The TruSight Myeloid Sequencing Panel uses expert-defined content and proven next-generation sequencing (NGS) technology to identify somatic mutations in myeloid malignancies.
The panel content was designed by a consortium of recognized experts in blood cancer disorders and targets genes frequently mutated in:
The TruSight Myeloid Sequencing Panel (96 samples) covers 15 full genes (exons only) and 39 additional genes where oncogenic hotspots are covered, providing a comprehensive assessment of the key genes involved in myeloid malignancies in a single test. The result is an accurate, cost-effective solution for profiling liquid tumors. View the gene list »
TruSight Myeloid libraries are ideally suited to run on a desktop sequencer and perform alignment and variant calling with the Somatic Variant Caller. Filtering and annotation can then be performed using Illumina’s annotation and filtering software, VariantStudio.
|Description||Document Type||File Info|
|TruSight Myeloid Sequencing Panel||Data Sheet||PDF< 1 MB|
Catalog IDs: FC-130-1010, FC-130-1003, FC-130-1006, FC-130-1007, MS-102-3003