CAJAL enables analysis and integration of single-cell morphological data using metric geometry

被引:6
|
作者
Govek, Kiya W. [1 ]
Nicodemus, Patrick [1 ]
Lin, Yuxuan [2 ]
Crawford, Jake [3 ]
Saturnino, Artur B. [2 ]
Cui, Hannah [2 ]
Zoga, Kristi [1 ]
Hart, Michael P. [1 ]
Camara, Pablo G. [1 ,4 ,5 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Arts & Sci, Dept Math, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Genom & Computat Biol Grad Grp, Philadelphia, PA 19104 USA
[4] Univ Penn, Inst Biomed Informat, Perelman Sch Med, Philadelphia, PA 19104 USA
[5] Univ Penn, Ctr Artificial Intelligence & Data Sci Integrated, Perelman Sch Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
RNA-SEQ; RECOGNITION; NEURONS;
D O I
10.1038/s41467-023-39424-2
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
Cell morphology is one of the most described phenotypes in biology, yet systematic quantification and classification of morphology remains limited. Here, the authors present a computational approach for cell morphometry and multi-modal analysis based on concepts from metric geometry. High-resolution imaging has revolutionized the study of single cells in their spatial context. However, summarizing the great diversity of complex cell shapes found in tissues and inferring associations with other single-cell data remains a challenge. Here, we present CAJAL, a general computational framework for the analysis and integration of single-cell morphological data. By building upon metric geometry, CAJAL infers cell morphology latent spaces where distances between points indicate the amount of physical deformation required to change the morphology of one cell into that of another. We show that cell morphology spaces facilitate the integration of single-cell morphological data across technologies and the inference of relations with other data, such as single-cell transcriptomic data. We demonstrate the utility of CAJAL with several morphological datasets of neurons and glia and identify genes associated with neuronal plasticity in C. elegans. Our approach provides an effective strategy for integrating cell morphology data into single-cell omics analyses.
引用
收藏
页数:17
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