Evidence map›Paper›PMID 39700149›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Toward optimal disease surveillance with graph-based active learning.

Joseph L-H Tsui, Mengyan Zhang, Prathyush Sambaturu, Simon Busch-Moreno, Marc A Suchard, Oliver G Pybus, Seth Flaxman, Elizaveta Semenova, Moritz U G Kraemer

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

9 authors.

Joseph L-H Tsui *Department of Biology, University of Oxford, Oxford OX1 3SZ, United Kingdom.ORCID 0000-0001-7871-8627
Mengyan Zhang *Department of Computer Science, University of Oxford, Oxford OX1 3QG, United Kingdom.
Prathyush SambaturuDepartment of Biology, University of Oxford, Oxford OX1 3SZ, United Kingdom.ORCID 0000-0003-1795-5287
Simon Busch-MorenoDepartment of Biology, University of Oxford, Oxford OX1 3SZ, United Kingdom.
Marc A SuchardDepartment of Biostatistics, University of California, Los Angeles, CA 90095.ORCID 0000-0001-9818-479X
Oliver G PybusDepartment of Biology, University of Oxford, Oxford OX1 3SZ, United Kingdom.ORCID 0000-0002-8797-2667
Seth Flaxman *Department of Computer Science, University of Oxford, Oxford OX1 3QG, United Kingdom.ORCID 0000-0002-2477-4217
Elizaveta Semenova *Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London SW7 2AZ, United Kingdom.
Moritz U G Kraemer *Department of Biology, University of Oxford, Oxford OX1 3SZ, United Kingdom.ORCID 0000-0001-8838-7147

Funding

Statistical Innovation to Integrate Sequences and Phenotypes for Scalable Phylodynamic InferenceR01AI153044 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Marc A. Suchard · 2021 to 2026
$2.4M
EC | ERC | HORIZON EUROPE European Research Council (ERC) 101086640EC | ERC | HORIZON EUROPE European Research Council (ERC) 874850NIAID NIH HHS R01 AI153044Schmidt Futures G-22-64476UK Research and Innovation (UKRI) APP8583UKRI | Engineering and Physical Sciences Research Council (EPSRC) EP/V002910/2UKRI | MRC | Medical Research Foundation MRF-RG-ICCH-2022-100069Wellcome TrustWellcome Trust (WT) 225288/Z/22/ZWellcome Trust (WT) 226052/Z/22/ZWellcome Trust (WT) 228186/Z/23/Z
6 · The paper itself

Abstract

Tracking the spread of emerging pathogens is critical to the design of timely and effective public health responses. Policymakers face the challenge of allocating finite resources for testing and surveillance across locations, with the goal of maximizing the information obtained about the underlying trends in prevalence and incidence. We model this decision-making process as an iterative node classification problem on an undirected and unweighted graph, in which nodes represent locations and edges represent movement of infectious agents among them. To begin, a single node is randomly selected for testing and determined to be either infected or uninfected. Test feedback is then used to update estimates of the probability of unobserved nodes being infected and to inform the selection of nodes for testing at the next iterations, until certain test budget is exhausted. Using this framework, we evaluate and compare the performance of previously developed active learning policies for node selection, including Node Entropy and Bayesian Active Learning by Disagreement. We explore the performance of these policies under different outbreak scenarios using simulated outbreaks on both synthetic and empirical networks. Further, we propose a policy that considers the distance-weighted average entropy of infection predictions among neighbors of each candidate node. Our proposed policy outperforms existing ones in most outbreak scenarios given small test budgets, highlighting the need to consider an exploration-exploitation trade-off in policy design. Our findings could inform the design of cost-effective surveillance strategies for emerging and endemic pathogens and reduce uncertainties associated with early risk assessments in resource-constrained situations.

Indexed as

Bayes TheoremDisease OutbreaksHumansMachine LearningPopulation Surveillanceactive learningdisease surveillanceepidemiologynetwork dynamicspublic health

Identifiers

PMID39700149
PMCPMC11670094

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.