Predicting gene regulatory regions with a convolutional neural network for processing double-strand genome sequence
Koh Onimaru1, Osamu Nishimura1, Shigehiro Kuraku1
1Laboratory for Phyloinformatics, RIKEN Center for Biosystems Dynamics Research (BDR), Chuo-ku, Kobe, Hyogo, Japan.
Deep learning models can now predict gene regulatory regions from genomic sequences. New forward- and reverse-sequence scan (FRSS) layers improve prediction accuracy, aiding genomic data interpretation.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- Advances in sequencing technology have generated vast amounts of genomic data.
- Annotating biological functions, especially in non-protein-coding regions, remains a significant challenge.
- Deep learning methods show promise for predicting gene regulatory regions from genomic sequences.
Purpose of the Study:
- To improve the prediction accuracy of gene regulatory regions using deep learning.
- To develop and introduce novel convolution layers for enhanced genomic sequence processing.
- To provide a software tool (DeepGMAP) for training and comparing deep learning models.
Main Methods:
- Designed novel convolution layers, termed forward- and reverse-sequence scan (FRSS) layers, to process genomic sequence information.
- Integrated both forward and reverse strand information within the convolution layers.
- Developed the DeepGMAP software for model training and comparison.
- Assessed previous studies to identify and address issues causing overfitting in data structures.
Main Results:
- The FRSS layers demonstrated enhanced capability in predicting gene regulatory regions.
- Identified and mitigated overfitting issues related to data structures in previous deep learning approaches.
- Developed visualization methods to interpret the learning process of the deep learning models.
Conclusions:
- The novel FRSS layers significantly improve the prediction accuracy for gene regulatory regions.
- DeepGMAP provides a valuable tool for researchers in genomics and bioinformatics.
- The findings contribute to better interpretation of genomic sequence data, particularly non-coding regions.
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