Evidence map›Paper›PMID 18617538›Full record

ArticleBioinformatics (Oxford, England)2008

Bayesian survival analysis in genetic association studies.

Ioanna Tachmazidou, Toby Andrew, Claudio J Verzilli, Michael R Johnson, Maria De Iorio

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

1 citing paper in PubMed.

  1. Review
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

5 authors.

Ioanna TachmazidouDepartment of Epidemiology and Public Health, Imperial College, London, UK. ioanna.tachmazidou@imperial.ac.uk
Toby Andrew
Claudio J Verzilli
Michael R Johnson
Maria De Iorio

Funding

Wellcome Trust
6 · The paper itself

Abstract

motivationLarge-scale genetic association studies are carried out with the hope of discovering single nucleotide polymorphisms involved in the etiology of complex diseases. There are several existing methods in the literature for performing this kind of analysis for case-control studies, but less work has been done for prospective cohort studies. We present a Bayesian method for linking markers to censored survival outcome by clustering haplotypes using gene trees. Coalescent-based approaches are promising for LD mapping, as the coalescent offers a good approximation to the evolutionary history of mutations.

resultsWe compare the performance of the proposed method in simulation studies to the univariate Cox regression and to dimension reduction methods, and we observe that it performs similarly in localizing the causal site, while offering a clear advantage in terms of false positive associations. Moreover, it offers computational advantages. Applying our method to a real prospective study, we observe potential association between candidate ABC transporter genes and epilepsy treatment outcomes. AVAILABILITY: R codes are available upon request. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Bayes TheoremGenetic Predisposition to DiseaseSurvival AnalysisATP-Binding Cassette TransportersComputer SimulationEpilepsyGenome, HumanHaplotypesHumansLinkage DisequilibriumPolymorphism, Single NucleotideATP-Binding Cassette Transporters

Identifiers

PMID18617538
PMCPMC2530885

What OpenQuestion holds

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LicenceCC BY-NC
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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.