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Human T-Lymphotropic Viruses

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Cover of 'Human T-Lymphotropic Viruses'

Table of Contents

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    Book Overview
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    Chapter 1 Serological and Molecular Methods to Study Epidemiological Aspects of Human T-Cell Lymphotropic Virus Type 1 Infection
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    Chapter 2 Molecular Epidemiology Database for Sequence Management and Data Mining
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    Chapter 3 Reporter Systems to Study HTLV-1 Transmission
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    Chapter 4 Quantitative Analysis of Human T-Lymphotropic Virus Type 1 (HTLV-1) Infection Using Co-Culture with Jurkat LTR-Luciferase or Jurkat LTR-GFP Reporter Cells
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    Chapter 5 Isolation of Exosomes from HTLV-Infected Cells
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    Chapter 6 A Luciferase Functional Quantitative Assay for Measuring NF-ĸB Promoter Transactivation Mediated by HTLV-1 and HTLV-2 Tax Proteins
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    Chapter 7 Generation of a Tet-On Expression System to Study Transactivation Ability of Tax-2
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    Chapter 8 EGF Uptake and Degradation Assay to Determine the Effect of HTLV Regulatory Proteins on the ESCRT-Dependent MVB Pathway
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    Chapter 9 Methods for Identifying and Examining HTLV-1 HBZ Post-translational Modifications
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    Chapter 10 High-Throughput Mapping and Clonal Quantification of Retroviral Integration Sites
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    Chapter 11 STR Profiling of HTLV-1-Infected Cell Lines
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    Chapter 12 Expression of HTLV-1 Genes in T-Cells Using RNA Electroporation
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    Chapter 13 Quantification of Cell Turnover in the Bovine Leukemia Virus Model
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    Chapter 14 Analysis of NK Cell Function and Receptor Expression During HTLV-1 and HTLV-2 Infection
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    Chapter 15 Overview of Targeted Therapies for Adult T-Cell Leukemia/Lymphoma
Attention for Chapter 10: High-Throughput Mapping and Clonal Quantification of Retroviral Integration Sites
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Chapter title
High-Throughput Mapping and Clonal Quantification of Retroviral Integration Sites
Chapter number 10
Book title
Human T-Lymphotropic Viruses
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6872-5_10
Pubmed ID
Book ISBNs
978-1-4939-6870-1, 978-1-4939-6872-5
Authors

Nicolas A. Gillet, Anat Melamed, Charles R. M. Bangham, Gillet, Nicolas A., Melamed, Anat, Bangham, Charles R. M.

Abstract

We describe here a method to identify the position of retroviral insertion sites and simultaneously to quantify the absolute abundance of each clone, i.e., the number of cells having the provirus inserted at a given place in the host genome. The method is based on random shearing of the host cell DNA, followed by a linker-mediated PCR to amplify the genomic regions flanking the proviruses, and high-throughput sequencing of the amplicons. The quantification of the abundance of each infected clone allowed us to develop two new metrics: i. the oligoclonality index, which quantifies the nonuniformity of the distribution of clone abundance, and ii. an estimator of the total number of clones in the body of the host. These new tools are valuable for the study of retroviral infections and can also be adapted for the tracking of gene-edited cells.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 12 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 12 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 42%
Student > Ph. D. Student 1 8%
Student > Bachelor 1 8%
Student > Doctoral Student 1 8%
Unknown 4 33%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 42%
Agricultural and Biological Sciences 2 17%
Immunology and Microbiology 1 8%
Unknown 4 33%