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Whole Genome Amplification

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Cover of 'Whole Genome Amplification'

Table of Contents

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    Book Overview
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    Chapter 1 Principles of Whole-Genome Amplification
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    Chapter 2 Bias in Whole Genome Amplification: Causes and Considerations.
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    Chapter 3 The Single-Cell Lab or How to Perform Single-Cell Molecular Analysis
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    Chapter 4 Sample Preparation Methods Following CellSearch Approach Compatible of Single-Cell Whole-Genome Amplification: An Overview
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    Chapter 5 Deterministic Whole-Genome Amplification of Single Cells.
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    Chapter 6 Construction of a DNA Library on Microbeads Using Whole Genome Amplification
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    Chapter 7 Heat-Induced Fragmentation and Adapter-Assisted Whole Genome Amplification Using GenomePlex ® Single-Cell Whole Genome Amplification Kit (WGA4)
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    Chapter 8 Whole Genome Amplification by Isothermal Multiple Strand Displacement Using Phi29 DNA Polymerase.
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    Chapter 9 Using Multiplex PCR for Assessing the Quality of Whole Genome Amplified DNA
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    Chapter 10 Quality Control of Isothermal Amplified DNA Based on Short Tandem Repeat Analysis
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    Chapter 11 Laser Microdissection of FFPE Tissue Areas and Subsequent Whole Genome Amplification by Ampli 1™
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    Chapter 12 Whole Genome Amplification from Blood Spot Samples
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    Chapter 13 Analysis of Whole Mitogenomes from Ancient Samples
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    Chapter 14 Copy Number Variation Analysis by Array Analysis of Single Cells Following Whole Genome Amplification.
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    Chapter 15 Whole Genome Amplification in Genomic Analysis of Single Circulating Tumor Cells.
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    Chapter 16 Whole Genome Amplification of Labeled Viable Single Cells Suited for Array-Comparative Genomic Hybridization
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    Chapter 17 Low-Volume On-Chip Single-Cell Whole Genome Amplification for Multiple Subsequent Analyses.
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    Chapter 18 Detection and Characterization of Circulating Tumor Cells by the CellSearch Approach
Attention for Chapter 18: Detection and Characterization of Circulating Tumor Cells by the CellSearch Approach
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Chapter title
Detection and Characterization of Circulating Tumor Cells by the CellSearch Approach
Chapter number 18
Book title
Whole Genome Amplification
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2990-0_18
Pubmed ID
Book ISBNs
978-1-4939-2989-4, 978-1-4939-2990-0
Authors

Frank Coumans, Leon Terstappen, Coumans, Frank, Terstappen, Leon

Abstract

Cancer metastasis occurs when cells shed from a primary or metastatic tumor, enter the circulation, and begin to grow in distant locations of the body. With current techniques it is possible to measure the presence of a few circulating tumor cells (CTC) in a blood sample. Detection of even the presence of a very small number (one or more) of these CTC in a 7.5 mL blood sample with the CellSearch system is associated with a significant decrease in survival of patients with metastatic carcinomas. The techniques and definitions used for the detection and enumeration of CTC with the CellSearch system were validated in series of preclinical and prospective multicenter studies. After enumeration of the CTC, the cells can be isolated from the cartridge for the purpose of downstream single-cell analysis. In this chapter, we will describe in detail the sample acquisition, sample preparation, data acquisition, and assignment of CTC used in the CellSearch system.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 41 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Netherlands 1 2%
Unknown 40 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 14 34%
Researcher 5 12%
Student > Master 3 7%
Student > Doctoral Student 2 5%
Student > Postgraduate 2 5%
Other 4 10%
Unknown 11 27%
Readers by discipline Count As %
Agricultural and Biological Sciences 9 22%
Medicine and Dentistry 8 20%
Biochemistry, Genetics and Molecular Biology 4 10%
Engineering 4 10%
Chemistry 2 5%
Other 3 7%
Unknown 11 27%