XCeloSeq
Pan Cancer cfDNA Kit
®
NGS Library Preparation kit for use with cell-free DNA from liquid biopsy
Use ATOM-Seq to capture cell-free DNA and enrich for mutation hotspots across 100 of the most frequently mutated genes across cancer for detection of even the rarest mutations.
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Product Details
Specifications
%Targeting primers are split between pool 1 which enriches sense DNA and pool 2 which enriches antisense DNA.
*Higher quantities will improve maximum sensitivity.
Target Genes
Targets mutation hotspots across 100 genes most frequently mutated across cancers
*Whole coding region coverage (NM_000546)
Benefits
Capture more of your patient sample with ATOM-Seq which captures all single stranded, double-stranded or nicked DNA of any length.
Detect even the rarest clinical signatures by using both UMIs and unique, error-reducing workflow optimisations
Simple, single-day protocols leveraging the inherent simplicity and efficiency of DNA polymerases
Unique Dual Indexes
Unique Dual Indexes (UDIs) are required to be purchased and are sold separately
Please contact us to discuss additional index options.
Resources
Product guide and protocol:
For Research Use Only (RUO).
Not for use in diagnostic procedures. Not intended to be used for treatment of human or animal diseases.