Analyzing scRNA-seq data by CCP-assisted UMAP and t-SNE

Yuta Hozumi; Gu-Wei Wei

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arXiv · 2306.13750

Analyzing scRNA-seq data by CCP-assisted UMAP and t-SNE

Yuta Hozumi·Gu-Wei Wei

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Abstract

Single-cell RNA sequencing (scRNA-seq) is widely used to reveal heterogeneity in cells, which has given us insights into cell-cell communication, cell differentiation, and differential gene expression. However, analyzing scRNA-seq data is a challenge due to sparsity and the large number of genes involved. Therefore, dimensionality reduction and feature selection are important for removing spurious signals and enhancing downstream analysis. Correlated clustering and projection (CCP) was recently introduced as an effective method for preprocessing scRNA-seq data. CCP utilizes gene-gene correlations to partition the genes and, based on the partition, employs cell-cell interactions to obtain super-genes. Because CCP is a data-domain approach that does not require matrix diagonalization, it can be used in many downstream machine learning tasks. In this work, we utilize CCP as an initialization tool for uniform manifold approximation and projection (UMAP) and t-distributed stochastic neighbor embedding (t-SNE). By using eight publicly available datasets, we have found that CCP significantly improves UMAP and t-SNE visualization and dramatically improve their accuracy.

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BibTeX RIS

Yuta Hozumi, Gu-Wei Wei. 2023-06-23. Analyzing scRNA-seq data by CCP-assisted UMAP and t-SNE. https://arxiv.org/abs/2306.13750

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