Difference between revisions of "Allele definition"
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==How to define PGx alleles== | ==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. | 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. | ||
| − | [[File:Variant tree outline.png| | + | [[File:Variant tree outline.png|miniature|The 16 possible haplotypes for a four loci, decomposed variant calling]] |
This means that | This means that | ||
*Patients may have a large, ambiguous number of matching PGx alleles | *Patients may have a large, ambiguous number of matching PGx alleles | ||
| Line 8: | Line 8: | ||
==The SNP array method== | ==The SNP array method== | ||
| − | [[File:Variant tree allele snp definition.png| | + | [[File:Variant tree allele snp definition.png|miniature|PGx alleles defined as collections of variants, with no requirement on loci that are not part of the definition, will assign the same PGx allele to several different haplotypes]] |
This definition only requires matches for variants explicitly included in PGx allele definitions. | This definition only requires matches for variants explicitly included in PGx allele definitions. | ||
| Line 17: | Line 17: | ||
==The PharmCAT method== | ==The PharmCAT method== | ||
This definition requires matches also for variants not explicitly included in PGx allele definitions. | This definition requires matches also for variants not explicitly included in PGx allele definitions. | ||
| − | [[File:Variant tree allele pharmcat definition.png| | + | [[File:Variant tree allele pharmcat definition.png|miniature|PGx alleles defined as complete haplotypes classifies the patient uniquely]] |
This means that | This means that | ||
*Only one PGx allele can exist simultaneously for the same patient | *Only one PGx allele can exist simultaneously for the same patient | ||
Revision as of 07:38, 8 August 2018
Contents
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
We illustrate some of the problems that we encountered when trying to match patient haplotypes to the PGx allele definitions, by an imagined four loci PGx gene
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 the patient
- But the presence of additional variants will have no effect on reported PGx alleles
The PharmCAT method
This definition requires matches also for variants not explicitly included in PGx allele definitions.
This means that
- Only one PGx allele can exist simultaneously for the same patient
- But whenever we have additional variants, no PGx alleles will be reported
Which definition should we stick to?
| Method | Advantages | Disadvantages |
|---|---|---|
| SNP array method | Compatible with previous SNP array methods. Assigns PGx alleles to the maximum number of patients | Multiple PGx alleles are possible |
| PharmCAT method | One PGx allele per patient | Less compatible with previous SNP array methods. Many patients are not assigned to a known PGx allele |
