| Literature DB >> 33413539 |
Fan Zheng1, She Zhang2, Christopher Churas3, Dexter Pratt3, Ivet Bahar2, Trey Ideker4.
Abstract
In any 'omics study, the scale of analysis can dramatically affect the outcome. For instance, when clustering single-cell transcriptomes, is the analysis tuned to discover broad or specific cell types? Likewise, protein communities revealed from protein networks can vary widely in sizes depending on the method. Here, we use the concept of persistent homology, drawn from mathematical topology, to identify robust structures in data at all scales simultaneously. Application to mouse single-cell transcriptomes significantly expands the catalog of identified cell types, while analysis of SARS-COV-2 protein interactions suggests hijacking of WNT. The method, HiDeF, is available via Python and Cytoscape.Entities:
Keywords: Community detection; Multiscale; Persistent homology; Protein-protein interaction network; Resolution; Single-cell clustering; Systems biology
Mesh:
Substances:
Year: 2021 PMID: 33413539 PMCID: PMC7789082 DOI: 10.1186/s13059-020-02228-4
Source DB: PubMed Journal: Genome Biol ISSN: 1474-7596 Impact factor: 13.583