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UK NEQAS provides External Quality Assessment/Proficiency Testing for all major aspects of clinical laboratory testing. To find the programme(s) to match your EQA/PT requirements please use the search function below.
Showing Results: 346 - 360 out of 426
Postnatal constitutional copy number variants (CNV) detection
|Genomics (GenQA)
Analysis and interpretation of copy number changes in postnatal samples: DNA for array or NGS studies.
Provided in collaboration with EMQN
Postnatal karyotyping
|Genomics (GenQA)
Prediction of 5-Fluorouracil Toxicity (DPYD)
|Genomics (GenQA)
Molecular testing of the DPYD gene.
Prediction of Thiopurine toxicity (TPMT) (Pilot)
|Genomics (GenQA)
Pregnancy loss (Molecular methods and G-banding)
|Genomics (GenQA)
Prenatal constitutional copy number variant (CNV) detection
|Genomics (GenQA)
Analysis and interpretation of copy number changes in prenatal samples: DNA for array or NGS studies.
Prenatal karyotyping
|Genomics (GenQA)
Analysis and interpretation of aneuploidy and structural chromosome rearrangements in prenatal samples (Amniotic fluid and CVS): online G-banded analysis with supplementary tests as applicable.
Primary Immunodeficiency disorders (PID)
|Genomics (GenQA)
Molecular testing for disorders associated with PID
Procalcitonin
|Immunology, Immunochemistry & Allergy (IIA)
Prostate Specific Antigen (PSA)
|Immunology, Immunochemistry & Allergy (IIA)
Oncology EQA scheme