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A comparative study of evaluating missing value imputation methods in label-free proteomics

The presence of missing values (MVs) in label-free quantitative proteomics greatly reduces the completeness of data. Imputation has been widely utilized to handle MVs, and selection of the proper method is critical for the accuracy and reliability of imputation. Here we present a comparative study t...

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Autores principales: Jin, Liang, Bi, Yingtao, Hu, Chenqi, Qu, Jun, Shen, Shichen, Wang, Xue, Tian, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815892/
https://www.ncbi.nlm.nih.gov/pubmed/33469060
http://dx.doi.org/10.1038/s41598-021-81279-4
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author Jin, Liang
Bi, Yingtao
Hu, Chenqi
Qu, Jun
Shen, Shichen
Wang, Xue
Tian, Yu
author_facet Jin, Liang
Bi, Yingtao
Hu, Chenqi
Qu, Jun
Shen, Shichen
Wang, Xue
Tian, Yu
author_sort Jin, Liang
collection PubMed
description The presence of missing values (MVs) in label-free quantitative proteomics greatly reduces the completeness of data. Imputation has been widely utilized to handle MVs, and selection of the proper method is critical for the accuracy and reliability of imputation. Here we present a comparative study that evaluates the performance of seven popular imputation methods with a large-scale benchmark dataset and an immune cell dataset. Simulated MVs were incorporated into the complete part of each dataset with different combinations of MV rates and missing not at random (MNAR) rates. Normalized root mean square error (NRMSE) was applied to evaluate the accuracy of protein abundances and intergroup protein ratios after imputation. Detection of true positives (TPs) and false altered-protein discovery rate (FADR) between groups were also compared using the benchmark dataset. Furthermore, the accuracy of handling real MVs was assessed by comparing enriched pathways and signature genes of cell activation after imputing the immune cell dataset. We observed that the accuracy of imputation is primarily affected by the MNAR rate rather than the MV rate, and downstream analysis can be largely impacted by the selection of imputation methods. A random forest-based imputation method consistently outperformed other popular methods by achieving the lowest NRMSE, high amount of TPs with the average FADR < 5%, and the best detection of relevant pathways and signature genes, highlighting it as the most suitable method for label-free proteomics.
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spelling pubmed-78158922021-01-21 A comparative study of evaluating missing value imputation methods in label-free proteomics Jin, Liang Bi, Yingtao Hu, Chenqi Qu, Jun Shen, Shichen Wang, Xue Tian, Yu Sci Rep Article The presence of missing values (MVs) in label-free quantitative proteomics greatly reduces the completeness of data. Imputation has been widely utilized to handle MVs, and selection of the proper method is critical for the accuracy and reliability of imputation. Here we present a comparative study that evaluates the performance of seven popular imputation methods with a large-scale benchmark dataset and an immune cell dataset. Simulated MVs were incorporated into the complete part of each dataset with different combinations of MV rates and missing not at random (MNAR) rates. Normalized root mean square error (NRMSE) was applied to evaluate the accuracy of protein abundances and intergroup protein ratios after imputation. Detection of true positives (TPs) and false altered-protein discovery rate (FADR) between groups were also compared using the benchmark dataset. Furthermore, the accuracy of handling real MVs was assessed by comparing enriched pathways and signature genes of cell activation after imputing the immune cell dataset. We observed that the accuracy of imputation is primarily affected by the MNAR rate rather than the MV rate, and downstream analysis can be largely impacted by the selection of imputation methods. A random forest-based imputation method consistently outperformed other popular methods by achieving the lowest NRMSE, high amount of TPs with the average FADR < 5%, and the best detection of relevant pathways and signature genes, highlighting it as the most suitable method for label-free proteomics. Nature Publishing Group UK 2021-01-19 /pmc/articles/PMC7815892/ /pubmed/33469060 http://dx.doi.org/10.1038/s41598-021-81279-4 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jin, Liang
Bi, Yingtao
Hu, Chenqi
Qu, Jun
Shen, Shichen
Wang, Xue
Tian, Yu
A comparative study of evaluating missing value imputation methods in label-free proteomics
title A comparative study of evaluating missing value imputation methods in label-free proteomics
title_full A comparative study of evaluating missing value imputation methods in label-free proteomics
title_fullStr A comparative study of evaluating missing value imputation methods in label-free proteomics
title_full_unstemmed A comparative study of evaluating missing value imputation methods in label-free proteomics
title_short A comparative study of evaluating missing value imputation methods in label-free proteomics
title_sort comparative study of evaluating missing value imputation methods in label-free proteomics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815892/
https://www.ncbi.nlm.nih.gov/pubmed/33469060
http://dx.doi.org/10.1038/s41598-021-81279-4
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