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Estimating Error Rates in Bioactivity Databases

delete2013-10-02
delete48
PRE
AI
L
Louisa J. Bellis
Y
Yvonne Light
L
Lutz Franke
DOI:10.1021/ci400099qdelete
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摘要

摘要

En 中文
Bioactivity databases are routinely used in drug discovery to look-up and, using prediction tools, to predict potential targets for small molecules. These databases are typically manually curated from patents and scientific articles. Apart from errors in the source document, the human factor can cause errors during the extraction process. These errors can lead to wrong decisions in the early drug discovery 0 process. In the current work, we have compared bioactivity data from three large databases (ChEMBL, Liceptor, and WOMBAT) who have curated data from the same source documents. As a result, we are able to report error rate estimates for individual activity parameters and individual bioactivity databases. Small molecule structures have the greatest estimated error rate followed by target, activity value, and activity type. This order is also reflected in supplier-specific error rate estimates. The results are also useful in identifying data points for recuration. We hope the results will lead to a more widespread awareness among scientists on the frequencies and types of errors in bioactivity data.
Keyword:
CURATION
QUALITY

期刊

Journal of Chemical Information and Modeling 封面图
Journal of Chemical Information and Modeling
IF:
5.3
论文数:
9.1K
被引数:
4.0W

机构

M
merz pharmaceuticals gmbh
学者数:
118
论文数: 88
被引数: 0
E
european molecular biology laboratory (embl)
学者数:
8.3K
论文数: 5.1K
被引数: 31
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引用论文

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