Tag Archives: Allele Frequency Community

Looking back at 2015 and ahead to 2016

In this post, we share some of the trends and milestones that mattered most to us in 2015, and dust off our crystal ball for a sneak peek at 2016. For the genomics community, 2015 kicked off with a bang: … Read More

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Data analysis with greater efficiency

The Fall release of Ingenuity® Variant Analysis™ enriches the analysis functionality, adding speed and power, and offers new tools for the organization and management of sample analysis. We are committed to providing the most comprehensive solutions to our customers, and we’re delighted to … Read More

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Highlights from ASHG 2015

ASHG 2015 was everything we hoped it would be: interesting and inspiring scientific presentations and a place to reconnect with friends and customers. When we weren’t manning a busy booth, our team had a wonderful time soaking in the latest and greatest … Read More

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Looking Ahead to the 65th ASHG

For more than six decades, the American Society of Human Genetics Annual Meeting has offered the latest news and views about all areas of human genetics. This year, in its 65th iteration, ASHG promises to uphold that tradition: it will … Read More

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QIAGEN Bioinformatics at Individualizing Medicine Conference 2015

In a few days we’ll be heading to Rochester, MN to attend the Individualizing Medicine Conference: 2015, an annual meeting hosted by the Mayo Clinic. It will be held from September 20-23 at the Mayo Clinic Civic Center, and will … Read More

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Big Data Getting Bigger: Analysis and Sharing Critical as Genomics Grows Up

Recently PLoS Biology published a paper about big data in genomics from lead author Zachary Stephens, senior author Gene Robinson, and their collaborators at the University of Illinois at Urbana-Champaign and Cold Spring Harbor Laboratory. The perspective offers a bold vision … Read More

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New Product – QIAGEN® Clinical Insight Launched!

We are very pleased to announce the general availability of QIAGEN® Clinical Insight, the most comprehensive, scalable bioinformatics platform for clinical labs interpreting and reporting on genomic variants identified using next-generation sequencing. The first two supported applications are in oncology, … Read More

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QIAGEN Supports New ACMG Guidelines with Integration into Data Interpretation Tools

The American College of Medical Genetics and Genomics (ACMG), in collaboration with the Association for Molecular Pathology (AMP), recently published new guidelines for the interpretation of sequence variants. These guidelines are significant in their inclusion of an evidence-based gene variant … Read More

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