Sammenlign metoder

	Single-cell RNA-seq Analyse	RNA-seq Differential Expression
Fagområde	Bioinformatik	Bioinformatik
Familie	Process / pipeline	Process / pipeline
Oprindelsesår	2009 (first scRNA-seq by Tang et al.); widely adopted 2015–2016	2008–2010 (RNA-seq DE methodology established)
Ophavsperson	Azim Surani, Barbara Treutlein, and the Regev/McCarroll groups (foundational droplet-based methods ~2015)	Multiple groups; foundational methods from Anders & Huber (DESeq, 2010), Robinson, McCarthy & Smyth (edgeR, 2010)
Type	High-throughput single-cell transcriptomic profiling pipeline	Quantitative genomics pipeline
Oprindelig kilde	Satija, R., Farrell, J. A., Gennert, D., Schier, A. F., & Regev, A. (2015). Spatial reconstruction of single-cell gene expression data. Nature Biotechnology, 33(5), 495–502.	Love, M. I., Huber, W., & Anders, S. (2014). Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biology, 15(12), 550.
Aliasser	scRNA-seq, single-cell transcriptomics, scRNAseq analysis, single-cell gene expression profiling	RNA-seq DE analysis, transcriptomic differential expression, bulk RNA-seq DE, DEA
Relaterede	5	6
Resumé	Single-cell RNA sequencing (scRNA-seq) analysis characterises gene expression at the resolution of individual cells, enabling discovery of cell types, states, and transitions that are invisible in bulk transcriptomics. Starting from raw sequencing reads, the workflow produces a cell-by-gene count matrix and proceeds through quality control, normalisation, dimensionality reduction, unsupervised clustering, cell-type annotation, and a range of downstream analyses such as trajectory inference and differential expression between cell populations.	RNA-seq differential expression (DE) analysis identifies genes whose transcript abundance differs significantly between two or more biological conditions — for example, treated versus control, or diseased versus healthy tissue. Starting from raw sequencing reads, the pipeline moves through alignment, count-based normalization, statistical modeling of count dispersion, hypothesis testing, and multiple-testing correction to produce a ranked list of differentially expressed genes accompanied by fold-change estimates and adjusted p-values.