Product Code: NGS(vSOMATIC)-25
From £715.00
Registration closed: 28/02/2025
Applicable to any labs using NGS (not requiring a matched normal control sample) as part of their somatic testing process. This is a pilot EQA.
Genomic, NGS, Panel testing, Single gene testing, Targeted testing, Whole exome sequencing, Whole genome sequencing
Not applicable
gDNA (from FFPE or fresh frozen sample)
No
The scheme is designed to assess the analytical process (genotyping) and quality of the raw data.
Please see our DNA SEQUENCING –
NGS (Somatic SNVs and indels + matched germline sample) EQA scheme if you require a matched sample.
One mock clinical case and matching tumour DNA sample will be provided.
Approximately 500ng DNA per sample is provided. Complete information will be
available in the scheme instructions.
Participants will receive a comprehensive individual
data quality report and a variant consensus analysis report for each
submission. A comprehensive summary scheme report is provided including
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.
No restrictions on number of participants. Open to laboratories from ALL countries (note: some restrictions may apply*)
*Sanctions, delivery network exceptions, restrictions on importation etc.
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