Evidence map›Paper›PMID 24984606›Full record

ArticleHeredity2014

Multiple-trait genome-wide association study based on principal component analysis for residual covariance matrix.

H Gao, Y Wu, T Zhang, Y Wu, L Jiang, J Zhan, J Li, R Yang

Erratum issuedAbstract read
In one paragraph

Article in Heredity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

H GaoInstitute of Animal Sciences, Chinese Academy of Agricultural Science, Beijing, People's Republic of China.
Y WuInstitute of Animal Sciences, Chinese Academy of Agricultural Science, Beijing, People's Republic of China.
T ZhangApplied and Computational Mathematics and Statistics, University of Notre Dame, Notre Dame, IN, USA.
Y WuSchool of Agriculture and Biology, Shanghai Jiaotong University, Shanghai, People's Republic of China.
L JiangResearch Centre for Aquatic Biotechnology, Chinese Academy of Fishery Sciences, Beijing, People's Republic of China.
J ZhanResearch Centre for Aquatic Biotechnology, Chinese Academy of Fishery Sciences, Beijing, People's Republic of China.
J LiInstitute of Animal Sciences, Chinese Academy of Agricultural Science, Beijing, People's Republic of China.
R YangResearch Centre for Aquatic Biotechnology, Chinese Academy of Fishery Sciences, Beijing, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Given the drawbacks of implementing multivariate analysis for mapping multiple traits in genome-wide association study (GWAS), principal component analysis (PCA) has been widely used to generate independent 'super traits' from the original multivariate phenotypic traits for the univariate analysis. However, parameter estimates in this framework may not be the same as those from the joint analysis of all traits, leading to spurious linkage results. In this paper, we propose to perform the PCA for residual covariance matrix instead of the phenotypical covariance matrix, based on which multiple traits are transformed to a group of pseudo principal components. The PCA for residual covariance matrix allows analyzing each pseudo principal component separately. In addition, all parameter estimates are equivalent to those obtained from the joint multivariate analysis under a linear transformation. However, a fast least absolute shrinkage and selection operator (LASSO) for estimating the sparse oversaturated genetic model greatly reduces the computational costs of this procedure. Extensive simulations show statistical and computational efficiencies of the proposed method. We illustrate this method in a GWAS for 20 slaughtering traits and meat quality traits in beef cattle.

Indexed as

Genetic Association StudiesModels, GeneticPrincipal Component AnalysisQuantitative Trait, HeritableAlgorithmsAnimalsCattleMeatMultivariate AnalysisPhenotypePolymorphism, Single Nucleotide

Identifiers

PMID24984606
PMCPMC4274615

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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.