| Literature DB >> 34530677 |
Abstract
The recent development of a high throughput single-cell RNA sequence devises the opportunity to study entire transcriptomes in the smallest detail. It also leads to the characterization of molecules and subtypes of a cell. Cancer epigenetics induced not only from individual molecules but also from the dysfunction of the system and the coupling effect of genes. While rapid advances are being made in the development of tools for single-cell RNA-seq data analysis, few slants are noticed in the potential advantages of single-cell network construction.Here, we used network perturbation theory with significant analysis to develop a cell-specific network that provides an insight into gene-gene association based on molecular expressions in a single-cell resolution. Besides, using this method, we can characterize each cell by inspecting how genes are connected and can identify the hub genes using network degree theory. Pathway & Gene enrichment analysis of the identified cell-specific high network degree genes supported the effectiveness of this method. This method could be beneficial for personalized drug design and even therapeutics.Entities:
Keywords: Single-cell RNA; embryonic stem cell; gene association; hub gene; perturbed network; significance analysis
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Year: 2021 PMID: 34530677 PMCID: PMC8794512 DOI: 10.1080/15384101.2021.1978265
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 5.173