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A streamlined platform for analyzing tera-scale DDA and DIA mass spectrometry data enables highly sensitive immunopeptidomics.
Xin, Lei; Qiao, Rui; Chen, Xin; Tran, Hieu; Pan, Shengying; Rabinoviz, Sahar; Bian, Haibo; He, Xianliang; Morse, Brenton; Shan, Baozhen; Li, Ming.
  • Xin L; Bioinformatics Solutions Inc., Waterloo, Ontario, Canada.
  • Qiao R; Bioinformatics Solutions Inc., Waterloo, Ontario, Canada.
  • Chen X; Bioinformatics Solutions Inc., Waterloo, Ontario, Canada.
  • Tran H; David R. Cheriton School of Computer Science, University of Waterloo, Waterloo, Ontario, Canada.
  • Pan S; Bioinformatics Solutions Inc., Waterloo, Ontario, Canada.
  • Rabinoviz S; Bioinformatics Solutions Inc., Waterloo, Ontario, Canada.
  • Bian H; Bioinformatics Solutions Inc., Waterloo, Ontario, Canada.
  • He X; Bioinformatics Solutions Inc., Waterloo, Ontario, Canada.
  • Morse B; Bioinformatics Solutions Inc., Waterloo, Ontario, Canada.
  • Shan B; Bioinformatics Solutions Inc., Waterloo, Ontario, Canada. bshan@bioinfor.com.
  • Li M; David R. Cheriton School of Computer Science, University of Waterloo, Waterloo, Ontario, Canada. mli@uwaterloo.ca.
Nat Commun ; 13(1): 3108, 2022 06 07.
Article in English | MEDLINE | ID: covidwho-1878525
ABSTRACT
Integrating data-dependent acquisition (DDA) and data-independent acquisition (DIA) approaches can enable highly sensitive mass spectrometry, especially for imunnopeptidomics applications. Here we report a streamlined platform for both DDA and DIA data analysis. The platform integrates deep learning-based solutions of spectral library search, database search, and de novo sequencing under a unified framework, which not only boosts the sensitivity but also accurately controls the specificity of peptide identification. Our platform identifies 5-30% more peptide precursors than other state-of-the-art systems on multiple benchmark datasets. When evaluated on immunopeptidomics datasets, we identify 1.7-4.1 and 1.4-2.2 times more peptides from DDA and DIA data, respectively, than previously reported results. We also discover six T-cell epitopes from SARS-CoV-2 immunopeptidome that might represent potential targets for COVID-19 vaccine development. The platform supports data formats from all major instruments and is implemented with the distributed high-performance computing technology, allowing analysis of tera-scale datasets of thousands of samples for clinical applications.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Proteomics / COVID-19 Type of study: Experimental Studies / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-022-30867-7

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Proteomics / COVID-19 Type of study: Experimental Studies / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-022-30867-7