Five Years of GWAS Discovery

全基因组关联研究 生物 单核苷酸多态性 计算生物学 遗传学 计算机科学 基因 基因型
作者
Peter M. Visscher,Matthew A. Brown,Mark I. McCarthy,Jian Yang
出处
期刊:American Journal of Human Genetics [Elsevier]
卷期号:90 (1): 7-24 被引量:2382
标识
DOI:10.1016/j.ajhg.2011.11.029
摘要

The past five years have seen many scientific and biological discoveries made through the experimental design of genome-wide association studies (GWASs). These studies were aimed at detecting variants at genomic loci that are associated with complex traits in the population and, in particular, at detecting associations between common single-nucleotide polymorphisms (SNPs) and common diseases such as heart disease, diabetes, auto-immune diseases, and psychiatric disorders. We start by giving a number of quotes from scientists and journalists about perceived problems with GWASs. We will then briefly give the history of GWASs and focus on the discoveries made through this experimental design, what those discoveries tell us and do not tell us about the genetics and biology of complex traits, and what immediate utility has come out of these studies. Rather than giving an exhaustive review of all reported findings for all diseases and other complex traits, we focus on the results for auto-immune diseases and metabolic diseases. We return to the perceived failure or disappointment about GWASs in the concluding section. The past five years have seen many scientific and biological discoveries made through the experimental design of genome-wide association studies (GWASs). These studies were aimed at detecting variants at genomic loci that are associated with complex traits in the population and, in particular, at detecting associations between common single-nucleotide polymorphisms (SNPs) and common diseases such as heart disease, diabetes, auto-immune diseases, and psychiatric disorders. We start by giving a number of quotes from scientists and journalists about perceived problems with GWASs. We will then briefly give the history of GWASs and focus on the discoveries made through this experimental design, what those discoveries tell us and do not tell us about the genetics and biology of complex traits, and what immediate utility has come out of these studies. Rather than giving an exhaustive review of all reported findings for all diseases and other complex traits, we focus on the results for auto-immune diseases and metabolic diseases. We return to the perceived failure or disappointment about GWASs in the concluding section.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
ming完成签到 ,获得积分10
1秒前
陈颖完成签到,获得积分10
2秒前
3秒前
阔达的凡完成签到 ,获得积分10
3秒前
曾曾曾完成签到 ,获得积分20
4秒前
tt完成签到,获得积分10
4秒前
CASPERWU完成签到,获得积分10
4秒前
wanci应助顺利山柏采纳,获得20
5秒前
梦菡发布了新的文献求助20
5秒前
6秒前
6秒前
汉堡包应助Nox采纳,获得10
6秒前
Shylie发布了新的文献求助10
7秒前
澜生发布了新的文献求助10
8秒前
kk完成签到,获得积分20
11秒前
11秒前
11秒前
易安发布了新的文献求助10
11秒前
11秒前
Lucas应助Liam采纳,获得10
11秒前
在水一方应助Viola采纳,获得10
12秒前
12秒前
任性的棒棒糖完成签到,获得积分10
13秒前
14秒前
完美世界应助zm采纳,获得10
14秒前
科研通AI2S应助hope采纳,获得10
16秒前
16秒前
所所应助哈哈采纳,获得30
16秒前
远方发布了新的文献求助10
16秒前
17秒前
17秒前
熊大对熊二说熊要有个熊样完成签到,获得积分10
17秒前
小二郎应助科研通管家采纳,获得10
18秒前
隐形曼青应助科研通管家采纳,获得10
18秒前
从容芮应助科研通管家采纳,获得10
18秒前
从容芮应助科研通管家采纳,获得10
18秒前
wanci应助科研通管家采纳,获得10
18秒前
JamesPei应助科研通管家采纳,获得10
18秒前
18秒前
高分求助中
Shape Determination of Large Sedimental Rock Fragments 2000
Sustainability in Tides Chemistry 2000
Rechtsphilosophie 1000
Bayesian Models of Cognition:Reverse Engineering the Mind 888
A Dissection Guide & Atlas to the Rabbit 600
Very-high-order BVD Schemes Using β-variable THINC Method 568
Mantiden: Faszinierende Lauerjäger Faszinierende Lauerjäger 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3129756
求助须知:如何正确求助?哪些是违规求助? 2780520
关于积分的说明 7748718
捐赠科研通 2435880
什么是DOI,文献DOI怎么找? 1294326
科研通“疑难数据库(出版商)”最低求助积分说明 623670
版权声明 600570