Evidence map›Paper›PMID 20823332›Full record

ArticleBioinformatics (Oxford, England)2010

Modeling associations between genetic markers using Bayesian networks.

Edwin Villanueva, Carlos Dias Maciel

Abstract readEvaluation Study
In one paragraph

Article in Bioinformatics (Oxford, England), 2010. 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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Edwin VillanuevaElectrical Engineering Department, Sao Carlos School of Engineering, University of Sao Paulo, Sao Carlos, Sao Paulo, Brazil.
Carlos Dias Maciel

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationUnderstanding the patterns of association between polymorphisms at different loci in a population (linkage disequilibrium, LD) is of fundamental importance in various genetic studies. Many coefficients were proposed for measuring the degree of LD, but they provide only a static view of the current LD structure. Generative models (GMs) were proposed to go beyond these measures, giving not only a description of the actual LD structure but also a tool to help understanding the process that generated such structure. GMs based in coalescent theory have been the most appealing because they link LD to evolutionary factors. Nevertheless, the inference and parameter estimation of such models is still computationally challenging.

resultsWe present a more practical method to build GM that describe LD. The method is based on learning weighted Bayesian network structures from haplotype data, extracting equivalence structure classes and using them to model LD. The results obtained in public data from the HapMap database showed that the method is a promising tool for modeling LD. The associations represented by the learned models are correlated with the traditional measure of LD D'. The method was able to represent LD blocks found by standard tools. The granularity of the association blocks and the readability of the models can be controlled in the method. The results suggest that the causality information gained by our method can be useful to tell about the conservability of the genetic markers and to guide the selection of subset of representative markers. AVAILABILITY: The implementation of the method is available upon request by email.

Indexed as

Genetic MarkersLinkage DisequilibriumModels, GeneticAlgorithmsBayes TheoremChromosome MappingHaplotypesHumansPolymorphism, Single NucleotideGenetic Markers

Identifiers

PMID20823332
PMCPMC2935421

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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.