HEREDITARY

Gene Variant Databases

Advances in Genomic Testing for Rare Disease Diagnostics

164 views March 26, 2024

Over the past decade, whole-exome and whole-genome sequencing have transformed the...

Clinical Summits

Part 2: AI-Powered Hereditary Disease Diagnostics: Closing the Gap in...

189 views November 30, 2023

Clinical exome sequencing (CES) is increasingly being adopted by small and mid-sized...

Clinical and Translational

Sample to Insight at LightSpeed: A barrier-breaking workflow for inherited...

248 views June 12, 2023

Next-generation sequencing (NGS) has transformed the field of genetic testing, enabling...

Clinical Summits

Emerging clinical trends in germline NGS testing: Expert Panel Discussion in USA

208 views November 17, 2022

Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline...

Clinical Summits

Emerging clinical trends in germline NGS testing: Expert Panel Discussion in...

144 views November 17, 2022

Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline...

Clinical Summits

Next-gen software workflow for germline testing: QIAGEN Expert talks in Europe

142 views October 18, 2022

Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline...

Clinical Summits

Next-gen software workflow for germline testing: QIAGEN Expert talks in USA

202 views October 18, 2022

Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline...

Web seminar recordings

Translational research: Find the needle in the haystack and access...

327 views December 15, 2020

Get connected to the industry’s most comprehensive collection of biological and...

Web seminar recordings

More effective and efficient routine exome and germline panel testing...

249 views October 29, 2020

See why laboratories across the globe choose QIAGEN solutions for routine testing...

Clinical Services

Fast tracking clinical NGS testing

483 views October 15, 2019

Discover a simpler and faster approach to implementing clinical NGS...

Web seminar recordings

Fast and easy identification of disease causing variants in hereditary diseases

1,793 views November 10, 2016

In this presentation, we will present our new one-step trio workflow, which...