ScholarGate
Assistent

Sammenlign metoder

Gennemgå dine valgte metoder side om side; rækker, der afviger, er fremhævet.

Proteomanalyse×Sekvensjustering×
FagområdeBioinformatikBioinformatik
FamilieProcess / pipelineProcess / pipeline
Oprindelsesår1994–2003 (term coined 1994; shotgun proteomics established early 2000s)1970 (global alignment); 1981 (local alignment)
OphavspersonMarc Wilkins, Matthias Mann, Ruedi Aebersold (proteome/mass spectrometry foundations)Saul B. Needleman & Christian D. Wunsch (global); Temple F. Smith & Michael S. Waterman (local)
TypeQuantitative omics pipelineComputational sequence analysis technique
Oprindelig kildeWilkins, M. R., Sanchez, J.-C., Gooley, A. A., Appel, R. D., Humphery-Smith, I., Hochstrasser, D. F., & Williams, K. L. (1996). Progress with proteome projects: Why all proteins expressed by a genome should be identified and how to do it. Biotechnology and Genetic Engineering Reviews, 13(1), 19–50. link ↗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 ↗
Aliasserproteomics, mass spectrometry-based proteomics, shotgun proteomics, quantitative proteomicspairwise alignment, multiple sequence alignment, MSA, sequence comparison
Relaterede66
ResuméProteomics analysis is a systematic pipeline for identifying and quantifying proteins in biological samples using mass spectrometry. Starting from raw spectral data, the workflow searches protein sequence databases, estimates abundance across conditions, applies statistical tests for differential expression, and maps findings onto biological pathways. It complements transcriptomics by capturing post-translational regulation and actual protein abundance, and is central to biomarker discovery, drug-target identification, and systems biology.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.
ScholarGateDatasæt
  1. v1
  2. 2 Kilder
  3. PUBLISHED
  1. v1
  2. 2 Kilder
  3. PUBLISHED

Gå til søgning Hent slides

ScholarGateSammenlign metoder: Proteomics Analysis · Sequence Alignment. Hentet 2026-06-15 fra https://scholargate.app/da/compare