Find a test tool

The National Genomic Test Directories specify which genomic tests are commissioned by the NHS in England, to be delivered by Genomic Laboratory Hubs.

This tool allows clinical teams to search all of the genomic tests available to patients through the National Testing Directory. From here you can find out more details about each test and information about how to order them. These tests can only be ordered by clinical teams, if you are a patient looking to request a test please speak to your clinical team directly.

Maternal cell contamination testing

Clinical Indication ID & Name

R321

Maternal cell contamination testing

Test Group

Core/Specialised

Test code

R321.1

Test name

N/A

Target genes

Genomewide

Test scope

n/a

Test method/ technology

Identity testing

Optimal Family Structure

n/a

Eligibility Criteria

Pregnancy requiring maternal cell contamination to inform interpretation of other testing, for example invasive prenatal testing, tests on fetal tissues or tests performed on cord blood
Testing will often be initiated by the testing laboratory but relevant samples will be required in advance of testing

Commissioning group

Core/Specialised

Overlapping idications

n/a

Address for samples/request forms

Please refer to the test request form.

Contact with queries

gos-tr.norththamesgenomics@nhs.net

Supporting documents

n/a

Education resources

n/a

Service updates

n/a

Request form download

Consent record

See consent guidance in test request form

Sample requirements

Sample Requirements Each sample must be sent labelled with 3 patient identifiers and must state the sample type clearly on the sample container. Sample Rejection Samples may be rejected for the following reasons: 1. Samples and request form do not show at least three identical patient identifiers 2. The sample is in the incorrect collection media 3. The request form is not sufficiently completed 4. The sample is not of sufficient volume 5. The sample is too old Sample Storage and Volume Required: For postnatal referrals: Peripheral blood (2-3ml) in an EDTA and lithium heparin bottles, or 3μg DNA. For Prenatal referrals: DNA sample (50ng), amniotic fluid in a dry sterile container (20ml), CVS (20mg) (please discuss with the laboratory). Storage, sample packing and transportation: Please notify the laboratory before sending prenatal samples. All prenatal samples must arrive in the laboratory on the day of sampling, preferably before 3pm. Patient/Clinician Instructions: N/A Factors affecting performance of test/interpretation of results: Do not spin down or freeze samples before sending.