genoCDS
Clinical Reference Tool — For Healthcare Professionals

Genomic Testing
Guidance for Oncology

genoCDS chronicles genomic testing indicated across all cancer disease states — organized by disease, subtype, and staging — with structured evidence tiers, reflex testing algorithms, and payer coverage across six major insurers.

Disease states
60+
in roadmap
Evidence sources
4
FDA, ASCO, ESMO, OncoKB
Payer policies tracked
6
CMS + 5 national payers
Standards aligned
5
SNOMED, LOINC, ICD-10, FHIR, CQL

Current Disease Coverage

Phase 1 covers four disease groups. Additional solid tumors and hematologic malignancies are added on a rolling basis.

How genoCDS Works

Step 01

Select Disease & Subtype

Browse by disease group (solid tumors or hematologic malignancies), then refine to the specific molecular or histologic subtype.

Step 02

Filter by Stage & Context

Specify the clinical context — pre-staging workup, at diagnosis, post-staging, or monitoring — and the applicable AJCC or WHO stage.

Step 03

Review Testing Recommendations

See prioritized test recommendations with evidence tiers (FDA, OncoKB, ASCO, ESMO), reflex algorithms, specimen requirements, and payer coverage.

API Access for Health Systems

Programmatic access to structured genomic testing guidance for EMR integration and clinical workflow tools. Free for qualified health systems; licensed for commercial use.

Request Access

Medical Disclaimer

genoCDS is a clinical reference tool for qualified healthcare professionals only. Content is derived from published guidelines and regulatory sources and may contain errors or outdated information. It is not a substitute for professional medical judgment, institutional protocols, or individual patient assessment. Always verify recommendations against current primary sources before making clinical decisions. Full disclaimer →