Evidence map›Paper›PMID 27966535›Full record

ArticleHeredity2017

Estimating parent-specific QTL effects through cumulating linked identity-by-state SNP effects in multiparental populations.

A Maurer, W Sannemann, J Léon, K Pillen

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Article in Heredity, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

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14citing papers in PubMed
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3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

A MaurerInstitute of Agricultural and Nutritional Sciences, Martin Luther University Halle-Wittenberg, Halle, Germany.
W SannemannInstitute of Agricultural and Nutritional Sciences, Martin Luther University Halle-Wittenberg, Halle, Germany.
J LéonInstitute for Crop Science and Resource Conservation, University Bonn, Bonn, Germany.
K PillenInstitute of Agricultural and Nutritional Sciences, Martin Luther University Halle-Wittenberg, Halle, Germany.ORCID 0000-0003-4646-6351

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The emergence of multiparental mapping populations enabled plant geneticists to gain deeper insights into the genetic architecture of major agronomic traits and to map quantitative trait loci (QTLs) controlling the expression of these traits. Although the investigated mapping populations are similar, one open question is whether genotype data should be modelled as identical by state (IBS) or identical by descent (IBD). Whereas IBS simply makes use of raw genotype scores to distinguish alleles, IBD data are derived from parental offspring information. We report on comparing IBS and IBD by applying two multiple regression models on four traits studied in the barley nested association mapping (NAM) population HEB-25. We observed that modelling parent-specific IBD genotypes produced a lower number of significant QTLs with increased prediction abilities compared with modelling IBS genotypes. However, at lower trait heritabilities the IBS model produced higher prediction abilities. We developed a method to estimate multiallelic QTL effects in multiparental populations from simple biallelic IBS data. This method is based on cumulating IBS-derived single-nucleotide polymorphism (SNP) effect estimates in a defined genetic region surrounding a QTL. Comparing the resulting parent-specific QTL effects with those obtained from IBD approaches revealed high accordance that could be confirmed through simulations. The method turned out to be also applicable to a barley multiparent advanced generation inter-cross (MAGIC) population. The 'cumulation method' represents a universal approach to differentiate parent-specific QTL effects in multiparental populations, even if no IBD information is available. In future, the method could further benefit from the availability of much denser SNP maps.

Indexed as

Genetics, PopulationPolymorphism, Single NucleotideQuantitative Trait LociAllelesChromosome MappingComputer SimulationCrosses, GeneticGenotypeHordeumModels, Genetic

Identifiers

PMID27966535
PMCPMC5520528

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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.