Recently, there have been many noteworthy papers citing QIAGEN CLC Genomics Workbench, a comprehensive, easy-to-use toolbox that ensures continuity in…

Publication Roundup: Biomedical Genomics Workbench Check out these recent articles citing Biomedical Genomics Workbench, a comprehensive, highly accurate NGS data…

Using new QIAseq DNA Targeted Panels with Biomedical Genomics Workbench increases the accuracy of detecting low frequency variants. We are…

We’re happy to announce that new releases of our products are now available. The releases offer a number of new features and improvements. You can…

We recently returned from beautiful Barcelona, where we attended the 49th annual meeting for the European Society of Human Genetics…

Looking back at ACMG 2016 where speakers looked ahead to improved variant analysis Inspiring talks at ACMG We recently attended the…

Living with a rare disease is often lonely and isolating for patients and caregivers alike. Through our work with researchers…

Your $1,000 genome will only cost $22 to analyze We’re committed to enabling our customers to analyze vast amounts of…

We are pleased to announce the launch of our new end-to-end solution for hereditary diseases; an offering including Biomedical Genomics Workbench, Biomedical…