Evidence map›Paper›PMID 25491445›Full record

ArticleBMC genetics2014

Integrative Bayesian variable selection with gene-based informative priors for genome-wide association studies.

Xiaoshuai Zhang, Fuzhong Xue, Hong Liu, Dianwen Zhu, Bin Peng, Joseph L Wiemels, Xiaowei Yang

Abstract read
In one paragraph

Article in BMC genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. New Algorithm and Software (BNOmics) for Inferring and Visualizing Bayesian Networks from Heterogeneous Big Biological and Genetic Data.Journal of computational biology : a journal of computational molecular cell biology · 2017
    Article
  5. 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

7 authors.

Xiaoshuai ZhangSchool of Public Health, Shandong University, Jinan, Shandong, 250012, China. zhxiaoshuai@gmail.com.
Fuzhong XueSchool of Public Health, Shandong University, Jinan, Shandong, 250012, China. xuefzh@sdu.edu.cn.
Hong LiuShandong Provincial Institute of Dermatology and Venereology, Shandong Academy of Medical Science, Jinan, Shandong, 250022, China. 1450407248@qq.com.
Dianwen ZhuBayessoft, Inc., 2221 Caravaggio Drive, Davis, CA, 95618, USA. dzhu2010@gmail.com.
Bin PengSchool of Public Health, Chongqing Medical University, Chongqing, 400016, China. cellepy@gmail.com.
Joseph L WiemelsDepartment of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA, 94158, USA. joe.wiemels@ucsf.edu.
Xiaowei YangBayessoft, Inc., 2221 Caravaggio Drive, Davis, CA, 95618, USA. dyang@bayessoft.com.

Funding

Use Mobile Devices and Cloud Computing Platforms for Real-time Data Solutions inR44DA026683 · NIDA · BAYESSOFT, INC. · PI LIN, EDWARD, YANG, XIAOWEI · 2012 to 2013
$1.2M
Bayesian Variable Selection in Generalized Linear Models with Missing VariblesR01HD061404 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI YANG, XIAOWEI · 2011 to 2013
$615k
NICHD NIH HHS 5R01HD061404NICHD NIH HHS R01 HD061404NIDA NIH HHS R44 DA026683NIDA NIH HHS R44DA026683
6 · The paper itself

Abstract

backgroundGenome-wide Association Studies (GWAS) are typically designed to identify phenotype-associated single nucleotide polymorphisms (SNPs) individually using univariate analysis methods. Though providing valuable insights into genetic risks of common diseases, the genetic variants identified by GWAS generally account for only a small proportion of the total heritability for complex diseases. To solve this "missing heritability" problem, we implemented a strategy called integrative Bayesian Variable Selection (iBVS), which is based on a hierarchical model that incorporates an informative prior by considering the gene interrelationship as a network. It was applied here to both simulated and real data sets.

resultsSimulation studies indicated that the iBVS method was advantageous in its performance with highest AUC in both variable selection and outcome prediction, when compared to Stepwise and LASSO based strategies. In an analysis of a leprosy case-control study, iBVS selected 94 SNPs as predictors, while LASSO selected 100 SNPs. The Stepwise regression yielded a more parsimonious model with only 3 SNPs. The prediction results demonstrated that the iBVS method had comparable performance with that of LASSO, but better than Stepwise strategies.

conclusionsThe proposed iBVS strategy is a novel and valid method for Genome-wide Association Studies, with the additional advantage in that it produces more interpretable posterior probabilities for each variable unlike LASSO and other penalized regression methods.

Indexed as

Genome-Wide Association StudyAlgorithmsArea Under CurveBayes TheoremChinaHumansLeprosyMultivariate AnalysisPolymorphism, Single NucleotideRegression AnalysisROC CurveStochastic Processes

Identifiers

PMID25491445
PMCPMC4275962

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.