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ER is the primary site for the maturation and folding of soluble and transmembrane secretory proteins. The calnexin cycle is a specific chaperone system that folds and assesses the confirmation of N-glycosylated proteins before they can exit the ER lumen. The primary players of this quality check pipeline are the lectins, ER-resident chaperones, and a glucosyl transferase enzyme. In case the calnexin system in the lumen fails to salvage a misfolded protein, it is transported to the cytoplasm...
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The Use of Reverse Phase Protein Arrays RPPA to Explore Protein Expression Variation within Individual Renal Cell Cancers
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RPPanalyzer toolbox: an improved R package for analysis of reverse phase protein array data.

Silvia von der Heyde1, Johanna Sonntag2, Daniel Kaschek3

  • 1Department of Medical Statistics, University Medical Center Göttingen, Göttingen, Germany.

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|September 12, 2014
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Summary

This study enhances the RPPanalyzer R package for analyzing proteomic data from reverse phase protein arrays (RPPA). The improved tool offers streamlined preprocessing, noise correction, and visualization for longitudinal RPPA studies.

Keywords:
RPPARPPanalyzerdata analysis toolboxopen-source softwareproteomics

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Area of Science:

  • Proteomics
  • Bioinformatics
  • Computational Biology

Background:

  • Large-scale proteomic data analysis necessitates specialized bioinformatics tools.
  • Existing software solutions for reverse phase protein array (RPPA) data require tailored approaches.
  • The R package RPPanalyzer was previously developed for RPPA data preprocessing, statistical analysis, and visualization.

Purpose of the Study:

  • To enhance the RPPanalyzer R package for improved analysis of RPPA data.
  • To integrate user-friendly functions for data preprocessing and noise correction.
  • To enable advanced visualization of longitudinal RPPA data, including time course plotting.

Main Methods:

  • Merging data preprocessing steps into a single user-friendly function.
  • Implementing novel methods for background noise correction and noise estimation.
  • Developing new techniques for averaging replicates to prepare data for time course analysis.
  • Utilizing the enhanced RPPanalyzer to analyze longitudinal RPPA data of MET receptor signaling.

Main Results:

  • The enhanced RPPanalyzer provides a streamlined workflow for RPPA data preprocessing.
  • New methods for noise correction and estimation improve data quality.
  • The updated package facilitates robust analysis of longitudinal RPPA data.
  • Successful application to MET receptor signaling data demonstrates platform robustness.

Conclusions:

  • The enhanced RPPanalyzer is a robust and user-friendly platform for analyzing longitudinal RPPA data.
  • The updated software facilitates comprehensive proteomic data analysis, from preprocessing to visualization.
  • This tool supports researchers in understanding signaling pathway dynamics using RPPA.