Cancer tests

I want to order a
Haemato-Oncology test

Including tests for Haematological Malignancies, transplantation
and bone marrow failure syndromes
This link will take you to the available tests, turnaround times, test request forms to use, and sample and transportation requirements for Haematological Malignancies.
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I want to order a
Solid Tumour test

Including NTRK testing and Whole Genome Sequencing
This link will take you to the available tests, turnaround times, test request forms to use, and sample and transportation requirements for Solid Tumours.
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I want to order an
Inherited Cancer test

Including testing for BRCA and Lynch Syndrome
This link will take you to the available tests, turnaround times, test request forms to use, and sample and transportation requirements for Inherited Cancers.
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I want to order a
Pharmacogenomics test

Including pharmacogenomic testing for DPYD polymorphisms with fluoropyrimidine therapies
This link will take you to the available tests, turnaround times, test request forms to use, and sample and transportation requirements for Pharmacogenomics.
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With any Whole Genome Sequencing (WGS) test ordered, a Record of Discussion (RoD) form will also need to be submitted. This document is to record the patient’s consent for genomic testing and their choice on taking part in research. Guidance on the patient choice conversation can be found here
 
This RoD form will be available for clinicians to download from this webpage. Once completed with the patient, it can be send to the lab with the corresponding test order form and sample.
Tests available to order will be listed in the National Genomic Test Directory. A test order form will soon be made available for clinicians on this webpage to download and complete. This form will include the address of the laboratory that the appropriate sample and completed form needs to be sent to.
 
Until the new Genomic Laboratory Service goes live, please continue to follow existing test order processes.
 
Later this year, the online test ordering tool for Whole Genome Sequencing will be integrated into the National Genomics Informatics System (NGIS) and clinicians will be able to search or filter to find a clinical indication, confirm eligibility criteria and start the test request process for their patient.