Skip to main navigation Skip to search Skip to main content

DANSE: A pipeline for dynamic modelling of time-series multi-omics data

Research output: Contribution to journalArticleAcademicpeer-review

37 Downloads (Pure)

Abstract

Background: Understanding time-dependent intracellular processes, such as cell differentiation, is key to developing new therapies for a wide range of diseases. Models that connect transcription factor activity to dynamic expression patterns are rare, despite the increased availability of time-series data.

Results: To identify key regulators of time-dependent biological processes, we present the pipeline DANSE: Dynamics inference Algorithm on Networks Specified by Enhancers. Starting from multi-omics data, our pipeline constructs a data-driven mechanistic transcription factor (TF) network and subsequently defines a dynamic model based on this TF network. The combination of a TF network and a mechanistic model allows for the identification of a small set of key transcription factors predicted to drive the modelled biological process. We showcase the result of our pipeline by applying DANSE to two different datasets that describe iPSC differentiation.

Conclusions: Models constructed using DANSE suggest testable hypotheses for the perturbation of gene expression, for example, knockdown or overexpression, that influence cell fate. In this way, DANSE is a powerful tool for generating novel hypotheses in a data-driven manner that take into account the dynamic nature of multi-omics time series data.

Original languageEnglish
Article number28
Number of pages22
JournalBMC bioinformatics
Volume27
Issue number1
Early online date30 Dec 2025
DOIs
Publication statusE-pub ahead of print/First online - 30 Dec 2025

Keywords

  • Data-driven
  • Gene regulatory network
  • Mechanistic modelling
  • Multi-omics
  • ODE modelling
  • Time series

Fingerprint

Dive into the research topics of 'DANSE: A pipeline for dynamic modelling of time-series multi-omics data'. Together they form a unique fingerprint.

Cite this