Difference between revisions of "GATK"
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[http://www.broadinstitute.org/gsa/wiki/index.php/GATK#Using_the_GATK Upstream documentation] for {{#var:app}}. | [http://www.broadinstitute.org/gsa/wiki/index.php/GATK#Using_the_GATK Upstream documentation] for {{#var:app}}. | ||
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{{#if: {{#var: exe}}|==How To Run== | {{#if: {{#var: exe}}|==How To Run== | ||
We provide two wrapper scripts AnalyzeCovariates and GenomeAnalysisTK that are equivalent to running | We provide two wrapper scripts AnalyzeCovariates and GenomeAnalysisTK that are equivalent to running | ||
Revision as of 16:55, 10 August 2012
Description
The GATK is a structured software library that 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.
We aim to work well with both samtools and Picard by providing complementary tools to those available in those two packages. Our SNP calling pipeline (Q score recalibration -> multiple sequence realignment -> snp/index calling) is a particular area of focus, and have been pushing to make these capabilities as general-purpose and powerful as possible. My group's mandate is to ensure the success of the human medical resequencing projects we've undertaken at the Broad over the next 2-3 years, which involves providing a robust, production-quality development library that underlies tools for common analysis problems (like SNP calling) as well as enabling exploratory research on NGS data. Upstream documentation for gatk.
Required Modules
Serial
- gatk
How To Run
We provide two wrapper scripts AnalyzeCovariates and GenomeAnalysisTK that are equivalent to running
java -jar $HPC_GATK_DIR/GenomeAnalysisTK.jar
and
java -jar $HPC_GATK_DIR/AnalyzeCovariates.jar