Read on for details from some recent publications. We enjoy learning how it’s being used to support a wide range of NGS bioinformatics applications, from veterinary research to wastewater treatment. CLC Genomics Workbench is developed by scientists, for scientists, to analyze and visualize next generation sequencing (NGS) data. Genome research scientists want a powerful, end-to-end solution that easily integrates into their existing NGS analysis workflows. Publications citing CLC Genomics Workbench On-demand webinar: Harnessing insight from real-world oncology cases : introducing HSMD – In this on-demand webinar, we will introduce you to the Human Somatic Mutation Database (HSMD)-a new somatic database developed by QIAGEN.On-demand Webinar: How you can simplify your NGS secondary analysis workflow to 5 easy steps – Find out how you can simplify your NGS secondary analysis workflow to 5 easy steps using QCI Secondary Analysis, a new cloud-based service f.On-demand webinar: Discover hidden relationships in your toxicological studies with QIAGEN IPA – Watch this informative past webinar on how QIAGEN IPA can help you dig deeper into your toxicogenomic studies!.10 – An expert panel of leading medical geneticists, variant scientists and bioinformaticians will discuss emerging scientific and clinical trend. Hereditary NGS Clinical Summit Series: Part II – Nov. 23 – Join us for a 90-minute training session for new users of QIAGEN IPA.
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