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Ingenuity Variant Analysis⢠enables Complete Genomics customers to rapidly analyze and interpret biologically relevant genetic variations and provides researchers with a unique, fully integrated, sample-to-insight workflow. Watch a short introductory video.
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Ingenuity Variant Analysis is intended for molecular biology applications. This product is not intended for the diagnosis, prevention or treatment of a disease. For up-to-date licensing information and product-specific disclaimers, see the respective Ingenuity product site. Further information can be requested from [email protected] or by ...
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Login Information: Email: Account activation email and Ingenuity communications will be sent to this address ... Register for access to Ingenuity Variant Analysis⢠All fields are required unless otherwise indicated. Login Information: Email: Account activation email and Ingenuity communications will be sent to this address ...
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Identifies causal variants from human sequencing data. Ingenuity Variant Analysis is a web-based application that combines analytical tools and integrated genomics content with user panel, exome, or genome data to rapidly identify and prioritize compelling causal variants using published biological evidence. The software enables prioritization of variants along biologically relevant filter ...Interface: Web user interface
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May 31, 2016 · Presented by Sohela Shah, Principle Genome Scientist. In this webinar Dr. Anika Joecker is going through the key features and...
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Iterative analysis Ingenuity Variant Analysis mirrors the investigative process, allowing rapid application of a hypothesis, visualization and evaluation of results, and reiteration of the hypothesis, providing immediate results that speed discovery. Sharing and publication tools Easy-to-use tools allow collaboration with colleagues and peers.
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Ingenuity Variant Analysis Identify causal variants, fast Find disease-causing variants faster and with fewer false leads using Ingenuity Variant Analysis (IVA), a software-as-a-service that taps into the knowledge of millions of scientific findings to help you zero-in on causal variants.
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