Abstract
The scRNA-seq technology enables high-resolution profiling and analysis of individual cells. The increasing availability of datasets and advancements in technology have prompted researchers to integrate existing annotated datasets with newly sequenced datasets for a more comprehensive analysis. It is important to ensure that the integration of new datasets does not alter the cell clusters defined in the old/reference datasets. Although several methods have been developed for scRNA-seq data integration, there is currently a lack of tools that can simultaneously achieve the aforementioned objectives. Therefore, in this study, we have introduced a novel tool called scDILT, which leverages a conditional autoencoder and deep embedding clustering to effectively remove batch effects among different datasets. Moreover, scDILT utilizes homogeneous constraints to preserve the cell-type/clustering patterns observed in the reference datasets, while employing heterogeneous constraints to map cells in the new datasets to the annotated cell clusters in the reference datasets. We have conducted extensive experiments to demonstrate that scDILT outperforms other methods in terms of data integration, as confirmed by evaluations on simulated and real datasets. Furthermore, we have shown that scDILT can be successfully applied to integrate multi-omics single-cell datasets. Based on these findings, we conclude that scDILT holds great promise as a tool for integrating single-cell datasets derived from different batches, experiments, times, or interventions.