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Dissecting Multi-protein Signaling Complexes by Bimolecular Complementation Affinity Purification (BiCAP)
Published on: June 15, 2018
Protein complex-based analysis is resistant to the obfuscating consequences of batch effects --- a case study in
Wilson Wen Bin Goh1,2, Limsoon Wong3,4
1School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin, 300072, People's Republic of China. wilson.goh@tju.edu.cn.
BMC Genomics
|April 1, 2017
Summary
Protein complex analysis offers a robust method to overcome batch effects in proteomics, ensuring data integrity and improving clinical relevance without complex data transformations.
Area of Science:
- Proteomics
- Bioinformatics
- Translational Research
Background:
- Batch effects in proteomics introduce technical variation, hindering clinical and translational research.
- Existing batch effect correction methods can be ineffective, compromise data integrity, and introduce false positives.
Purpose of the Study:
- To introduce and validate batch-effect resistant methods for proteomics data analysis.
- To demonstrate the efficacy of protein complex-based analyses in mitigating batch effects.
Main Methods:
- Utilized simulated and real proteomics data.
- Evaluated existing batch effect correction techniques and Principal Component Analysis (PCA).
- Introduced and assessed protein complex-based analysis as a batch-effect resistant approach.
Main Results:
- Standard batch effect correction and PCA methods may fail to remove all batch effects or can distort data.
- Protein complex-based analyses demonstrate innate resistance to subtle batch effects.
- These complex-based methods protect data integrity by avoiding data transformation.
Conclusions:
- Protein complex-based analyses provide high reproducibility and prediction accuracy in proteomics.
- These methods are inherently resistant to batch effects, preserving data integrity.
- The constituent proteins of identified complexes are strongly associated with phenotype, indicating clinical relevance.
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