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Authoritative and easily accessible, Array Comparative Genomic Hybridization: Protocols and Applications provides researchers with well-honed methodologies to learn these techniques for their own use in research or clinical diagnostic laboratories.
Authoritative and easily accessible, Array Comparative Genomic Hybridization: Protocols and Applications provides researchers with well-honed methodologies to learn these techniques for their own use in research or clinical diagnostic laboratories.
Includes cutting-edge methods and protocols
Provides step-by-step detail essential for reproducible results
Contains key notes and implementation advice from the experts
Includes supplementary material: [...]
Array Comparative Genomic Hybridization: An Overview of Protocols, Applications and Technology Trends.- Ultra Dense Array CGH and Discovery of Micro-Copy Number Alterations and Gene Fusions in the Cancer Genome.- Epigenomics: Sequencing the Methylome.- Application of Array Comparative Genomic Hybridization in Chronic Myeloid Leukemia.- The Use of Cytogenetic Microarrays in Myelodysplastic Syndrome Characterization.- CGH Protocols - Chronic Lymphocytic Leukemia.- Analysis of Acquire Genomic Copy Number Aberrations and Regions of Loss of Heterozygosity in Acute Myelogenous Leukemia Fenomes using Affymetrix SNP 6.0 Arrays and Supporting Software Tools.- Clinical Applications of BAC Array-CGH to the Study of Diffuse Large B-Cell Lymphomas.- Genomic Profiling of Mantle Cell Lymphoma.- Copy Number Analysis in EBV-Positive Nodal Peripheral T-Cell Lymphoma, Unspecified.- Mycosis Fungoides and Sézary Syndrome.- Array CGH Reveals Clonal Evolution of Adult T Cell Leukemia/Lymphoma.- Array-CGH Analysis of Cutaneous Anaplastic Large Cell Lymphoma.- Genome Wide DNA-Profiling of HIV-Related B-Cell Lymphomas.- Array Comparative Genomic Hybridization in Osteosarcoma.- Comparative Genomic Hybridization of Wilms' Tumor.- Array-CGH in Childhood MDS.- Non-Familial Breast Cancer Subtypes.- Applications of Array-CGH for Lung Cancer.- Array CGH in Brain Tumours.- Finding Common Regions of Alteration in Copy Number Data.- Distinguishing Somatic and Germline Copy Number Events in Cancer Patient DNA Hybridized to Whole Genome SNP Genotyping Arrays.
Erscheinungsjahr: | 2013 |
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Fachbereich: | Andere Fachgebiete |
Genre: | Importe, Medizin |
Rubrik: | Wissenschaften |
Medium: | Buch |
Inhalt: |
xii
382 S. |
ISBN-13: | 9781627032803 |
ISBN-10: | 1627032800 |
Sprache: | Englisch |
Einband: | Gebunden |
Redaktion: |
Shah, Sohrab P.
Banerjee, Diponkar |
Herausgeber: | Diponkar Banerjee/Sohrab P Shah |
Hersteller: | Humana Press |
Verantwortliche Person für die EU: | Humana Press in Springer Science + Business Media, Heidelberger Platz 3, D-14197 Berlin, juergen.hartmann@springer.com |
Maße: | 260 x 183 x 25 mm |
Von/Mit: | Sohrab P. Shah (u. a.) |
Erscheinungsdatum: | 15.02.2013 |
Gewicht: | 0,939 kg |