Analytes/procedures in
bold type are regulated for proficiency testing by the Centers for Medicare & Medicaid Services (CMS).
CAP accredited laboratories that perform testing for the detection of somatic single nucleotide variants, insertions, and deletions in BRAF, EGFR, and KRAS by non-NGS methods are required to enroll in either MTP or the respective single gene programs. This includes laboratories that perform non-NGS-based multiplexed assays, and nonmultiplexed assays (eg, Sanger sequencing). Laboratories that perform NGS-based testing of somatic single nucleotide variants, insertions, and deletions in BRAF, KRAS, EGFR, and/or other genes are required to enroll in NGSST.
Program Information
- Three 2.0‑μg gDNA (50ng/‑μL) specimens for laboratories performing molecular testing on multiple targets
Shipping Schedule
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Shipment A: February 13
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Shipment B: August 21