RareVariantVis 2.20.0
:: DESCRIPTION
RareVariantVis is a new tool for analysis of genome sequence data (including non-coding regions) for both germ line and somatic variants.
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::DEVELOPER
Tomasz Stokowy <tomasz.stokowy at k2.uib.no>
:: SCREENSHOTS
N/A
:: REQUIREMENTS
- Linux / WIndows/ MacOsX
- R
- BioConductor
:: DOWNLOAD
:: MORE INFORMATION
Citation
RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data.
Stokowy T, Garbulowski M, Fiskerstrand T, Holdhus R, Labun K, Sztromwasser P, Gilissen C, Hoischen A, Houge G, Petersen K, Jonassen I, Steen VM.
Bioinformatics. 2016 Jun 10. pii: btw359.