Evidence map›Paper›PMID 23782975›Full record

ArticleGenetics, selection, evolution : GSE2013

QTL fine mapping with Bayes C(π): a simulation study.

Irene van den Berg, Sébastien Fritz, Didier Boichard

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Article in Genetics, selection, evolution : GSE, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

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18citing papers in PubMed
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3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Review
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  4. Accuracy of genomic prediction of maternal traits in pigs using Bayesian variable selection methods.Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie · 2022
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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Irene van den BergINRA, UMR1313 Génétique animale et biologie intégrative, Domaine de Vilvert, 78350 Jouy-en-Josas, France. irene.vanderberg@jouy.inra.fr
Sébastien Fritz
Didier Boichard

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate QTL mapping is a prerequisite in the search for causative mutations. Bayesian genomic selection models that analyse many markers simultaneously should provide more accurate QTL detection results than single-marker models. Our objectives were to (a) evaluate by simulation the influence of heritability, number of QTL and number of records on the accuracy of QTL mapping with Bayes Cπ and Bayes C; (b) estimate the QTL status (homozygous vs. heterozygous) of the individuals analysed. This study focussed on the ten largest detected QTL, assuming they are candidates for further characterization.

methodsOur simulations were based on a true dairy cattle population genotyped for 38,277 phased markers. Some of these markers were considered biallelic QTL and used to generate corresponding phenotypes. Different numbers of records (4387 and 1500), heritability values (0.1, 0.4 and 0.7) and numbers of QTL (10, 100 and 1000) were studied. QTL detection was based on the posterior inclusion probability for individual markers, or on the sum of the posterior inclusion probabilities for consecutive markers, estimated using Bayes C or Bayes Cπ. The QTL status of the individuals was derived from the contrast between the sums of the SNP allelic effects of their chromosomal segments.

resultsThe proportion of markers with null effect (π) frequently did not reach convergence, leading to poor results for Bayes Cπ in QTL detection. Fixing π led to better results. Detection of the largest QTL was most accurate for medium to high heritability, for low to moderate numbers of QTL, and with a large number of records. The QTL status was accurately inferred when the distribution of the contrast between chromosomal segment effects was bimodal.

conclusionsQTL detection is feasible with Bayes C. For QTL detection, it is recommended to use a large dataset and to focus on highly heritable traits and on the largest QTL. QTL statuses were inferred based on the distribution of the contrast between chromosomal segment effects.

Indexed as

Bayes TheoremChromosome MappingModels, GeneticQuantitative Trait LociAlgorithmsAllelesAnimalsCattleComputer SimulationGenotypeMutationPolymorphism, Single Nucleotide

Identifiers

PMID23782975
PMCPMC3700753

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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.