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Resource Name
RRID:SCR_001876 RRID Copied      
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GATK (RRID:SCR_001876)
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Resource Information

URL: https://software.broadinstitute.org/gatk/

Proper Citation: GATK (RRID:SCR_001876)

Description: A software package to analyze next-generation resequencing data. The toolkit offers a wide variety of tools, with a primary focus on variant discovery and genotyping as well as strong emphasis on data quality assurance. Its robust architecture, powerful processing engine and high-performance computing features make it capable of taking on projects of any size. This software library makes writing efficient analysis tools using next-generation sequencing data very easy, and second it's a suite of tools for working with human medical resequencing projects such as 1000 Genomes and The Cancer Genome Atlas. These tools include things like a depth of coverage analyzers, a quality score recalibrator, a SNP/indel caller and a local realigner. (entry from Genetic Analysis Software)

Abbreviations: GATK

Synonyms: Genome Analysis ToolKit

Resource Type: data analysis software, software application, software toolkit, software library, data processing software, software resource

Defining Citation: PMID:21478889

Keywords: gene, genetic, genomic, next-generation resequencing, bio.tools

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This resource

is used by

Halvade Somatic

is listed by

OMICtools

is listed by

Genetic Analysis Software

is listed by

bio.tools

is listed by

Debian

is listed by

SoftCite

is related to

SnpEff

has parent organization

Broad Institute

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