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Open AccessJournal ArticleDOI

miRCancer: a microRNA-cancer association database constructed by text mining on literature

Boya Xie, +3 more
- 01 Mar 2013 - 
- Vol. 29, Iss: 5, pp 638-644
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TLDR
This work proposes to extract microRNA-cancer associations by text mining and store them in a database called miRCancer, which documents 878 relationships between 236 microRNAs and 79 human cancers through the processing of >26 000 published articles.
Abstract
Motivation: Research interests in microRNAs have increased rapidly in the past decade. Many studies have showed that microRNAs have close relationships with various human cancers, and they potentially could be used as cancer indicators in diagnosis or as a suppressor for treatment purposes. There are several databases that contain microRNA–cancer associations predicted by computational methods but few from empirical results. Despite the fact that abundant experiments investigating microRNA expressions in cancer cells have been carried out, the results have remain scattered in the literature. We propose to extract microRNA–cancer associations by text mining and store them in a database called miRCancer. Results: The text mining is based on 75 rules we have constructed, which represent the common sentence structures typically used to state microRNA expressions in cancers. The microRNA–cancer association database, miRCancer, is updated regularly by running the text mining algorithm against PubMed. All miRNA–cancer associations are confirmed manually after automatic extraction. miRCancer currently documents 878 relationships between 236 microRNAs and 79 human cancers through the processing of426 000 published articles. Availability: miRCancer is freely available on the web at http://mircan

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Colorectal Carcinoma: A General Overview and Future Perspectives in Colorectal Cancer

TL;DR: The choice of first-line treatment in CRC follows a multimodal approach based on tumour-related characteristics and usually comprises surgical resection followed by chemotherapy combined with monoclonal antibodies or proteins against vascular endothelial growth factor (VEGF) and epidermal growth receptor (EGFR).
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MicroRNAs and complex diseases: from experimental results to computational models.

TL;DR: Twenty state-of-the-art computational models of predicting miRNA-disease associations from different perspectives are reviewed, including five feasible and important research schemas, and future directions for further development of computational models are summarized.
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DIABLO: an integrative approach for identifying key molecular drivers from multi-omics assays

TL;DR: DIABLO is a multi-omics integrative method that seeks for common information across different data types through the selection of a subset of molecular features, while discriminating between multiple phenotypic groups, while achieving predictive performance comparable to state-of-the-art supervised approaches.
References
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MicroRNAs Modulate Hematopoietic Lineage Differentiation

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