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Cancer Cytogenetics

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Cover of 'Cancer Cytogenetics'

Table of Contents

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    Book Overview
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    Chapter 1 Cancer Cytogenetics: An Introduction.
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    Chapter 2 Chromosome Preparation for Myeloid Malignancies.
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    Chapter 3 Chromosome Preparation for Acute Lymphoblastic Leukemia.
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    Chapter 4 Chromosome Preparation for Chronic Lymphoid Malignancies.
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    Chapter 5 Cytogenetic Harvesting of Cancer Cells and Cell Lines.
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    Chapter 6 Chromosome Bandings.
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    Chapter 7 Chromosome Recognition.
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    Chapter 8 Applications of Fluorescence In Situ Hybridization Technology in Malignancies.
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    Chapter 9 Fluorescence In Situ Hybridization Probe Preparation.
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    Chapter 10 Fluorescence In Situ Hybridization Probe Validation for Clinical Use.
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    Chapter 11 Fluorescence In Situ Hybridization on Tissue Sections.
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    Chapter 12 Cytoplasmic Immunoglobulin Light Chain Revelation and Interphase Fluorescence In Situ Hybridization in Myeloma.
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    Chapter 13 Quantitative Fluorescence In Situ Hybridization (QFISH).
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    Chapter 14 High Resolution Fiber-Fluorescence In Situ Hybridization.
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    Chapter 15 Array-Based Comparative Genomic Hybridization (aCGH).
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    Chapter 16 Multicolor Karyotyping and Fluorescence In Situ Hybridization-Banding (MCB/mBAND).
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    Chapter 17 Cytogenetics for Biological Dosimetry.
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    Chapter 18 Recurrent Cytogenetic Abnormalities in Myelodysplastic Syndromes.
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    Chapter 19 Recurrent Cytogenetic Abnormalities in Acute Myeloid Leukemia.
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    Chapter 20 Recurrent Cytogenetic Abnormalities in Myeloproliferative Neoplasms and Chronic Myeloid Leukemia.
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    Chapter 21 Recurrent Cytogenetic Abnormalities in Acute Lymphoblastic Leukemia.
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    Chapter 22 Recurrent Cytogenetic Abnormalities in Non-Hodgkin's Lymphoma and Chronic Lymphocytic Leukemia.
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    Chapter 23 Recurrent Cytogenetic Abnormalities in Multiple Myeloma.
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    Chapter 24 Cytogenetic Nomenclature and Reporting.
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    Chapter 25 Cytogenetic Resources and Information.
Attention for Chapter 15: Array-Based Comparative Genomic Hybridization (aCGH).
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Chapter title
Array-Based Comparative Genomic Hybridization (aCGH).
Chapter number 15
Book title
Cancer Cytogenetics
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6703-2_15
Pubmed ID
Book ISBNs
978-1-4939-6701-8, 978-1-4939-6703-2
Authors

Chengsheng Zhang M.D., Ph.D., Eliza Cerveira, Mallory Romanovitch, Qihui Zhu, Chengsheng Zhang

Editors

Thomas S.K. Wan

Abstract

Copy number variations (CNVs) in the genomes have been suggested to play important roles in human evolution, genetic diversity, and disease susceptibility. A number of assays have been developed for the detection of CNVs, including fluorescent in situ hybridization (FISH), array-based comparative genomic hybridization (aCGH), PCR-based assays, and next-generation sequencing (NGS). In this chapter, we describe a microarray method that has been used for the detection of genome-wide CNVs, loss of heterozygosity (LOH), and uniparental disomy (UPD) associated with constitutional and neoplastic disorders.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 152 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 <1%
United States 1 <1%
Slovenia 1 <1%
Egypt 1 <1%
Unknown 148 97%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 33 22%
Student > Master 24 16%
Researcher 21 14%
Student > Ph. D. Student 20 13%
Student > Postgraduate 10 7%
Other 20 13%
Unknown 24 16%
Readers by discipline Count As %
Agricultural and Biological Sciences 46 30%
Biochemistry, Genetics and Molecular Biology 34 22%
Medicine and Dentistry 27 18%
Pharmacology, Toxicology and Pharmaceutical Science 4 3%
Computer Science 2 1%
Other 8 5%
Unknown 31 20%