Evidence map›Paper›PMID 39197015›Full record

ArticleG3 (Bethesda, Md.)2024

Prediction of additive genetic variances of descendants for complex families based on Mendelian sampling variances.

Tobias A M Niehoff, Jan Ten Napel, Mario P L Calus

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Practical Considerations When Using Mendelian Sampling Variances for Selection Decisions in Genomic Selection Programs.Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie · 2025
    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.

Tobias A M NiehoffAnimal Breeding and Genomics, Wageningen University & Research, Droevendaalsesteeg 1, P.O. Box 338, 6700 AH Wageningen, The Netherlands.ORCID 0000-0003-3046-6699
Jan Ten NapelAnimal Breeding and Genomics, Wageningen University & Research, Droevendaalsesteeg 1, P.O. Box 338, 6700 AH Wageningen, The Netherlands.ORCID 0000-0002-1918-9080
Mario P L CalusAnimal Breeding and Genomics, Wageningen University & Research, Droevendaalsesteeg 1, P.O. Box 338, 6700 AH Wageningen, The Netherlands.ORCID 0000-0002-3213-704X

Funding

Breed4Food partners Cobb EuropeCRVDutch Ministry of Economic AffairsHendrix GeneticsTopigs Norsvin
6 · The paper itself

Abstract

The ability to predict the outcome of selection and mating decisions enables breeders to make strategically better selection decisions. To improve genetic progress, those individuals need to be selected whose offspring can be expected to show high genetic variance next to high breeding values. Previously published approaches enable to predict the variance of descendants of 2 future generations for up to 4 founding haplotypes, or 2 outbred individuals, based on phased genotypes, allele effects, and recombination frequencies. The purpose of this study was to develop a general approach for the analytical calculation of the genetic variance in any future generation. The core development is an equation for the prediction of the variance of double haploid lines, under the assumption of no selection and negligible drift, stemming from an arbitrary number of founder haplotypes. This double haploid variance can be decomposed into gametic Mendelian sampling variances (MSVs) of ancestors of the double haploid lines allowing usage for non-double haploid genotypes that enables application in animal breeding programs as well as in plant breeding programs. Together with the breeding values of the founders, the gametic MSV may be used in new selection criteria. We present our idea of such a criterion that describes the genetic level of selected individuals in 4 generations. Since breeding programs do select, the assumption made for predicting variances is clearly violated, which decreases the accuracy of predicted gametic MSV caused by changes in allele frequency and linkage disequilibrium. Despite violating the assumption, we found high predictive correlations of our criterion to the true genetic level that was obtained by means of simulation for the "corn" and "cattle" genome models tested in this study (0.90 and 0.97). In practice, the genotype phases, genetic map, and allele effects all need to be estimated meaning inaccuracies in their estimation will lead to inaccurate variance prediction. Investigation of variance prediction accuracy when input parameters are estimated was not part of this study.

Indexed as

Genetic VariationHaploidyModels, GeneticAnimalsBreedingGene FrequencyGenotypeHaplotypesSelection, Geneticgenetic variancegenomic selectionIndex5Mendelian samplingMendelian sampling variancemultiparental crossesprogeny varianceresponse to selectionusefulness criterionwithin-family selection

Identifiers

PMID39197015
PMCPMC11540313

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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 Socratic graph.