检索结果 - O'Rawe, Jason

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  1. 1
    Genome-wide variant analysis of simplex autism families with an integrative clinical-bioinformatics pipeline

    Genome-wide variant analysis of simplex autism families with an integrative clinical-bioinformatics pipeline 由 Jiménez-Barrón, Laura T., O'Rawe, Jason A., Wu, Yiyang, Yoon, Margaret, Fang, Han, Iossifov, Ivan, Lyon, Gholson J.

    出版 2015
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  2. 2
    Integrating precision medicine in the study and clinical treatment of a severely mentally ill person

    Integrating precision medicine in the study and clinical treatment of a severely mentally ill person 由 O’Rawe, Jason A., Fang, Han, Rynearson, Shawn, Robison, Reid, Kiruluta, Edward S., Higgins, Gerald, Eilbeck, Karen, Reese, Martin G., Lyon, Gholson J.

    出版 2013
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  3. 3
    Accurate detection of de novo and transmitted indels within exome-capture data using micro-assembly

    Accurate detection of de novo and transmitted indels within exome-capture data using micro-assembly 由 Narzisi, Giuseppe, O'Rawe, Jason A., Iossifov, Ivan, Fang, Han, Lee, Yoon-ha, Wang, Zihua, Wu, Yiyang, Lyon, Gholson J., Wigler, Michael, Schatz, Michael C.

    出版 2014
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  4. 4
    Reducing INDEL calling errors in whole genome and exome sequencing data

    Reducing INDEL calling errors in whole genome and exome sequencing data 由 Fang, Han, Wu, Yiyang, Narzisi, Giuseppe, O’Rawe, Jason A, Barrón, Laura T Jimenez, Rosenbaum, Julie, Ronemus, Michael, Iossifov, Ivan, Schatz, Michael C, Lyon, Gholson J

    出版 2014
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  5. 5
    Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

    Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing 由 O'Rawe, Jason, Jiang, Tao, Sun, Guangqing, Wu, Yiyang, Wang, Wei, Hu, Jingchu, Bodily, Paul, Tian, Lifeng, Hakonarson, Hakon, Johnson, W Evan, Wei, Zhi, Wang, Kai, Lyon, Gholson J

    出版 2013
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  6. 6
    SeqHBase: a big data toolset for family based sequencing data analysis

    SeqHBase: a big data toolset for family based sequencing data analysis 由 He, Min, Person, Thomas N, Hebbring, Scott J, Heinzen, Ethan, Ye, Zhan, Schrodi, Steven J, McPherson, Elizabeth W, Lin, Simon M, Peissig, Peggy L, Brilliant, Murray H, O'Rawe, Jason, Robison, Reid J, Lyon, Gholson J, Wang, Kai

    出版 2015
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  7. 7
    Indel variant analysis of short-read sequencing data with Scalpel

    Indel variant analysis of short-read sequencing data with Scalpel 由 Fang, Han, Bergmann, Ewa A, Arora, Kanika, Vacic, Vladimir, Zody, Michael C, Iossifov, Ivan, O’Rawe, Jason A, Wu, Yiyang, Barron, Laura T Jimenez, Rosenbaum, Julie, Ronemus, Michael, Lee, Yoon-ha, Wang, Zihua, Dikoglu, Esra, Jobanputra, Vaidehi, Lyon, Gholson J, Wigler, Michael, Schatz, Michael C, Narzisi, Giuseppe

    出版 2016
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