Clinical diagnostics
Choose a genetic test from the case, specimen, and clinical question.
Review testing routes for inherited disease, prevention, prenatal genetics, oncology, liquid biopsy, and treatment interpretation.
Choose how to search
Start from the case, a known test, or a gene.
Use the route that matches the information already available.
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 starting points
Choose the route that matches the case.
The same gene can require a different method depending on the clinical setting, specimen, and question.
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.
Case review
Discuss a case that needs individual review.
Share a non-identifying clinical summary, phenotype, family structure, previous testing, and available material. We will use it to prepare the diagnostic discussion.