Actionable mutation detection with multiplex PCR based targeted enrichment for NGS

>> YOUR LINK HERE: ___ http://youtube.com/watch?v=FeH65s9sTp0

Watch on LabRoots at http://labroots.com/user/webinars/det... • Next-generation sequencing (NGS) has revolutionized extraction of genomic information, facilitating rapid advances in the fields of basic and clinical research, molecular diagnostics, and drug development. However, certain bottlenecks in the NGS workflow still pose challenges to researchers. To meet these challenges, QIAGEN introduces GeneRead DNAseq Targeted Panels V2, targeting an extensive range of cancer-related genes or genomic regions. The gene panels use multiplex PCR-based target enrichment and enable ultra-deep sequencing of specific genes. They are compatible with any NGS sequencer and customizable to include other genes based on your research interests. The panels use as little as 10 ng starting DNA material per pool, require only 3 hours to enrich for targets, and substantially reduce the time to go from isolated DNA sample to sequencing-ready libraries. They are compatible for use with FFPE samples, do not require specialized instruments, and achieve industry-leading coverage (gt 96% of coding regions), specificity ( gt 90% of reads on-target), and uniformity (gt 90% of bases covered by at least 20% of the mean coverage depth).

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