"RareVariantVis: new tool for visualization of causative variants in rare ..."

Tomasz Stokowy et al. (2016)

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DOI: 10.1093/BIOINFORMATICS/BTW359

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type: Journal Article

metadata version: 2024-10-06

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Tomasz Stokowy, Mateusz Garbulowski, Torunn Fiskerstrand, Rita Holdhus, Kornel Labun, Pawel Sztromwasser, Christian Gilissen, Alexander Hoischen, Gunnar Houge, Kjell Petersen, Inge Jonassen, Vidar M. Steen:
RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data. Bioinform. 32(19): 3018-3020 (2016)

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