Allele definition

How to define PGx alleles

PGx alleles are defined as collections of one or more SNPs, INDELs or structural variants. When a patient is sequenced by next generation sequencing (NGS) we may typically observe more variants than those which are included in any individual PGx allele definitions. This means that

• Patients may have a large, ambiguous number of matching PGx alleles
• Patients may have additional variants that may modify the effect of a known PGx allele

The SNP array method

This definition only requires matches for variants explicitly included in PGx allele definitions. This means that

• Several PGx alleles may match to the patient
• But the presence of additional variants will have no effect on reported PGx alleles

The PharmCAT method

This definition require matches also for variants not explicitly included in PGx allele definitions. This means that

• Several PGx alleles may not be simultaneously reported for the same patient
• But whenever we have additional variants, no PGx alleles will be reported