Technical Note:  Advancing pharmacogenomics with NGS and CNV analysis

Published on 29/06/25
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Routine pharmacogenomic (PGx) testing has significant potential to improve drug efficacy and safety.
Home breadcrumb-arrow Technical Note:  Advancing pharmacogenomics with NGS and CNV analysis
Routine pharmacogenomic (PGx) testing has significant potential to improve drug efficacy and safety.

This Technical Note explores key considerations for PGx analysis, with a focus on the advantages of copy number variation (CNV) detection and next-generation sequencing (NGS) over traditional methodologies.

We introduce the SOPHiA DDM™ Community Pharmacogenomics Solution, expertly designed for rapid and accurate identification of PGx-related variants, enhancing precision medicine through advanced analytics.

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