The Ion AmpliSeq™ Cancer Panel provides a fast & easy, cost effective sequencing workflow for single-tube preparation of amplicon libraries from genomic "hotspot" regions that frequently mutate in human cancer genes. These high quality libraries are prepared rapidly by PCR with as little as 10 ng of FFPE DNA or genomic DNA.
This cancer panel was designed to detect 739 COSMIC mutations in 604 loci from 46 oncogenes and tumor suppressor genes with emphasis on the deep coverage of KRAS, BRAF, and EGFR genes for the detection of somatic mutations in archived cancer samples. View the Ion AmpliSeq™ Cancer Panel Mutations List of targeted genes and mutations.
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Member since: 2008
Organization: National Institute of Biomedical Genomics