Rezultati - 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 od Jiménez-Barrón, Laura T., O'Rawe, Jason A., Wu, Yiyang, Yoon, Margaret, Fang, Han, Iossifov, Ivan, Lyon, Gholson J.

    Izdano 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 od O’Rawe, Jason A., Fang, Han, Rynearson, Shawn, Robison, Reid, Kiruluta, Edward S., Higgins, Gerald, Eilbeck, Karen, Reese, Martin G., Lyon, Gholson J.

    Izdano 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 od 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.

    Izdano 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 od 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

    Izdano 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 od 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

    Izdano 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 od 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

    Izdano 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 od 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

    Izdano 2016
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