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, 11:18, 3 November 2011
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− | This page documents how to perform variant calling from low-coverage sequencing data using glfmultiples and thunder. The pipeline was originally developed by [mailto:yunli@med.unc.edu Yun Li] for the 1000 Genomes Low Coverage Pilot Project. | + | This page documents how to perform variant calling from low-coverage sequencing data using glfmultiples and thunder. The pipeline was originally developed by [mailto:yunli@med.unc.edu Yun Li] and for [mailto:goncalo@umich.edu Goncalo Abecasis] the 1000 Genomes Low Coverage Pilot Project. |
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| == Input Data == | | == Input Data == |