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DeepIso: A Deep Learning Model for Peptide Feature Detection from LC-MS map
Liquid chromatography with tandem mass spectrometry (LC-MS/MS) based quantitative proteomics provides the relative different protein abundance in healthy and disease-afflicted patients, which offers the information for molecular interactions, signaling pathways, and biomarker identification to serve...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868186/ https://www.ncbi.nlm.nih.gov/pubmed/31748623 http://dx.doi.org/10.1038/s41598-019-52954-4 |
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author | Zohora, Fatema Tuz Rahman, M. Ziaur Tran, Ngoc Hieu Xin, Lei Shan, Baozhen Li, Ming |
author_facet | Zohora, Fatema Tuz Rahman, M. Ziaur Tran, Ngoc Hieu Xin, Lei Shan, Baozhen Li, Ming |
author_sort | Zohora, Fatema Tuz |
collection | PubMed |
description | Liquid chromatography with tandem mass spectrometry (LC-MS/MS) based quantitative proteomics provides the relative different protein abundance in healthy and disease-afflicted patients, which offers the information for molecular interactions, signaling pathways, and biomarker identification to serve the drug discovery and clinical research. Typical analysis workflow begins with the peptide feature detection and intensity calculation from LC-MS map. We are the first to propose a deep learning based model, DeepIso, that combines recent advances in Convolutional Neural Network (CNN) and Recurrent Neural Network (RNN) to detect peptide features of different charge states, as well as, estimate their intensity. Existing tools are designed with limited engineered features and domain-specific parameters, which are hardly updated despite a huge amount of new coming proteomic data. On the other hand, DeepIso consisting of two separate deep learning based modules, learns multiple levels of representation of high dimensional data itself through many layers of neurons, and adaptable to newly acquired data. The peptide feature list reported by our model matches with 97.43% of high quality MS/MS identifications in a benchmark dataset, which is higher than the matching produced by several widely used tools. Our results demonstrate that novel deep learning tools are desirable to advance the state-of-the-art in protein identification and quantification. |
format | Online Article Text |
id | pubmed-6868186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68681862019-12-04 DeepIso: A Deep Learning Model for Peptide Feature Detection from LC-MS map Zohora, Fatema Tuz Rahman, M. Ziaur Tran, Ngoc Hieu Xin, Lei Shan, Baozhen Li, Ming Sci Rep Article Liquid chromatography with tandem mass spectrometry (LC-MS/MS) based quantitative proteomics provides the relative different protein abundance in healthy and disease-afflicted patients, which offers the information for molecular interactions, signaling pathways, and biomarker identification to serve the drug discovery and clinical research. Typical analysis workflow begins with the peptide feature detection and intensity calculation from LC-MS map. We are the first to propose a deep learning based model, DeepIso, that combines recent advances in Convolutional Neural Network (CNN) and Recurrent Neural Network (RNN) to detect peptide features of different charge states, as well as, estimate their intensity. Existing tools are designed with limited engineered features and domain-specific parameters, which are hardly updated despite a huge amount of new coming proteomic data. On the other hand, DeepIso consisting of two separate deep learning based modules, learns multiple levels of representation of high dimensional data itself through many layers of neurons, and adaptable to newly acquired data. The peptide feature list reported by our model matches with 97.43% of high quality MS/MS identifications in a benchmark dataset, which is higher than the matching produced by several widely used tools. Our results demonstrate that novel deep learning tools are desirable to advance the state-of-the-art in protein identification and quantification. Nature Publishing Group UK 2019-11-20 /pmc/articles/PMC6868186/ /pubmed/31748623 http://dx.doi.org/10.1038/s41598-019-52954-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zohora, Fatema Tuz Rahman, M. Ziaur Tran, Ngoc Hieu Xin, Lei Shan, Baozhen Li, Ming DeepIso: A Deep Learning Model for Peptide Feature Detection from LC-MS map |
title | DeepIso: A Deep Learning Model for Peptide Feature Detection from LC-MS map |
title_full | DeepIso: A Deep Learning Model for Peptide Feature Detection from LC-MS map |
title_fullStr | DeepIso: A Deep Learning Model for Peptide Feature Detection from LC-MS map |
title_full_unstemmed | DeepIso: A Deep Learning Model for Peptide Feature Detection from LC-MS map |
title_short | DeepIso: A Deep Learning Model for Peptide Feature Detection from LC-MS map |
title_sort | deepiso: a deep learning model for peptide feature detection from lc-ms map |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868186/ https://www.ncbi.nlm.nih.gov/pubmed/31748623 http://dx.doi.org/10.1038/s41598-019-52954-4 |
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