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Resource Name
SVA
RRID:SCR_002155 RRID Copied      
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SVA (RRID:SCR_002155)
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Resource Information

URL: http://www.omicsexpress.com/sva.php

Proper Citation: SVA (RRID:SCR_002155)

Description: Software package to annotate, visualize, and analyze the genetic variants identified through next-generation sequencing studies, including whole-genome sequencing (WGS) and exome sequencing studies. SVA aims to provide the research community with a user-friendly and efficient tool to analyze large amount of genetic variants, and to facilitate the identification of the genetic causes of human diseases and related traits.

Abbreviations: SVA

Synonyms: Sequence Variant Analyzer, SVA: Sequence Variant Analyzer

Resource Type: commercial organization, software resource, software application

Defining Citation: PMID:21624899

Keywords: gene, genetic, genomic, annotate, visualize, genetic variant, next-generation sequencing, whole-genome sequencing, exome, sequencing, genome, disease, trait, bio.tools

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This resource

is listed by

OMICtools

is listed by

Genetic Analysis Software

is listed by

bio.tools

is listed by

Debian

has parent organization

Duke University School of Medicine; North Carolina; USA

Usage and Citation Metrics

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Data and Source Information