Abstract
A novel framework for the automated evaluation of various deep learning-based splice site detectors is presented. The framework eliminates time-consuming development and experimenting activities for different codebases, architectures, and configurations to obtain the best models for a given RNA splice site dataset. RNA splicing is a cellular process in which pre-mRNAs are processed into mature mRNAs and used to produce multiple mRNA transcripts from a single gene sequence. Since the advancement of sequencing technologies, many splice site variants have been identified and associated with the diseases. So, RNA splice site prediction is essential for gene finding, genome annotation, disease-causing variants, and identification of potential biomarkers. Recently, deep learning models performed highly accurately for classifying genomic signals. Convolutional Neural Network (CNN), Long Short-Term Memory (LSTM) and its bidirectional version (BLSTM), Gated Recurrent Unit (GRU), and its bidirectional version (BGRU) are promising models. During genomic data analysis, CNN's locality feature helps where each nucleotide correlates with other bases in its vicinity. In contrast, BLSTM can be trained bidirectionally, allowing sequential data to be processed from forward and reverse directions. Therefore, it can process 1-D encoded genomic data effectively. Even though both methods have been used in the literature, a performance comparison was missing. To compare selected models under similar conditions, we have created a blueprint for a series of networks with five different levels. As a case study, we compared CNN and BLSTM models' learning capabilities as building blocks for RNA splice site prediction in two different datasets. Overall, CNN performed better with [Formula: see text] accuracy ([Formula: see text] improvement), [Formula: see text] F1 score ([Formula: see text] improvement), and [Formula: see text] AUC-PR ([Formula: see text] improvement) in human splice site prediction. Likewise, an outperforming performance with [Formula: see text] accuracy ([Formula: see text] improvement), [Formula: see text] F1 score ([Formula: see text] improvement), and [Formula: see text] AUC-PR ([Formula: see text] improvement) is achieved in C. elegans splice site prediction. Overall, our results showed that CNN learns faster than BLSTM and BGRU. Moreover, CNN performs better at extracting sequence patterns than BLSTM and BGRU. To our knowledge, no other framework is developed explicitly for evaluating splice detection models to decide the best possible model in an automated manner. So, the proposed framework and the blueprint would help selecting different deep learning models, such as CNN vs. BLSTM and BGRU, for splice site analysis or similar classification tasks and in different problems.