Literature DB >> 22717648

wANNOVAR: annotating genetic variants for personal genomes via the web.

Xiao Chang1, Kai Wang.   

Abstract

BACKGROUND: High-throughput DNA sequencing platforms have become widely available. As a result, personal genomes are increasingly being sequenced in research and clinical settings. However, the resulting massive amounts of variants data pose significant challenges to the average biologists and clinicians without bioinformatics skills. METHODS AND
RESULTS: We developed a web server called wANNOVAR to address the critical needs for functional annotation of genetic variants from personal genomes. The server provides simple and intuitive interface to help users determine the functional significance of variants. These include annotating single nucleotide variants and insertions/deletions for their effects on genes, reporting their conservation levels (such as PhyloP and GERP++ scores), calculating their predicted functional importance scores (such as SIFT and PolyPhen scores), retrieving allele frequencies in public databases (such as the 1000 Genomes Project and NHLBI-ESP 5400 exomes), and implementing a 'variants reduction' protocol to identify a subset of potentially deleterious variants/genes. We illustrated how wANNOVAR can help draw biological insights from sequencing data, by analysing genetic variants generated on two Mendelian diseases.
CONCLUSIONS: 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.

Entities:  

Mesh:

Year:  2012        PMID: 22717648      PMCID: PMC3556337          DOI: 10.1136/jmedgenet-2012-100918

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  29 in total

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  187 in total

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Journal:  Genetics       Date:  2017-07-24       Impact factor: 4.562

4.  Phenolyzer: phenotype-based prioritization of candidate genes for human diseases.

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5.  Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing.

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Journal:  Eur J Hum Genet       Date:  2019-06-21       Impact factor: 4.246

6.  Whole-exome sequencing indicates FLG2 variant associated with leg ulcers in Brazilian sickle cell anemia patients.

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Review 9.  Clinical analysis and interpretation of cancer genome data.

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