ArticleBioData mining2009
Spatially uniform relieff (SURF) for computationally-efficient filtering of gene-gene interactions.
Article in BioData mining, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.
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Who cites it
67 citing papers in PubMed.
- Differential Radiomics-Based Signature Predicts Lung Cancer Risk Accounting for Imaging Parameters in NLST Cohort.Cancer medicine · 2024Article
- Assessing the limitations of relief-based algorithms in detecting higher-order interactions.BioData mining · 2024Article
- Assessing the Limitations of Relief-Based Algorithms in Detecting Higher-Order Interactions.Research square · 2024Article
- Multi-institutional prognostic modeling of survival outcomes in NSCLC patients treated with first-line immunotherapy using radiomics.Journal of translational medicine · 2024Article
- RGIE: A Gene Selection Method Related to Radiotherapy Resistance in Head and Neck Squamous Cell Carcinoma.Current radiopharmaceuticals · 2024Article
- Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets.American journal of human genetics · 2023Article
- What makes a good prediction? Feature importance and beginning to open the black box of machine learning in genetics.Human genetics · 2022Review
- A Review of Feature Selection Methods for Machine Learning-Based Disease Risk Prediction.Frontiers in bioinformatics · 2022Review
- Hierarchical Information Criterion for Variable Abstraction.Proceedings of machine learning research · 2021Article
- Statistical and Machine Learning Link Selection Methods for Brain Functional Networks: Review and Comparison.Brain sciences · 2021Article
- Article
- Application of data mining for predicting hemodynamics instability during pheochromocytoma surgery.BMC medical informatics and decision making · 2020Article
- A parallelized strategy for epistasis analysis based on Empirical Bayesian Elastic Net models.Bioinformatics (Oxford, England) · 2020Article
- Genomics models in radiotherapy: From mechanistic to machine learning.Medical physics · 2020Review
- Nearest-neighbor Projected-Distance Regression (NPDR) for detecting network interactions with adjustments for multiple tests and confounding.Bioinformatics (Oxford, England) · 2020Article
- Embracing study heterogeneity for finding genetic interactions in large-scale research consortia.Genetic epidemiology · 2020Article
- Automatic Identification and Intuitive Map Representation of the Epiretinal Membrane Presence in 3D OCT Volumes.Sensors (Basel, Switzerland) · 2019Article
- Discovering genetic interactions bridging pathways in genome-wide association studies.Nature communications · 2019Article
- STatistical Inference Relief (STIR) feature selection.Bioinformatics (Oxford, England) · 2019Article
- How to increase our belief in discovered statistical interactions via large-scale association studies?Human genetics · 2019Review
7 more citing papers are in PubMed but not listed here.
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Authors and funding
4 authors.
Funding
Abstract
backgroundGenome-wide association studies are becoming the de facto standard in the genetic analysis of common human diseases. Given the complexity and robustness of biological networks such diseases are unlikely to be the result of single points of failure but instead likely arise from the joint failure of two or more interacting components. The hope in genome-wide screens is that these points of failure can be linked to single nucleotide polymorphisms (SNPs) which confer disease susceptibility. Detecting interacting variants that lead to disease in the absence of single-gene effects is difficult however, and methods to exhaustively analyze sets of these variants for interactions are combinatorial in nature thus making them computationally infeasible. Efficient algorithms which can detect interacting SNPs are needed. ReliefF is one such promising algorithm, although it has low success rate for noisy datasets when the interaction effect is small. ReliefF has been paired with an iterative approach, Tuned ReliefF (TuRF), which improves the estimation of weights in noisy data but does not fundamentally change the underlying ReliefF algorithm. To improve the sensitivity of studies using these methods to detect small effects we introduce Spatially Uniform ReliefF (SURF).
resultsSURF's ability to detect interactions in this domain is significantly greater than that of ReliefF. Similarly SURF, in combination with the TuRF strategy significantly outperforms TuRF alone for SNP selection under an epistasis model. It is important to note that this success rate increase does not require an increase in algorithmic complexity and allows for increased success rate, even with the removal of a nuisance parameter from the algorithm.
conclusionResearchers performing genetic association studies and aiming to discover gene-gene interactions associated with increased disease susceptibility should use SURF in place of ReliefF. For instance, SURF should be used instead of ReliefF to filter a dataset before an exhaustive MDR analysis. This change increases the ability of a study to detect gene-gene interactions. The SURF algorithm is implemented in the open source Multifactor Dimensionality Reduction (MDR) software package available from http://www.epistasis.org.
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Registered trials
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.