Evidence map›Paper›PMID 29624574›Full record

ArticlePLoS computational biology2018

Need for speed: An optimized gridding approach for spatially explicit disease simulations.

Stefan Sellman, Kimberly Tsao, Michael J Tildesley, Peter Brommesson, Colleen T Webb, Uno Wennergren, Matt J Keeling, Tom Lindström

Abstract read
In one paragraph

Article in PLoS computational biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Stefan SellmanDepartment of Physics, Chemistry and Biology, Division of Theoretical Biology, Linköping University, Linköping, Sweden.ORCID 0000-0002-5595-8780
Kimberly TsaoDepartment of Biology, Colorado State University, Fort Collins, CO, United States of America.ORCID 0000-0002-5616-1888
Michael J TildesleyZeeman Institute (SBIDER), School of Life Sciences and Mathematics Institute, University of Warwick, Gibbet Hill Road, Coventry, CV4 7AL, UK.
Peter BrommessonDepartment of Physics, Chemistry and Biology, Division of Theoretical Biology, Linköping University, Linköping, Sweden.
Colleen T WebbDepartment of Biology, Colorado State University, Fort Collins, CO, United States of America.
Uno WennergrenDepartment of Physics, Chemistry and Biology, Division of Theoretical Biology, Linköping University, Linköping, Sweden.
Matt J KeelingZeeman Institute (SBIDER), School of Life Sciences and Mathematics Institute, University of Warwick, Gibbet Hill Road, Coventry, CV4 7AL, UK.ORCID 0000-0003-4639-4765
Tom LindströmDepartment of Physics, Chemistry and Biology, Division of Theoretical Biology, Linköping University, Linköping, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Numerical models for simulating outbreaks of infectious diseases are powerful tools for informing surveillance and control strategy decisions. However, large-scale spatially explicit models can be limited by the amount of computational resources they require, which poses a problem when multiple scenarios need to be explored to provide policy recommendations. We introduce an easily implemented method that can reduce computation time in a standard Susceptible-Exposed-Infectious-Removed (SEIR) model without introducing any further approximations or truncations. It is based on a hierarchical infection process that operates on entire groups of spatially related nodes (cells in a grid) in order to efficiently filter out large volumes of susceptible nodes that would otherwise have required expensive calculations. After the filtering of the cells, only a subset of the nodes that were originally at risk are then evaluated for actual infection. The increase in efficiency is sensitive to the exact configuration of the grid, and we describe a simple method to find an estimate of the optimal configuration of a given landscape as well as a method to partition the landscape into a grid configuration. To investigate its efficiency, we compare the introduced methods to other algorithms and evaluate computation time, focusing on simulated outbreaks of foot-and-mouth disease (FMD) on the farm population of the USA, the UK and Sweden, as well as on three randomly generated populations with varying degree of clustering. The introduced method provided up to 500 times faster calculations than pairwise computation, and consistently performed as well or better than other available methods. This enables large scale, spatially explicit simulations such as for the entire continental USA without sacrificing realism or predictive power.

Indexed as

Computer SimulationModels, BiologicalAlgorithmsAnimalsCluster AnalysisComputational BiologyDisease OutbreaksFarmsFoot-and-Mouth DiseaseLivestock

Identifiers

PMID29624574
PMCPMC5906030

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Registered trials

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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.