Powerful and accurate detection of temporal gene expression patterns from multi-sample multi-stage single-cell transcriptomics data with TDEseq.
Yue FanLei LiShiquan SunPublished in: Genome biology (2024)
We present a non-parametric statistical method called TDEseq that takes full advantage of smoothing splines basis functions to account for the dependence of multiple time points in scRNA-seq studies, and uses hierarchical structure linear additive mixed models to model the correlated cells within an individual. As a result, TDEseq demonstrates powerful performance in identifying four potential temporal expression patterns within a specific cell type. Extensive simulation studies and the analysis of four published scRNA-seq datasets show that TDEseq can produce well-calibrated p-values and up to 20% power gain over the existing methods for detecting temporal gene expression patterns.
Keyphrases
- single cell
- gene expression
- rna seq
- dna methylation
- high throughput
- genome wide
- induced apoptosis
- poor prognosis
- oxidative stress
- cell cycle arrest
- machine learning
- randomized controlled trial
- electronic health record
- endoplasmic reticulum stress
- systematic review
- artificial intelligence
- deep learning
- sensitive detection
- meta analyses