Computing Identity Co-Reference Across Drug Discovery Datasets
نویسندگان
چکیده
This paper presents the rules used within the Open PHACTS (http://www.openphacts.org) Identity Management Service to compute co-reference chains across multiple datasets. The web of (linked) data has encouraged a proliferation of identifiers for the concepts captured in datasets; with each dataset using their own identifier. A key data integration challenge is linking the co-referent identifiers, i.e. identifying and linking the equivalent concept in every dataset. Exacerbating this challenge, the datasets model the data differently, so when is one representation truly the same as another? Finally, different users have their own task and domain specific notions of equivalence that are driven by their operational knowledge. Consumers of the data need to be able to choose the notion of operational equivalence to be applied for the context of their application. We highlight the challenges of automatically computing co-reference and the need for capturing the context of the equivalence. This context is then used to control the co-reference computation. Ultimately, the context will enable data consumers to decide which co-references to include in their applications.
منابع مشابه
HEDD: the human epigenetic drug database
Epigenetic drugs are chemical compounds that target disordered post-translational modification of histone proteins and DNA through enzymes, and the recognition of these changes by adaptor proteins. Epigenetic drug-related experimental data such as gene expression probed by high-throughput sequencing, co-crystal structure probed by X-RAY diffraction and binding constants probed by bio-assay have...
متن کاملSimBoost: a read-across approach for predicting drug–target binding affinities using gradient boosting machines
Computational prediction of the interaction between drugs and targets is a standing challenge in the field of drug discovery. A number of rather accurate predictions were reported for various binary drug-target benchmark datasets. However, a notable drawback of a binary representation of interaction data is that missing endpoints for non-interacting drug-target pairs are not differentiated from...
متن کاملSurvey on Perception of People Regarding Utilization of Computer Science & Information Technology in Manipulation of Big Data, Disease Detection & Drug Discovery
this research explores the manipulation of biomedical big data and diseases detection using automated computing mechanisms. As efficient and cost effective way to discover disease and drug is important for a society so computer aided automated system is a must. This paper aims to understand the importance of computer aided automated system among the people. The analysis result from collected da...
متن کاملCorrection: Identification of Druggable Cancer Driver Genes Amplified across TCGA Datasets
The Cancer Genome Atlas (TCGA) projects have advanced our understanding of the driver mutations, genetic backgrounds, and key pathways activated across cancer types. Analysis of TCGA datasets have mostly focused on somatic mutations and translocations, with less emphasis placed on gene amplifications. Here we describe a bioinformatics screening strategy to identify putative cancer driver genes ...
متن کاملSecurely Measuring the Overlap between Private Datasets with Cryptosets
Many scientific questions are best approached by sharing data--collected by different groups or across large collaborative networks--into a combined analysis. Unfortunately, some of the most interesting and powerful datasets--like health records, genetic data, and drug discovery data--cannot be freely shared because they contain sensitive information. In many situations, knowing if private data...
متن کامل