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The genome
revolution

is here.
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Powering Discovery
Delivering genomic insights to genetics research and everyday medical practice through a robust, secure, clinical-grade web application.
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Next-Generation Medicine
By the creator of ANNOVAR, the gold-standard in whole genome interpretation with over 700 scientific citations
Tute pulls in over 125 annotation types, more than any other software
Tute uses proprietary machine-learning algorithms to help rapidly prioritize genetic variants
Tute takes your genome variant data in a variety of common formats (VCF, CG masterVar, and more)
For each genetic variant, Tute presents a human-readable annotation with links to external supporting evidence
Tute supports disease gene finding, biomarker discovery, pharmacogenetics and more
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Data You Can See
Tute Genomics has a broad set of features that allow you to quickly understand and visualize your data. With Tute Genomics you can literally view your samples, allowing rapid application of a hypothesis, visualization and evaluation of results and re-iteration of the hypothesis for immediate results that speed discovery.
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Tute Genomics is opening a new door for precision medicine by enabling researchers and clinicians to utilize human genome data for scientific discovery and individualized treatment.

What people are saying about Tute

"It’s extremely difficult to find experienced help with next-generation sequencing right now. We were glad to find Tute Genomics as our outsourced partner in biomarker discovery projects."

Senior Director, Translational Informatics
Top 10 Big Pharma

"It used to take my lab over 10 hours to analyze a human genome. With Tute's cloud browser-based software we can now do all of this in a matter of minutes."

Medical Director
CLIA-certified NGS Laboratory

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