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Author Notes:

Tianwei Yu, Email: yutianwei@cuhk.edu.cn

T.Y. designed the method. D.W, K.U., C.M., V.T., S.L., D.J. provided the data. Q.L., D.W. conducted testing on the data. Q.L., Z.L. and T.Y. drafted the manuscript. All authors reviewed the manuscript.

The authors declare no competing interests.

Subjects:

Research Funding:

This work was partially supported by NIH grants R01GM124061 and U01CA235493, National Key R&D Program of China Grant No. 2018YFB0505000, Emory/Georgia Tech Center for Health Discovery and Well Being (CHDWB), and a grant from the University Development Fund of CUHK-Shenzhen.

Keywords:

  • Science & Technology
  • Multidisciplinary Sciences
  • Science & Technology - Other Topics
  • SPECTROMETRY DATA
  • MASS
  • ANNOTATION
  • EXTRACTION
  • ALIGNMENT
  • CHROMATOGRAPHY

Addressing the batch effect issue for LC/MS metabolomics data in data preprocessing

Tools:

Journal Title:

SCIENTIFIC REPORTS

Volume:

Volume 10, Number 1

Publisher:

, Pages 13856-13856

Type of Work:

Article | Final Publisher PDF

Abstract:

With the growth of metabolomics research, more and more studies are conducted on large numbers of samples. Due to technical limitations of the Liquid Chromatography–Mass Spectrometry (LC/MS) platform, samples often need to be processed in multiple batches. Across different batches, we often observe differences in data characteristics. In this work, we specifically focus on data generated in multiple batches on the same LC/MS machinery. Traditional preprocessing methods treat all samples as a single group. Such practice can result in errors in the alignment of peaks, which cannot be corrected by post hoc application of batch effect correction methods. In this work, we developed a new approach that address the batch effect issue in the preprocessing stage, resulting in better peak detection, alignment and quantification. It can be combined with down-stream batch effect correction methods to further correct for between-batch intensity differences. The method is implemented in the existing workflow of the apLCMS platform. Analyzing data with multiple batches, both generated from standardized quality control (QC) plasma samples and from real biological studies, the new method resulted in feature tables with better consistency, as well as better down-stream analysis results. The method can be a useful addition to the tools available for large studies involving multiple batches. The method is available as part of the apLCMS package. Download link and instructions are at https://mypage.cuhk.edu.cn/academics/yutianwei/apLCMS/.

Copyright information:

© The Author(s) 2020

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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