Evidence map›Paper›PMID 32612939›Full record

ArticleMethodsX2020

Size matters: Sample size assessments for chronic wasting disease surveillance using an agent-based modeling framework.

Aniruddha Belsare, Matthew Gompper, Barbara Keller, Jason Sumners, Lonnie Hansen, Joshua Millspaugh

Open access · goldAbstract read
In one paragraph

Article in MethodsX, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 34% of its field
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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

6 authors at 5 institutions in 1 country.

Aniruddha BelsareBoone & Crockett Quantitative Wildlife Center, Michigan State University, East Lansing, MI 48824, United States.
Matthew GompperDepartment of Fish, Wildlife and Conservation Ecology, New Mexico State University, Las Cruces, NM 88003, United States.
Barbara KellerMinnesota Department of Natural Resources, St. Paul, MN 55155, United States.
Jason SumnersMissouri Department of Conservation, 3500 East Gans Road, Columbia, MO 65201, United States.
Lonnie HansenMissouri Department of Conservation, 3500 East Gans Road, Columbia, MO 65201, United States.
Joshua MillspaughW.A. Franke College of Forestry and Conservation, University of Montana, Missoula, MT 59812, United States.
Missouri Department of Conservation · USMichigan State University · USMinnesota Department of Natural Resources · USNew Mexico State University · USUniversity of Montana · US

Funding

Sequence-structure-function relationships in human visual photopigmentsP20GM104420 · NIGMS · UNIVERSITY OF IDAHO · PI WICHMAN, HOLLY A · 2015 to 2024
$22.9M
NIGMS NIH HHS P20 GM104420
6 · The paper itself

Abstract

Epidemiological surveillance for many important wildlife diseases relies on samples obtained from hunter-harvested animals. Statistical methods used to calculate sample size requirements assume that the target population is randomly sampled, and therefore the samples are representative of the population. But hunter-harvested samples may not be representative of the population due to disease distribution heterogeneities (e.g. spatial clustering of infected individuals), and harvest-related non-random processes like regulations, hunter selectivity, variable land access, and uneven hunter distribution. Consequently, sample sizes necessary for detection of disease are underestimated and disease detection probabilities are overestimated, resulting in erroneous inferences about disease presence and distribution. We have developed a modeling framework to support the design of efficient disease surveillance programs for wildlife populations. The constituent agent-based models can incorporate real-world heterogeneities associated with disease distribution, harvest, and harvest-based sampling, and can be used to determine population-specific sample sizes necessary for prompt detection of important wildlife diseases like chronic wasting disease and bovine tuberculosis. The modeling framework and its application has been described in detail by Belsare et al. [1]. Here we describe how model scenarios were developed and implemented, and how model outputs were analyzed. The main objectives of this methods paper are to provide users the opportunity to a) assess the reproducibility of the published model results, b) gain an in-depth understanding of model analysis, and c) facilitate adaptation of this modeling framework to other regions and other wildlife disease systems.•The two agent-based models, MO

Indexed as

Agent-based modelingHarvest-based surveillanceIterative model analysisNetLogo

Identifiers

PMID32612939
PMCPMC7317228
OpenAlexW3035728602

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.