Evidence map›Paper›PMID 35303797›Full record

ArticleGenetics, selection, evolution : GSE2022

Effect of genotyping strategies on the sustained benefit of single-step genomic BLUP over multiple generations.

Milagros Sánchez-Mayor, Valentina Riggio, Pau Navarro, Beatriz Gutiérrez-Gil, Chris S Haley, Luis Fernando De la Fuente, Juan-José Arranz, Ricardo Pong-Wong

Abstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

8 authors.

Milagros Sánchez-MayorDpto. Producción Animal, Universidad de León, 24071, León, Spain.
Valentina RiggioThe Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush Campus, Edinburgh, EH25 9RG, UK.
Pau NavarroMRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.
Beatriz Gutiérrez-GilDpto. Producción Animal, Universidad de León, 24071, León, Spain.
Chris S HaleyThe Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush Campus, Edinburgh, EH25 9RG, UK.
Luis Fernando De la FuenteDpto. Producción Animal, Universidad de León, 24071, León, Spain.
Juan-José ArranzDpto. Producción Animal, Universidad de León, 24071, León, Spain.
Ricardo Pong-WongThe Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush Campus, Edinburgh, EH25 9RG, UK. ricardo.pong-wong@roslin.ed.ac.uk.ORCID http://orcid.org/0000-0001-9808-2742

Funding

Biotechnology and Biological Sciences Research Council BBS/E/D/30002275Biotechnology and Biological Sciences Research Council (GB) BBS/E/D/30002276Horizon 2020 Framework Programme 772787Horizon 2020 Framework Programme () 772787Medical Research Council MC_PC_U127561128Medical Research Council MC_PC_U127592696Medical Research Council MC_UU_00007/10Medical Research Council (GB) MC_PC_U127561128Medical Research Council (GB) MC_PC_U127592696Ministerio de Ciencia, Innovación y Universidades RTI2018-093535-B-I00Ministerio de Ciencia, Innovación y Universidades (ES) RTI2018-093535-B-I00Ministerio de Economía y Competitividad BES-2013-063614
6 · The paper itself

Abstract

backgroundSingle-step genomic best linear unbiased prediction (ssGBLUP) allows the inclusion of information from genotyped and ungenotyped individuals in a single analysis. This avoids the need to genotype all candidates with the potential benefit of reducing overall costs. The aim of this study was to assess the effect of genotyping strategies, the proportion of genotyped candidates and the genotyping criterion to rank candidates to be genotyped, when using ssGBLUP evaluation. A simulation study was carried out assuming selection over several discrete generations where a proportion of the candidates were genotyped and evaluation was done using ssGBLUP. The scenarios compared were: (i) three genotyping strategies defined by their protocol for choosing candidates to be genotyped (RANDOM: candidates were chosen at random; TOP: candidates with the best genotyping criterion were genotyped; and EXTREME: candidates with the best and worse criterion were genotyped); (ii) eight proportions of genotyped candidates (p); and (iii) two genotyping criteria to rank candidates to be genotyped (candidates' own phenotype or estimated breeding values). The criteria of the comparison were the cumulated gain and reliability of the genomic estimated breeding values (GEBV).

resultsThe genotyping strategy with the greatest cumulated gain was TOP followed by RANDOM, with EXTREME behaving as RANDOM at low p and as TOP with high p. However, the reliability of GEBV was higher with RANDOM than with TOP. This disparity between the trend of the gain and the reliability is due to the TOP scheme genotyping the candidates with the greater chances of being selected. The extra gain obtained with TOP increases when the accuracy of the selection criterion to rank candidates to be genotyped increases.

conclusionsThe best strategy to maximise genetic gain when only a proportion of the candidates are to be genotyped is TOP, since it prioritises the genotyping of candidates which are more likely to be selected. However, the strategy with the greatest GEBV reliability does not achieve the largest gain, thus reliability cannot be considered as an absolute and sufficient criterion for determining the scheme which maximises genetic gain.

Indexed as

GenomeGenomicsGenotypePhenotypeReproducibility of Results

Identifiers

PMID35303797
PMCPMC8931970

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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.