Differential detection workflows for multi-sample single-cell RNA-seq data.
Jeroen GilisLaura PerinMilan MalfaitLieven ClementAlemu Takele AssefaBie VerbistDavide RissoLieven ClementPublished in: bioRxiv : the preprint server for biology (2023)
In single-cell transcriptomics, differential gene expression (DE) analyses typically focus on testing differences in the average expression of genes between cell types or conditions of interest. Single-cell transcriptomics, however, also has the promise to prioritise genes for which the expression differ in other aspects of the distribution. Here we develop a workflow for assessing differential detection (DD), which tests for differences in the average fraction of samples or cells in which a gene is detected. After benchmarking eight different DD data analysis strategies, we provide a unified workflow for jointly assessing DE and DD. Using simulations and two case studies, we show that DE and DD analysis provide complementary information, both in terms of the individual genes they report and in the functional interpretation of those genes.
Keyphrases
- single cell
- rna seq
- genome wide
- data analysis
- genome wide identification
- gene expression
- high throughput
- poor prognosis
- bioinformatics analysis
- dna methylation
- electronic health record
- genome wide analysis
- loop mediated isothermal amplification
- big data
- transcription factor
- molecular dynamics
- long non coding rna
- binding protein
- stem cells
- machine learning
- cell proliferation
- cell death
- bone marrow
- social media
- cell therapy
- health information
- sensitive detection
- cell cycle arrest
- pi k akt