NimaGen offers two versions of its CE-IVD approved EasySeq™ NGS CFTR Library Prep kit powered by Reverse Complement PCR technology to aid in the diagnosis of (or the congenital predisposition to) cystic fibrosis by detecting sequence variants of the CFTR gene:
Illumina® sequencing of the human CFTR gene coding exons, including a minimum of 20 bases upstream and downstream of each exon, as well as includes 2 intronic hotspot mutations
Illumina® sequencing of 50 hotspot mutations of the human CFTR gene, including the most common mutations found in the European population