Literature DB >> 25701572

Unified representation of genetic variants.

Adrian Tan1, Gonçalo R Abecasis1, Hyun Min Kang1.   

Abstract

UNLABELLED: A genetic variant can be represented in the Variant Call Format (VCF) in multiple different ways. Inconsistent representation of variants between variant callers and analyses will magnify discrepancies between them and complicate variant filtering and duplicate removal. We present a software tool vt normalize that normalizes representation of genetic variants in the VCF. We formally define variant normalization as the consistent representation of genetic variants in an unambiguous and concise way and derive a simple general algorithm to enforce it. We demonstrate the inconsistent representation of variants across existing sequence analysis tools and show that our tool facilitates integration of diverse variant types and call sets.
AVAILABILITY AND IMPLEMENTATION: The source code is available for download at http://github.com/atks/vt. More detailed documentation is available at http://genome.sph.umich.edu/wiki/Variant_Normalization. CONTACT: hmkang@umich.edu SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
© The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Mesh:

Year:  2015        PMID: 25701572      PMCID: PMC4481842          DOI: 10.1093/bioinformatics/btv112

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  5 in total

1.  dbSNP: the NCBI database of genetic variation.

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2.  Natural genetic variation caused by small insertions and deletions in the human genome.

Authors:  Ryan E Mills; W Stephen Pittard; Julienne M Mullaney; Umar Farooq; Todd H Creasy; Anup A Mahurkar; David M Kemeza; Daniel S Strassler; Chris P Ponting; Caleb Webber; Scott E Devine
Journal:  Genome Res       Date:  2011-04-01       Impact factor: 9.043

3.  A framework for variation discovery and genotyping using next-generation DNA sequencing data.

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Journal:  Nat Genet       Date:  2011-04-10       Impact factor: 38.330

4.  The variant call format and VCFtools.

Authors:  Petr Danecek; Adam Auton; Goncalo Abecasis; Cornelis A Albers; Eric Banks; Mark A DePristo; Robert E Handsaker; Gerton Lunter; Gabor T Marth; Stephen T Sherry; Gilean McVean; Richard Durbin
Journal:  Bioinformatics       Date:  2011-06-07       Impact factor: 6.937

5.  An integrated map of genetic variation from 1,092 human genomes.

Authors:  Goncalo R Abecasis; Adam Auton; Lisa D Brooks; Mark A DePristo; Richard M Durbin; Robert E Handsaker; Hyun Min Kang; Gabor T Marth; Gil A McVean
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  5 in total
  158 in total

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