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Related Concept Videos

Proteomics01:33

Proteomics

A proteome is the entire set of proteins that a cell type produces. We can study proteomes using the knowledge of genomes because genes code for mRNAs, and the mRNAs encode proteins. Although mRNA analysis is a step in the right direction, not all mRNAs are translated into proteins.
Proteomics is the study of proteomes' function. It involves the large-scale systematic study of the proteome to denote the protein complement expressed by a genome. Scientist Mark Wilkins coined the term proteomics...

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Updated: Jun 6, 2026

Deep Proteome Profiling by Isobaric Labeling, Extensive Liquid Chromatography, Mass Spectrometry, and Software-assisted Quantification
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Deep Proteome Profiling by Isobaric Labeling, Extensive Liquid Chromatography, Mass Spectrometry, and Software-assisted Quantification

Published on: November 15, 2017

Multiple hypothesis testing in proteomics: A strategy for experimental work.

Angel P Diz1, Antonio Carvajal-Rodriguez, David O F Skibinski

  • 1University of Vigo, Spain;

Molecular & Cellular Proteomics : MCP
|December 9, 2010
PubMed
Summary
This summary is machine-generated.

Quantitative proteomics often involves multiple hypothesis testing, leading to false positives. This study presents a strategy using false discovery rate (FDR) methods to improve the reliability of proteomics results from two-dimensional electrophoresis (2-DE).

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TMT Sample Preparation for Proteomics Facility Submission and Subsequent Data Analysis
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Last Updated: Jun 6, 2026

Deep Proteome Profiling by Isobaric Labeling, Extensive Liquid Chromatography, Mass Spectrometry, and Software-assisted Quantification
10:37

Deep Proteome Profiling by Isobaric Labeling, Extensive Liquid Chromatography, Mass Spectrometry, and Software-assisted Quantification

Published on: November 15, 2017

TMT Sample Preparation for Proteomics Facility Submission and Subsequent Data Analysis
07:44

TMT Sample Preparation for Proteomics Facility Submission and Subsequent Data Analysis

Published on: June 8, 2020

Area of Science:

  • Proteomics
  • Statistical analysis
  • Biotechnology

Background:

  • Quantitative proteomics involves analyzing numerous protein expression differences between experimental conditions.
  • Multiple hypothesis testing is a common issue, increasing the risk of false positive results due to chance.
  • Statistical methods like the false discovery rate (FDR) exist but are underutilized in techniques like two-dimensional electrophoresis (2-DE).

Purpose of the Study:

  • To address the underutilization of multiple hypothesis testing methods in quantitative proteomics, specifically in 2-DE.
  • To provide a practical strategy for experimental scientists to implement these statistical methods.
  • To enhance the accuracy and reliability of findings in quantitative proteomics research.

Main Methods:

  • Review and selection of various multiple hypothesis testing methods, including well-established and less common approaches.
  • Development of a straightforward strategy for applying these methods in quantitative proteomics.
  • Demonstration of the strategy using both experimental and simulated data sets.

Main Results:

  • A significant gap exists in the application of FDR and other multiple hypothesis testing corrections in 2-DE proteomics studies.
  • The proposed strategy offers a flexible framework for scientists to choose and combine methods based on research needs.
  • Case scenarios illustrate the practical utility and benefits of the strategy in real-world and simulated data.

Conclusions:

  • Implementing multiple hypothesis testing corrections is crucial for robust quantitative proteomics, particularly with 2-DE.
  • A strategic, multi-method approach enhances the validity of identifying significant protein expression changes.
  • This work encourages wider adoption of rigorous statistical practices in proteomics research.