Review, evaluation, and discussion of the challenges of missing value imputation for mass spectrometry-based label-free global proteomics

J Proteome Res. 2015 May 1;14(5):1993-2001. doi: 10.1021/pr501138h. Epub 2015 Apr 22.

Abstract

In this review, we apply selected imputation strategies to label-free liquid chromatography-mass spectrometry (LC-MS) proteomics datasets to evaluate the accuracy with respect to metrics of variance and classification. We evaluate several commonly used imputation approaches for individual merits and discuss the caveats of each approach with respect to the example LC-MS proteomics data. In general, local similarity-based approaches, such as the regularized expectation maximization and least-squares adaptive algorithms, yield the best overall performances with respect to metrics of accuracy and robustness. However, no single algorithm consistently outperforms the remaining approaches, and in some cases, performing classification without imputation sometimes yielded the most accurate classification. Thus, because of the complex mechanisms of missing data in proteomics, which also vary from peptide to protein, no individual method is a single solution for imputation. On the basis of the observations in this review, the goal for imputation in the field of computational proteomics should be to develop new approaches that work generically for this data type and new strategies to guide users in the selection of the best imputation for their dataset and analysis objectives.

Keywords: Imputation; accuracy; classification; label free; mean-square error; peak intensity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Algorithms
  • Animals
  • Blood Proteins / analysis*
  • Chromatography, Liquid / statistics & numerical data*
  • Humans
  • Lung / chemistry
  • Mass Spectrometry / statistics & numerical data*
  • Mice
  • Peptides / analysis*
  • Proteomics / methods
  • Proteomics / statistics & numerical data*

Substances

  • Blood Proteins
  • Peptides