Discovering Genomics, Proteomics and Bioinformatics, 2/e (Paperback)
暫譯: 探索基因組學、蛋白質組學與生物資訊學,第二版 (平裝本)
A. Malcolm Campbell, Laurie J. Heyer
- 出版商: Benjamin Cummins
- 出版日期: 2006-03-12
- 售價: $1,100
- 貴賓價: 9.8 折 $1,078
- 語言: 英文
- 頁數: 464
- 裝訂: Paperback
- ISBN: 0805382194
- ISBN-13: 9780805382198
-
相關分類:
生物資訊 Bioinformatics
無法訂購
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相關主題
商品描述
Discovering Genomics is the first genomics text that combines web activities and case studies with a problem-solving approach to teach upper-level undergraduates and first-year graduate students the fundamentals of genomic analysis. More of a workbook than a traditional text, Discovering Genomics, Second Edition allows students to work with real genomic data in solving problems and provides the user with an active learning experience.
The Second Edition has been thoroughly revised and updated to incorporate the latest scientific findings on popular topics such as disease-causing organisms and genetic defects. Case study chapters have been placed throughout the book to tie real-life scenarios into the concepts that follow. Two of the book’s key pedagogical features, Discovery Questions and Math Minutes, have also been updated and expanded.
The interactive companion website has been reprogrammed with JMOL, the latest 3-D software used to view DNA structures.
Table of Contents
1. Genomic Medicine Case Study: What’s wrong with my child?
2. Genome Sequence Acquisition and Analysis
3. Comparative Genomics in Evolution and Medicine
4. Genome Variations
5. Genomic Medicine Case Study: Why Can’t I Just Take a Pill to Lose Weight?
6. Basic Research with DNA Microarrays
7. Applied Research with DNA Microarrays
8. Proteomics
9. Genomic Medicine Case Study: Why Can’t We Cure More Diseases?
10. Genomic Circuits in Single Genes
11. Integrated Genomic Circuits
12. Modeling Whole-Genome Circuits
商品描述(中文翻譯)
描述
《發現基因組學》(Discovering Genomics)是第一本將網路活動和案例研究結合問題解決方法的基因組學教材,旨在教授高年級本科生和一年級研究生基因組分析的基本原理。《發現基因組學,第二版》更像是一本工作手冊,而非傳統教材,讓學生能夠使用真實的基因組數據來解決問題,並提供主動學習的體驗。
第二版已全面修訂和更新,納入了最新的科學發現,涵蓋疾病致病生物和遺傳缺陷等熱門主題。案例研究章節分佈於全書,將現實情境與後續概念相結合。書中的兩個關鍵教學特徵——探索問題(Discovery Questions)和數學分鐘(Math Minutes)也已更新和擴展。
互動伴隨網站已重新編程,使用JMOL,這是最新的3D軟體,用於查看DNA結構。
目錄
1. 基因組醫學案例研究:我的孩子怎麼了?
2. 基因組序列獲取與分析
3. 進化與醫學中的比較基因組學
4. 基因組變異
5. 基因組醫學案例研究:為什麼我不能只吃藥減肥?
6. 使用DNA微陣列的基礎研究
7. 使用DNA微陣列的應用研究
8. 蛋白質組學
9. 基因組醫學案例研究:為什麼我們不能治療更多疾病?
10. 單基因中的基因組電路
11. 整合基因組電路
12. 全基因組電路建模
