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dc.contributor.authorSebastiani, Paola
dc.contributor.authorZhao, Zhenming
dc.contributor.authorAbad Grau, María Del Mar 
dc.contributor.authorRiva, Alberto
dc.contributor.authorHartley, Stephen W.
dc.contributor.authorSedgewick, Amanda E.
dc.contributor.authorDoria, Alessandro
dc.contributor.authorMontano, Monty
dc.contributor.authorMelista, Efthymia
dc.contributor.authorTerry, Dellara
dc.contributor.authorPerls, Thomas T.
dc.contributor.authorSteinberg, Martin H.
dc.contributor.authorBaldwin, Clinton T.
dc.date.accessioned2014-04-02T09:17:22Z
dc.date.available2014-04-02T09:17:22Z
dc.date.issued2008
dc.identifier.citationSabastiani, P.; et al. A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples. BMC Genetics, 9: 6 (2008). [http://hdl.handle.net/10481/31188]es_ES
dc.identifier.issn1471-2156
dc.identifier.otherdoi: 10.1186/1471-2156-9-6
dc.identifier.urihttp://hdl.handle.net/10481/31188
dc.description.abstract[Background] One of the challenges of the analysis of pooling-based genome wide association studies is to identify authentic associations among potentially thousands of false positive associations. [Results] We present a hierarchical and modular approach to the analysis of genome wide genotype data that incorporates quality control, linkage disequilibrium, physical distance and gene ontology to identify authentic associations among those found by statistical association tests. The method is developed for the allelic association analysis of pooled DNA samples, but it can be easily generalized to the analysis of individually genotyped samples. We evaluate the approach using data sets from diverse genome wide association studies including fetal hemoglobin levels in sickle cell anemia and a sample of centenarians and show that the approach is highly reproducible and allows for discovery at different levels of synthesis. [Conclusion] Results from the integration of Bayesian tests and other machine learning techniques with linkage disequilibrium data suggest that we do not need to use too stringent thresholds to reduce the number of false positive associations. This method yields increased power even with relatively small samples. In fact, our evaluation shows that the method can reach almost 70% sensitivity with samples of only 100 subjects.es_ES
dc.description.sponsorshipSupported by NHLBI grants R21 HL080463 (PS); R01 HL68970 (MHS); K-24, AG025727 (TP); K23 AG026754 (D.T.).es_ES
dc.language.isoenges_ES
dc.publisherBiomed Centrales_ES
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs 3.0 Licensees_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es_ES
dc.subjectBayes theoremes_ES
dc.subjectComputational biologyes_ES
dc.subjectDNA es_ES
dc.subjectFetal hemoglobines_ES
dc.subjectGene frequencyes_ES
dc.subjectGenetic markers es_ES
dc.subjectGenomees_ES
dc.subjectGenotypees_ES
dc.subjectLinkage disequilibriumes_ES
dc.subjectSensitivity and specificityes_ES
dc.titleA hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA sampleses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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