单核苷酸多态性
遗传学
生物
外显子组
人类基因组
外显子组测序
遗传关联
基因组
基因
计算生物学
基因型
突变
作者
Chunling Liu,Dianke Yu
出处
期刊:Chinese Journal of Laboratory Medicine
[Chinese Medical Association]
日期:2012-07-11
卷期号:35 (07): 579-584
标识
DOI:10.3760/cma.j.issn.1009-9158.2012.07.002
摘要
Single nucleotide polymorphisms (SNPs) are the most common genetic variants in human genome.Candidate gene, genome-wide association studies (GWASs) and exome sequencing which base on SNPs have made a great progress in identifying cancer susceptibility.The development and application of high resolutions in SNPs has played an important role in clarifying the mechanism, prevention, diagnosis and targeted therapy in cancers.(Chin J Lab Med, 2012, 35:579-584)
科研通智能强力驱动
Strongly Powered by AbleSci AI