ILoReg: a tool for high-resolution cell population identification from single-cell RNA-seq data

被引:5
|
作者
Smolander, Johannes [1 ,2 ]
Junttila, Sini [1 ,2 ]
Venalainen, Mikko S. [1 ,2 ]
Elo, Laura L. [1 ,2 ,3 ]
机构
[1] Univ Turku, Turku Biosci Ctr, FIN-20520 Turku, Finland
[2] Abo Akad Univ, FIN-20520 Turku, Finland
[3] Univ Turku, Inst Biomed, Turku, Finland
基金
芬兰科学院; 欧洲研究理事会;
关键词
D O I
10.1093/bioinformatics/btaa919
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Single-cell RNA-seq allows researchers to identify cell populations based on unsupervised clustering of the transcriptome. However, subpopulations can have only subtle transcriptomic differences and the high dimensionality of the data makes their identification challenging. Results: We introduce ILoReg, an R package implementing a new cell population identification method that improves identification of cell populations with subtle differences through a probabilistic feature extraction step that is applied before clustering and visualization. The feature extraction is performed using a novel machine learning algorithm, called iterative clustering projection (ICP), that uses logistic regression and clustering similarity comparison to iteratively cluster data. Remarkably, ICP also manages to integrate feature selection with the clustering through L1-regularization, enabling the identification of genes that are differentially expressed between cell populations. By combining solutions of multiple ICP runs into a single consensus solution, ILoReg creates a representation that enables investigating cell populations with a high resolution. In particular, we show that the visualization of ILoReg allows segregation of immune and pancreatic cell populations in a more pronounced manner compared with current state-of-the-art methods.
引用
收藏
页码:1107 / 1114
页数:8
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