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Pseudomonas graminis Behrendt et al. 1999|微生物学数据集|生物信息学数据集
收藏DataCite Commons2025-01-07 更新2025-03-18 收录
下载链接：
https://bacdive.dsmz.de/index.php?site=pdf_view&id=13062&doi=doi:10.13145/bacdive13062.20240916.9.1
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The range of data encompasses taxonomy, morphology, physiology, sampling and concomitant environmental conditions as well as molecular biology.
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DSMZ
创建时间：
2024-09-17
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全国 1∶200 000 数字地质图（公开版）空间数据库
As the only one of its kind, China National Digital Geological Map (Public Version at 1∶200 000 scale) Spatial Database (CNDGM-PVSD) is based on China' s former nationwide measured results of regional geological survey at 1∶200 000 scale, and is also one of the nationwide basic geosciences spatial databases jointly accomplished by multiple organizations of China. Spatially, it embraces 1 163 geological map-sheets (at scale 1: 200 000) in both formats of MapGIS and ArcGIS, covering 72% of China's whole territory with a total data volume of 90 GB. Its main sources is from 1∶200 000 regional geological survey reports, geological maps, and mineral resources maps with an original time span from mid-1950s to early 1990s. Approved by the State's related agencies, it meets all the related technical qualification requirements and standards issued by China Geological Survey in data integrity, logic consistency, location acc racy, attribution fineness, and collation precision, and is hence of excellent and reliable quality. The CNDGM-PVSD is an important component of China' s national spatial database categories, serving as a spatial digital platform for the information construction of the State's national economy, and providing informationbackbones to the national and provincial economic planning, geohazard monitoring, geological survey, mineral resources exploration as well as macro decision-making.
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CatMeows
该数据集包含440个声音样本，由21只属于两个品种（缅因州库恩猫和欧洲短毛猫）的猫在三种不同情境下发出的喵声组成。这些情境包括刷毛、在陌生环境中隔离和等待食物。每个声音文件都遵循特定的命名约定，包含猫的唯一ID、品种、性别、猫主人的唯一ID、录音场次和发声计数。此外，还有一个额外的zip文件，包含被排除的录音（非喵声）和未剪辑的连续发声序列。
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The Brain & Body Genetic Resource Exchange (BBGRE) provides a resource for investigating the genetic basis of neurodisability. It combines phenotype information from patients with neurodevelopmental and behavioural problems with clinical genetic data, and displays this information on the human genome map.
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