Evidence map›Paper›PMID 27107720›Full record

ArticleGenetics, selection, evolution : GSE2016

Mendelian sampling covariability of marker effects and genetic values.

Sarah Bonk, Manuela Reichelt, Friedrich Teuscher, Dierck Segelke, Norbert Reinsch

Open access · goldAbstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.9field-weighted citation impact, top 7% of its field
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

31 citing papers in PubMed, 46 citations in OpenAlex.

  1. A comparative study on recombination activity in cattle.Genetics, selection, evolution : GSE · 2026
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  8. A Similarity Matrix for Preserving Haplotype Diversity Amongst Parents in Genomic Selection.Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie · 2025
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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

5 authors at 1 institution in 1 country.

Sarah BonkInstitute of Genetics and Biometry, Leibniz-Institute for Farm Animal Biology (FBN), Wilhelm-Stahl-Allee 2, 18196, Dummerstorf, Germany.
Manuela ReicheltInstitute of Genetics and Biometry, Leibniz-Institute for Farm Animal Biology (FBN), Wilhelm-Stahl-Allee 2, 18196, Dummerstorf, Germany.
Friedrich TeuscherInstitute of Genetics and Biometry, Leibniz-Institute for Farm Animal Biology (FBN), Wilhelm-Stahl-Allee 2, 18196, Dummerstorf, Germany.
Dierck SegelkeVereinigte Informationssysteme Tierhaltung w.V., Heideweg 1, 27283, Verden, Germany.
Norbert ReinschInstitute of Genetics and Biometry, Leibniz-Institute for Farm Animal Biology (FBN), Wilhelm-Stahl-Allee 2, 18196, Dummerstorf, Germany. reinsch@fbn-dummerstorf.de.
Research Institute for Farm Animal Biology (FBN) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMeasures of the expected genetic variability among full-sibs are of practical relevance, such as in the context of mating decisions. An important application field in animal and plant breeding is the selection and allocation of mates when large or small amounts of genetic variability among offspring are desired, depending on user-specific goals. Estimates of the Mendelian sampling variance can be obtained by simulating gametes from parents with known diplotypes. Knowledge of recombination rates and additive marker effects is also required. In this study, we aimed at developing an exact method that can account for both additive and dominance effects.

resultsWe derived parent-specific covariance matrices that exactly quantify the within-family (co-)variability of additive and dominance marker effects. These matrices incorporate prior knowledge of the parental diplotypes and recombination rates. When combined with additive marker effects, they allow the exact derivation of the Mendelian sampling (co-)variances of (estimated) breeding values for several traits, as well for the aggregate genotype. A comparative analysis demonstrated good average agreement between the exact values and the simulation results for a practical dataset (74,353 German Holstein cattle).

conclusionsThe newly derived method is suitable for calculating the exact amount of intra-family variation of the estimated breeding values and genetic values (comprising additive and dominance effects).

Indexed as

BreedingGenetic MarkersGenetic VariationModels, GeneticAnimalsCattleFemaleGenotypeMalePhenotypeGenetic Markers

Identifiers

PMID27107720
PMCPMC4842306
OpenAlexW2337645233

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.