Target: whether the next 4 weeks carry above-median confirmed burden. Trained on real, cross-validated NCDC weekly data (train ≤2023, test 2024). The model beats a naive persistence baseline by only ~0.03 AUROC; the dominant predictor is dry-season timing. All metrics are retrospective — prospective validation is the pre-registered next step.
National Early-Warning Model
Clinical Copilot
| Item | Value |
|---|---|
| Time period | 2020–2025 (national weekly) |
| Observations | 313 epidemiological weeks |
| Confirmed cases (2020–25) | 6,456 |
| Case source | NCDC Weekly Epidemiological Reports (cross-validated) |
| Per-state / clinical | SORMAS 2018–2021 (CC-BY, DOI 10.5281/zenodo.7309567) |
| Elevated-week rate | 56% (balanced, non-degenerate target) |
| Preprint (open access) | Zenodo, CC-BY · DOI 10.5281/zenodo.21122486 |
Dry-season timing dominates (52.6% gain importance) — the model is learning the real November–April Lassa season, not a data artefact. Recent case history and trend supply the rest. The national model uses no meteorological covariates; national-average weather is not epidemiologically meaningful.
We are preparing a NIH Fogarty International Center R21 application (up to $275,000 / 2 years) with two aims:
Application deadline: October 16, 2026 (LOI due September 16, 2026)
From the individual-level SORMAS 2018–2021 data, the endemic states rank Edo > Ondo > Ebonyi > Bauchi, consistent with published NCDC reporting. Edo (ISTH Irrua) and Ondo (FMC Owo / ILFRC) host the principal treatment and reference centres.
Validated per-state weekly case counts are not yet available — NCDC publishes them as image tables not amenable to extraction. Obtaining structured per-state data (proposed in partnership with NCDC) to build and prospectively validate a per-state model is the immediate next step. No per-state cumulative totals are shown here because none have been validated.
(1) Retrospective only — prospective validation not yet complete. (2) Confirmed cases only — true Lassa incidence substantially higher. (3) State-capital weather — rural microclimates may differ. (4) Reporting variability — testing capacity varies by state and year. (5) Clinical Copilot — not validated in a prospective clinical study; not a diagnostic device.