Evidence map›Paper›PMID 37561812›Full record

ArticlePLoS computational biology2023

Call detail record aggregation methodology impacts infectious disease models informed by human mobility.

Hamish Gibbs, Anwar Musah, Omar Seidu, William Ampofo, Franklin Asiedu-Bekoe, Jonathan Gray, Wole A Adewole, James Cheshire, Michael Marks, Rosalind M Eggo

Abstract read
In one paragraph

Article in PLoS computational biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Characterizing the impact of incorporating spatially aggregated human mobility data into infectious disease models.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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

10 authors.

Hamish GibbsDepartment of Geography, University College London, London, United Kingdom.ORCID 0000-0003-4413-453X
Anwar MusahDepartment of Geography, University College London, London, United Kingdom.
Omar SeiduGhana Statistical Service, Accra, Ghana.
William AmpofoNoguchi Memorial Institute for Medical Research, University of Ghana, Legon, Accra, Ghana.
Franklin Asiedu-BekoeGhana Health Service, Ministry of Health, Accra, Ghana.
Jonathan GrayFlowminder Foundation, Stockholm, Sweden.
Wole A AdewoleFlowminder Foundation, Stockholm, Sweden.
James CheshireDepartment of Geography, University College London, London, United Kingdom.
Michael MarksDepartment of Clinical Research, London School of Hygiene & Tropical Medicine, London, United Kingdom.
Rosalind M EggoDepartment of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, United Kingdom.

Funding

Medical Research Council MC_PC_19065
6 · The paper itself

Abstract

This paper demonstrates how two different methods used to calculate population-level mobility from Call Detail Records (CDR) produce varying predictions of the spread of epidemics informed by these data. Our findings are based on one CDR dataset describing inter-district movement in Ghana in 2021, produced using two different aggregation methodologies. One methodology, "all pairs," is designed to retain long distance network connections while the other, "sequential" methodology is designed to accurately reflect the volume of travel between locations. We show how the choice of methodology feeds through models of human mobility to the predictions of a metapopulation SEIR model of disease transmission. We also show that this impact varies depending on the location of pathogen introduction and the transmissibility of infections. For central locations or highly transmissible diseases, we do not observe significant differences between aggregation methodologies on the predicted spread of disease. For less transmissible diseases or those introduced into remote locations, we find that the choice of aggregation methodology influences the speed of spatial spread as well as the size of the peak number of infections in individual districts. Our findings can help researchers and users of epidemiological models to understand how methodological choices at the level of model inputs may influence the results of models of infectious disease transmission, as well as the circumstances in which these choices do not alter model predictions.

Indexed as

Communicable DiseasesEpidemicsGhanaHumansTravel

Identifiers

PMID37561812
PMCPMC10443843

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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.