RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data.
Resource URI: https://dblp.l3s.de/d2r/resource/publications/journals/bioinformatics/StokowyGFHLSGHH16
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2016
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RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data.
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RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data.
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