Talos was built to help resolve a major bottleneck in genomic medicine: human review time. The open-source system recovered 90% of in-scope diagnoses while surfacing just 1.3 candidate variants per patient for expert review. https://msft.it/6014vUBwK
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#1629Medical diagnoses can be improved by reanalyzing genomic data in rare disease cases. This is normally very burdensome, but today in @NatureMedicine we present Talos, a tool that in iterative monthly reanalysis reduces the burden to 1 variant per 200 cases https://www.nature.com/articles/s41591-026-04477-5
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