CLINICAL DIAGNOSTICS
A clearer route from the clinical question to the right test.
Built for clinician-led selection across inherited disease, prevention, prenatal genetics, oncology, liquid biopsy, and treatment interpretation.
CHOOSE HOW TO BEGIN
Three focused tools. No overloaded single page.
The selector, portfolio, and gene directory now have different jobs and separate pages.
Select from the clinical question
A four-step route for cases where the most appropriate assay has not yet been established.
Start clinical selector →02Find a known test
Search the complete portfolio by indication, method, sample, biomarker, product code, or test name.
Open test portfolio →03Check a gene or panel scope
Enter an HGNC gene symbol and see which published panels include it, then inspect the complete analytical scope.
Search genes & scopes →CLINICAL ENTRY POINTS
Start with the case—not a product name.
These routes narrow the portfolio before a test appears. The same gene may require a different method depending on the clinical setting and specimen.
Preventive inherited-risk assessment
Actionable predisposition or medication-response assessment in an unaffected individual.
Established cancer diagnosis
Tumor profiling, liquid biopsy, MRD, neoantigens, or therapy review.
Unexplained phenotype or suspected rare disease
Panel, exome, copy-number, or single-gene diagnosis.
Ongoing pregnancy or prenatal indication
Time-sensitive fetal exome, array, or familial-variant testing.
Preconception, carrier, or fertility assessment
Couple carrier screening, fertility genetics, or familial clarification.
Known gene or documented familial variant
Focused confirmation instead of broad discovery testing.
This selector organizes the portfolio for discussion. A qualified clinician must confirm the indication, consent, validated scope, specimen, and interpretation pathway before ordering.
NEED A HUMAN REVIEW?
Complex cases should not be forced through an algorithm.
Share a non-identifying clinical summary, phenotype, family structure, previous testing, and available material. We will help prepare the appropriate diagnostic discussion.