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MaxDIA enables library-based and library-free data-independent acquisition proteomics
MaxDIA is a software platform for analyzing data-independent acquisition (DIA) proteomics data within the MaxQuant software environment. Using spectral libraries, MaxDIA achieves deep proteome coverage with substantially better coefficients of variation in protein quantification than other software....
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668435/ https://www.ncbi.nlm.nih.gov/pubmed/34239088 http://dx.doi.org/10.1038/s41587-021-00968-7 |
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author | Sinitcyn, Pavel Hamzeiy, Hamid Salinas Soto, Favio Itzhak, Daniel McCarthy, Frank Wichmann, Christoph Steger, Martin Ohmayer, Uli Distler, Ute Kaspar-Schoenefeld, Stephanie Prianichnikov, Nikita Yılmaz, Şule Rudolph, Jan Daniel Tenzer, Stefan Perez-Riverol, Yasset Nagaraj, Nagarjuna Humphrey, Sean J. Cox, Jürgen |
author_facet | Sinitcyn, Pavel Hamzeiy, Hamid Salinas Soto, Favio Itzhak, Daniel McCarthy, Frank Wichmann, Christoph Steger, Martin Ohmayer, Uli Distler, Ute Kaspar-Schoenefeld, Stephanie Prianichnikov, Nikita Yılmaz, Şule Rudolph, Jan Daniel Tenzer, Stefan Perez-Riverol, Yasset Nagaraj, Nagarjuna Humphrey, Sean J. Cox, Jürgen |
author_sort | Sinitcyn, Pavel |
collection | PubMed |
description | MaxDIA is a software platform for analyzing data-independent acquisition (DIA) proteomics data within the MaxQuant software environment. Using spectral libraries, MaxDIA achieves deep proteome coverage with substantially better coefficients of variation in protein quantification than other software. MaxDIA is equipped with accurate false discovery rate (FDR) estimates on both library-to-DIA match and protein levels, including when using whole-proteome predicted spectral libraries. This is the foundation of discovery DIA—hypothesis-free analysis of DIA samples without library and with reliable FDR control. MaxDIA performs three- or four-dimensional feature detection of fragment data, and scoring of matches is augmented by machine learning on the features of an identification. MaxDIA’s bootstrap DIA workflow performs multiple rounds of matching with increasing quality of recalibration and stringency of matching to the library. Combining MaxDIA with two new technologies—BoxCar acquisition and trapped ion mobility spectrometry—both lead to deep and accurate proteome quantification. |
format | Online Article Text |
id | pubmed-8668435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-86684352021-12-29 MaxDIA enables library-based and library-free data-independent acquisition proteomics Sinitcyn, Pavel Hamzeiy, Hamid Salinas Soto, Favio Itzhak, Daniel McCarthy, Frank Wichmann, Christoph Steger, Martin Ohmayer, Uli Distler, Ute Kaspar-Schoenefeld, Stephanie Prianichnikov, Nikita Yılmaz, Şule Rudolph, Jan Daniel Tenzer, Stefan Perez-Riverol, Yasset Nagaraj, Nagarjuna Humphrey, Sean J. Cox, Jürgen Nat Biotechnol Article MaxDIA is a software platform for analyzing data-independent acquisition (DIA) proteomics data within the MaxQuant software environment. Using spectral libraries, MaxDIA achieves deep proteome coverage with substantially better coefficients of variation in protein quantification than other software. MaxDIA is equipped with accurate false discovery rate (FDR) estimates on both library-to-DIA match and protein levels, including when using whole-proteome predicted spectral libraries. This is the foundation of discovery DIA—hypothesis-free analysis of DIA samples without library and with reliable FDR control. MaxDIA performs three- or four-dimensional feature detection of fragment data, and scoring of matches is augmented by machine learning on the features of an identification. MaxDIA’s bootstrap DIA workflow performs multiple rounds of matching with increasing quality of recalibration and stringency of matching to the library. Combining MaxDIA with two new technologies—BoxCar acquisition and trapped ion mobility spectrometry—both lead to deep and accurate proteome quantification. Nature Publishing Group US 2021-07-08 2021 /pmc/articles/PMC8668435/ /pubmed/34239088 http://dx.doi.org/10.1038/s41587-021-00968-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sinitcyn, Pavel Hamzeiy, Hamid Salinas Soto, Favio Itzhak, Daniel McCarthy, Frank Wichmann, Christoph Steger, Martin Ohmayer, Uli Distler, Ute Kaspar-Schoenefeld, Stephanie Prianichnikov, Nikita Yılmaz, Şule Rudolph, Jan Daniel Tenzer, Stefan Perez-Riverol, Yasset Nagaraj, Nagarjuna Humphrey, Sean J. Cox, Jürgen MaxDIA enables library-based and library-free data-independent acquisition proteomics |
title | MaxDIA enables library-based and library-free data-independent acquisition proteomics |
title_full | MaxDIA enables library-based and library-free data-independent acquisition proteomics |
title_fullStr | MaxDIA enables library-based and library-free data-independent acquisition proteomics |
title_full_unstemmed | MaxDIA enables library-based and library-free data-independent acquisition proteomics |
title_short | MaxDIA enables library-based and library-free data-independent acquisition proteomics |
title_sort | maxdia enables library-based and library-free data-independent acquisition proteomics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668435/ https://www.ncbi.nlm.nih.gov/pubmed/34239088 http://dx.doi.org/10.1038/s41587-021-00968-7 |
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