Product Code: POSTNATAL CNV-25
From £471.00
Registration closed: 28/02/2025
Applicable to all labs undertaking Postnatal Constitutional CNV Detection using array based, or NGS approaches.
Array based, NGS, Whole genome analysis (CNV)
English
DNA (in TE Buffer)
Yes
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.
Two mock clinical cases with matching samples will be
provided. Approximately 1µg DNA per sample is provided. Complete information will be
available in the scheme instructions.
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.
Open to laboratories from ALL countries (note: some restrictions may apply*)
*Sanctions, delivery network exceptions, restrictions on importation etc.
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