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| Format: | Preprint |
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2026
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| Online Access: | https://arxiv.org/abs/2601.23077 |
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| _version_ | 1866911411393789952 |
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| author | Bernal-Alvarado, Jose de Jesus Delepine, David |
| author_facet | Bernal-Alvarado, Jose de Jesus Delepine, David |
| contents | Traditional compartmental models, including SIR, SEIR, and SIRS frameworks, remain the analytical standard for epidemic forecasting. However, real-world data validation consistently reveals significant predictive failures, such as peak underestimations of up to 50%. This research identifies a persistent fundamental methodological error: the calibration of prevalence-based (stock) models using raw daily incidence (flow) data without proper transformation. We propose an integrated protocol utilizing an exponentially weighted convolution to reconstruct active cases from reported incidence: $I(t) \approx \frac{1}{p} \int_{0}^{t} NDC(τ) e^{-γ(t-τ)} dτ$. This transformation accounts for the recovery rate $γ$ and the ascertainment rate $p$. We demonstrate that increasing structural complexity, such as adding latency (SEIR) or waning immunity (SIRS), fails to resolve the incidence-prevalence gap. Simulation results show that without the proposed universal pre-processor, these advanced models inherit the systematic biases of misaligned data types, leading to significant errors in estimating latent periods and the "heavy tail" of endemicity. The proposed convolution transformation must serve as a universal prerequisite for any compartmental framework, bridging the gap between clinical reporting and mechanistic modeling. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2601_23077 |
| institution | arXiv |
| publishDate | 2026 |
| record_format | arxiv |
| spellingShingle | A Universal Convolution-Based Pre-processor to Correct the Prevalence-Incidence Gap in SIR, SEIR, and SIRS Modeling Bernal-Alvarado, Jose de Jesus Delepine, David Physics and Society Biological Physics Traditional compartmental models, including SIR, SEIR, and SIRS frameworks, remain the analytical standard for epidemic forecasting. However, real-world data validation consistently reveals significant predictive failures, such as peak underestimations of up to 50%. This research identifies a persistent fundamental methodological error: the calibration of prevalence-based (stock) models using raw daily incidence (flow) data without proper transformation. We propose an integrated protocol utilizing an exponentially weighted convolution to reconstruct active cases from reported incidence: $I(t) \approx \frac{1}{p} \int_{0}^{t} NDC(τ) e^{-γ(t-τ)} dτ$. This transformation accounts for the recovery rate $γ$ and the ascertainment rate $p$. We demonstrate that increasing structural complexity, such as adding latency (SEIR) or waning immunity (SIRS), fails to resolve the incidence-prevalence gap. Simulation results show that without the proposed universal pre-processor, these advanced models inherit the systematic biases of misaligned data types, leading to significant errors in estimating latent periods and the "heavy tail" of endemicity. The proposed convolution transformation must serve as a universal prerequisite for any compartmental framework, bridging the gap between clinical reporting and mechanistic modeling. |
| title | A Universal Convolution-Based Pre-processor to Correct the Prevalence-Incidence Gap in SIR, SEIR, and SIRS Modeling |
| topic | Physics and Society Biological Physics |
| url | https://arxiv.org/abs/2601.23077 |