Department of Genetics, Stanford University Medical Center, Stanford, CA 94305-5120, USA.
Pharmacogenomics. 2010 Apr;11(4):501-5. doi: 10.2217/pgs.10.15.
The NIH initiated the PharmGKB in April 2000. The primary mission was to create a repository of primary data, tools to track associations between genes and drugs, and to catalog the location and frequency of genetic variations known to impact drug response. Over the past 10 years, new technologies have shifted research from candidate gene pharmacogenetics to phenotype-based pharmacogenomics with a consequent explosion of data. PharmGKB has refocused on curating knowledge rather than housing primary genotype and phenotype data, and now, captures more complex relationships between genes, variants, drugs, diseases and pathways. Going forward, the challenges are to provide the tools and knowledge to plan and interpret genome-wide pharmacogenomics studies, predict gene-drug relationships based on shared mechanisms and support data-sharing consortia investigating clinical applications of pharmacogenomics.
NIH 于 2000 年 4 月启动了 PharmGKB。其主要任务是创建一个主要数据存储库,用于跟踪基因与药物之间的关联的工具,并对已知影响药物反应的遗传变异的位置和频率进行编目。在过去的 10 年中,新技术已将研究从候选基因药物遗传学转移到基于表型的药物基因组学,随之而来的数据呈爆炸式增长。PharmGKB 已将重点重新调整为管理知识,而不是存储主要基因型和表型数据,现在,它可以捕捉到基因、变体、药物、疾病和途径之间更复杂的关系。未来的挑战是提供工具和知识,以规划和解释全基因组药物基因组学研究,基于共享机制预测基因-药物关系,并支持调查药物基因组学临床应用的数据共享联盟。