Evidence map›Paper›PMID 32533106›Full record

ArticleHeredity2020

Novel approach to incorporate information about recessive lethal genes increases the accuracy of genomic prediction for mortality traits.

Grum Gebreyesus, Goutam Sahana, A Christian Sørensen, Mogens S Lund, Guosheng Su

Open access · hybridAbstract read
In one paragraph

Article in Heredity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

5 authors at 1 institution in 1 country.

Grum GebreyesusCenter for Quantitative Genetics and Genomics, Aarhus University, Blichers Alle, 8830, Tjele, Denmark.ORCID http://orcid.org/0000-0003-4757-3060
Goutam SahanaCenter for Quantitative Genetics and Genomics, Aarhus University, Blichers Alle, 8830, Tjele, Denmark.ORCID http://orcid.org/0000-0001-7608-7577
A Christian SørensenCenter for Quantitative Genetics and Genomics, Aarhus University, Blichers Alle, 8830, Tjele, Denmark.
Mogens S LundCenter for Quantitative Genetics and Genomics, Aarhus University, Blichers Alle, 8830, Tjele, Denmark.
Guosheng SuCenter for Quantitative Genetics and Genomics, Aarhus University, Blichers Alle, 8830, Tjele, Denmark. guosheng.su@qgg.au.dk.
Aarhus University · DK

Funding

Miljø- og Fødevareministeriet (Ministry of Environment and Food of Denmark) 34009-16-1101
6 · The paper itself

Abstract

The genetic underpinnings of calf mortality can be partly polygenic and partly due to deleterious effects of recessive lethal alleles. Prediction of the genetic merits of selection candidates should thus take into account both genetic components contributing to calf mortality. However, simultaneously modeling polygenic risk and recessive lethal allele effects in genomic prediction is challenging due to effects that behave differently. In this study, we present a novel approach where mortality risk probabilities from polygenic and lethal allele components are predicted separately to compute the total risk probability of an individual for its future offspring as a basis for selection. We present methods for transforming genomic estimated breeding values of polygenic effect into risk probabilities using normal density and cumulative distribution functions and show computations of risk probability from recessive lethal alleles given sire genotypes and population recessive allele frequencies. Simulated data were used to test the novel approach as implemented in probit, logit, and linear models. In the simulation study, the accuracy of predicted risk probabilities was computed as the correlation between predicted mortality probabilities and observed calf mortality for validation sires. The results indicate that our novel approach can greatly increase the accuracy of selection for mortality traits compared with the accuracy of predictions obtained without distinguishing polygenic and lethal gene effects.

Indexed as

Genes, LethalGenes, RecessiveModels, GeneticAnimalsCattleGenomeGenomicsGenotypeMortalityPhenotype

Identifiers

PMID32533106
PMCPMC7426854
OpenAlexW3035723688

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.