Cell type identification plays a vital role in single-cell RNA sequencing (scRNA-seq) data analysis. Although many deep embedded methods to cluster scRNA-seq data have been proposed, they still fail in elucidating the intrinsic properties of cells and genes. Here, we present a novel end-to-end deep graph clustering model for single-cell transcriptomics data based on unsupervised Gene-cell Collective representation learning and Optimal Transport (scGCOT) which integrates both cell and gene correlations. Specifically, scGCOT learns the latent embedding of cells and genes simultaneously and reconstructs the cell graph, the gene graph, and the gene expression count matrix. A zero-inflated negative binomial (ZINB) model is estimated via the reconstructed count matrix to capture the essential properties of scRNA-seq data. By leveraging the optimal transport-based joint representation alignment, scGCOT learns the clustering process and the latent representations through a mutually supervised self optimization strategy. Extensive experiments with 14 competing methods on 15 real scRNA-seq datasets demonstrate the competitive edges of scGCOT.

Unsupervised Gene-Cell Collective Representation Learning with Optimal Transport | VIDEO

Cell clustering is a critical step in analyzing single-cell RNA sequencing (scRNA-seq) data, which allows us to characterize the cellular heterogeneity of transcriptional profiling at the single-cell level. Single-cell deep embedded representation models have recently become popular since they can learn feature representation and clustering simultaneously. However, the model still suffers from a variety of significant challenges, including the massive amount of data, pervasive dropout events, and complicated noise patterns in transcriptional profiling. Here, we propose a Single-Cell Deep Embedding Fusion Representation (scDEFR) model, which develop a deep embedded fusion representation to learn fused heterogeneous latent embedding that contains both the transcriptome gene-level information and the cell topology information. We first fuse them layer by layer to obtain compressed representations of intercellular relationships and transcriptome information. After that, the zero-inflated negative binomial model (ZINB)-based decoder is proposed to capture the global probabilistic structure of the data and reconstruct the final gene expression information and cell graph. Finally, by simultaneously integrating the clustering loss, crossentropy loss, ZINB loss, and the cell graph reconstruction loss,
scDEFR can optimize clustering performance and learn the latent representation in fused information under a joint mutual supervised strategy. We conducted extensive and comprehensive experiments on 15 single-cell RNA-seq datasets from different sequencing platforms to demonstrate the superiority of scDEFR over a variety of state-of-the-art methods. 


Unsupervised Deep Embedded Fusion Representation of Single-cell Transcriptomics

Single-cell RNA sequencing (scRNA-seq) provides high-throughput information about the genome-wide gene expression levels at the single-cell resolution, bringing a precise understanding on the transcriptome of individual cells. Unfortunately, the rapidly growing scRNA-seq data and the prevalence of dropout events pose substantial challenges for cell type annotation. Here, we propose a single-cell model-based deep graph embedding clustering (scTAG) method, which simultaneously learns cellâ€“cell topology representations and identifies cell clusters based on deep graph convolutional network. scTAG integrates the zero-inflated negative binomial (ZINB) model into a topology adaptive graph convolutional autoencoder to learn the low-dimensional latent representation and adopts Kullbackâ€“Leibler (KL) divergence for the clustering tasks. By simultaneously optimizing the clustering loss, ZINB loss, and the cell graph reconstruction loss, scTAG jointly optimizes cluster label assignment and feature learning with the topological structures preserved in an end-to-end manner. Extensive experiments on 16 single-cell RNA-seq datasets from diverse yet representative single-cell sequencing platforms demonstrate the superiority of scTAG over various state-of-the-art clustering methods.

ZINB-Based Graph Embedding Autoencoder for Single-Cell RNA-Seq Interpretations

Main track - Applications

technical paper

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The purpose of the AAAI conference series is to promote research in Artificial Intelligence (AI) and foster scientific exchange between researchers, practitioners, scientists, students, and engineers across the entirety of AI and its affiliated disciplines. 

AI: Applications 1

poster

The purpose of the AAAI conference series is to promote research in Artificial Intelligence (AI) and foster scientific exchange between researchers, practitioners, scientists, students, and engineers across the entirety of AI and its affiliated disciplines. AAAI-23 is the Thirty-Seventh AAAI Conference on Artificial Intelligence. The theme of this conference is to create collaborative bridges within and beyond AI. Like previous AAAI conferences, AAAI-23 will feature technical paper presentations, special tracks, invited speakers, workshops, tutorials, poster sessions, senior member presentations, competitions, and exhibit programs, and two new activities: a Bridge Program and a Lab Program. Many of these activities are tailored to the theme of bridges and all are selected according to the highest standards, with additional programs for students and young researchers. 
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AAAI 2023

The purpose of the AAAI conference series is to promote research in Artificial Intelligence (AI) and foster scientific exchange between researchers, practitioners, scientists, students, and engineers across the entirety of AI and its affiliated disciplines.

Main_Track

The purpose of the AAAI conference is to promote research in artificial intelligence (AI) and scientific exchange among AI researchers, practitioners, scientists, and engineers in affiliated disciplines. 

Xiangtao Li

3

24

SHORT BIO

Presentations

Unsupervised Gene-Cell Collective Representation Learning with Optimal Transport | VIDEO

Unsupervised Deep Embedded Fusion Representation of Single-cell Transcriptomics

ZINB-Based Graph Embedding Autoencoder for Single-Cell RNA-Seq Interpretations

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