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APCanalysis: an R package for identifying active factors using the APC method
Abu Zar Md Shafiullah1,2, Arden Miller1
1Department of Statistics, University of Auckland, Auckland, New Zealand.
The APCanalysis R package introduces the All Possible Comparisons (APC) method for robust screening experiments, reliably identifying active factors while controlling error rates like the individual error rate (IER) and experiment-wise error rate (EER). This tool enhances statistical analysis for complex experimental designs, offering precise control over false discoveries.
Area of Science:
- Statistics
- Experimental Design
- Bioinformatics
Background:
- Unreplicated two-level designs, such as Plackett-Burman designs (PBDs) and fractional factorial designs (2^(k-p)), are crucial for screening experiments.
- Classical statistical methods like t-tests are inadequate for saturated models in these designs due to insufficient degrees of freedom.
- Controlling error rates, including the individual error rate (IER) and experiment-wise error rate (EER), is essential for reliable identification of significant effects.
Purpose of the Study:
- To introduce APCanalysis, a novel R package implementing the All Possible Comparisons (APC) method for statistical screening experiments.
- To provide a user-friendly tool for objective identification of significant effects in complex experimental designs, controlling false positive rates.
- To extend error control beyond IER and EER to include the false discovery rate (FDR) using an advanced penalty algorithm.
Main Methods:
- Implementation of the APC method within the APCanalysis R package, utilizing a tailored AIC-type model selection criterion (APC-criterion).
- Application of an advanced penalty algorithm to extend error control to the false discovery rate (FDR).
- Support for various experimental designs including PBDs, full factorial (2^k), resolution-V (2^(k-p)V), resolution-IV (2^(k-p)IV), and resolution-III (2^(k-p)III) designs.
Main Results:
- The APC-criterion reliably identifies active factors across different experimental designs while adhering to user-specified error thresholds (IER, EER, FDR).
- Simulations and real-world data examples demonstrate the effectiveness and accuracy of the APCanalysis package.
- Benchmarking against Lenth's method shows strong agreement in screening power and accuracy, validating the APC-criterion's performance.
Conclusions:
- APCanalysis offers a robust and user-friendly solution for identifying significant effects in screening experiments using unreplicated two-level designs.
- The package effectively controls various error rates, providing reliable results for complex experimental data analysis.
- APCanalysis is a valuable tool for researchers seeking accurate and statistically sound methods for experimental screening, available on CRAN.
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