Topic: annovar Goto Github
Some thing interesting about annovar
Some thing interesting about annovar
annovar,Highly Open Workflow for Annotation & Ranking toward genomic variant Discovery. HOWARD annotates and prioritizes genetic variations, calculates and normalizes annotations, translates files in multiple formats (e.g. vcf, tsv, parquet) and generates variants statistics.
User: bioinfo-chru-strasbourg
annovar,anor: an annotation and visualization system based on R and Shiny framework
Organization: clindet
Home Page: https://jhuanglab.github.io/anor/
annovar,bionano annovar annotation
User: daaaaande
annovar,2016 Genomics Epidemiology Workshop
User: geniusphil
Home Page: http://www.genomics.sinica.edu.tw/genomicepi2016/
annovar,2017 Genomics Epidemiology Workshop at Academia Sinica
User: geniusphil
annovar,2018 Genomic Epidemiology Workshop at Academia Sinica
User: geniusphil
Home Page: https://sites.google.com/gate.sinica.edu.tw/genomicepi
annovar,Reference pipeline for somatic SNP detection using BWA for mapping, Mutect2 for calling and Annovar for annotation
Organization: gustaveroussy
annovar,
User: jianhuig
annovar,Clinical machine-learning based interpreter of germline mutations.
User: mazzalab-ieo
annovar,automatic update Clinvar db for ANNOVAR
User: ryuzheng
annovar,tool for converting between dash and non-dash INDEL format using docker
User: shanghungshih
annovar,Scripts for .bed file genomic region annotation with various tools
User: stevekm
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