Analytes/procedures in bold
type are regulated for proficiency testing by the Centers for Medicare & Medicaid Services (CMS).
All laboratories subject to US Clinical Laboratory Improvement Amendments (CLIA) Regulations:
Proficiency testing (PT) challenges must NOT be referred to another laboratory for any portion of NGS testing, even if this is how patient testing is routinely performed. For PT challenges, any referral is strictly prohibited by CMS.
- Laboratories will have the ability to analyze up to 200 preselected chromosomal positions or intervals in hg19 (GRCh37) and hg38 (GRCh38) coordinates within various genes; for the full list of genes in this program, click here.
- One 10.0‑µg extracted DNA specimen; one educational variant interpretation paper challenge
- Methods-based challenge for germline variants for laboratories using gene panels, exome, and whole genome sequencing
- Results for this program must be submitted online through e-LAB Solutions Suite
Shipment A: March 1
Shipment B: September 13