Evidence map›Paper›PMID 33711929›Full record

ArticleGenetics, selection, evolution : GSE2021

Imputation accuracy to whole-genome sequence in Nellore cattle.

Gerardo A Fernandes Júnior, Roberto Carvalheiro, Henrique N de Oliveira, Mehdi Sargolzaei, Roy Costilla, Ricardo V Ventura, Larissa F S Fonseca, Haroldo H R Neves, Ben J Hayes, Lucia G de Albuquerque

Open access · goldAbstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
6.9field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 56 citations in OpenAlex.

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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

10 authors at 5 institutions in 3 countries.

Gerardo A Fernandes JúniorSchool of Agricultural and Veterinarian Sciences, UNESP, Jaboticabal, SP, 14884-900, Brazil. gerardojjunior@yahoo.com.br.ORCID http://orcid.org/0000-0002-0391-003X
Roberto CarvalheiroSchool of Agricultural and Veterinarian Sciences, UNESP, Jaboticabal, SP, 14884-900, Brazil.
Henrique N de OliveiraSchool of Agricultural and Veterinarian Sciences, UNESP, Jaboticabal, SP, 14884-900, Brazil.
Mehdi SargolzaeiOntario Veterinary College, UG, Guelph, Canada.
Roy CostillaQueensland Alliance for Agriculture and Food Innovation, UQ, Brisbane, QLD, 4072, Australia.
Ricardo V VenturaSchool of Veterinary Medicine and Animal Science, USP, Pirassununga, SP, 13635-900, Brazil.
Larissa F S FonsecaSchool of Agricultural and Veterinarian Sciences, UNESP, Jaboticabal, SP, 14884-900, Brazil.
Haroldo H R NevesGenSys Associated Consultants, Porto Alegre, RS, 90680-000, Brazil.
Ben J HayesQueensland Alliance for Agriculture and Food Innovation, UQ, Brisbane, QLD, 4072, Australia.
Lucia G de AlbuquerqueSchool of Agricultural and Veterinarian Sciences, UNESP, Jaboticabal, SP, 14884-900, Brazil. galvao.albuquerque@unesp.br.
National Council for Scientific and Technological Development · BRAgriculture and Food · AUNúcleo de Pesquisas Aplicadas (Brazil) · BRAssociated Research (United States) · USOntario Veterinary College

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2017/10630-2
6 · The paper itself

Abstract

backgroundA cost-effective strategy to explore the complete DNA sequence in animals for genetic evaluation purposes is to sequence key ancestors of a population, followed by imputation mechanisms to infer marker genotypes that were not originally reported in a target population of animals genotyped with single nucleotide polymorphism (SNP) panels. The feasibility of this process relies on the accuracy of the genotype imputation in that population, particularly for potential causal mutations which may be at low frequency and either within genes or regulatory regions. The objective of the present study was to investigate the imputation accuracy to the sequence level in a Nellore beef cattle population, including that for variants in annotation classes which are more likely to be functional.

methodsInformation of 151 key sequenced Nellore sires were used to assess the imputation accuracy from bovine HD BeadChip SNP (~ 777 k) to whole-genome sequence. The choice of the sires aimed at optimizing the imputation accuracy of a genotypic database, comprised of about 10,000 genotyped Nellore animals. Genotype imputation was performed using two computational approaches: FImpute3 and Minimac4 (after using Eagle for phasing). The accuracy of the imputation was evaluated using a fivefold cross-validation scheme and measured by the squared correlation between observed and imputed genotypes, calculated by individual and by SNP. SNPs were classified into a range of annotations, and the accuracy of imputation within each annotation classification was also evaluated.

resultsHigh average imputation accuracies per animal were achieved using both FImpute3 (0.94) and Minimac4 (0.95). On average, common variants (minor allele frequency (MAF) > 0.03) were more accurately imputed by Minimac4 and low-frequency variants (MAF ≤ 0.03) were more accurately imputed by FImpute3. The inherent Minimac4 Rsq imputation quality statistic appears to be a good indicator of the empirical Minimac4 imputation accuracy. Both software provided high average SNP-wise imputation accuracy for all classes of biological annotations.

conclusionsOur results indicate that imputation to whole-genome sequence is feasible in Nellore beef cattle since high imputation accuracies per individual are expected. SNP-wise imputation accuracy is software-dependent, especially for rare variants. The accuracy of imputation appears to be relatively independent of annotation classification.

Indexed as

AnimalsCattleGenome-Wide Association StudyPolymorphism, Single NucleotideReproducibility of ResultsSoftwareWhole Genome Sequencing

Identifiers

PMID33711929
PMCPMC7953568
OpenAlexW3135522965

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.