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Single Nucleotide Polymorphisms / Methods and Protocols, Kwok Pui-Yan


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Цена: 38730.00T
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Автор: Kwok Pui-Yan
Название:  Single Nucleotide Polymorphisms / Methods and Protocols
Перевод названия: Полиморфизм нуклеотида / методы и протоколы
ISBN: 9780896039681
Издательство: Springer
Классификация:
ISBN-10: 0896039684
Обложка/Формат: Hardcover
Страницы: 288
Вес: 0.59 кг.
Дата издания: 2003
Серия: Methods in Molecular Biology
Язык: English
Размер: 23.52 x 15.85 x 2.08 cm
Ссылка на Издательство: Link
Поставляется из: Германии
Описание: Pui-Yan Kwok, MD, PhD, has assembled a comprehensive collection of readily reproducible techniques for the difficult process of single nucleotide polymorphisms (SNP) discovery and genotyping. These cutting-edge protocols for mutation/SNP detection utilize denaturing high-performance liquid chromatography (dHPLC), single-strand conformation polymorphism (SSCP), conformation-sensitive gel electrophoresis (CSGE), chemical cleavage, and direct sequencing. Equally powerful and up-to-date methods are given for genotyping SNPs, including molecular beacons, the Taqman assay, single-base extension approaches, pyrosequencing, ligation, the Invader assay, and primer extension with mass spectrometry detection.
Дополнительное описание: Формат: 229x152
Илюстрации: 60
Круг читателей: Researchers interested in genetic studies, including association studies of common diseases in humans, DNA diagnostics, forensics, and agricultural biotechnology
Ключевые слова:
Язык: eng



Human Chromosome Variation: Heteromorphism and Polymorphism

Автор: Wyandt
Название: Human Chromosome Variation: Heteromorphism and Polymorphism
ISBN: 9400708955 ISBN-13(EAN): 9789400708952
Издательство: Springer
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Цена: 156720.00 T
Наличие на складе: Поставка под заказ.
Описание: Human Chromosome Variation: Heteromorphism and Polymorphism was formerly printed under the title “Atlas of Human Chromosome Heteromorphism”. The Atlas has become a standard reference book in most cytogenetic laboratories and is cited as a significant reference in ISCN 2009. This revised version has updated and retained the most useful pictorial sections of the first edition, including the comprehensive review of normal and “not-so-normal” variations of the human karyotype with summaries and extensive reference lists organized by chromosome number. This updated edition features concise background information on chromosome methods and applications, essential information on heteromorphism frequencies in normal and clinical populations as well as new listing and discussions of euchromatic, subtelomeric and FISH variants. The addition of two new sections make this an even more valuable reference than before. A section on common and rare fragile sites includes a short historical discussion, definitions and an extensive table of officially recognized sites that includes the HUGO name, chromosomal location, methods of induction, genes and references to the most recent molecular characterization. A new section on array CGH discusses the clinical challenge of interpreting copy number variations (CNVs) revealed by this newest technology, gives examples of various levels of interpretation and lists the several most common websites used in this interpretation.


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