Evidence map›Paper›PMID 19208195›Full record

ArticleBMC bioinformatics2009

Phenotype forecasting with SNPs data through gene-based Bayesian networks.

Alberto Malovini, Angelo Nuzzo, Fulvia Ferrazzi, Annibale A Puca, Riccardo Bellazzi

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Article in BMC bioinformatics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Latent variable modeling paradigms for genotype-trait association studies.Biometrical journal. Biometrische Zeitschrift · 2011
    Article
  5. An efficient bayesian method for predicting clinical outcomes from genome-wide data.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2010
    Article
  6. Article
4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Alberto MaloviniIRCCS Multimedica, Via Fantoli 16/15, I-20138 Milano, Italy. alberto.malovini@unipv.it
Angelo Nuzzo
Fulvia Ferrazzi
Annibale A Puca
Riccardo Bellazzi

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBayesian networks are powerful instruments to learn genetic models from association studies data. They are able to derive the existing correlation between genetic markers and phenotypic traits and, at the same time, to find the relationships between the markers themselves. However, learning Bayesian networks is often non-trivial due to the high number of variables to be taken into account in the model with respect to the instances of the dataset. Therefore, it becomes very interesting to use an abstraction of the variable space that suitably reduces its dimensionality without losing information. In this paper we present a new strategy to achieve this goal by mapping the SNPs related to the same gene to one meta-variable. In order to assign states to the meta-variables we employ an approach based on classification trees.

resultsWe applied our approach to data coming from a genome-wide scan on 288 individuals affected by arterial hypertension and 271 nonagenarians without history of hypertension. After pre-processing, we focused on a subset of 24 SNPs. We compared the performance of the proposed approach with the Bayesian network learned with SNPs as variables and with the network learned with haplotypes as meta-variables. The results were obtained by running a hold-out experiment five times. The mean accuracy of the new method was 64.28%, while the mean accuracy of the SNPs network was 58.99% and the mean accuracy of the haplotype network was 54.57%.

conclusionThe new approach presented in this paper is able to derive a gene-based predictive model based on SNPs data. Such model is more parsimonious than the one based on single SNPs, while preserving the capability of highlighting predictive SNPs configurations. The prediction performance of this approach was consistently superior to the SNP-based and the haplotype-based one in all the test sets of the evaluation procedure. The method can be then considered as an alternative way to analyze the data coming from association studies.

Indexed as

Gene Regulatory NetworksPhenotypeBayes TheoremGenome, HumanHaplotypesHumansModels, GeneticPolymorphism, Single Nucleotide

Identifiers

PMID19208195
PMCPMC2646249

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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.