Single-cell RNA-sequencing (scRNA-seq) technologies offer the opportunity to understand regulatory mechanisms at single-cell resolution. Gene regulatory networks (GRNs) provide a crucial blueprint of regulatory mechanisms in cellular systems and thus play a central role in biological research. It's therefore imperative to develop an accurate tool for inferring GRNs from scRNA-seq data.
Researchers from the Wuhan Botanical Garden of the Chinese Academy of Sciences have developed a novel method, namely STGRNS, for constructing GRNs from scRNA-seq data using a deep learning model. The tool and tutorial are publicly available at https://github.com/zhanglab-wbgcas/STGRNS.
In this algorithm, a gene expression motif technique was proposed to convert each gene pair into a form that can be received as a transformer encoder. By avoiding missing phase-specific regulations in a network, STGRNS can accurately infer GRNs from static, pseudo-time, or time series single-cell transcriptome data.
The researchers showed that STGRNS outperforms other state-of-the-art deep learning methods on 48 benchmark datasets, including 21 static scRNA-seq datasets and 27 time-series scRNA-seq datasets.
Unlike other "black box" deep learning-based methods, which are often characterized by their opacity and the associated difficulty in providing clear justifications for their predictions, STGRNS is more reliable and can interpret the predictions.
In addition, STGRNS has fewer hyperparameters compared to other GRN reconstruction methods based on deep learning models, which is one of the main reasons for its excellent generalization.
Results have been published in Bioinformatics entitled "STGRNS: an interpretable transformer-based method for inferring gene regulatory networks from single-cell transcriptomic data."
This study was funded by the National Natural Science Foundation of China.
