Genomic Structural Variants in Nervous System Disorders
Genomic Structural Variants in Nervous System Disorders by Christos Proukakis, published by Springer US on June 1, 2022, is a comprehensive volume consisting of 272 pages. This edition focuses on the detection of structural variants (SVs) in the context of nervous system disorders, emphasizing the need for distinct strategies compared to single nucleotide variants (SNVs). The book presents a blend of the latest laboratory methods and computational pipelines aimed at addressing all classes of SVs.
Readers will find detailed chapters that cover a range of topics, including the detection of transposable elements from short read data, long read sequencing for variable number tandem repeat analysis, and genomic mosaicism in the nervous system. The content is designed to provide key insights and practical advice from specialists, making it a valuable resource for scientists and researchers in the fields of biological sciences and medicine, particularly those focused on diseases such as Parkinson’s disease.
Official synopsis Publisher
This volume covers the detection of structural variants (SVs), which require different strategies than the ones used for single nucleotide variants (SNVs). This book aims to provide readers with a combination of the latest “wet lab” methods and computational pipelines that target all SV classes. The chapters in this book cover topics such as detection of transposable elements (TEs) from short read data; long read sequencing used for multiple variable number tandem repeat analysis; genomic mosaicism in the nervous system; and optical genome mapping. In the Neuromethods series style, chapters include the kind of detail and key advice from the specialists needed to get successful results in your laboratory.
Cutting-edge and comprehensive, Genomic Structural Variants in Nervous System Disorders is a valuable resource for scientists and researchers interested in learning more about this important field.
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