Next generation sequencing and data analysis [electronic resource] / edited by Melanie Kappelmann-Fenzl.
- 其他作者：
- 其他題名：
- Learning materials in biosciences.
- 出版： Cham : Springer International Publishing :Imprint: Springer 2021.
- 叢書名： Learning materials in biosciences,
- 主題： Sequence alignment (Bioinformatics) , Computational biology. , Genetics and Genomics. , Bioinformatics. , Biomedicine, general.
- ISBN： 9783030624903 (electronic bk.) 、 9783030624897 (paper)
- URL：
電子書(校內)
點擊此處查看電子書
- 一般註：E1103學校採購電子書 Chapter 1. Next Generation Sequencing (NGS)- What can be sequenced? -- Opportunities and Perspectives of NGS Applications in Cancer Research -- Chapter 3. Library Construction for NGS -- Chapter 4. NGS Technologies -- Chapter 5. Computer Setup -- Chapter 6. Introduction to Command Line -- Chapter 7. NGS Data -- Chapter 8. Reference Genome -- Chapter 9. Alignment -- Chapter 10. Identification of Genetic Variants and de novo Mutations Based on NGS -- Chapter 11. Design and Analysis of RNA Sequencing Data -- Chapter 12. Design and Analysis of Epigenetics and ChIP-Sequencing Data -- APPENDIX.
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讀者標籤：
- 系統號： 000293544 | 機讀編目格式
館藏資訊
This textbook provides step-by-step protocols and detailed explanations for RNA Sequencing, ChIP-Sequencing and Epigenetic Sequencing applications. The reader learns how to perform Next Generation Sequencing data analysis, how to interpret and visualize the data, and acquires knowledge on the statistical background of the used software tools. Written for biomedical scientists and medical students, this textbook enables the end user to perform and comprehend various Next Generation Sequencing applications and their analytics without prior understanding in bioinformatics or computer sciences.
摘要註
This textbook provides step-by-step protocols and detailed explanations for RNA Sequencing, ChIP-Sequencing and Epigenetic Sequencing applications. The reader learns how to perform Next Generation Sequencing data analysis, how to interpret and visualize the data, and acquires knowledge on the statistical background of the used software tools. Written for biomedical scientists and medical students, this textbook enables the end user to perform and comprehend various Next Generation Sequencing applications and their analytics without prior understanding in bioinformatics or computer sciences.