GiniClust: detecting rare cell types from single-cell gene expression data with Gini index

被引:180
作者
Jiang, Lan [1 ,2 ,3 ]
Chen, Huidong [1 ,2 ,4 ]
Pinello, Luca [1 ,2 ]
Yuan, Guo-Cheng [1 ,2 ,5 ]
机构
[1] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02215 USA
[2] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[3] Boston Childrens Hosp, Boston, MA 02115 USA
[4] Tongji Univ, Dept Comp Sci & Technol, Shanghai, Peoples R China
[5] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
来源
GENOME BIOLOGY | 2016年 / 17卷
关键词
Clustering; Single-cell analysis; RNA-seq; qPCR; Gini index; Rare cell type; CHARACTERIZING HETEROGENEITY;
D O I
10.1186/s13059-016-1010-4
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
High-throughput single-cell technologies have great potential to discover new cell types; however, it remains challenging to detect rare cell types that are distinct from a large population. We present a novel computational method, called GiniClust, to overcome this challenge. Validation against a benchmark dataset indicates that GiniClust achieves high sensitivity and specificity. Application of GiniClust to public single-cell RNA-seq datasets uncovers previously unrecognized rare cell types, including Zscan4-expressing cells within mouse embryonic stem cells and hemoglobin-expressing cells in the mouse cortex and hippocampus. GiniClust also correctly detects a small number of normal cells that are mixed in a cancer cell population.
引用
收藏
页数:13
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