| Literature DB >> 34285968 |
Thomas Luh1, Kimberly Lucero1, Wenji Ma2, Jaeyop Lee1, Yu Jerry Zhou1, Yufeng Shen2, Kang Liu1.
Abstract
The ability to conduct investigation of cellular transcription, signaling, and function at the single-cell level has opened opportunities to examine heterogeneous populations at unprecedented resolutions. Although methods have been developed to evaluate high-dimensional transcriptomic and proteomic data (relating to cellular mRNA and protein), there has not been a method to evaluate corresponding high-dimensional functionomic data (relating to cellular functions) from single cells. Here, we present a protocol to quantitatively measure the differentiation potentials of single human hematopoietic stem and progenitor cells, and then cluster the cells according to these measurements. High dimensional functionomic analysis of cell potential allows cell function to be linked to molecular mechanisms within the same progenitor population.Entities:
Keywords: CD34+ hematopoietic stem and progenitor cells ; Barnes-Hut t-SNE; Differentiation; Dimension reduction; Quantitative clonal output; Single cell culture
Year: 2018 PMID: 34285968 PMCID: PMC8275246 DOI: 10.21769/BioProtoc.2851
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325