ArticleBioinformatics (Oxford, England)2009
Efficiently finding genome-wide three-way gene interactions from transcript- and genotype-data.
Article in Bioinformatics (Oxford, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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10 citing papers in PubMed.
- DRaCOon: a novel algorithm for pathway-level differential co-expression analysis in transcriptomics.BMC bioinformatics · 2025Article
- A dynamic co-expression approach reveals Gins2 as a potential upstream modulator of HNSCC metastasis.Scientific reports · 2025Article
- Article
- Differential Co-Expression Analyses Allow the Identification of Critical Signalling Pathways Altered during Tumour Transformation and Progression.International journal of molecular sciences · 2020Review
- Differential co-expression-based detection of conditional relationships in transcriptional data: comparative analysis and application to breast cancer.Genome biology · 2019Article
- Three-way interaction model to trace the mechanisms involved in Alzheimer's disease transgenic mice.PloS one · 2017Article
- xSyn: A Software Tool for Identifying Sophisticated 3-Way Interactions From Cancer Expression Data.Cancer informatics · 2017Article
- Identification of markers associated with global changes in DNA methylation regulation in cancers.BMC bioinformatics · 2012Article
- ROS-DET: robust detector of switching mechanisms in gene expression.Nucleic acids research · 2011Article
- Article
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5 authors.
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Abstract
motivationWe address the issue of finding a three-way gene interaction, i.e. two interacting genes in expression under the genotypes of another gene, given a dataset in which expressions and genotypes are measured at once for each individual. This issue can be a general, switching mechanism in expression of two genes, being controlled by categories of another gene, and finding this type of interaction can be a key to elucidating complex biological systems. The most suitable method for this issue is likelihood ratio test using logistic regressions, which we call interaction test, but a serious problem of this test is computational intractability at a genome-wide level.
resultsWe developed a fast method for this issue which improves the speed of interaction test by around 10 times for any size of datasets, keeping highly interacting genes with an accuracy of approximately 85%. We applied our method to approximately 3 x 10(8) three-way combinations generated from a dataset on human brain samples and detected three-way gene interactions with small P-values. To check the reliability of our results, we first conducted permutations by which we can show that the obtained P-values are significantly smaller than those obtained from permuted null examples. We then used GEO (Gene Expression Omnibus) to generate gene expression datasets with binary classes to confirm the detected three-way interactions by using these datasets and interaction tests. The result showed us some datasets with significantly small P-values, strongly supporting the reliability of the detected three-way interactions. AVAILABILITY: Software is available from http://www.bic.kyoto-u.ac.jp/pathway/kayano/bioinfo_three-way.html CONTACT: kayano@kuicr.kyoto-u.ac.jp SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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