Evidence map›Paper›PMID 26658140›Full record

ArticlePloS one2015

An Effective Method to Identify Heritable Components from Multivariate Phenotypes.

Jiangwen Sun, Henry R Kranzler, Jinbo Bi

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Collaborative Phenotype Inference from Comorbid Substance Use Disorders and Genotypes.Proceedings. IEEE International Conference on Bioinformatics and Biomedicine · 2017
    Article
  3. VIGAN: Missing View Imputation with Generative Adversarial Networks.Proceedings : ... IEEE International Conference on Big Data. IEEE International Conference on Big Data · 2017
    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

3 authors.

Jiangwen SunDepartment of Computer Science and Engineering, University of Connecticut, Storrs, Connecticut, United States of America.
Henry R KranzlerTreatment Research Center, University of Pennsylvania Perelman School of Medicine and Philadelphia VAMC, Philadelphia, Pennsylvania, United States of America.
Jinbo BiDepartment of Computer Science and Engineering, University of Connecticut, Storrs, Connecticut, United States of America.

Funding

Study of Addiction: Genetics and EnvironmentU01HG004422 · NHGRI · WASHINGTON UNIVERSITY · PI BIERUT, LAURA J. · 2007 to 2010
$1.2M
Quantitative methods to subtype drug dependence and detect novel genetic variantsR01DA037349 · NIDA · UNIVERSITY OF CONNECTICUT STORRS · PI BI, JINBO · 2015 to 2018
$1.1M
NHGRI NIH HHS U01 HG004422NIDA NIH HHS R01 DA037349NIDA NIH HHS R01DA037349
6 · The paper itself

Abstract

Multivariate phenotypes may be characterized collectively by a variety of low level traits, such as in the diagnosis of a disease that relies on multiple disease indicators. Such multivariate phenotypes are often used in genetic association studies. If highly heritable components of a multivariate phenotype can be identified, it can maximize the likelihood of finding genetic associations. Existing methods for phenotype refinement perform unsupervised cluster analysis on low-level traits and hence do not assess heritability. Existing heritable component analytics either cannot utilize general pedigrees or have to estimate the entire covariance matrix of low-level traits from limited samples, which leads to inaccurate estimates and is often computationally prohibitive. It is also difficult for these methods to exclude fixed effects from other covariates such as age, sex and race, in order to identify truly heritable components. We propose to search for a combination of low-level traits and directly maximize the heritability of this combined trait. A quadratic optimization problem is thus derived where the objective function is formulated by decomposing the traditional maximum likelihood method for estimating the heritability of a quantitative trait. The proposed approach can generate linearly-combined traits of high heritability that has been corrected for the fixed effects of covariates. The effectiveness of the proposed approach is demonstrated in simulations and by a case study of cocaine dependence. Our approach was computationally efficient and derived traits of higher heritability than those by other methods. Additional association analysis with the derived cocaine-use trait identified genetic markers that were replicated in an independent sample, further confirming the utility and advantage of the proposed approach.

Indexed as

Genetic Predisposition to DiseaseQuantitative Trait, HeritableAlgorithmsCocaine-Related DisordersComputer SimulationFemaleGenetic Association StudiesGenetic MarkersGenetic VariationHumansLikelihood FunctionsMaleModels, GeneticPhenotypeGenetic Markers

Identifiers

PMID26658140
PMCPMC4678282

What OpenQuestion holds

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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.