FREE Webinar: Hybridisation capture for variant detection in DNA and RNA - 21st of April
Hybridisation capture enables the detection of all variant types: SNV’s, InDel, CNV, rearrangements. Celemics provide custom design and pre-set hybridisation capture tools for DNA and RNA analysis. Celemics’ Target Enrichment Panel utilise our intrinsic probe design, rebalancing, and molecular barcode technologies to efficiently analyse not only hard-to-capture areas such as GC-rich and homologous regions but also tiny amounts of damaged DNA or RNA originated from circulating tumour cells or FFPE samples.
- Celemics custom design build and capture
- Uniformity of capture
- Dealing with Homologous and GC rich regions
- FFPE and poor quality DNA
- Questions and answers