RareVariantVis statistics

To access cutting-edge analytics on consensus tools, life science contexts and associated fields, you will need to subscribe to our premium service.

Subscribe
info

Citations per year

Citations chart
info

Popular tool citations

chevron_left Variant visualization chevron_right
Popular tools chart
info

Tool usage distribution map

Tool usage distribution map
info

Associated diseases

Associated diseases

RareVariantVis specifications

Information


Unique identifier OMICS_12127
Name RareVariantVis
Software type Package/Module
Interface Command line interface
Restrictions to use None
Operating system Unix/Linux, Mac OS, Windows
Programming languages R
License Artistic License version 2.0
Computer skills Advanced
Version 1.6.2
Stability Stable
Requirements
BiocGenerics, IRanges, GenomicRanges, S4Vectors, GenomeInfoDb, knitr, VariantAnnotation, googleVis, AshkenazimSonChr21
Maintained Yes

Versioning


Add your version

Documentation


Maintainer


  • person_outline Tomasz Stokowy <>

Publication for RareVariantVis

RareVariantVis institution(s)
Department of Clinical Science, University of Bergen, Bergen, Norway; Computational Biology Unit, Department of Informatics, University of Bergen, Bergen, Norway; Department of Informatics, Silesian University of Technology, Gliwice, Poland; Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, Bergen, Norway; Department of Human Genetics, Radboud University Medical Center, Nijmegen, Netherlands
RareVariantVis funding source(s)
Supported by Bergen Research Foundation grant no. 807964, Meltzer Foundation grant ID 7761, POIG.02.03.01-24-099/13 grant: "GCONiI - Upper-Silesian Center for Scientific Computation", and the Research Council of Norway (Centres of Excellence funding scheme, grant no. 223273; NORMENT CoE).

RareVariantVis reviews

star_border star_border star_border star_border star_border
star star star star star

Be the first to review RareVariantVis