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Titlebook: Genomic Structural Variants; Methods and Protocol Lars Feuk Book 2012 Springer Science+Business Media, LLC 2012 copy number variation (CNV)

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發(fā)表于 2025-3-21 18:18:34 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Genomic Structural Variants
副標(biāo)題Methods and Protocol
編輯Lars Feuk
視頻videohttp://file.papertrans.cn/383/382904/382904.mp4
概述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 materia
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Genomic Structural Variants; Methods and Protocol Lars Feuk Book 2012 Springer Science+Business Media, LLC 2012 copy number variation (CNV)
描述.The completion of a consensus draft sequence for the human genome was the starting point for more thorough investigations of individual genome variation.? The development of array-based strategies made it possible to look at our genome in new ways and for new types of variation to be discovered and characterized. Characterization of copy number variation and other forms of structural genetic variation has highlighted the complexity of human genetic variation and also provided significant insight into the evolution and dynamic nature of our genome. .Genomic Structural Variants: Methods and Protocols. provides an in-depth description of the developments in our understanding of structural genetic variation and its implications for human disease, from the introduction of microarrays up to current state-of-the-art sequencing strategies. It covers the major technologies used for research and diagnostics as well as web-based resources for variation data, and it then goes into depth regarding specific regions of the genome that differ in variation content. Specific patient groups where copy number variation has been shown to be of great importance are highlighted, and implications for bot
出版日期Book 2012
關(guān)鍵詞copy number variation (CNV); genomic disorders; genomic structural variation; human genome; personal gen
版次1
doihttps://doi.org/10.1007/978-1-61779-507-7
isbn_softcover978-1-4939-6189-4
isbn_ebook978-1-61779-507-7Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media, LLC 2012
The information of publication is updating

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Genomic Structural Variants978-1-61779-507-7Series ISSN 1064-3745 Series E-ISSN 1940-6029
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1064-3745 ation advice from the experts.Includes supplementary materia.The completion of a consensus draft sequence for the human genome was the starting point for more thorough investigations of individual genome variation.? The development of array-based strategies made it possible to look at our genome in
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1064-3745 regarding specific regions of the genome that differ in variation content. Specific patient groups where copy number variation has been shown to be of great importance are highlighted, and implications for bot978-1-4939-6189-4978-1-61779-507-7Series ISSN 1064-3745 Series E-ISSN 1940-6029
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