Evidence map›Paper›PMID 26058849›Full record

ArticleGenetics2015

Gene Level Meta-Analysis of Quantitative Traits by Functional Linear Models.

Ruzong Fan, Yifan Wang, Michael Boehnke, Wei Chen, Yun Li, Haobo Ren, Iryna Lobach, Momiao Xiong

Abstract read
In one paragraph

Article in Genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

8 authors.

Ruzong FanBiostatistics and Bioinformatics Branch, Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892 fanr@mail.nih.gov.
Yifan WangBiostatistics and Bioinformatics Branch, Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
Michael BoehnkeDepartment of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Michigan 48109.
Wei ChenDivision of Pulmonary Medicine, Allergy, and Immunology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania 15224.
Yun LiDepartment of Genetics, Department of Biostatistics, University of North Carolina, Chapel Hill, North Carolina 27599.
Haobo RenRegeneron Pharmaceuticals, Basking Ridge, New Jersey 07920.
Iryna LobachDivision of Biostatistics, Department of Epidemiology and Biostatistics, University of California, San Francisco, California 94185.
Momiao XiongHuman Genetics Center, University of Texas, Houston, Texas 77225.

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Design and Analysis of Sequencing-based Studies for Complex Human TraitsR01HG006292 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LI, YUN · 2011 to 2015
$1.8M
Statistical methods for population and family-based whole-genome sequence dataR01HG007358 · NHGRI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHEN, WEI · 2014 to 2018
$1.7M
Unified Statistical Methods for Sequence-Based Association StudiesR01GM104411 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI XIONG, MOMIAO · 2013 to 2016
$1.3M
Statistical Methods for Association Analysis of Complex TraitsZIAHD008918 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI FAN, RUZONG · 2011 to 2016
$1.1M
Imputation and Analysis of Rare Variants in Admixed PopulationsR01HG006703 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LI, YUN · 2012 to 2014
$931k
AMD genetics: methods and analysis for progression, prediction, and associationR01EY024226 · NEI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHEN, WEI · 2014 to 2016
$899k
NEI NIH HHS R01 EY024226NEI NIH HHS R01EY024226NHGRI NIH HHS R01 HG006292NHGRI NIH HHS R01HG006292NHGRI NIH HHS R01 HG006703NHGRI NIH HHS R01HG006703NHGRI NIH HHS R01 HG007358NHGRI NIH HHS R01HG007358NIDDK NIH HHS P30 DK020572NIGMS NIH HHS R01 GM104411
6 · The paper itself

Abstract

Meta-analysis of genetic data must account for differences among studies including study designs, markers genotyped, and covariates. The effects of genetic variants may differ from population to population, i.e., heterogeneity. Thus, meta-analysis of combining data of multiple studies is difficult. Novel statistical methods for meta-analysis are needed. In this article, functional linear models are developed for meta-analyses that connect genetic data to quantitative traits, adjusting for covariates. The models can be used to analyze rare variants, common variants, or a combination of the two. Both likelihood-ratio test (LRT) and F-distributed statistics are introduced to test association between quantitative traits and multiple variants in one genetic region. Extensive simulations are performed to evaluate empirical type I error rates and power performance of the proposed tests. The proposed LRT and F-distributed statistics control the type I error very well and have higher power than the existing methods of the meta-analysis sequence kernel association test (MetaSKAT). We analyze four blood lipid levels in data from a meta-analysis of eight European studies. The proposed methods detect more significant associations than MetaSKAT and the P-values of the proposed LRT and F-distributed statistics are usually much smaller than those of MetaSKAT. The functional linear models and related test statistics can be useful in whole-genome and whole-exome association studies.

Indexed as

Meta-Analysis as TopicQuantitative Trait, HeritableAnalysis of VarianceCohort StudiesHumansLikelihood FunctionsLinear ModelsLipid MetabolismMaleassociation mappingcommon variantscomplex traitsfunctional data analysismeta-analysisquantitative trait locirare variants

Identifiers

PMID26058849
PMCPMC4574252

What OpenQuestion holds

Textmetadata
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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.