ArticleClinical and translational science2026
A Serverless Pharmacogenomic Risk Dashboard: Translating Ensemble Models and Model-Based Scenario Rules to Clinical Decision Support.
Article in Clinical and translational science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The "last mile" problem in healthcare AI-translating high-performance models into accessible, privacy-preserving point-of-care tools-remains unsolved for pharmacogenomic (PGx) risk assessment. No existing platform integrates opioid and polypharmacy risk scoring, model-based scenario analysis, and CPIC-based PGx patient cards within a single privacy-first serverless architecture. We designed, developed, and implemented the PGx Risk Dashboard: a serverless system combining an S3-hosted static frontend with AWS Lambda containerized backends. Fifty-six bin-level ensembles (2 cohorts × 7 age bands × 4 density bins), each comprising CatBoost/XGBoost/XGBoost-RF base learners, are packaged within an AWS Lambda container, with aggregate fallback artifacts used for sparse cells. Partial-input imputation using training-set medians handles real-world data sparsity; the PGx Patient Card executes stateless CPIC lookups for 573 deterministic gene-drug logic-verification cases without storing any PII. Lambda cold-start latency was mean 2100 ms (SD 250 ms); warm inference latency was mean 6 ms (SD 1 ms), meeting the sub-100 ms target. Prediction stability was maintained under sparse inputs (≤ 5 features provided): mean |Δp̂| = 0.10 vs. full-feature baseline. The PGx Risk Dashboard demonstrates technical feasibility for low-latency, privacy-first PGx risk decision support without EHR integration. We maintain the association-versus-causation distinction to support safer clinical use, avoid overstating treatment-effect evidence from observational outputs, and preserve a clear path to prospective causal-effect validation as next steps.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.