Products & ReviewLife Sciences
SureSeq CLL + CNV Panel
Oxford Gene Technology LtdAvailable: Worldwide
The SureSeq™ CLL + CNV Panel has been designed in collaboration with recognised cancer experts to detect 13 key genes and 5 chromosomal regions implicated in CLL progression (Table 1). The SureSeq CLL + CNV Panel alleviates the burden of running multiple assays and streamlines your CLL research to deliver a comprehensive genomic profile for each CLL sample using a single workflow
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Features
- Unparalleled uniformity and high depth of coverage
- Detect low-frequency SNVs and indels with confidence CNV detection ranging from loss of single exons to full chromosome arms and trisomy 12
- Profile your samples for CNVs in the 5 most commonly aberrant regions in CLL
- Time savings
- Replace multiple assays with a single NGS panel, increasing throughput and reducing turnaround time
- Complimentary data analysis software
- Analyse your data with Interpret, OGT’s powerful and easy-to-use analysis solution for accurate identification of all variants and CNVs
