De-novo reconstruction and identification of transcriptional gene regulatory network modules differentiating single-cell clusters.
Mhaned OubounytMaria L ElkjaerTanja LaskeAlexander G B GrønningMarcus J MoellerJan BaumbachPublished in: NAR genomics and bioinformatics (2023)
Single-cell RNA sequencing (scRNA-seq) technology provides an unprecedented opportunity to understand gene functions and interactions at single-cell resolution. While computational tools for scRNA-seq data analysis to decipher differential gene expression profiles and differential pathway expression exist, we still lack methods to learn differential regulatory disease mechanisms directly from the single-cell data. Here, we provide a new methodology, named DiNiro, to unravel such mechanisms de novo and report them as small, easily interpretable transcriptional regulatory network modules. We demonstrate that DiNiro is able to uncover novel, relevant, and deep mechanistic models that not just predict but explain differential cellular gene expression programs. DiNiro is available at https://exbio.wzw.tum.de/diniro/.
Keyphrases
- single cell
- rna seq
- gene expression
- data analysis
- transcription factor
- high throughput
- genome wide
- dna methylation
- poor prognosis
- genome wide identification
- copy number
- network analysis
- public health
- oxidative stress
- computed tomography
- magnetic resonance
- magnetic resonance imaging
- binding protein
- bioinformatics analysis