Cell identity revealed by precise cell cycle state mapping links data modalities

Saeed Alahmari, Andrew Schultz, Jordan Albrecht, Vural Tagal, Zaid Siddiqui, Sadhya Prabhakaran, Issam El Naqa, Alexander Anderson, Laura Heiser, Noemi Andor
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引用次数: 0

Abstract

Several methods for cell cycle inference from sequencing data exist and are widely adopted. In contrast, methods for classification of cell cycle state from imaging data are scarce. We have for the first time integrated sequencing and imaging derived cell cycle pseudo-times for assigning 449 imaged cells to 693 sequenced cells at an average resolution of 3.4 and 2.4 cells for sequencing and imaging data respectively. Data integration revealed thousands of pathways and organelle features that are correlated with each other, including several previously known interactions and novel associations. The ability to assign the transcriptome state of a profiled cell to its closest living relative, which is still actively growing and expanding opens the door for genotype-phenotype mapping at single cell resolution forward in time.
通过精确的细胞周期状态映射揭示细胞身份,将数据模式联系起来
目前已有几种从测序数据推断细胞周期的方法,并被广泛采用。相比之下,从成像数据中对细胞周期状态进行分类的方法却很少。我们首次整合了测序和成像得出的细胞周期伪时间,将 449 个成像细胞分配给 693 个测序细胞,测序和成像数据的平均分辨率分别为 3.4 个细胞和 2.4 个细胞。数据整合揭示了数以千计相互关联的通路和细胞器特征,包括一些以前已知的相互作用和新的关联。将剖析细胞的转录组状态分配给仍在积极生长和扩张的近亲细胞的能力,为以单细胞分辨率进行基因型-表型映射打开了一扇大门。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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