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Clinical Applications of PCR

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Cover of 'Clinical Applications of PCR'

Table of Contents

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    Book Overview
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    Chapter 1 A Targeted Q-PCR-Based Method for Point Mutation Testing by Analyzing Circulating DNA for Cancer Management Care.
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    Chapter 2 COLD-PCR: Applications and Advantages
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    Chapter 3 PCR-Based Detection of DNA Copy Number Variation.
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    Chapter 4 Emulsion PCR: Techniques and Applications
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    Chapter 5 Digital PCR: Principles and Applications
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    Chapter 6 Quantitative PCR for Plasma Epstein-Barr Virus Loads in Cancer Diagnostics
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    Chapter 7 High-Resolution Melt Curve Analysis in Cancer Mutation Screen
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    Chapter 8 Locked Nucleic Acid Probes (LNA) for Enhanced Detection of Low-Level, Clinically Significant Mutations
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    Chapter 9 Genotyping of Frequent Mutations in Solid Tumors by PCR-Based Single-Base Extension and MassARRAY Analysis
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    Chapter 10 Microfluidics-Based PCR for Fusion Transcript Detection.
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    Chapter 11 Polymerase Chain Reaction Diagnosis of Leishmaniasis: A Species-Specific Approach
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    Chapter 12 Detection of Trypanosoma cruzi by Polymerase Chain Reaction
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    Chapter 13 PCR Techniques in Next-Generation Sequencing.
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    Chapter 14 Single-Cell Quantitative PCR: Advances and Potential in Cancer Diagnostics
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    Chapter 15 Quantitative Real-Time PCR: Recent Advances
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    Chapter 16 PCR Techniques in Characterizing DNA Methylation.
Attention for Chapter 3: PCR-Based Detection of DNA Copy Number Variation.
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Chapter title
PCR-Based Detection of DNA Copy Number Variation.
Chapter number 3
Book title
Clinical Applications of PCR
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3360-0_3
Pubmed ID
Book ISBNs
978-1-4939-3358-7, 978-1-4939-3360-0
Authors

Mehrotra, Meenakshi, Meenakshi Mehrotra

Editors

Rajyalakshmi Luthra, Rajesh R. Singh, Keyur P. Patel

Abstract

Copy number variations are important polymorphisms that can influence gene expression within and close to the rearranged region, and results in phenotypic variation. Techniques that detect abnormalities in DNA copy number are therefore useful for studying the associations between DNA aberrations and disease phenotype and for locating critical genes. PCR-based detection of copy number of target gene using TaqMan copy number assay offers a reliable method to measure copy number variation in human genome.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 13 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 13 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 38%
Student > Master 2 15%
Researcher 1 8%
Student > Bachelor 1 8%
Unknown 4 31%
Readers by discipline Count As %
Agricultural and Biological Sciences 3 23%
Computer Science 2 15%
Biochemistry, Genetics and Molecular Biology 2 15%
Veterinary Science and Veterinary Medicine 1 8%
Pharmacology, Toxicology and Pharmaceutical Science 1 8%
Other 1 8%
Unknown 3 23%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 05 February 2016.
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#18,437,241
of 22,842,950 outputs
Outputs from Methods in molecular biology
#7,921
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Outputs of similar age
#284,426
of 393,571 outputs
Outputs of similar age from Methods in molecular biology
#846
of 1,470 outputs
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