Evidence map›Paper›PMID 39003468›Full record

ArticleBMC genomics2024

Evaluation of heritability partitioning approaches in livestock populations.

Can Yuan, José Luis Gualdrón Duarte, Haruko Takeda, Michel Georges, Tom Druet

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Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Can YuanUnit of Animal Genomics, GIGA-R & Faculty of Veterinary Medicine, University of Liège, Avenue de L'Hôpital, 1, 4000, Liège, Belgium. can.yuan@uliege.be.
José Luis Gualdrón DuarteWalloon Breeders Association, Rue Des Champs Elysées, 4, Ciney, 5590, Belgium.
Haruko TakedaUnit of Animal Genomics, GIGA-R & Faculty of Veterinary Medicine, University of Liège, Avenue de L'Hôpital, 1, 4000, Liège, Belgium.
Michel GeorgesUnit of Animal Genomics, GIGA-R & Faculty of Veterinary Medicine, University of Liège, Avenue de L'Hôpital, 1, 4000, Liège, Belgium.
Tom DruetUnit of Animal Genomics, GIGA-R & Faculty of Veterinary Medicine, University of Liège, Avenue de L'Hôpital, 1, 4000, Liège, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHeritability partitioning approaches estimate the contribution of different functional classes, such as coding or regulatory variants, to the genetic variance. This information allows a better understanding of the genetic architecture of complex traits, including complex diseases, but can also help improve the accuracy of genomic selection in livestock species. However, methods have mainly been tested on human genomic data, whereas livestock populations have specific characteristics, such as high levels of relatedness, small effective population size or long-range levels of linkage disequilibrium.

resultsHere, we used data from 14,762 cows, imputed at the whole-genome sequence level for 11,537,240 variants, to simulate traits in a typical livestock population and evaluate the accuracy of two state-of-the-art heritability partitioning methods, GREML and a Bayesian mixture model. In simulations where a single functional class had increased contribution to heritability, we observed that the estimators were unbiased but had low precision. When causal variants were enriched in variants with low (< 0.05) or high (> 0.20) minor allele frequency or low (below 1st quartile) or high (above 3rd quartile) linkage disequilibrium scores, it was necessary to partition the genetic variance into multiple classes defined on the basis of allele frequencies or LD scores to obtain unbiased results. When multiple functional classes had variable contributions to heritability, estimators showed higher levels of variation and confounding between certain categories was observed. In addition, estimators from small categories were particularly imprecise. However, the estimates and their ranking were still informative about the contribution of the classes. We also demonstrated that using methods that estimate the contribution of a single category at a time, a commonly used approach, results in an overestimation. Finally, we applied the methods to phenotypes for muscular development and height and estimated that, on average, variants in open chromatin regions had a higher contribution to the genetic variance (> 45%), while variants in coding regions had the strongest individual effects (> 25-fold enrichment on average). Conversely, variants in intergenic or intronic regions showed lower levels of enrichment (0.2 and 0.6-fold on average, respectively).

conclusionsHeritability partitioning approaches should be used cautiously in livestock populations, in particular for small categories. Two-component approaches that fit only one functional category at a time lead to biased estimators and should not be used.

Indexed as

Linkage DisequilibriumLivestockAnimalsBayes TheoremCattleGene FrequencyGenetic VariationGenomicsModels, GeneticPhenotypePolymorphism, Single NucleotideQuantitative Trait, HeritableComplex traitsFunctional annotationGenetic architectureHeritability partitioningVariance components

Identifiers

PMID39003468
PMCPMC11246585

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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.