Neuroblastoma (Pilot)
ACCREDITATION STATUS:
Pilot - Not Accredited.
CLINICAL APPLICATION:
Neuroblastoma Tumour testing using array/FISH.
PURPOSE OF PROGRAMME:
To establish the cytogenomic analytical and interpretative capabilities of the participating laboratory in Neuroblastoma tumour testing.
ANALYTES:
Analyte | Default Unit |
---|---|
Array results | Qualitative detection of absence/presence of abnormality |
FISH images | Qualitative detection of absence/presence of abnormality |
Pathology information online | Qualitative detection of absence/presence of abnormality |
MATERIAL PROVIDED: Online images of Array and FISH results plus other tests as applicable.
DISTRIBUTIONS PER YEAR: 1
SAMPLES PER DISTRIBUTION: 1
FREQUENCY OF DISTRIBUTION: 1 distribution in accordance with the annual EQA timetable.
PROGRAMME OF ANALYSIS:
FISH images and array results are presented for analysis together with a referral card and additional clinical information to mimic a routine diagnostic case. Instructions and a user guide are available on the website. The scheme is not prescriptive as to the technique used (e.g. array, NGS) provided the limitations of the test used are stated in the report (ISO15189). The participant analyses the images, interprets the results and reports via the CEQAS website. The EQA is open for 5 weeks. Results can be entered at any time during this period. Any non-submitting labs will be contacted and given 24 hours to submit a late result.
DATA ANALYSIS:
All EQA cases are validated prior to release. Results are assessed by a panel of experts against set marking criteria based upon professional guidelines. There are three marking categories, Analytical, Interpretation and Clerical Accuracy. Each category carries two points. Deductions are made in accordance with the severity of the omission. A “critical error” is an error made in either the analytical or interpretive category that could lead to serious clinical consequences or imply a significant lack of diagnostic skill or scientific knowledge on the part of the participating laboratory. All critical errors are given a zero score and are designated as poor performance. A critical error in one category may result in the remaining categories being left unmarked. Any poor performance is ratified by the Oncology Specialist Advisory Group.
PERFORMANCE SCORING:
Pilot EQA – no performance designation.
PERFORMANCE MONITORING:
Pilot EQA – no performance designation.
Genomics (GenQA)
GenQA (Genomics Quality Assessment) provides external quality assessment (EQA) / proficiency testing (PT) to the genomics community worldwide. GenQA EQAs cover the entire clinical genomics service from patient counselling, sample preparation, testing processes, results interpretation and reporting. Laboratories and individual clinicians have access to more than 100 unique EQAs available for a range of rare and inherited disorders and acquired diseases. Please click here for an overview of GenQA For the most up-to-date scheme information (including any pilot schemes) please contact the centre directly.
Contact Details
- GenQA (Edinburgh)
- Nine, Edinburgh Bioquarter
- Little France Road
- Edinburgh
- EH16 4UX
Genomics (GenQA)
- Telephone: +44 (0) 131 2426898
- Fax: +44 (0) 131 2426882
- Email: info@genqa.org
- Web: https://www.genqa.org/