Validation Program (Prerequisite)
The Validation Program is a prerequisite to the use of SOPHiA DDM® for a given NGS test. We support you to be ready in routine within a maximum of 21 days. You will gain access to the world’s largest clinical genomics community and entitle your lab for ISO 15189 certification.
Dr. López-Guerrero, Head of the Molecular Biology Laboratory of IVO: “As a provider of clinical BRCA analysis for cancer patients, we were looking for a standardised dry lab solution to certify our laboratory and achieve the best analytical performance. For us, only SOPHiA could provide this at the required standard.”
As experts in genomics data analyses, our technologies offer you the best analytical performance to treat your raw NGS data. Within a few quick steps, we validate your lab for an NGS test (7 or 21 days). You are then able to use our SOPHiA DDM® platform for routine diagnostics to achieve top analytical performance and shorten your turn around time. Thus, being able to diagnose more patients, more efficiently. It's as simple as that.
Through the analysis of thousands of clinical samples we have been exposed to dozens of NGS enrichment technologies. We have discovered and solved the biases of these technologies and we are now in the privileged position to offer your packaged kits bundled with analytics for robust and accurate patient diagnosis. The results are improved turn around time and a top analytical performance, all brought to you by our SOPHiA DDM® platform.
From sample to variant report
With Integrated Diagnostic Solutions you can be part of the genetic revolution, benefit from your peers through our Clinical Genomics Community that allows knowledge sharing and offer your patients the highest standards in NGS clinical routine diagnostic with no investment from your side. You simply have to send us your samples and we take care of the rest.