Search Results - Steinberg, Karyn M.

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  1. 1
    Complete Haplotype Sequence of the Human Immunoglobulin Heavy-Chain Variable, Diversity, and Joining Genes and Characterization of Allelic and Copy-Number Variation

    Complete Haplotype Sequence of the Human Immunoglobulin Heavy-Chain Variable, Diversity, and Joining Genes and Characterization of Allelic and Copy-Number Variation by Watson, Corey T., Steinberg, Karyn M., Huddleston, John, Warren, Rene L., Malig, Maika, Schein, Jacqueline, Willsey, A. Jeremy, Joy, Jeffrey B., Scott, Jamie K., Graves, Tina A., Wilson, Richard K., Holt, Robert A., Eichler, Evan E., Breden, Felix

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  2. 2
    Exome-Based Mapping and Variant Prioritization for Inherited Mendelian Disorders

    Exome-Based Mapping and Variant Prioritization for Inherited Mendelian Disorders by Koboldt, Daniel C., Larson, David E., Sullivan, Lori S., Bowne, Sara J., Steinberg, Karyn M., Churchill, Jennifer D., Buhr, Aimee C., Nutter, Nathan, Pierce, Eric A., Blanton, Susan H., Weinstock, George M., Wilson, Richard K., Daiger, Stephen P.

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  3. 3
    Combining Microarray‐based Genomic Selection (MGS) with the Illumina Genome Analyzer Platform to Sequence Diploid Target Regions

    Combining Microarray‐based Genomic Selection (MGS) with the Illumina Genome Analyzer Platform to Sequence Diploid Target Regions by Okou, David T., Locke, Adam E., Steinberg, Karyn M., Hagen, Katie, Athri, Prashanth, Shetty, Amol C., Patel, Viren, Zwick, Michael E.

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  4. 4
    SeqAnt: a web service to rapidly identify and annotate DNA sequence variations

    SeqAnt: a web service to rapidly identify and annotate DNA sequence variations by Shetty, Amol Carl, Athri, Prashanth, Mondal, Kajari, Horner, Vanessa L, Steinberg, Karyn Meltz, Patel, Viren, Caspary, Tamara, Cutler, David J, Zwick, Michael E

    Published in BMC bioinformatics
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