Variant Analysis Fall 2017 Release

This release is a minor release including slight improvements in the Phenotype Driven Ranking feature which now further sub-ranks variants that have identical scores. If you’re an existing customer, you can log in here.

Release summary

Ingenuity Variant Analysis

With Ingenuity Variant Analysis™, you can find disease-causing variants faster, and with fewer false leads, by tapping into the knowledge of millions of scientific findings. Based on 16+ years of expert manual curation of the scientific literature, our Knowledge Base is the gold standard for genome interpretation. By indexing all known disease-causing biological processes, we can deliver new insights and increased likelihood of homing in on the causal variant you’re seeking.

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Insights driving publications

Scientists all over the world have accelerated their research by analyzing more than 400,000 human samples using Ingenuity Variant Analysis. Our Knowledge Base has contributed to more than 5,500 peer-reviewed genomics publications from leading labs across the globe. Read a case study and learn why Ingenuity Variant Analysis is quickly becoming the industry standard for NGS variant interpretation.



Access thousands of genomes instantly

It can be expensive and time-consuming to study the number of genomes it takes to understand a disease. Ingenuity Variant Analysis is your gateway to extensive cohorts of high-quality, ethnically and phenotypically diverse human genome samples. They provide a set of healthy controls for rapid discovery and validation of causal elements of disease.



By using the filtering in Ingenuity Variant Analysis, we were able to find the gene which then led to the identification of this syndrome.

Dr. Hywel Williams, Centre for Translational Omics in the University College London’s Institute of Child Health (GOSgene)

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System requirements

Windows Internet Browsers

  • Internet Explorer v.9 or later
  • Firefox v.6 or later
  • Chrome v18 or later
Mac Internet Browsers

  • Safari v.5 or later
  • Firefox v.11 or later
  • Chrome v.18 or later

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