Developing solid tumor and hematological panels for a flexible and automated microfluidic workflow that improves efficiency of NGS library preparation for cancer research

In this study, Fluidigm designed two amplicon-based, targeted NGS library preparation (LP) panels for detecting single-nucleotide variants, insertions and deletions, copy number variants, and RNA fusions. This workflow, coupled with relevant panel content and performance, offers a solution for investigators requiring economical NGS testing of FFPE and blood samples.