Kick start your variant discovery research with over 7,000 phenotypically and ethnically diverse genome samples from more than 2,100 consenting families – minus the investment in sample acquisition costs and time. Whether you’re searching to unravel the complexities of disease inheritance or to tie identified variants to changes in RNA expression or protein function, Inova Genomes provides you with access to a wealth of high quality pre-annotated and pre-computed experimental data for easy and rapid hypothesis generation and validation.
Benefit from instant access to an expanding pool of scientifically validated genomes that can be filtered by disease, ethnicity, and familial relationship with the unprecedented ability to drill down to the genotypic details that enable you to distinguish and prioritize causal from non-causal variants. Inova Genomes helps you quickly isolate trends in inheritance, or validate research findings against a verified reference dataset for accelerated biomedical case solve rates.
Integration with Ingenuity® Variant Analysis™ allows you to directly mine the preloaded Inova Genomes data or work side-by-side with your own data to facilitate rapid and accurate isolation of causal variants.
Learn more about Ingenuity Variant Analysis.
Complementary data sets provide immediate possibilities for exploration of downstream effects of identified genetic variation, while access to fully consented study participants gives the flexibility to design your own follow up surveys, experiments and therapeutic programs.
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