Evidence map›Paper›PMID 25519515›Full record

ArticleBMC proceedings2014

XVI(th) QTLMAS: simulated dataset and comparative analysis of submitted results for QTL mapping and genomic evaluation.

M Graziano Usai, Giustino Gaspa, Nicolò Pp Macciotta, Antonello Carta, Sara Casu

Abstract read
In one paragraph

Article in BMC proceedings, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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.

M Graziano UsaiSettore Genetica e Biotecnologie, Dipartimento per la Ricerca nelle Produzioni Animali, AGRIS-Sardegna, 07040 Olmedo, Italy.
Giustino GaspaDipartimento di AGRARIA, Sezione Scienze Zootecniche, Università di Sassari, 07100 Sassari, Italy.
Nicolò Pp MacciottaDipartimento di AGRARIA, Sezione Scienze Zootecniche, Università di Sassari, 07100 Sassari, Italy.
Antonello CartaSettore Genetica e Biotecnologie, Dipartimento per la Ricerca nelle Produzioni Animali, AGRIS-Sardegna, 07040 Olmedo, Italy.
Sara CasuSettore Genetica e Biotecnologie, Dipartimento per la Ricerca nelle Produzioni Animali, AGRIS-Sardegna, 07040 Olmedo, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA common dataset was simulated and made available to participants of the XVI(th) QTL-MAS workshop. Tasks for the participants were to detect QTLs affecting three traits, to assess their possible pleiotropic effects, and to evaluate the breeding values in a candidate population without phenotypes using genomic information.

methodsFour generations consisting of 20 males and 1000 females were generated by mating each male with 50 females. The genome consisted of 5 chromosomes, each of 100 Mb size and carrying 2,000 equally distributed SNPs. Three traits were simulated in order to mimic milk yield, fat yield and fat content. Genetic (co)variances were generated from 50 QTLs with pleiotropic effects. Phenotypes for all traits were expressed only in females, and were provided for the first 3 generations. Fourteen methods for detecting single-trait QTL and 3 methods for investigating their pleiotropic nature were proposed. QTL mapping results were compared according to the following criteria: number of true QTL detected; number of false positives; and the proportion of the true genetic variance explained by submitted positions. Eleven methods for estimating direct genomic values of the candidate population were proposed. Accuracies and bias of predictions were assessed by comparing estimated direct genomic values with true breeding values.

resultsThe number of true detections ranged from 0 to 8 across methods and traits, false positives from 0 to 15, and the proportion of genetic variance captured from 0 to 0.82, respectively. The accuracy and bias of genomic predictions varied from 0.74 to 0.85 and from 0.86 to 1.34 across traits and methods, respectively.

conclusionsThe best results in terms of detection power were obtained by ridge regression that, however, led to a large number of false positives. Good results both in terms of true detections and false positives were obtained by the approaches that fit polygenic effects in the model. The investigation of the pleiotropic nature of the QTL permitted the identification of few additional markers compared to the single-trait analyses. Bayesian and grouped regularized regression methods performed similarly for genomic prediction while GBLUP produced the poorest results.

Identifiers

PMID25519515
PMCPMC4195410

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.