Complete NGS workflow for ultra-rare cfDNA variant detection

What are the key considerations when working with cfDNA? How can I use NGS to detect ultra-rare variants at 0.1% variant allele frequency from cfDNA samples? Let us help you figure it all out. From cfDNA isolation to NGS and data analysis, we’ve developed a highly sensitive end-to-end workflow that delivers the data you need. Dive into the details in our application note.
QIAGEN products shown in the Application Note are intended for molecular biology applications. These products are not intended for the diagnosis, prevention or treatment of a disease.