Hotspot Cancer Panel Sequencing Library Preparation Kit

The Atila Hotspot Cancer Panel Sequencing Library Preparation Kit targets amplicon regions of more than 50 cancer related genes, including BRAF, KRAS, and EGFR etc, and provides superior sensitivity for detection of more than 2700 cancer mutation hotspots.

The resulting sample library is compatible with Illumina NGS sequencing. The current method employs novel primer design strategies, greatly simplifies sample preparation procedures, and enables rapid screening and discovering genetic variations.

Cancer hotspots are commonly observed mutations in known oncogenes and tumor suppressor genes across different cancer types.

Cancer is a type of diseases caused by accumulation of genetic changes, which results in abnormal cell growth and invasive behaviors that potentially spread to other body parts. Most common nucleotide sequence changes in cancer involve single-nucleotide variants and small insertions or deletions.