白鸟 (2023-05-30 09:20):
#paper https://doi.org/10.1093/nar/gkaa1027 Open Targets Platform: supporting systematic drug–target identification and prioritisation 1.靶标-疾病知识库: (1)20 个不同数据源的靶标-疾病关系的证据; (2)关键数据集的新证据:全基因组CRISPR敲除筛选数据, GWAS/UK BioBank统计遗传分析证据; (3)已知药物不良信息:上市后药物不良反应的评估,以及有关靶标成药性和安全性的新精选信息; 2.改进证据评分: 改进了证据评分框架以改进靶标识别 3.Open Targets平台开发: 更新10个版本,开发了用户界面和后端技术以提高性能和可用性
IF:16.600Q1 Nucleic acids research, 2021-01-08. DOI: 10.1093/nar/gkaa1027 PMID: 33196847
Open Targets Platform: supporting systematic drug-target identification and prioritisation
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Abstract:
The Open Targets Platform (https://www.targetvalidation.org/) provides users with a queryable knowledgebase and user interface to aid systematic target identification and prioritisation for drug discovery based upon underlying evidence. It is publicly available and the underlying code is open source. Since our last update two years ago, we have had 10 releases to maintain and continuously improve evidence for target-disease relationships from 20 different data sources. In addition, we have integrated new evidence from key datasets, including prioritised targets identified from genome-wide CRISPR knockout screens in 300 cancer models (Project Score), and GWAS/UK BioBank statistical genetic analysis evidence from the Open Targets Genetics Portal. We have evolved our evidence scoring framework to improve target identification. To aid the prioritisation of targets and inform on the potential impact of modulating a given target, we have added evaluation of post-marketing adverse drug reactions and new curated information on target tractability and safety. We have also developed the user interface and backend technologies to improve performance and usability. In this article, we describe the latest enhancements to the Platform, to address the fundamental challenge that developing effective and safe drugs is difficult and expensive.
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