Sample Reqs

A

Turnaround

2 weeks

Special instructions

No special instructions.

Test details

This next-generation sequencing (NGS) panel analyses RNA samples for single nucleotide variants (SNVs), short insertions/deletions (indels), or fusion transcripts associated with leukaemias, lymphomas and other haematological malignancies.

The panel encompasses targets in over 199 genes relating to lymphoid and myeloid malignancies. By using gene-specific primers to amplify into molecular barcodes ligated onto the cDNA fragment ends, both known and novel fusions can be identified.

Additional information

• How to order a test
• HSL Genetics specimens
• HSL Genetics specialties
• HSL Genetics request procedures
• Guidance on specimen collection
• Specimen transport
• Sample rejection criteria
• Request Forms

Last-updated: 13/03/23

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