wANNOVAR 20190509 – Annotating Genetic Variants with respect to Disease Phenotypes

wANNOVAR 20190509

:: DESCRIPTION

ANNOVAR is a rapid, efficient tool to annotate functional consequences of genetic variation from high-throughput sequencing data. wANNOVAR provides easy and intuitive web-based access to the most popular functionalities of the ANNOVAR software, to facilitate biologists without bioinformatics skills taking full advantage of the sequencing data.

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::DEVELOPER

Wang Genomics Lab

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • WEb Browser

:: DOWNLOAD

 NO

:: MORE INFORMATION

Citation

J Med Genet. 2012 Jul;49(7):433-6. doi: 10.1136/jmedgenet-2012-100918. Epub 2012 Jun 20.
wANNOVAR: annotating genetic variants for personal genomes via the web.
Chang X1, Wang K.