The Jackson Laboratory, Bar Harbor, Maine 04609, USA.
Nucleic Acids Res. 2018 Jan 4;46(D1):D843-D850. doi: 10.1093/nar/gkx1082.
The Mouse Phenome Database (MPD; https://phenome.jax.org) is a widely used resource that provides access to primary experimental trait data, genotypic variation, protocols and analysis tools for mouse genetic studies. Data are contributed by investigators worldwide and represent a broad scope of phenotyping endpoints and disease-related traits in naïve mice and those exposed to drugs, environmental agents or other treatments. MPD houses individual animal data with detailed, searchable protocols, and makes these data available to other resources via API. MPD provides rigorous curation of experimental data and supporting documentation using relevant ontologies and controlled vocabularies. Most data in MPD are from inbreds and other reproducible strains such that the data are cumulative over time and across laboratories. The resource has been expanded to include the QTL Archive and other primary phenotype data from mapping crosses as well as advanced high-diversity mouse populations including the Collaborative Cross and Diversity Outbred mice. Furthermore, MPD provides a means of assessing replicability and reproducibility across experimental conditions and protocols, benchmarking assays in users' own laboratories, identifying sensitized backgrounds for making new mouse models with genome editing technologies, analyzing trait co-inheritance, finding the common genetic basis for multiple traits and assessing sex differences and sex-by-genotype interactions.
鼠表型数据库(MPD;https://phenome.jax.org)是一个广泛使用的资源,提供了对小鼠遗传研究的原始实验特征数据、基因型变异、方案和分析工具的访问。数据由世界各地的研究人员提供,代表了在未处理的小鼠和暴露于药物、环境剂或其他处理的小鼠中广泛的表型终点和与疾病相关的特征。MPD 存储具有详细、可搜索方案的个体动物数据,并通过 API 将这些数据提供给其他资源。MPD 使用相关本体论和受控词汇表对实验数据和支持文档进行严格的编目。MPD 中的大多数数据来自近交系和其他可重复的品系,因此数据随着时间的推移和实验室的不同而累积。该资源已扩展到包括 QTL 档案和来自映射杂交的其他原始表型数据,以及高级高多样性小鼠群体,包括合作交叉和多样性杂交小鼠。此外,MPD 提供了一种评估在不同实验条件和方案下的可重复性和再现性的方法,在用户自己的实验室中对测定进行基准测试,为使用基因组编辑技术制造新的小鼠模型确定敏感的背景,分析特征的共同遗传基础,找到多个特征的常见遗传基础,并评估性别差异和性别-基因型相互作用。