ArticleBMC bioinformatics2017
KNN-MDR: a learning approach for improving interactions mapping performances in genome wide association studies.
Article in BMC bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
7 citing papers in PubMed.
- Searching for gene-gene interactions through variance quantitative trait loci of 29 continuous Taiwan Biobank phenotypes.Frontiers in genetics · 2024Article
- Article
- What makes a good prediction? Feature importance and beginning to open the black box of machine learning in genetics.Human genetics · 2022Review
- GEP-EpiSeeker: a gene expression programming-based method for epistatic interaction detection in genome-wide association studies.BMC genomics · 2021Article
- Synergistic effect of genetic polymorphisms inInnate immunity · 2021Article
- Aggregation of experts: an application in the field of "interactomics" (detection of interactions on the basis of genomic data).BMC bioinformatics · 2018Article
- Heterogeneity Analysis and Diagnosis of Complex Diseases Based on Deep Learning Method.Scientific reports · 2018Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
backgroundFinding epistatic interactions in large association studies like genome-wide association studies (GWAS) with the nowadays-available large volume of genomic data is a challenging and largely unsolved issue. Few previous studies could handle genome-wide data due to the intractable difficulties met in searching a combinatorial explosive search space and statistically evaluating epistatic interactions given a limited number of samples. Our work is a contribution to this field. We propose a novel approach combining K-Nearest Neighbors (KNN) and Multi Dimensional Reduction (MDR) methods for detecting gene-gene interactions as a possible alternative to existing algorithms, e especially in situations where the number of involved determinants is high. After describing the approach, a comparison of our method (KNN-MDR) to a set of the other most performing methods (i.e., MDR, BOOST, BHIT, MegaSNPHunter and AntEpiSeeker) is carried on to detect interactions using simulated data as well as real genome-wide data.
resultsExperimental results on both simulated data and real genome-wide data show that KNN-MDR has interesting properties in terms of accuracy and power, and that, in many cases, it significantly outperforms its recent competitors.
conclusionsThe presented methodology (KNN-MDR) is valuable in the context of loci and interactions mapping and can be seen as an interesting addition to the arsenal used in complex traits analyses.
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Registered trials
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