Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies.
作者:
主题词
等位基因(Alleles);数据库, 遗传学(Databases, Genetic);基因频率(Gene Frequency);疾病遗传易感性(Genetic Predisposition to Disease);遗传变异(Genetic Variation);基因组学(Genomics);人类(Humans);遗传药理学(Pharmacogenetics);软件(Software)
DOI
10.1093/nar/gkw949
PMID
27924022
发布时间
2018-11-13
- 浏览20

Nucleic acids research
D846-D853页
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