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URL: http://www.openbioinformatics.org/annovar/
Proper Citation: ANNOVAR (RRID:SCR_012821)
Description: An efficient software tool to utilize update-to-date information to functionally annotate genetic variants detected from diverse genomes (including human genome hg18, hg19, as well as mouse, worm, fly, yeast and many others). Given a list of variants with chromosome, start position, end position, reference nucleotide and observed nucleotides, ANNOVAR can perform: 1. gene-based annotation. 2. region-based annotation. 3. filter-based annotation. 4. other functionalities. (entry from Genetic Analysis Software)
Abbreviations: ANNOVAR
Synonyms: functional ANNOtation of genetic VARiants, ANNOVAR: Functional annotation of genetic variants
Resource Type: software resource, software application
Defining Citation: PMID:20601685
Keywords: genomic analysis, imaging genomics, next generation sequencing, snp, gene, bio.tools
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