Difference between revisions of "Pharmcat"

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[[Category:Software]][[Category:Bioinformatics]][[Category:Biology]][[Category:Phylogenetics]]
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[[Category:Software]][[Category:Biology]][[Category:Phylogenetics]]
 
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|{{#vardefine:app|pharmcat}}
 
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Latest revision as of 20:19, 12 August 2022

Description

pharmcat website  

PharmCAT: Pharmacogenomics Clinical Annotation Tool. A tool to extract all CPIC guideline gene variants from a genetic dataset (represented as a VCF file), interpret the variant alleles, and generate a report.

Environment Modules

Run module spider pharmcat to find out what environment modules are available for this application.

System Variables

  • HPC_PHARMCAT_DIR - installation directory

Additional Information

$ pharmcat -vcf <sample_file> -o <output_dir>



Citation

If you publish research that uses pharmcat you have to cite it as follows:

Commentary: TE Klein, MD Ritchie. PharmCAT: A Pharmacogenomics Clinical Annotation Tool. Clinical Pharmacology & Therapeutics (2018) 104(1):19-22. Methods paper: K Sangkuhl & M Whirl-Carrillo, et al. Pharmacogenomics Clinical Annotation Tool (PharmCAT). Clinical Pharmacology & Therapeutics (2020) 107(1):203-210.