Bleed to read - from blood samples to ready-to-use library for NGS

Automating both nucleic acid (NA) purification from biological samples and library preparation for next-generation sequencing (NGS) is a crucial challenge in streamlining NGS protocols. While NGS has become more accessible and widely used, these manual processes can be time-consuming, error-prone, and labour-intensive.

This application note is focused on utilizing the chemagic™ Body Fluid 1k Kit and BioQule™ NGS System for Whole Genome Sequencing (WGS) with enzymatic fragmentation.