Content by Qiagen

Scientists can optimize variant annotation with the Human Somatic Mutation Database (HSMD) and Human Germline Mutation Database (HGMD).

Discover the importance of automation and software solutions for standardizing NGS-based clinical diagnostics.

Learn where scientists need to exercise awareness when interpreting next-generation sequencing data for cancer screening.

Improving the reliability of genetic variant annotation and clinical interpretation

Researchers consult a continuously curated database to determine a variant’s clinical significance.

color = "#939598";.pullquote_left1, .pullquote_right1, .pullquote_left, .pullquote_right { color: #FEF8F6; background: #939598 } .breakhead { color: #000000; border-bottom: 1px solid #000000; } SPONSOR PROFILE About QIAGEN It all starts with the sample. Genetic material must be extracted from a biological sample and specifically processed before scientists from academia and industry can actually work with it. QIAGEN has made the hand