Solve-RD's collaborative “Solvathons” show how structured data reanalysis and joint interpretation can drive diagnosis and how GHGA tools help enable secure, scalable workflows.
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Discussion around expectations and needs towards patient communication. The aim is to build a comprehensive online information hub for patients, care-givers, and the interested public. Registration for focus groups is open.
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A new study introduces a workflow with the clinical implementation of RNA sequencing in conjunction with DNA sequencing to diagnose patients with rare genetic disorders.
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