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Convolutional neural networks (CNNs) have been widely used in hyperspectral image classification in recent years. The training of CNNs relies on a large amount of labeled sample data. However, the number of labeled samples of hyperspectral data is relatively small. Moreover, for hyperspectral images, fully extracting spectral and spatial feature information is the key to achieve high classification performance. To solve the above issues, a deep spectral spatial inverted residuals network (DSSIRNet) is proposed. In this network, a data block random erasing strategy is introduced to alleviate the problem of limited labeled samples by data augmentation of small spatial blocks. In addition, a deep inverted residuals (DIR) module for spectral spatial feature extraction is proposed, which locks the effective features of each layer while avoiding network degradation. Furthermore, a global 3D attention module is proposed, which can realize the fine extraction of spectral and spatial global context information under the condition of the same number of input and output feature maps. Experiments are carried out on four commonly used hyperspectral datasets. A large number of experimental results show that compared with some state-of-the-art classification methods, the proposed method can provide higher classification accuracy for hyperspectral images.

Single-cell RNA (scRNA-seq) sequencing technologies trigger the study of individual cell gene expression and reveal the diversity within cell populations. To measure cell-to-cell similarity based on their transcription and gene expression, many dimension reduction methods are employed to retrieve the corresponding low-dimensional embeddings of input scRNA-seq data to conduct clustering. However, the methods lack explainability and may not perform well with scRNA-seq data because they are often migrated from other fields and not customized for high-dimensional sparse scRNA-seq data. In this study, we propose an explainable t-SNE: cell-driven t-SNE (c-TSNE) that fuses the cell differences reflected from biologically meaningful distance metrics for input scRNA-seq data. Our study shows that the proposed method not only enhances the interpretation of the original t-SNE visualization for scRNA-seq data but also demonstrates favorable single cell segregation performance on benchmark datasets compared to the state-of-the-art peers. The robustness analysis shows that the proposed cell-driven t-SNE demonstrates robustness to dropout and noise in dimension reduction and clustering. It provides a novel and practical way to investigate the interpretability of t-SNE in scRNA-seq data analysis. Unlike the general assumption that the explainanbility of a machine learning method needs to compromise with the learning efficiency, the proposed explainable t-SNE improves both clustering efficiency and explainanbility in scRNA-seq analysis. More importantly, our work suggests that widely used t-SNE can be easily misused in the existing scRNA-seq analysis, because its default Euclidean distance can bring biases or meaningless results in cell difference evaluation for high-dimensional sparse scRNA-seq data. To the best of our knowledge, it is the first explainable t-SNE proposed in scRNA-seq analysis and will inspire other explainable machine learning method development in the field.

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