Single-cell omics technologies are currently solving biological and medical problems that earlier have remained elusive, such as discovery of new cell types, cellular differentiation trajectories and communication networks across cells and tissues. Current advances especially in single-cell multi-omics hold high potential for breakthroughs by integration of multiple different omics layers. To pair with the recent biotechnological developments, many computational approaches to process and analyze single-cell multi-omics data have been proposed. In this review, we first introduce recent developments in single-cell multi-omics in general and then focus on the available data integration strategies. The integration approaches are divided into three categories: early, intermediate, and late data integration. For each category, we describe the underlying conceptual principles and main characteristics, as well as provide examples of currently available tools and how they have been applied to analyze single-cell multi-omics data. Finally, we explore the challenges and prospective future directions of single-cell multi-omics data integration, including examples of adopting multi-view analysis approaches used in other disciplines to single-cell multi-omics.

Computational strategies for single-cell multi-omics integration.

Machine Learning and Big Data Provide Crucial Insight for Future Biomaterials Discovery and Research.

Deep learning applications in single-cell genomics and transcriptomics data analysis.

Motivation The rapid development of single-cell RNA sequencing (scRNA-seq) technologies allows us to explore tissue heterogeneity at the cellular level. The identification of cell types plays an essential role in the analysis of scRNA-seq data, which, in turn, influences the discovery of regulatory genes that induce heterogeneity. As the scale of sequencing data increases, the classical method of combining clustering and differential expression analysis to annotate cells becomes more costly in terms of both labor and resources. Existing scRNA-seq supervised classification method can alleviate this issue through learning a classifier trained on the labeled reference data and then making a prediction based on the unlabeled target data. However, such label transference strategy carries with risks, such as susceptibility to batch effect and further compromise of inherent discrimination of target data. Results In this article, inspired by unsupervised domain adaptation, we propose a flexible single cell semi-supervised clustering and annotation framework, scSemiCluster, which integrates the reference data and target data for training. We utilize structure similarity regularization on the reference domain to restrict the clustering solutions of the target domain. We also incorporates pairwise constraints in the feature learning process such that cells belonging to the same cluster are close to each other, and cells belonging to different clusters are far from each other in the latent space. Notably, without explicit domain alignment and batch effect correction, scSemiCluster outperforms other state-of-the-art, single-cell supervised classification and semi-supervised clustering annotation algorithms in both simulation and real data. To the best of our knowledge, we are the first to use both deep discriminative clustering and deep generative clustering techniques in the single-cell field. Availabilityand implementation An implementation of scSemiCluster is available from https://github.com/xuebaliang/scSemiCluster. Supplementary information Supplementary data are available at Bioinformatics online.

Single-cell RNA-seq data semi-supervised clustering and annotation via structural regularized domain adaptation.

Abstract Motivation The rapid development of single-cell RNA sequencing (scRNA-seq) makes it possible to study the heterogeneity of individual cell characteristics. Cell clustering is a vital procedure in scRNA-seq analysis, providing insight into complex biological phenomena. However, the noisy, high-dimensional and large-scale nature of scRNA-seq data introduces challenges in clustering analysis. Up to now, many deep learning-based methods have emerged to learn underlying feature representations while clustering. However, these methods are inefficient when it comes to rare cell type identification and barely able to fully utilize gene dependencies or cell similarity integrally. As a result, they cannot detect a clear cell type structure which is required for clustering accuracy as well as downstream analysis. Results Here, we propose a novel scRNA-seq clustering algorithm called scNAME which incorporates a mask estimation task for gene pertinence mining and a neighborhood contrastive learning framework for cell intrinsic structure exploitation. The learned pattern through mask estimation helps reveal uncorrupted data structure and denoise the original single-cell data. In addition, the randomly created augmented data introduced in contrastive learning not only helps improve robustness of clustering, but also increases sample size in each cluster for better data capacity. Beyond this, we also introduce a neighborhood contrastive paradigm with an offline memory bank, global in scope, which can inspire discriminative feature representation and achieve intra-cluster compactness, yet inter-cluster separation. The combination of mask estimation task, neighborhood contrastive learning and global memory bank designed in scNAME is conductive to rare cell type detection. The experimental results of both simulations and real data confirm that our method is accurate, robust and scalable. We also implement biological analysis, including marker gene identification, gene ontology and pathway enrichment analysis, to validate the biological significance of our method. To the best of our knowledge, we are among the first to introduce a gene relationship exploration strategy, as well as a global cellular similarity repository, in the single-cell field. Availability and implementation An implementation of scNAME is available from https://github.com/aster-ww/scNAME. Supplementary information Supplementary data are available at Bioinformatics online. 

OUP accepted manuscript

As single-cell RNA sequencing technologies mature, massive gene expression profiles can be obtained. Consequently, cell clustering and annotation become two crucial and fundamental procedures affecting other specific downstream analyses. Most existing single-cell RNA-seq (scRNA-seq) data clustering algorithms do not take into account the available cell annotation results on the same tissues or organisms from other laboratories. Nonetheless, such data could assist and guide the clustering process on the target dataset. Identifying marker genes through differential expression analysis to manually annotate large amounts of cells also costs labor and resources. Therefore, in this paper, we propose a novel end-to-end cell supervised clustering and annotation framework called scAnCluster, which fully utilizes the cell type labels available from reference data to facilitate the cell clustering and annotation on the unlabeled target data. Our algorithm integrates deep supervised learning, self-supervised learning and unsupervised learning techniques together, and it outperforms other customized scRNA-seq supervised clustering methods in both simulation and real data. It is particularly worth noting that our method performs well on the challenging task of discovering novel cell types that are absent in the reference data.

https://www.mdpi.com/2073-4425/11/7/792/pdf

Integrating Deep Supervised, Self-Supervised and Unsupervised Learning for Single-Cell RNA-seq Clustering and Annotation

Microbes can affect processes from food production to human health. Such microbes are not isolated, but rather interact with each other and establish connections with their living environments. Understanding these interactions is essential to an understanding of the organization and complex interplay of microbial communities, as well as the structure and dynamics of various ecosystems. A common and essential approach toward this objective involves the inference of microbiome interaction networks. Although network inference methods in other fields have been studied before, applying these methods to estimate microbiome associations based on compositional data will not yield valid results. On the one hand, features of microbiome data such as compositionality, sparsity and high-dimensionality challenge the data normalization and the design of computational methods. On the other hand, several issues like microbial community heterogeneity, external environmental interference and biological concerns also make it more difficult to deal with the network inference. In this paper, we provide a comprehensive review of emerging microbiome interaction network inference methods. According to various assumptions and research targets, estimated networks are divided into four main categories: correlation networks, conditional correlation networks, mixture networks and differential networks. Their scope of applications, advantages and limitations are presented in this review. Since real microbial interactions can be complex and dynamic, no unifying method has captured all the aspects of interest to date. In addition, we discuss the challenges now confronting current microbial associations study and future prospects. Finally, we highlight that the research in microbial network inference requires the joint promotion of statistical computation methods and experimental techniques.

Statistical computation methods for microbiome compositional data network inference

Microbes can be found almost everywhere in the world. They are not isolated, but rather interact with each other and establish connections with their living environments. Studying these interactions is essential to an understanding of the organization and complex interplay of microbial communities, as well as the structure and dynamics of various ecosystems. A widely used approach toward this objective involves the inference of microbiome interaction networks. However, owing to the compositional, high-dimensional, sparse, and heterogeneous nature of observed microbial data, applying network inference methods to estimate their associations is challenging. In addition, external environmental interference and biological concerns also make it more difficult to deal with the network inference. In this article, we provide a comprehensive review of emerging microbiome interaction network inference methods. According to various research targets, estimated networks are divided into four main categories: correlation networks, conditional correlation networks, mixture networks, and differential networks. Their assumptions, high-level ideas, advantages, as well as limitations, are presented in this review. Since real microbial interactions can be complex and dynamic, no unifying method has, to date, captured all the aspects of interest. In addition, we discuss the challenges now confronting current microbial interaction study and future prospects. Finally, we point out several feasible directions of microbial network inference analysis and highlight that future research requires the joint promotion of statistical computation methods and experimental techniques.

Statistical Methods for Microbiome Compositional Data Network Inference: A Survey

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Single-cell RNA-seq data semi-supervised clustering and annotation via structural regularized domain adaptation.

Integrating Deep Supervised, Self-Supervised and Unsupervised Learning for Single-Cell RNA-seq Clustering and Annotation

Statistical computation methods for microbiome compositional data network inference

Statistical Methods for Microbiome Compositional Data Network Inference: A Survey