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学习扩散模型的极限

The Limits to Learning a Diffusion Model
Management Science · 2025 · Jackie Baek、Vivek F. Farias、Andreea Georgescu、Retsef Levi、Tianyi Peng、Deeksha Sinha

中文摘要

本文首次给出了简单扩散模型估计的样本复杂度下界,这些模型包括 Bass 模型(用于建模消费者采纳)和易感—感染—康复(SIR)模型(用于建模流行病)。我们表明,在扩散过程相当晚期之前,人们无法指望学习这类模型。具体而言,我们表明,收集数量超过我们样本复杂度下界的观测值所需的时间很长。对于 Bass 模型,我们的结果意味着,当新采纳者主要由模仿驱动时,在至少走完通往新采纳者速率达到峰值之时三分之二路程之前,人们无法指望预测最终的采纳顾客数量。类似地,我们的结果意味着,在 SIR 模型的情形下,在大约走完通往感染率峰值之时三分之二路程之前,人们无法指望预测最终的感染人数。这一估计上的下界进一步转化为流行病干预决策中遗憾的下界。我们的结果将准确预测的挑战形式化,并凸显了纳入额外数据来源的重要性。为此,我们分析了一项流行病血清流行率研究的益处,其中我们刻画了改进 SIR 模型估计所需的研究规模。针对产品采纳与流行病数据的大量实证分析支持了我们的理论发现。

Abstract

This paper provides the first sample complexity lower bounds for the estimation of simple diffusion models, including the Bass model (used in modeling consumer adoption) and the Susceptible-Infected-Recovered (SIR) model (used in modeling epidemics). We show that one cannot hope to learn such models until quite late in the diffusion. Specifically, we show that the time required to collect a number of observations that exceeds our sample complexity lower bounds is large. For the Bass model, our results imply that when new adopters are predominantly driven by imitation, one cannot hope to predict the eventual number of adopting customers until one is at least two-thirds of the way to the time at which the rate of new adopters is at its peak. In a similar vein, our results imply that in the case of an SIR model, one cannot hope to predict the eventual number of infections until one is approximately two-thirds of the way to the time at which the infection rate has peaked. This lower bound in estimation further translates into a lower bound in regret for decision making in epidemic interventions. Our results formalize the challenge of accurate forecasting and highlight the importance of incorporating additional data sources. To this end, we analyze the benefit of a seroprevalence study in an epidemic, where we characterize the size of the study needed to improve SIR model estimation. Extensive empirical analyses on product adoption and epidemic data support our theoretical findings.
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