Abstract
Machine learning-guided protein engineering is a rapidly advancing field. Despite major experimental and computational advances, collecting protein genotype (sequence) and phenotype (function) data remains time- and resource-intensive. As a result, the quality and quantity of training data are often a limiting factor in developing machine learning models. Data augmentation techniques have been successfully applied to the fields of computer vision and natural language processing; however, there is a lack of such augmentation techniques for biological sequence data. Towards this end, we develop nucleotide augmentation (NTA), which leverages natural nucleotide codon degeneracy to augment protein sequence data via synonymous codon substitution. As a proof of concept for protein engineering, we test several online and offline augmentation implementations to train machine learning models with benchmark datasets of protein genotype and phenotype, revealing performance gains on par and surpassing benchmark models using a fraction of the training data. NTA also enables substantial improvements for classification tasks under heavy class imbalance.
Cite
CITATION STYLE
Minot, M., & Reddy, S. T. (2023). Nucleotide augmentation for machine learning-guided protein engineering. Bioinformatics Advances, 3(1). https://doi.org/10.1093/bioadv/vbac094
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