ArticleHealthcare informatics research2014
Drug similarity search based on combined signatures in gene expression profiles.
Article in Healthcare informatics research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
8 citing papers in PubMed.
- Analysis and identification of drug similarity through drug side effects and indications data.BMC medical informatics and decision making · 2023Article
- Computing Drug-Drug Similarity from Patient-Centric Data.Bioengineering (Basel, Switzerland) · 2023Article
- Identification and ranking of important bio-elements in drug-drug interaction by Market Basket Analysis.BioImpacts : BI · 2020Article
- Synergy from gene expression and network mining (SynGeNet) method predicts synergistic drug combinations for diverse melanoma genomic subtypes.NPJ systems biology and applications · 2019Article
- Entropy-based divergent and convergent modular pattern reveals additive and synergistic anticerebral ischemia mechanisms.Experimental biology and medicine (Maywood, N.J.) · 2016Article
- Quantitative Identification of Compound-Dependent On-Modules and Differential Allosteric Modules From Homologous Ischemic Networks.CPT: pharmacometrics & systems pharmacology · 2016Article
- NFFinder: an online bioinformatics tool for searching similar transcriptomics experiments in the context of drug repositioning.Nucleic acids research · 2015Article
- Health avatar: an informatics platform for personal and private big data.Healthcare informatics research · 2014Article
Corrections and comments
- Erratum issued
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectivesRecently, comparison of drug responses on gene expression has been a major approach to identifying the functional similarity of drugs. Previous studies have mostly focused on a single feature, the expression differences of individual genes. We provide a more robust and accurate method to compare the functional similarity of drugs by diversifying the features of comparison in gene expression and considering the sample dependent variations.
methodsFor differentially expressed gene measurement, we modified the conventional t-test to normalize variations in diverse experimental conditions of individual samples. To extract significant differentially co-expressed gene modules, we searched maximal cliques among the co-expressed gene network. Finally, we calculated a combined similarity score by averaging the two scaled scores from the above two measurements.
resultsThis method shows significant performance improvement in comparison to other approaches in the test with Connectivity Map data. In the test to find the drugs based on their own expression profiles with leave-one-out cross validation, the proposed method showed an area under the curve (AUC) score of 0.99, which is much higher than scores obtained with previous methods, ranging from 0.71 to 0.93. In the drug networks, we could find well clustered drugs having the same target proteins and novel relations among drugs implying the possibility of drug repurposing.
conclusionsInclusion of the features of a co-expressed module provides more implications to infer drug action. We propose that this method be used to find collaborative cellular mechanisms associated with drug action and to simply identify drugs having similar responses.
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