Gene regulation varies across different cell types and developmental stages, leading to distinct cellular roles across cellular populations. Investigating cell type-specific gene coexpression is therefore crucial for understanding gene functions and disease pathology. However, reconstructing gene coexpression networks from single-cell transcriptome data is challenging due to artifacts, noise, and data sparsity. Here, we present an efficient method for inference of gene coexpression networks via variance decomposition analysis (GCNVDA) to explore the underlying gene regulatory mechanisms from single-cell transcriptome data. Our model incorporates multiple sources of variability, including a random effect term $G$ to capture gene-level variance and a random effect term $E$ to account for residual errors. We applied GCNVDA to three real-world single-cell datasets, demonstrating that our method outperforms existing state-of-the-art algorithms in both sensitivity and specificity for identifying tissue- or state-specific gene regulations. Furthermore, GCNVDA facilitates the discovery of functional modules that play critical roles in key biological processes such as embryonic development. These findings provide new insights into cell-specific regulatory mechanisms and have the potential to significantly advance research in developmental biology and disease pathology.

Deep neural networks (DNN) based Channel state information (CSI) fingerprint indoor localization schemes have been widely investigated. However, existing DNN based schemes usually require to collect massive amount of training data samples, which is labor intensive and time consuming. In order to reduce the labor effort and time consumption, in this paper, we propose a Siamese network based CSI fingerprint indoor localization scheme with WiFi (SiFi), which only requires small number of training data samples to achieve a higher localization accuracy. Specifically, in our experiments, with only limited number of training data samples, for localization error less than 0.4m, the proposed SiFi scheme has the probability 82% to fall into this range, while the CNN based scheme only has the probability 67%. The experiment results demonstrate the proposed SiFi scheme has distinct advantages when only small number of training data samples are available.

SUMMARY: Single-cell multi-omics technologies provide a unique platform for characterizing cell states and reconstructing developmental process by simultaneously quantifying and integrating molecular signatures across various modalities, including genome, transcriptome, epigenome, and other omics layers. However, there is still an urgent unmet need for novel computational tools in this nascent field, which are critical for both effective and efficient interrogation of functionality across different omics modalities. Scbean represents a user-friendly Python library, designed to seamlessly incorporate a diverse array of models for the examination of single-cell data, encompassing both paired and unpaired multi-omics data. The library offers uniform and straightforward interfaces for tasks, such as dimensionality reduction, batch effect elimination, cell label transfer from well-annotated scRNA-seq data to scATAC-seq data, and the identification of spatially variable genes. Moreover, Scbean's models are engineered to harness the computational power of GPU acceleration through Tensorflow, rendering them capable of effortlessly handling datasets comprising millions of cells. AVAILABILITY AND IMPLEMENTATION: Scbean is released on the Python Package Index (PyPI) (https://pypi.org/project/scbean/) and GitHub (https://github.com/jhu99/scbean) under the MIT license. The documentation and example code can be found at https://scbean.readthedocs.io/en/latest/.

MOTIVATION: Single-cell multimodal assays allow us to simultaneously measure two different molecular features of the same cell, enabling new insights into cellular heterogeneity, cell development and diseases. However, most existing methods suffer from inaccurate dimensionality reduction for the joint-modality data, hindering their discovery of novel or rare cell subpopulations. RESULTS: Here, we present VIMCCA, a computational framework based on variational-assisted multi-view canonical correlation analysis to integrate paired multimodal single-cell data. Our statistical model uses a common latent variable to interpret the common source of variances in two different data modalities. Our approach jointly learns an inference model and two modality-specific non-linear models by leveraging variational inference and deep learning. We perform VIMCCA and compare it with 10 existing state-of-the-art algorithms on four paired multi-modal datasets sequenced by different protocols. Results demonstrate that VIMCCA facilitates integrating various types of joint-modality data, thus leading to more reliable and accurate downstream analysis. VIMCCA improves our ability to identify novel or rare cell subtypes compared to existing widely used methods. Besides, it can also facilitate inferring cell lineage based on joint-modality profiles. AVAILABILITY AND IMPLEMENTATION: The VIMCCA algorithm has been implemented in our toolkit package scbean (≥0.5.0), and its code has been archived at https://github.com/jhu99/scbean under MIT license. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.