Description
Detect low-frequency variants incl. rearrangements in somatic cancer
• Targets 13 genes associated with somatic cancer mutations
• Target Size 61 kb (Whole CDS incl. rearrangements for selected genes)
• Gene-Add-On Service when needed- contact us with your wish list
• Probes targeting mitochondrial or intronic/regulatory regions can also be spiked in – please inquire!
• Celemics´probe design ensures superior on-target performance, coverage, and uniformity
• Hard to capture sequences such as GC-rich, AT-rich and homologous sequences are equally represented
• Detection of SNV, Indel, CNV, Rearrangement, MSI, TMB
• Full Bioinformatics Support available when needed
• Input: >50 ng fragmented DNA (FFPE, frozen tissue, cfDNA, RNA converted to cDNA)
Celemics´ CancerScreen Core Panel was developed to target genes involved in somatic tumor mutations for cost-efficient and sensitive sequencing.
The All-In-One-Kit for pre-capture library pooling includes the NGS Library Kit developed for the Illumina Sequencing platform – user manual see here – and all accessories such as magnetic beads, Streptavidin beads, and Polymerase. For 64, 128, 384, and 768 samples kit sizes please contact us. All-In-One KIts for pre-capture library pooling for Ion Torrent and MGI platforms can also be ordered – please inquire!
The hyb capture panel – which is suitable for any sequencing platform including Illumina, Ion Torrent, MGI, PacBio and Oxford Nanopore – is also available without accessories and without library prep kit – please contact us us for pricing.