Pharmacogenomics

VSPGx is a pharmacogenomics interpretation software based on CPIC recommendations

The PGx Variant Detection and Recommendation algorithm identifies pharmacogenomic diplotypes and annotates them with drug recommendations. By default, diplotypes are annotated against recommendations provided by the Clinical Pharmacogenetics Implementation Consortium (CPIC).

Identify Alleles: Identifying the named alleles present at all positions required according to the CPIC guidelines to define a diplotype for a given gene.
Matching to Recommendations: Once diplotypes have been assigned for each gene, VSPGx matches these diplotypes to phenotypes and recommendations.
Structural Variations: PGx Variant Detection and Recommendation algorithm can be used to report on phenotypic data and treatment recommendations for structural variations and copy number deletions or duplications.

Reporting: After running PGx Variant Detection and Recommendations, a clinical report can be generated using VSPGX's customizable reporting system. VSPGX comes shipped with an initial PGx Word®-based report template that serves as a starting point for creating custom reports.

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Recommended Learning Materials

We have a variety of supplemental learning materials that are an excellent resource for anyone interested in the industry or our software solutions. Here are some of our recommended materials for you to check out related to VarSeq!