Precision diagnostics work happens at two altitudes. One is a person wondering whether their family history is worth a conversation. The other is a partner deciding which variant biology is worth funding. Both start with the same discipline — interpret the signal correctly before anyone acts on it.
Neither portal below provides a diagnosis. Each is designed to get the right person to the right next conversation.
For patients and clients
A short history checklist and an optional genetic result lookup — built against published hereditary-risk referral criteria, not a proprietary score. The output is a plain-language flag: does this pattern typically warrant a genetic counseling conversation.
For biopharma & diagnostics partners
Computational pre-screen (JAK) in progressCausal, functional variant stratification across exhaustion & persistence, TME & stress, antigen & escape, and safety & manufacturing — applied to specific franchises, not a generic biomarker pitch.
OpenOnco is a free, open, vendor-neutral comparison of 100+ liquid biopsy tests across MRD, early detection, and comprehensive genomic profiling. Once someone's history warrants a conversation, comparing which confirmatory test fits is exactly the problem OpenOnco already solves well. We link to it rather than rebuild it.
It doesn't diagnose, score risk numerically, or replace a clinician. It flags patterns against published referral criteria and points toward a genetic counselor. Anyone with a personal health concern should talk to a healthcare provider regardless of what the intake returns.