Start with the case.
Create a case, add the sample details, and upload variants. Keep the genome build, assay, and biomarkers together from the start.
Connect molecular findings with therapy evidence. Review every association in context, then bring your reasoning together in a traceable report.
Non-small cell lung cancer
Move from an uploaded file to a reviewed report in one workspace. Your case context and review decisions travel with you.
Create a case, add the sample details, and upload variants. Keep the genome build, assay, and biomarkers together from the start.
See the alteration, therapy association, evidence direction, and source together. Record what belongs in the report and what does not.
Create a report snapshot from your review. Keep resistance cautions, source records, and limitations visible alongside the findings.
Drugmarker keeps the path from a molecular finding to its supporting record visible, so the review can be understood beyond a single result.
Sensitivity and resistance are distinct, visible signals.
Included, excluded, and pending findings remain distinguishable.
A report captures a review snapshot; later changes are flagged.
DM-2026-008 · Non-small cell lung cancer
Researchers and clinical teams working with molecular findings and therapy evidence. The workspace is organized around case review, interpretation, and reporting.
Request access with your role and organization. The flow is request review, an invitation, then account setup.
No. Its case and review decisions are illustrative. Evidence associations do not represent current prescribing guidance or a treatment recommendation.
VEP, ClinVar, CIViC, ClinicalTrials.gov, report generation, audit, and email are connected to the research platform. OncoKB is enabled when a licensed token is available.
Request access for your research team, or sign in to continue a review.