scSID: A lightweight algorithm for identifying rare cell types by capturing differential expression from single-cell sequencing data

Shudong Wang, Hengxiao Li, Kuijie Zhang, Hao Wu, Shanchen Pang*, Wenhao Wu, Lan Ye, Jionglong Su, Yulin Zhang

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Single-cell RNA sequencing (scRNA-seq) is currently an important technology for identifying cell types and studying diseases at the genetic level. Identifying rare cell types is biologically important as one of the downstream data analyses of single-cell RNA sequencing. Although rare cell identification methods have been developed, most of these suffer from insufficient mining of intercellular similarities, low scalability, and being time-consuming. In this paper, we propose a single-cell similarity division algorithm (scSID) for identifying rare cells. It takes cell-to-cell similarity into consideration by analyzing both inter-cluster and intra-cluster similarities, and discovers rare cell types based on the similarity differences. We show that scSID outperforms other existing methods by benchmarking it on different experimental datasets. Application of scSID to multiple datasets, including 68K PBMC and intestine, highlights its exceptional scalability and remarkable ability to identify rare cell populations.

Original languageEnglish
Pages (from-to)589-600
Number of pages12
JournalComputational and Structural Biotechnology Journal
Volume23
DOIs
Publication statusPublished - Dec 2024

Keywords

  • Rare cell types
  • Scalability
  • Similarity analysis
  • Single-cell RNA sequencing

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