Publication: An omnibus permutation test on ensembles of two-locus analyses for the detection of purely epistatic multi-locus interactions
dc.contributor.author | Waranyu Wongseree | en_US |
dc.contributor.author | Anunchai Assawamakin | en_US |
dc.contributor.author | Theera Piroonratana | en_US |
dc.contributor.author | Saravudh Sinsomros | en_US |
dc.contributor.author | Chanin Limwongse | en_US |
dc.contributor.author | Nachol Chaiyaratana | en_US |
dc.contributor.other | King Mongkut's University of Technology North Bangkok | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-09-13T06:33:40Z | |
dc.date.available | 2018-09-13T06:33:40Z | |
dc.date.issued | 2009-12-01 | en_US |
dc.description.abstract | Purely epistatic multi-locus interactions cannot generally be detected via single-locus analysis in case-control studies of complex diseases. Recently, many two-locus and multi-locus analysis techniques have been shown to be promising for the epistasis detection. However, exhaustive multi-locus analysis requires prohibitively large computational efforts when problems involve large-scale or genome-wide data. Furthermore, there is no explicit proof that a combination of multiple two-locus analyses can lead to the correct identification of multi-locus interactions. 2LOmb which performs an omnibus permutation test on ensembles of two-locus analyses is proposed. The algorithm consists of four main steps: two-locus analysis, a permutation test, global p-value determination and a progressive search for the best ensemble. 2LOmb is benchmarked against a set association approach, a correlation-based feature selection technique and a tuned ReliefF technique. The simulation results from multi-locus interaction problems indicate that 2LOmb has a low false-positive error. Moreover, 2LOmb has the best performance in terms of an ability to identify all causative single nucleotide polymorphisms (SNPs), which signifies a high detection power. 2LOmb is subsequently applied to type 1 and type 2 diabetes mellitus (T1D and T2D) data sets, which are obtained as a part of the UK genome-wide genetic epidemiology study by the Wellcome Trust Case Control Consortium. After primarily screening for SNPs that locate within or near candidate genes and exhibit no marginal single-locus effects, the T1D and T2D data sets are reduced to 2,359 SNPs from 350 genes and 7,065 SNPs from 370 genes, respectively. The 2LOmb search reveals that 28 SNPs in 21 genes are associated with T1D while 11 SNPs in four genes are associated with T2D. The findings provide an alternative explanation for the aetiology of T1D and T2D in a UK population. © 2009 Springer-Verlag Berlin Heidelberg. | en_US |
dc.identifier.citation | Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). Vol.5864 LNCS, No.PART 2 (2009), 493-502 | en_US |
dc.identifier.doi | 10.1007/978-3-642-10684-2_55 | en_US |
dc.identifier.issn | 16113349 | en_US |
dc.identifier.issn | 03029743 | en_US |
dc.identifier.other | 2-s2.0-76249132689 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/27474 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=76249132689&origin=inward | en_US |
dc.subject | Computer Science | en_US |
dc.subject | Mathematics | en_US |
dc.title | An omnibus permutation test on ensembles of two-locus analyses for the detection of purely epistatic multi-locus interactions | en_US |
dc.type | Conference Paper | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=76249132689&origin=inward | en_US |