PAnno is a Pharmacogenomics Annotation tool for clinical genomic testing.
conda install lyaqing::panno
PAnno reports drug responses and prescribing recommendations by parsing the germline variant call format (VCF) file from NGS and the population to which the individual belongs. PAnno provides an end-to-end clinical pharmacogenomics decision support solution by resolving, annotating, and reporting germline variants in individuals.