2013
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    Artigo
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  3. 3
    Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutations

    Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutations od Jean-François Spinella, Pauline Cassart, Chantal Richer, Virginie Saillour, Manon Ouimet, Sylvie Langlois, Pascal St-Onge, Thomas Sontag, Jasmine Healy, Mark D. Minden, Daniel Sinnett

    Wydane 2016
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  4. 4
    Rare allelic forms of <i>PRDM9</i> associated with childhood leukemogenesis

    Rare allelic forms of <i>PRDM9</i> associated with childhood leukemogenesis od Julie Hussin, Daniel Sinnett, Ferrán Casals, Youssef Idaghdour, Vanessa Bruat, Virginie Saillour, Jasmine Healy, Jean‐Christophe Grenier, Thibault de Malliard, Stephan Busche, Jean-François Spinella, Mathieu Larivière, Greg Gibson, Anna Andersson, Linda Holmfeldt, Jing Ma, Lei Wei, Jinghui Zhang, Grégor Andelfinger, James R. Downing, Charles G. Mullighan, Philip Awadalla

    Wydane 2012
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  5. 5
    Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans

    Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans od Ferrán Casals, Alan Hodgkinson, Julie Hussin, Youssef Idaghdour, Vanessa Bruat, Thibault de Maillard, Jean‐Christophe Grenier, Elias Gbeha, Fadi F. Hamdan, Simon Girard, Jean-François Spinella, Mathieu Larivière, Virginie Saillour, Jasmine Healy, Isabel Fernández, Daniel Sinnett, Jacques L. Michaud, Guy A. Rouleau, Élie Haddad, Françoise Le Deist, Philip Awadalla

    Wydane 2013
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