Evidence map›Paper›PMID 37311810›Full record

ArticleScientific reports2023

Population size in QTL detection using quantile regression in genome-wide association studies.

Gabriela França Oliveira, Ana Carolina Campana Nascimento, Camila Ferreira Azevedo, Maurício de Oliveira Celeri, Laís Mayara Azevedo Barroso, Isabela de Castro Sant'Anna, José Marcelo Soriano Viana, Marcos Deon Vilela de Resende, Moysés Nascimento

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Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

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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

9 authors.

Gabriela França OliveiraDepartment of Statistics, Federal University of Viçosa, Av. Peter Henry Rolfs, S/N, Campus Universitário, 36570.900, Viçosa, Minas Gerais, Brazil. gabriela.franca@ufv.br.
Ana Carolina Campana NascimentoDepartment of Statistics, Federal University of Viçosa, Av. Peter Henry Rolfs, S/N, Campus Universitário, 36570.900, Viçosa, Minas Gerais, Brazil.
Camila Ferreira AzevedoDepartment of Statistics, Federal University of Viçosa, Av. Peter Henry Rolfs, S/N, Campus Universitário, 36570.900, Viçosa, Minas Gerais, Brazil.
Maurício de Oliveira CeleriDepartment of Statistics, Federal University of Viçosa, Av. Peter Henry Rolfs, S/N, Campus Universitário, 36570.900, Viçosa, Minas Gerais, Brazil.
Laís Mayara Azevedo BarrosoFederal Institute of Education, Science and Technology of Mato Grosso, Sorriso, Mato Grosso, Brazil.
Isabela de Castro Sant'AnnaRubber Tree and Agroforestry Systems Research Center, Campinas Agronomy Institute (IAC), Votuporanga, São Paulo, Brazil.
José Marcelo Soriano VianaDepartment of General Biology, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil.
Marcos Deon Vilela de ResendeBrazilian Agricultural Research Corporation, Embrapa Coffee, Brasília, DF, Brazil.
Moysés NascimentoDepartment of Statistics, Federal University of Viçosa, Av. Peter Henry Rolfs, S/N, Campus Universitário, 36570.900, Viçosa, Minas Gerais, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to evaluate the performance of Quantile Regression (QR) in Genome-Wide Association Studies (GWAS) regarding the ability to detect QTLs (Quantitative Trait Locus) associated with phenotypic traits of interest, considering different population sizes. For this, simulated data was used, with traits of different levels of heritability (0.30 and 0.50), and controlled by 3 and 100 QTLs. Populations of 1,000 to 200 individuals were defined, with a random reduction of 100 individuals for each population. The power of detection of QTLs and the false positive rate were obtained by means of QR considering three different quantiles (0.10, 0.50 and 0.90) and also by means of the General Linear Model (GLM). In general, it was observed that the QR models showed greater power of detection of QTLs in all scenarios evaluated and a relatively low false positive rate in scenarios with a greater number of individuals. The models with the highest detection power of true QTLs at the extreme quantils (0.10 and 0.90) were the ones with the highest detection power of true QTLs. In contrast, the analysis based on the GLM detected few (scenarios with larger population size) or no QTLs in the evaluated scenarios. In the scenarios with low heritability, QR obtained a high detection power. Thus, it was verified that the use of QR in GWAS is effective, allowing the detection of QTLs associated with traits of interest even in scenarios with few genotyped and phenotyped individuals.

Indexed as

Genome-Wide Association StudyQuantitative Trait LociGenotypeHumansLinear ModelsPopulation Density

Identifiers

PMID37311810
PMCPMC10264463

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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.