Compară metode
Examinează metodele selectate una lângă alta; rândurile care diferă sunt evidențiate.
| Aliniere de secvențe× | Analiza ARN-seq monocelular× | |
|---|---|---|
| Domeniu | Bioinformatică | Bioinformatică |
| Familie | Process / pipeline | Process / pipeline |
| Anul apariției≠ | 1970 (global alignment); 1981 (local alignment) | 2009 (first scRNA-seq by Tang et al.); widely adopted 2015–2016 |
| Autorul original≠ | Saul B. Needleman & Christian D. Wunsch (global); Temple F. Smith & Michael S. Waterman (local) | Azim Surani, Barbara Treutlein, and the Regev/McCarroll groups (foundational droplet-based methods ~2015) |
| Tip≠ | Computational sequence analysis technique | High-throughput single-cell transcriptomic profiling pipeline |
| Sursa seminală≠ | Needleman, 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 ↗ | 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. DOI ↗ |
| Denumiri alternative | pairwise alignment, multiple sequence alignment, MSA, sequence comparison | scRNA-seq, single-cell transcriptomics, scRNAseq analysis, single-cell gene expression profiling |
| Înrudite≠ | 6 | 5 |
| Rezumat≠ | Sequence 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. | 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. |
| ScholarGateSet de date ↗ |
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