VIASURE Cystic fibrosis NGS Solution

VIASURE Cystic Fibrosis NGS Solution is a comprehensive solution that integrates both library preparation, amplicon based, and downstream bioinformatic analysis. It is specifically designed to streamline the simultaneous detection of clinically relevant mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene, the primary cause of cystic fibrosis—a severe genetic disorder. The kit is compatible with human samples, including blood and buccal swabs.

VIASURE Cystic Fibrosis NGS Solution enables the identification of single nucleotide variants (SNVs) and small insertions or deletions (indels). It supports the multiplexing of up to 48 samples in a single sequencing run. For optimal performance, each library should receive approximately 150,000 paired-end reads. Sequencing is recommended using a 2×150 bp paired-end configuration.