APEC: an accesson-based method for single-cell chromatin accessibility analysis

被引:15
作者
Li, Bin [1 ]
Li, Young [1 ]
Li, Kun [1 ]
Zhu, Lianbang [1 ]
Yu, Qiaoni [1 ]
Cai, Pengfei [1 ]
Fang, Jingwen [1 ,2 ]
Zhang, Wen [1 ]
Du, Pengcheng [1 ]
Jiang, Chen [1 ]
Lin, Jun [1 ]
Qu, Kun [1 ,3 ]
机构
[1] Univ Sci & Technol China, Affiliated Hosp 1, Hefei Natl Lab Phys Sci Microscale, Div Life Sci & Med,Div Mol Med,Dept Oncol, Hefei 230001, Anhui, Peoples R China
[2] HanGene Biotech, Xiaoshan Innovat Polis, Hangzhou 3CAS, Zhejiang, Peoples R China
[3] Univ Sci & Technol China, CAS Ctr Excellence Mol Cell Sci, CAS Key Lab Innate Immun & Chron Dis, Hefei 230027, Anhui, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
scATAC-seq; Cell clustering; Accesson; Regulome; Pseudotime trajectory; RNA-SEQ; TRANSCRIPTION FACTORS; REVEALS PRINCIPLES; STEM-CELLS; CTCF; GENOME; THYMOCYTES; EXPRESSION; LANDSCAPE; APOPTOSIS;
D O I
10.1186/s13059-020-02034-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The development of sequencing technologies has promoted the survey of genome-wide chromatin accessibility at single-cell resolution. However, comprehensive analysis of single-cell epigenomic profiles remains a challenge. Here, we introduce an accessibility pattern-based epigenomic clustering (APEC) method, which classifies each cell by groups of accessible regions with synergistic signal patterns termed "accessons". This python-based package greatly improves the accuracy of unsupervised single-cell clustering for many public datasets. It also predicts gene expression, identifies enriched motifs, discovers super-enhancers, and projects pseudotime trajectories. APEC is available at .
引用
收藏
页数:27
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