Evidence map›Paper›PMID 19736252›Full record

ArticleBioinformatics (Oxford, England)2009

Efficiently finding genome-wide three-way gene interactions from transcript- and genotype-data.

Mitsunori Kayano, Ichigaku Takigawa, Motoki Shiga, Koji Tsuda, Hiroshi Mamitsuka

Abstract read
In one paragraph

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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0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Mitsunori KayanoBioinformatics Center, Institute for Chemical Research, Kyoto University, Gokasho, Uji 611-0011, Japan. kayano@kuicr.kyoto-u.ac.jp
Ichigaku Takigawa
Motoki Shiga
Koji Tsuda
Hiroshi Mamitsuka

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

GenomeGenotypeDatabases, GeneticGene ExpressionGene Expression ProfilingGenomicsLogistic ModelsSoftware

Identifiers

PMID19736252
PMCPMC2781753

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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.