Parametry
- 395 stron
- 14 godzin czytania
Więcej o książce
This volume provides an interdisciplinary perspective of applying Next Generation Sequencing (NGS) technology to cancer research. It aims to systematically introduce the concept of NGS, a variety of NGS platforms and their practical implications in cancer biology.This unique and comprehensive text will integrate the unprecedented NGS technology into various cancer research projects as opposed to most books which offer a detailed description of the technology. This volume will present true experimental results with concrete data processing pipelines, discuss the bottleneck of each platform for real project in cancer research. In additional, single cancer cell sequencing as the proof of concept will be introduced in this book, along with cutting-edge information provided will help the intended audience to develop a comprehensive understanding of the NGS technology and practical whole genome sequencing data analysis and rapidly translate into their own research, specifically in the field of cancer biology.
Zakup książki
Next Generation Sequencing in Cancer Research, Wei Wu, Hani Choudhry
- Język
- Rok wydania
- 2013
- Oprawa
- (twarda)
Metody płatności
Nikt jeszcze nie ocenił.
- Tytuł
- Next Generation Sequencing in Cancer Research
- Podtytuł
- Decoding the Cancer Genome
- Język
- angielski
- Autorzy
- Wei Wu, Hani Choudhry
- Wydawca
- Springer New York
- Rok wydania
- 2013
- Oprawa
- twarda
- Liczba stron
- 395
- ISBN10
- 1461476445
- ISBN13
- 9781461476443
- Seria
- Kategorie
- Tagi
- Nauki przyrodnicze, Nauka, USA, Tematyka medyczna, Badania naukowe, Genetyka, Biochemia, Onkologia, Badania medyczne, Cytologia
- Opis
- This volume provides an interdisciplinary perspective of applying Next Generation Sequencing (NGS) technology to cancer research. It aims to systematically introduce the concept of NGS, a variety of NGS platforms and their practical implications in cancer biology.This unique and comprehensive text will integrate the unprecedented NGS technology into various cancer research projects as opposed to most books which offer a detailed description of the technology. This volume will present true experimental results with concrete data processing pipelines, discuss the bottleneck of each platform for real project in cancer research. In additional, single cancer cell sequencing as the proof of concept will be introduced in this book, along with cutting-edge information provided will help the intended audience to develop a comprehensive understanding of the NGS technology and practical whole genome sequencing data analysis and rapidly translate into their own research, specifically in the field of cancer biology.