A geometric approach to characterize the functional identity of single cells

被引:38
作者
Mohammadi, Shahin [1 ,2 ]
Ravindra, Vikram [3 ]
Gleich, David F. [3 ]
Grama, Ananth [3 ]
机构
[1] MIT, Comp Sci & Artificial Intelligence Lab, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] MIT & Harvard, Broad Inst, Cambridge, MA 02142 USA
[3] Purdue Univ, Dept Comp Sci, W Lafayette, IN 47907 USA
基金
美国国家科学基金会;
关键词
GENE-EXPRESSION DATA; RNA-SEQ; MELANOMA; HETEROGENEITY; GENOMICS; E2F1;
D O I
10.1038/s41467-018-03933-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Single-cell transcriptomic data has the potential to radically redefine our view of cell-type identity. Cells that were previously believed to be homogeneous are now clearly distinguishable in terms of their expression phenotype. Methods for automatically characterizing the functional identity of cells, and their associated properties, can be used to uncover processes involved in lineage differentiation as well as sub-typing cancer cells. They can also be used to suggest personalized therapies based on molecular signatures associated with pathology. We develop a new method, called ACTION, to infer the functional identity of cells from their transcriptional profile, classify them based on their dominant function, and reconstruct regulatory networks that are responsible for mediating their identity. Using ACTION, we identify novel Melanoma subtypes with differential survival rates and therapeutic responses, for which we provide biomarkers along with their underlying regulatory networks.
引用
收藏
页数:10
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