Products & ReviewLife Sciences
SureSeq Myeloid Plus Workflow
Oxford Gene Technology LtdAvailable: Worldwide
The SureSeq™ Myeloid Plus NGS Complete Workflow combines the rapid Universal NGS Workflow hybridisation-based target enrichment method together with OGT’s expert bait design to detect 49 key genes implicated in myeloid disorders.
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Designed in collaboration with recognised
cancer experts
- Detect SNVs and indels in 49 genes
- implicated in a variety of Myeloid
- malignancies, together with 44 SNPs as ID
- markers and 4 sex chromosome genes
- Unparalleled uniformity and high depth of
- coverage
- Detect low-frequency variants down to
- 2.5% VAF with confidence
- Robust detection of FLT3-ITDs and
- KMT2A-PTDs
- Replace multiple single gene assays with
- one comprehensive panel
- Fast and easy workflow
- Streamlined library preparation, rapid
- hybridisation and intuitive software
- allowing easy variant analysis
