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Improved identification and quantification of peptides in mass spectrometry data via chemical and random additive noise elimination (CRANE)

MOTIVATION: The output of electrospray ionization–liquid chromatography mass spectrometry (ESI-LC-MS) is influenced by multiple sources of noise and major contributors can be broadly categorized as baseline, random and chemical noise. Noise has a negative impact on the identification and quantificat...

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Autores principales: Seneviratne, Akila J, Peters, Sean, Clarke, David, Dausmann, Michael, Hecker, Michael, Tully, Brett, Hains, Peter G, Zhong, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711017/
https://www.ncbi.nlm.nih.gov/pubmed/34323970
http://dx.doi.org/10.1093/bioinformatics/btab563
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author Seneviratne, Akila J
Peters, Sean
Clarke, David
Dausmann, Michael
Hecker, Michael
Tully, Brett
Hains, Peter G
Zhong, Qing
author_facet Seneviratne, Akila J
Peters, Sean
Clarke, David
Dausmann, Michael
Hecker, Michael
Tully, Brett
Hains, Peter G
Zhong, Qing
author_sort Seneviratne, Akila J
collection PubMed
description MOTIVATION: The output of electrospray ionization–liquid chromatography mass spectrometry (ESI-LC-MS) is influenced by multiple sources of noise and major contributors can be broadly categorized as baseline, random and chemical noise. Noise has a negative impact on the identification and quantification of peptides, which influences the reliability and reproducibility of MS-based proteomics data. Most attempts at denoising have been made on either spectra or chromatograms independently, thus, important 2D information is lost because the mass-to-charge ratio and retention time dimensions are not considered jointly. RESULTS: This article presents a novel technique for denoising raw ESI-LC-MS data via 2D undecimated wavelet transform, which is applied to proteomics data acquired by data-independent acquisition MS (DIA-MS). We demonstrate that denoising DIA-MS data results in the improvement of peptide identification and quantification in complex biological samples. AVAILABILITY AND IMPLEMENTATION: The software is available on Github (https://github.com/CMRI-ProCan/CRANE). The datasets were obtained from ProteomeXchange (Identifiers—PXD002952 and PXD008651). Preliminary data and intermediate files are available via ProteomeXchange (Identifiers—PXD020529 and PXD025103). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-87110172022-01-04 Improved identification and quantification of peptides in mass spectrometry data via chemical and random additive noise elimination (CRANE) Seneviratne, Akila J Peters, Sean Clarke, David Dausmann, Michael Hecker, Michael Tully, Brett Hains, Peter G Zhong, Qing Bioinformatics Original Papers MOTIVATION: The output of electrospray ionization–liquid chromatography mass spectrometry (ESI-LC-MS) is influenced by multiple sources of noise and major contributors can be broadly categorized as baseline, random and chemical noise. Noise has a negative impact on the identification and quantification of peptides, which influences the reliability and reproducibility of MS-based proteomics data. Most attempts at denoising have been made on either spectra or chromatograms independently, thus, important 2D information is lost because the mass-to-charge ratio and retention time dimensions are not considered jointly. RESULTS: This article presents a novel technique for denoising raw ESI-LC-MS data via 2D undecimated wavelet transform, which is applied to proteomics data acquired by data-independent acquisition MS (DIA-MS). We demonstrate that denoising DIA-MS data results in the improvement of peptide identification and quantification in complex biological samples. AVAILABILITY AND IMPLEMENTATION: The software is available on Github (https://github.com/CMRI-ProCan/CRANE). The datasets were obtained from ProteomeXchange (Identifiers—PXD002952 and PXD008651). Preliminary data and intermediate files are available via ProteomeXchange (Identifiers—PXD020529 and PXD025103). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2021-07-29 /pmc/articles/PMC8711017/ /pubmed/34323970 http://dx.doi.org/10.1093/bioinformatics/btab563 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Papers
Seneviratne, Akila J
Peters, Sean
Clarke, David
Dausmann, Michael
Hecker, Michael
Tully, Brett
Hains, Peter G
Zhong, Qing
Improved identification and quantification of peptides in mass spectrometry data via chemical and random additive noise elimination (CRANE)
title Improved identification and quantification of peptides in mass spectrometry data via chemical and random additive noise elimination (CRANE)
title_full Improved identification and quantification of peptides in mass spectrometry data via chemical and random additive noise elimination (CRANE)
title_fullStr Improved identification and quantification of peptides in mass spectrometry data via chemical and random additive noise elimination (CRANE)
title_full_unstemmed Improved identification and quantification of peptides in mass spectrometry data via chemical and random additive noise elimination (CRANE)
title_short Improved identification and quantification of peptides in mass spectrometry data via chemical and random additive noise elimination (CRANE)
title_sort improved identification and quantification of peptides in mass spectrometry data via chemical and random additive noise elimination (crane)
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711017/
https://www.ncbi.nlm.nih.gov/pubmed/34323970
http://dx.doi.org/10.1093/bioinformatics/btab563
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