ScholarGate
Pembantu

Bandingkan kaedah

Semak kaedah pilihan anda secara bersebelahan; baris yang berbeza akan diserlahkan.

Sequence Alignment×Analisis scRNA-seq×
BidangBioinformatikBioinformatik
KeluargaProcess / pipelineProcess / pipeline
Tahun asal1970 (global alignment); 1981 (local alignment)2009 (first scRNA-seq by Tang et al.); widely adopted 2015–2016
PengasasSaul 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)
JenisComputational sequence analysis techniqueHigh-throughput single-cell transcriptomic profiling pipeline
Sumber perintisNeedleman, 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 ↗
Aliaspairwise alignment, multiple sequence alignment, MSA, sequence comparisonscRNA-seq, single-cell transcriptomics, scRNAseq analysis, single-cell gene expression profiling
Berkaitan65
RingkasanSequence 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 data
  1. v1
  2. 2 Sumber
  3. PUBLISHED
  1. v1
  2. 2 Sumber
  3. PUBLISHED

Pergi ke carian Muat turun slaid

ScholarGateBandingkan kaedah: Sequence Alignment · Single-cell RNA-seq analysis. Dicapai 2026-06-15 daripada https://scholargate.app/ms/compare