Evidence map›Paper›PMID 31142813›Full record

ArticleHeredity2019

Bayesian model selection for the study of Hardy-Weinberg proportions and homogeneity of gender allele frequencies.

Xavier Puig, Josep Ginebra, Jan Graffelman

Abstract read
In one paragraph

Article in Heredity, 2019. 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. 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

3 authors.

Xavier PuigDepartment of Statistics and Operations Research, Universitat Politècnica de Catalunya, Barcelona, Spain.
Josep GinebraDepartment of Statistics and Operations Research, Universitat Politècnica de Catalunya, Barcelona, Spain.
Jan GraffelmanDepartment of Statistics and Operations Research, Universitat Politècnica de Catalunya, Barcelona, Spain. jan.graffelman@upc.edu.ORCID http://orcid.org/0000-0003-3900-0780

Funding

Theoretical Population Genetics SupplementR01GM075091 · NIGMS · UNIVERSITY OF WASHINGTON · PI WEIR, BRUCE S. · 2006 to 2020
$4.7M
Ministerio de Economía y Competitividad (Ministry of Economy and Competitiveness) MTM2013-43992-RMinisterio de Economía y Competitividad (Ministry of Economy and Competitiveness) MTM2015-65016-C2-2-RNIGMS NIH HHS R01 GM075091
6 · The paper itself

Abstract

Standard statistical tests for Hardy-Weinberg equilibrium assume the equality of allele frequencies in the sexes, whereas tests for the equality of allele frequencies in the sexes assume Hardy-Weinberg equilibrium. This produces a circularity in the testing of genetic variants, which has recently been resolved with new frequentist likelihood and exact procedures. In this paper, we tackle the same problem by posing it as a Bayesian model comparison problem. We formulate an exhaustive set of ten alternative scenarios for biallelic genetic variants. Using Dirichlet and Beta priors for genotype and allele frequencies, we derive marginal likelihoods for all scenarios, and select the most likely scenario using the posterior probabilities that each of these scenarios is the one in place. Different from the usual frequentist testing approach, the Bayesian approach allows one to compare any number of models, and not just two at a time, and the models compared do not have to be nested. We illustrate our Bayesian approach with genetic data from the 1,000 genomes project and through a simulation study.

Indexed as

AllelesGene FrequencyGenotypeModels, GeneticAnimalsFemaleHumansMale

Identifiers

PMID31142813
PMCPMC6972714

What OpenQuestion holds

Textmetadata
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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.