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"RareVariantVis: new tool for visualization of causative variants in rare ..."
Tomasz Stokowy et al. (2016)
- 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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