article Open AccessTop 1% cited
wANNOVAR: annotating genetic variants for personal genomes via the web
Journal of Medical Genetics · 2012 · Vol. 49(7) · pp. 433–436
Xiao Chang(University of Southern California)Kai Wang✉(University of Southern California)
Abstract
We conclude that wANNOVAR will help biologists and clinicians take advantage of the personal genome information to expedite scientific discoveries. The wANNOVAR server is available at http://wannovar.usc.edu, and will be continuously updated to reflect the latest annotation information.
Genomics and Rare DiseasesGenomics and Phylogenetic StudiesCancer Genomics and DiagnosticsAnnotationGenomeGenome browserPersonal genomicsExome1000 Genomes ProjectBiologyDNA sequencingExome sequencingComputational biology
MeSH terms
Abnormalities, MultipleHumansMaleMandibulofacial DysostosisMicrognathismSoftwareGenetic VariationGenome, HumanSequence Analysis, DNALimb Deformities, CongenitalInternetGenomicsDatabases, GeneticHigh-Throughput Nucleotide SequencingExome
Citations
456
FWCI
16.33
field-weighted impact
References
31
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99%
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