Evidence map›Paper›PMID 23419378›Full record

ArticleBioinformatics (Oxford, England)2013

PleioGRiP: genetic risk prediction with pleiotropy.

Stephen W Hartley, Paola Sebastiani

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Multivariate Analysis and Modelling of multiple Brain endOphenotypes: Let's MAMBO!Computational and structural biotechnology journal · 2021
    Review
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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Stephen W HartleyNational Institutes of Health/National Human Genome Research Institute, 5625 Fishers Lane, Rockville, MD 20850, USA. stephen.hartley@nih.gov
Paola Sebastiani

Funding

Systems BiologyU19AG023122 · NIA · TRANSLATIONAL GENOMICS RESEARCH INST · PI PAOLA SEBASTIANI · 2004 to 2026
$102.6M
Effect of non genetic factors on genetic signatures of complex traitsR21HL114237 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SEBASTIANI, PAOLA · 2012 to 2014
$480k
NHLBI NIH HHS R21 HL114237NHLBI NIH HHS R21HL114237NIA NIH HHS U19 AG023122NIA NIH HHS U19AG023122
6 · The paper itself

Abstract

motivationAlthough several studies have used Bayesian classifiers for risk prediction using genome-wide single nucleotide polymorphism (SNP) datasets, no software can efficiently perform these analyses on massive genetic datasets and can accommodate multiple traits.

resultsWe describe the program PleioGRiP that performs a genome-wide Bayesian model search to identify SNPs associated with a discrete phenotype and uses SNPs ranked by Bayes factor to produce nested Bayesian classifiers. These classifiers can be used for genetic risk prediction, either selecting the classifier with optimal number of features or using an ensemble of classifiers. In addition, PleioGRiP implements an extension to the Bayesian search and classification and can search for pleiotropic relationships in which SNPs are simultaneously associated with two or more distinct phenotypes. These relationships can be used to generate connected Bayesian classifiers to predict the phenotype of interest either using genetic data alone or in combination with the secondary phenotype(s). AVAILABILITY: PleioGRiP is implemented in Java, and it is available from http://hdl.handle.net/2144/4367. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

PhenotypePolymorphism, Single NucleotideSoftwareBayes TheoremGenome-Wide Association StudyHumansRisk

Identifiers

PMID23419378
PMCPMC3624803

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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.