Skip to main navigation Skip to search Skip to main content

HiDeF: identifying persistent structures in multiscale ‘omics data

  • Fan Zheng
  • , She Zhang
  • , Christopher Churas
  • , Dexter Pratt
  • , Ivet Bahar
  • , Trey Ideker
  • University of California at San Diego
  • University of Pittsburgh

Research output: Contribution to journalArticlepeer-review

39 Scopus citations

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.

Original languageEnglish
Article number21
JournalGenome Biology
Volume22
Issue number1
DOIs
StatePublished - Dec 2021

Keywords

  • Community detection
  • Multiscale
  • Persistent homology
  • Protein-protein interaction network
  • Resolution
  • Single-cell clustering
  • Systems biology

Fingerprint

Dive into the research topics of 'HiDeF: identifying persistent structures in multiscale ‘omics data'. Together they form a unique fingerprint.

Cite this