TREAT: a bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing data
- PMID: 22088845
- PMCID: PMC3259432
- DOI: 10.1093/bioinformatics/btr612
TREAT: a bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing data
Abstract
TREAT (Targeted RE-sequencing Annotation Tool) is a tool for facile navigation and mining of the variants from both targeted resequencing and whole exome sequencing. It provides a rich integration of publicly available as well as in-house developed annotations and visualizations for variants, variant-hosting genes and host-gene pathways.
Availability and implementation: TREAT is freely available to non-commercial users as either a stand-alone annotation and visualization tool, or as a comprehensive workflow integrating sequencing alignment and variant calling. The executables, instructions and the Amazon Cloud Images of TREAT can be downloaded at the website: http://ndc.mayo.edu/mayo/research/biostat/stand-alone-packages.cfm.
References
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- Ansorge W.J. Next-generation DNA sequencing techniques. New Biotechnol. 2009;25:195–203. - PubMed
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