Evidence map›Paper›PMID 22640591›Full record

ArticleBMC proceedings2012

Comparison of the analyses of the XVth QTLMAS common dataset II: QTL analysis.

Olivier Demeure, Olivier Filangi, Jean-Michel Elsen, Pascale Le Roy

Open access · goldAbstract read
In one paragraph

Article in BMC proceedings, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 87% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

4 authors at 3 institutions in 1 country.

Olivier DemeureINRA, UMR1348 PEGASE, Domaine de la Prise, 35590 Saint-Gilles, France. olivier.demeure@rennes.inra.fr.
Olivier Filangi
Jean-Michel Elsen
Pascale Le Roy
Physiologie Environnement et Génétique pour l'Animal et les Systèmes d'Elevage · FRGénétique Physiologie et Systèmes d'Elevage · FRInstitut Agro Rennes-Angers · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe QTLMAS XVth dataset consisted of the pedigrees, marker genotypes and quantitative trait performances of 2,000 phenotyped animals with a half-sib family structure. The trait was regulated by 8 QTL which display additive, imprinting or epistatic effects. This paper aims at comparing the QTL mapping results obtained by six participants of the workshop.

methodsDifferent regression, GBLUP, LASSO and Bayesian methods were applied for QTL detection. The results of these methods are compared based on the number of correctly mapped QTL, the number of false positives, the accuracy of the QTL location and the estimation of the QTL effect.

resultsAll the simulated QTL, except the interacting QTL on Chr5, were identified by the participants. Depending on the method, 3 to 7 out of the 8 QTL were identified. The distance to the real location and the accuracy of the QTL effect varied to a large extent depending on the methods and complexity of the simulated QTL.

conclusionsWhile all methods were fairly efficient in detecting QTL with additive effects, it was clear that for non-additive situations, such as parent-of-origin effects or interactions, the BayesC method gave the best results by detecting 7 out of the 8 simulated QTL, with only two false positives and a good precision (less than 1 cM away on average). Indeed, if LASSO could detect QTL even in complex situations, it was associated with too many false positive results to allow for efficient GWAS. GENMIX, a method based on the phylogenies of local haplotypes, also appeared as a promising approach, which however showed a few more false positives when compared with the BayesC method.

Identifiers

PMID22640591
PMCPMC3363156
OpenAlexW2125014740

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.