TY - JOUR
T1 - Context-dependent representation of within- and between-model uncertainty
T2 - Aggregating probabilistic predictions in infectious disease epidemiology
AU - Howerton, Emily
AU - Runge, Michael C.
AU - Bogich, Tiffany L.
AU - Borchering, Rebecca K.
AU - Inamine, Hidetoshi
AU - Lessler, Justin
AU - Mullany, Luke C.
AU - Probert, William J.M.
AU - Smith, Claire P.
AU - Truelove, Shaun
AU - Viboud, Cécile
AU - Shea, Katriona
N1 - Funding Information:
This work was supported by the National Science Foundation (COVID-19 RAPID awards DEB-2028301, DEB-2037885 and DEB-2126278), the Eberly College of Science Barbara McClintock Science Achievement Graduate Scholarship in Biology at the Pennsylvania State University, and the Huck Institutes for the Life Sciences. Additional support was received from the US Department of Health and Human Services Centers for Disease Control and Prevention. Acknowledgements
Publisher Copyright:
© 2023 The Authors.
PY - 2023/1/25
Y1 - 2023/1/25
N2 - Probabilistic predictions support public health planning and decision making, especially in infectious disease emergencies. Aggregating outputs from multiple models yields more robust predictions of outcomes and associated uncertainty. While the selection of an aggregation method can be guided by retrospective performance evaluations, this is not always possible. For example, if predictions are conditional on assumptions about how the future will unfold (e.g. possible interventions), these assumptions may never materialize, precluding any direct comparison between predictions and observations. Here, we summarize literature on aggregating probabilistic predictions, illustrate various methods for infectious disease predictions via simulation, and present a strategy for choosing an aggregation method when empirical validation cannot be used. We focus on the linear opinion pool (LOP) and Vincent average, common methods that make different assumptions about between-prediction uncertainty. We contend that assumptions of the aggregation method should align with a hypothesis about how uncertainty is expressed within and between predictions from different sources. The LOP assumes that between-prediction uncertainty is meaningful and should be retained, while the Vincent average assumes that between-prediction uncertainty is akin to sampling error and should not be preserved. We provide an R package for implementation. Given the rising importance of multi-model infectious disease hubs, our work provides useful guidance on aggregation and a deeper understanding of the benefits and risks of different approaches.
AB - Probabilistic predictions support public health planning and decision making, especially in infectious disease emergencies. Aggregating outputs from multiple models yields more robust predictions of outcomes and associated uncertainty. While the selection of an aggregation method can be guided by retrospective performance evaluations, this is not always possible. For example, if predictions are conditional on assumptions about how the future will unfold (e.g. possible interventions), these assumptions may never materialize, precluding any direct comparison between predictions and observations. Here, we summarize literature on aggregating probabilistic predictions, illustrate various methods for infectious disease predictions via simulation, and present a strategy for choosing an aggregation method when empirical validation cannot be used. We focus on the linear opinion pool (LOP) and Vincent average, common methods that make different assumptions about between-prediction uncertainty. We contend that assumptions of the aggregation method should align with a hypothesis about how uncertainty is expressed within and between predictions from different sources. The LOP assumes that between-prediction uncertainty is meaningful and should be retained, while the Vincent average assumes that between-prediction uncertainty is akin to sampling error and should not be preserved. We provide an R package for implementation. Given the rising importance of multi-model infectious disease hubs, our work provides useful guidance on aggregation and a deeper understanding of the benefits and risks of different approaches.
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U2 - 10.1098/rsif.2022.0659
DO - 10.1098/rsif.2022.0659
M3 - Article
C2 - 36695018
AN - SCOPUS:85147047791
SN - 1742-5689
VL - 20
JO - Journal of the Royal Society Interface
JF - Journal of the Royal Society Interface
IS - 198
M1 - 20220659
ER -