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Sequenz-Alignment×RNA-seq Differential Expression×
FachgebietBioinformatikBioinformatik
FamilieProcess / pipelineProcess / pipeline
Entstehungsjahr1970 (global alignment); 1981 (local alignment)2008–2010 (RNA-seq DE methodology established)
UrheberSaul B. Needleman & Christian D. Wunsch (global); Temple F. Smith & Michael S. Waterman (local)Multiple groups; foundational methods from Anders & Huber (DESeq, 2010), Robinson, McCarthy & Smyth (edgeR, 2010)
TypComputational sequence analysis techniqueQuantitative genomics pipeline
Wegweisende QuelleNeedleman, S. B., & Wunsch, C. D. (1970). A general method applicable to the search for similarities in the amino acid sequence of two proteins. Journal of Molecular Biology, 48(3), 443–453. DOI ↗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. DOI ↗
Aliasnamenpairwise alignment, multiple sequence alignment, MSA, sequence comparisonRNA-seq DE analysis, transcriptomic differential expression, bulk RNA-seq DE, DEA
Verwandt66
ZusammenfassungSequence alignment is a foundational bioinformatics technique that arranges two or more DNA, RNA, or protein sequences to reveal regions of similarity, infer evolutionary relationships, identify functional domains, and map sequencing reads to reference genomes. It underpins virtually every downstream genomic analysis, from variant calling and gene expression quantification to phylogenetics and structural annotation.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.
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ScholarGateMethoden vergleichen: Sequence Alignment · RNA-seq Differential Expression. Abgerufen am 2026-06-15 von https://scholargate.app/de/compare