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Empirical Performance of Cross-Validation With Oracle Methods in a Genomics Context
Josue G Martinez1, Raymond J Carroll, Samuel Müller
1Department of Epidemiology & Biostatistics, School of Rural Public Health, Texas A&M Health Science Center, 1266 TAMU, College Station, TX 77843-1266.
Cross-validation for sparse genomic data with small signals, using methods like SCAD and Adaptive Lasso, shows high variable selection variability. A single cross-validation run is insufficient for reliable model selection in SNP regression.
Area of Science:
- Statistical modeling
- Genomic data analysis
- Machine learning in bioinformatics
Background:
- Model selection methods like SCAD and Adaptive Lasso are commonly used with m-fold cross-validation.
- These methods perform well when regression functions are sparse with large signals.
- Genomic studies using Single Nucleotide Polymorphisms (SNP) present sparse regression functions with small signals.
Purpose of the Study:
- To investigate the performance of model selection methods in genomic regression with sparse signals.
- To evaluate the variability of variable selection in SCAD and Adaptive Lasso using cross-validation for SNP data.
- To question the reliability of single-run cross-validation for oracle methods in such contexts.
Main Methods:
- Empirical demonstration of variable selection performance.
- Utilizing m-fold cross-validation (m=10) with SCAD and Adaptive Lasso.
- Comparison with non-oracle methods like Lasso.
Main Results:
- Cross-validation exhibits considerable and surprising variation in selected variables for SCAD and Adaptive Lasso on SNP data.
- This variability persists even for non-oracle methods like Lasso.
- Small signal strengths in genomic data contribute to this instability.
Conclusions:
- A single run of m-fold cross-validation is questionable for oracle model selection methods in genomic studies.
- The reliability of variable selection is compromised by high variability in sparse, small-signal scenarios.
- Further research is needed to develop more robust cross-validation strategies for genomic data analysis.
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