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2-D PAGE Map Analysis

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Cover of '2-D PAGE Map Analysis'

Table of Contents

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    Book Overview
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    Chapter 1 Sources of Experimental Variation in 2-D Maps: The Importance of Experimental Design in Gel-Based Proteomics
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    Chapter 2 Decoding 2-D Maps by Autocovariance Function
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    Chapter 3 Two-Dimensional Gel Electrophoresis Image Analysis via Dedicated Software Packages
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    Chapter 4 Comparative Evaluation of Software Features and Performances
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    Chapter 5 Image Pretreatment Tools I: Algorithms for Map Denoising and Background Subtraction Methods
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    Chapter 6 Image Pretreatment Tools II: Normalization Techniques for 2-DE and 2-D DIGE
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    Chapter 7 Spot Matching of 2-DE Images Using Distance, Intensity, and Pattern Information
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    Chapter 8 Algorithms for Warping of 2-D PAGE Maps
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    Chapter 9 2-DE Gel Analysis: The Spot Detection
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    Chapter 10 2-D PAGE Map Analysis
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    Chapter 11 Detection and Quantification of Protein Spots by Pinnacle
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    Chapter 12 A Novel Gaussian Extrapolation Approach for 2-D Gel Electrophoresis Saturated Protein Spots
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    Chapter 13 Multiple Testing and Pattern Recognition in 2-DE Proteomics
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    Chapter 14 Chemometric Multivariate Tools for Candidate Biomarker Identification: LDA, PLS-DA, SIMCA, Ranking-PCA
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    Chapter 15 The Use of Legendre and Zernike Moment Functions for the Comparison of 2-D PAGE Maps
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    Chapter 16 Nonlinear Dimensionality Reduction by Minimum Curvilinearity for Unsupervised Discovery of Patterns in Multidimensional Proteomic Data
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    Chapter 17 Differential Analysis of 2-D Maps by Pixel-Based Approaches
Attention for Chapter 13: Multiple Testing and Pattern Recognition in 2-DE Proteomics
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Chapter title
Multiple Testing and Pattern Recognition in 2-DE Proteomics
Chapter number 13
Book title
2-D PAGE Map Analysis
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3255-9_13
Pubmed ID
Book ISBNs
978-1-4939-3254-2, 978-1-4939-3255-9
Authors

Sebastien C. Carpentier

Abstract

After separation through two-dimensional gel electrophoresis (2-DE), several hundreds of individual protein abundances can be quantified in a cell population or sample tissue. However, gel-based proteomics has the reputation of being a slow and cumbersome art. But art is not dead! While 2-DE may no longer be the tool of choice in high-throughput differential proteomics, it is still very effective to identify and quantify protein species caused by genetic variations, alternative splicing, and/or PTMs. This chapter reviews some typical statistical exploratory and confirmatory tools available and suggests case-specific guidelines for (1) the discovery of potentially interesting protein spots, and (2) the further characterization of protein families and their possible PTMs.

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Mendeley readers

The data shown below were compiled from readership statistics for 8 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 8 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 2 25%
Lecturer 1 13%
Professor 1 13%
Student > Doctoral Student 1 13%
Student > Master 1 13%
Other 1 13%
Unknown 1 13%
Readers by discipline Count As %
Agricultural and Biological Sciences 4 50%
Biochemistry, Genetics and Molecular Biology 1 13%
Pharmacology, Toxicology and Pharmaceutical Science 1 13%
Computer Science 1 13%
Medicine and Dentistry 1 13%
Other 0 0%