Suppr超能文献

A brief history of genetic variation analysis.

作者信息

Ahmadian Afshin, Lundeberg Joakim

机构信息

Department of Biotechnology, The Royal Institute of Technology, Stockholm, Sweden.

出版信息

Biotechniques. 2002 May;32(5):1122-4, 1126, 1128 passim.

Abstract

As the human genome sequence is determined, there is an emerging need for the analysis of human sequence variations as genetic markers in diagnosis, linkage and association studies, cancer research, and pharmacogenomics. There are several different techniques and approaches for detecting these genetic variations, and here we review some of these techniques and their application fields. However, all the techniques have advantages and disadvantages, andfactors such as laboratory instrumentation, personnel experience, required accuracy, required throughput, and cost often have to be taken into account before selecting a method.

摘要

相似文献

1
A brief history of genetic variation analysis.
Biotechniques. 2002 May;32(5):1122-4, 1126, 1128 passim.
3
Human genome mapping and its medical perspectives.人类基因组图谱及其医学前景。
Southeast Asian J Trop Med Public Health. 1997;28 Suppl 2:25-46.
8
Who cares about the double helix?谁在乎双螺旋结构?
Nature. 2003 Apr 24;422(6934):803-4. doi: 10.1038/422803a.
9
Establishing the triplet nature of the genetic code.确定遗传密码的三联体性质。
Cell. 2007 Mar 9;128(5):815-8. doi: 10.1016/j.cell.2007.02.029.
10
Human genomics: implications for health.人类基因组学:对健康的影响。
Southeast Asian J Trop Med Public Health. 1997;28 Suppl 2:19-24.

引用本文的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验