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Titlebook: Clinical Bioinformatics; Ronald Trent Book 2014Latest edition Springer Science+Business Media New York 2014 DNA sequencing.analytes.bioinf

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发表于 2025-3-21 16:56:25 | 显示全部楼层 |阅读模式
书目名称Clinical Bioinformatics
编辑Ronald Trent
视频video
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
丛书名称Methods in Molecular Biology
图书封面Titlebook: Clinical Bioinformatics;  Ronald Trent Book 2014Latest edition Springer Science+Business Media New York 2014 DNA sequencing.analytes.bioinf
描述.In .Clinical Bioinformatics, Second Edition.,. .leading experts in the field provide a series of articles focusing on software applications used to translate information into outcomes of clinical relevance. Recent developments in .omics., such as increasingly sophisticated analytic platforms allowing changes in diagnostic strategies from the traditional focus on single or small number of analytes to what might be possible when large numbers or all analytes are measured, are now impacting patient care. Covering such topics as gene discovery, gene function (microarrays), DNA sequencing, online approaches and resources, and informatics in clinical practice, this volume concisely yet thoroughly explores this cutting-edge subject. Written in the successful .Methods in Molecular Biology. series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible protocols, and notes on troubleshooting and avoiding known pitfalls..Authoritative and easily accessible, .Clinical Bioinformatics, Second Edition. serves as an ideal guide for scientists and health professionals working in genetics and genomics..
出版日期Book 2014Latest edition
关键词DNA sequencing; analytes; bioinformatics; gene discovery; gene function
版次2
doihttps://doi.org/10.1007/978-1-4939-0847-9
isbn_softcover978-1-4939-4700-3
isbn_ebook978-1-4939-0847-9Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media New York 2014
The information of publication is updating

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Production and Analytic Bioinformatics for Next-Generation DNA Sequencing,dictable. At the same time, the bewildering amount of information produced during these analyses needs to be carefully managed, used and interpreted correctly. The challenge for clinical laboratories now is to implement production analytical processes that are capable of handling different experimen
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Analyzing the Metabolome,prediction of the phenotype and the nature of a disease. Mass spectrometry now allows thousands of metabolites to be quantitated. The targeted or untargeted data from metabolic profiling can be combined with either supervised or unsupervised approaches to improve interpretation. These sophisticated
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Statistical Perspectives for Genome-Wide Association Studies (GWAS),well (Subheading 3.1), paying particular attention to case and control selection and achieving adequate sample size to deal with the large burden of multiple testing. Second, we focus on the crucial step of applying stringent quality control (Subheading 3.2) to genotyping results. The most crucial p
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Bioinformatics Challenges in Genome-Wide Association Studies (GWAS),netic architecture of diseases and open up new opportunities for treatment and prevention. However, despite its successes, GWAS have not been able to identify genetic loci that are effective classifiers of disease, limiting their value for genetic testing. This chapter highlights the challenges that
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Studying Cancer Genomics Through Next-Generation DNA Sequencing and Bioinformatics,o distinguish them from inherited germline mutations, can include single-nucleotide substitutions, insertions, deletions, copy number alterations, and structural rearrangements. A patient’s cancer can contain a combination of these aberrations, and the ability to generate a comprehensive genetic pro
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Using Bioinformatics Tools to Study the Role of microRNA in Cancer, groups have described transcript variants as well as discovering new transcribed loci and noncoding RNAs, including microRNAs. In oncology, expression profiling of microRNAs in matched tumor and normal tissues has been used to detect differential expression of microRNAs in cancer. We present one ap
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Bioinformatics Approach to Understanding Interacting Pathways in Neuropsychiatric Disorders,th the increasing interest in the molecular aspect of neuropsychiatry and the availability of high-throughput discovery and analysis tools have encouraged the incorporation of bioinformatics and neurosystems biology techniques into psychiatry and neuroscience research. As applied to neuropsychiatry,
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