Peer-reviewed evidence
Publications and manuscripts that support EvoClin’s scientific foundation, including cancer evolution, molecular modelling, clinical endpoints and disease-specific validation.
EvoClin combines international guidelines, peer-reviewed publications, curated molecular cohorts and evolution-informed models to support NGS prescription, appropriateness assessment, molecular interpretation and outcome prediction.
EvoClin’s scientific layer connects evidence-based oncology knowledge with patient-level molecular and clinical data.
Publications and manuscripts that support EvoClin’s scientific foundation, including cancer evolution, molecular modelling, clinical endpoints and disease-specific validation.
The methodological layer combines cohort-trained machine learning, curated guideline logic and evolution-derived features to assist molecular decisions.
Molecular and clinical datasets are used to train, test and validate models for risk stratification, disease trajectories and clinically meaningful outcomes.
The same scientific architecture supports physicians and molecular biologists before, during and after molecular testing.
EvoClin uses guideline-aware and literature-aware AI to help evaluate which molecular tests are appropriate for a clinical context and when repeating NGS or ctDNA is likely to be useful.
Molecular findings are interpreted alongside clinical variables, longitudinal history and published evidence so that complex results become readable for clinical decision making.
Cohort-trained and evolution-informed models support prediction of clinically relevant outcomes, including prognosis, relapse, disease-free survival, metastasis and therapy resistance.