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Data Imputation in Merged Isobaric Labeling-Based Relative Quantification Datasets.

Nicolai Bjødstrup Palstrøm1, Rune Matthiesen2, Hans Christian Beck3

  • 1Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense C, Denmark.

Methods in Molecular Biology (Clifton, N.J.)
|September 26, 2019
PubMed
Summary
This summary is machine-generated.

Missing values in mass spectrometry proteomics data hinder clinical research. k-Nearest Neighbors imputation effectively addresses these gaps in shotgun clinical proteomics, improving downstream analysis for disease-related protein discovery.

Keywords:
Clinical proteomicsData imputationIsobaric tagsMissing valuesRelative quantification

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Area of Science:

  • Proteomics
  • Clinical Mass Spectrometry
  • Bioinformatics

Background:

  • Shotgun clinical proteomics using isobaric labeling (iTRAQ, TMT) generates large datasets.
  • Missing values are common in these datasets, complicating statistical analysis and biomarker discovery.
  • Accurate imputation is crucial for linking protein expression to clinical traits.

Purpose of the Study:

  • To evaluate data imputation methods for mass spectrometry-based proteomics.
  • To assess the effectiveness of microarray-derived imputation techniques in shotgun clinical proteomics.
  • To identify robust methods for handling missing values in quantitative proteomic datasets.

Main Methods:

  • Tested three data imputation approaches originally developed for microarray data.
  • Applied methods to quantitative proteomic datasets using isobaric tags (iTRAQ and TMT).
  • Evaluated performance on datasets with varying percentages of missing values.

Main Results:

  • k-Nearest Neighbors (kNN) imputation demonstrated success in handling missing values.
  • The kNN method effectively imputed data in datasets with up to 50% missing values.
  • Imputation improved the integrity of proteomic data for downstream analysis.

Conclusions:

  • k-Nearest Neighbors imputation is a viable strategy for addressing missing values in quantitative proteomics.
  • This approach enhances the reliability of clinical proteomics studies.
  • Successful imputation facilitates the identification of disease-associated proteins for diagnostic and prognostic applications.