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Histones

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Cover of 'Histones'

Table of Contents

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    Book Overview
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    Chapter 1 In Vitro Assembly of Nucleosomes for Binding/Remodeling Assays.
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    Chapter 2 An Assay for Measuring Histone Variant Exchange within Nucleosomes In Vitro.
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    Chapter 3 Purification of Yeast Native Reagents for the Analysis of Chromatin Function-I: Nucleosomes for Reconstitution and Manipulation of Histone Marks.
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    Chapter 4 Purification of Yeast Native Reagents for the Analysis of Chromatin Function-II: Multiprotein Complexes and Biochemical Assays.
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    Chapter 5 Histone Purification from Saccharomyces cerevisiae.
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    Chapter 6 Analytical Ultracentrifuge Analysis of Nucleosomes Assembled from Recombinant, Acid-Extracted, HPLC-Purified Histones.
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    Chapter 7 SILAC-Based Quantitative Strategies for Accurate Histone Posttranslational Modification Profiling Across Multiple Biological Samples.
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    Chapter 8 Characterization of Individual Histone Posttranslational Modifications and Their Combinatorial Patterns by Mass Spectrometry-Based Proteomics Strategies.
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    Chapter 9 Production and Purification of Antibodies Against Histone Modifications.
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    Chapter 10 Immunofluorescence of Histone Proteins.
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    Chapter 11 Acid-Urea Gel Electrophoresis and Western Blotting of Histones.
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    Chapter 12 Chromatin Immunoprecipitation of Histone Modifications in Fission Yeast.
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    Chapter 13 A Spiking Strategy for ChIP-chip Data Normalization in S. cerevisiae.
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    Chapter 14 High-Resolution Genome-Wide Mapping of Nucleosome Positioning and Occupancy Level Using Paired-End Sequencing Technology.
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    Chapter 15 Physarum polycephalum for Studying the Function of Histone Modifications In Vivo.
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    Chapter 16 A Method for Large-Scale Screening of Random Sequence Libraries to Determine the Function of Unstructured Regions from Essential Proteins.
Attention for Chapter 14: High-Resolution Genome-Wide Mapping of Nucleosome Positioning and Occupancy Level Using Paired-End Sequencing Technology.
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Chapter title
High-Resolution Genome-Wide Mapping of Nucleosome Positioning and Occupancy Level Using Paired-End Sequencing Technology.
Chapter number 14
Book title
Histones
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6630-1_14
Pubmed ID
Book ISBNs
978-1-4939-6628-8, 978-1-4939-6630-1
Authors

Mylène Brunelle, Sébastien Rodrigue, Pierre-Étienne Jacques, Nicolas Gévry

Editors

Benoit Guillemette, Luc R. Gaudreau

Abstract

Because of its profound influence on DNA accessibility for protein binding and thus on the regulation of diverse biological processes, nucleosome positioning has been studied for many years. In the past decade, high-throughput sequencing technologies have opened new perspectives in this research field by allowing the study of nucleosome positioning and occupancy on a genome-wide scale, therefore providing understanding on important aspects of chromatin packaging, as well as on various chromatin-template processes like transcription. In this chapter, we provide the protocol of MNase sequencing for the genome-wide mapping of nucleosomes using MNase to generate mononucleosomal DNA fragments and next-generation sequencing technology to identify their individual location.

Mendeley readers

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 %
Researcher 2 25%
Student > Ph. D. Student 1 13%
Other 1 13%
Student > Master 1 13%
Professor > Associate Professor 1 13%
Other 0 0%
Unknown 2 25%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 38%
Agricultural and Biological Sciences 2 25%
Medicine and Dentistry 1 13%
Unknown 2 25%