Automated DNA extraction for NGS using the MagNA Pure System family

Presented by

Mariana Fitarelli Kiehl, PhD, Senior Applications Scientist at Roche Sequencing and Life Science

About this talk

High-throughput NGS library preparation and expanded sequencing capacity demand greater scalability in nucleic acid extraction workflows, with less hands-on time. In this webinar, we: - Demonstrate that the MagNA Pure System’s hands-free workflows yield NGS-ready DNA - Present sequencing data from libraries prepared with genomic DNA (from whole blood) and cell-free DNA (from plasma) using the MagNA Pure 24 and the MagNA Pure 96 Systems - Compare sequencing metrics of data yielded by both manual extraction and the MagNA Pure Systems - Discuss the advantages of using MagNA Pure Systems to extract DNA for NGS MC-US-09885
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Next-generation sequencing (NGS) is driving advances in translational and clinical research. From expanding our understanding of cancer, reproductive and developmental biology to unravelling complex microbial populations, NGS is touching all facets of human disease and well­being. Sample prep for NGS holds the key to unlocking the potential of every sample. Explore our integrated Roche Sample Preparation Solutions, encompassing all the steps required to convert a sample to a sequencing-ready library. From sample collection to library quantification, we offer sample prep solutions for different sample types and sequencing applications that are proven, simple, and complete.