Evidence map›Paper›PMID 27247027›Full record

ArticleGenetic epidemiology2016

Analyzing Association Mapping in Pedigree-Based GWAS Using a Penalized Multitrait Mixed Model.

Jin Liu, Can Yang, Xingjie Shi, Cong Li, Jian Huang, Hongyu Zhao, Shuangge Ma

Abstract read
In one paragraph

Article in Genetic epidemiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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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

7 citing papers in PubMed.

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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

7 authors.

Jin LiuCenter of Quantitative Medicine, Duke-NUS Medical School, Singapore, Singapore.
Can YangDepartment of Mathematics, Hong Kong Baptist University, Kowloon Tong, Hong Kong.
Xingjie ShiDepartment of Statistics, Nanjing University of Finance and Economics, Nanjing, Jiangsu, China.
Cong LiComputational Biology and Bioinformatics, Yale University, New Haven, Connecticut, United States of America.
Jian HuangDepartment of Statistics & Actuarial Science, University of Iowa, Iowa City, Iowa, United States of America.
Hongyu ZhaoDepartment of Biostatistics, Yale University, New Haven, Connecticut, United States of America.
Shuangge MaDepartment of Biostatistics, Yale University, New Haven, Connecticut, United States of America.

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI DAVID L RIMM · 1985 to 2026
$85.0M
STATISTICAL METHODS TO MAP GENES FOR COMPLEX TRAITSR01GM059507 · NIGMS · YALE UNIVERSITY · PI ZHAO, HONGYU · 1999 to 2013
$3.6M
Novel Methods for Integrative Analysis of Cancer Genomic DataR01CA142774 · NCI · YALE UNIVERSITY · PI MA, SHUANGGE · 2010 to 2013
$1.3M
NCI NIH HHS P30 CA016359NCI NIH HHS R01 CA142774NIGMS NIH HHS R01 GM059507
6 · The paper itself

Abstract

Genome-wide association studies (GWAS) have led to the identification of many genetic variants associated with complex diseases in the past 10 years. Penalization methods, with significant numerical and statistical advantages, have been extensively adopted in analyzing GWAS. This study has been partly motivated by the analysis of Genetic Analysis Workshop (GAW) 18 data, which have two notable characteristics. First, the subjects are from a small number of pedigrees and hence related. Second, for each subject, multiple correlated traits have been measured. Most of the existing penalization methods assume independence between subjects and traits and can be suboptimal. There are a few methods in the literature based on mixed modeling that can accommodate correlations. However, they cannot fully accommodate the two types of correlations while conducting effective marker selection. In this study, we develop a penalized multitrait mixed modeling approach. It accommodates the two different types of correlations and includes several existing methods as special cases. Effective penalization is adopted for marker selection. Simulation demonstrates its satisfactory performance. The GAW 18 data are analyzed using the proposed method.

Indexed as

Genome-Wide Association StudyModels, GeneticPedigreeQuantitative Trait, HeritableArea Under CurveComputer SimulationHumansPhenotypePolymorphism, Single NucleotideROC CurveGWASmixed modelingmultitrait analysispedigreepenalization

Identifiers

PMID27247027
PMCPMC5582543

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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.