Product Code: 02-MELAN-26
From £655.00 Early Bird
Early Bird Deadline: 31/01/2026
Deadline to order: 28/02/2026
BRAF, NRAS and KIT gene testing in melanoma (FFPE).
Variants in the BRAF, NRAS, KIT genes.
NGS, Panel testing, PCR based, Whole exome sequencing, Whole genome sequencing
English, French, German, Italian, Spanish
FFPE
Yes
June 2026
June - August 2026
December 2026 - January 2027
You can complete purchase on our secure partner site.
The scheme is designed to assess the analytical process (genotyping), and reporting (biological and clinical interpretation of the test result) including the overall report layout, content and clerical accuracy.
Five mock clinical cases with matching human tumour tissue paraffin embedded (FFPE) and/or artificial FFPE (designed to simulate real patient samples). One 10um or 15um FFPE section per case is provided.
Samples are provided as cut sections (rolled scrolls / curls) only – we cannot provide slide mounted materials. Variant allele frequencies of any artificial FFPE reference materials have been validated using ddPCR. There is an option to purchase additional sets of samples at the time of scheme purchase. For example, for laboratories requiring more sample material to complete testing of the EQA e.g., users of Biocartis IdyllaTM.
There is a maximum of 3 x additional sets of samples per participant.
Participants will receive an individual report including educational advice and a scheme report which includes additional information from the cohort of participants including geographical spread, methodologies employed, common errors, learning points and scheme statistics allowing participants to benchmark their results.
Each laboratory will also receive a single certificate listing all EQAs participated in with performance result for each year.
The minimum requirement is BRAF gene testing. If you provide a clinical service for the NRAS and/or KIT genes, these should be included. These samples are not suitable for an RNA-based methodology only.
Participants are expected to test samples according to their routine strategy. For case 1, participants are expected to return a clinical report. The remaining four cases require genotyping only. For all cases, mandatory completion of an online data collection form is required.
No restrictions on number of participants. Open to laboratories from ALL countries (note: some restrictions may apply due to sanctions, delivery network exceptions, restrictions on importation etc).
added wishlist!
View Wishlist
View Wishlist
Express your interest in ''.