计算生物学
可扩展性
鉴定(生物学)
相似性(几何)
电池类型
计算机科学
标杆管理
细胞
核糖核酸
DNA测序
RNA序列
数据挖掘
生物
生物信息学
人工智能
遗传学
基因
基因表达
转录组
数据库
植物
营销
业务
图像(数学)
作者
Shudong Wang,Hengxiao Li,Kuijie Zhang,Hao Wu,Shanchen Pang,Wenhao Wu,Lan Ye,Jionglong Su,Yulin Zhang
标识
DOI:10.1016/j.csbj.2023.12.043
摘要
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.
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