Variant Analysis
Identify causal variants from human sequencing data in just hours Rapidly Identify and Prioritize Variants Ingenuity Variant Analysis combines analytical tools and integrated content to help you rapidly identify and prioritize variants by drilling down to a small, targeted subset of compelling variants based both upon published biological evidence and your own knowledge of disease biology. Biological Interpretation of your Var…

The supplier does not provide quotations for this product through SelectScience. You can search for similar products in our Product Directory.
Identify causal variants from human sequencing data in just hours
Rapidly Identify and Prioritize Variants
Ingenuity Variant Analysis combines analytical tools and integrated content to help you rapidly identify and prioritize variants by drilling down to a small, targeted subset of compelling variants based both upon published biological evidence and your own knowledge of disease biology.
Biological Interpretation of your Variant Data
With Variant Analysis, you can interrogate your variants from multiple biological perspectives, explore different biological hypotheses, and identify the most promising variants for follow-up.
In Sickle Cell Project, Baylor Scientist Discovers Link to Fetal Hemoglobin Production with Ingenuity Variant Analysis from QIAGEN
Just two decades ago, there were virtually no therapeutic treatments for patients with sickle cell anemia, a severe condition in which blood cells form rigid sickle shapes, damaging several organs in the body. Today, there’s not only a medication, but thanks to new research from Vivien Sheehan and data interpretation from QIAGEN’s Ingenuity Variant Analysis, scientists also have a promising new lead for another treatment option.
Introducing Ingenuity Variant Analysis Software for the Rapid Identification of Causal Variants in NGS Data
Discover how Variant Analysis from Ingenuity combines analytical tools and integrated content to help you rapidly identify and prioritize variants. See how by drilling down to a small, targeted subset of compelling variants based both upon published biological evidence and your own knowledge of disease biology causal variants can easily be identified. Watch this video to learn about some of the key features of the software.












