TruSight Lymphoma 40 uses expert-defined content and proven next-generation sequencing (NGS) technology to identify somatic variants associated with lymphomas.
The panel content was designed by a consortium of recognized lymphoma experts with input from industry guidelines1,2 and relevant literature.3 The panel targets genes frequently mutated in lymphomas, including:
- Classical Hodgkin lymphoma
- Diffuse large B cell lymphoma
- Chronic lymphocytic leukemia
- Hairy cell leukemia
- Waldenstrom’s macroglobulinemia
TruSight Lymphoma 40 covers 9 fullgenes (exons only) and exonic hotspots on 31 additional genes, providing a comprehensive assessment of key genes known to be associated with lymphomas in a single test. The result is an accurate, cost-effective solution that enables researchers to profile this class of hematological malignancies.
View the gene list
TruSight Lymphoma 40 libraries are ideally suited to run on the MiSeq System. Sequence data generated from TruSight Lymphoma 40 libraries are analyzed using on-instrument MiSeqReporter software or the Amplicon DS BaseSpace App. Filtering and annotation can then be performed using BaseSpace Variant Interpreter or Variant StudioSoftware.