CAMUR: Knowledge extraction from RNA-seq cancer data through equivalent classification rules.
Where this comes from
- Record sourced from PubMed, PMID 26519501.
- Also identified by DOI 10.1093/bioinformatics/btv635 and PMC identifier 4795614.
- Licence recorded as CC BY-NC.
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Abstract
Nowadays, knowledge extraction methods from Next Generation Sequencing data are highly requested. In this work, we focus on RNA-seq gene expression analysis and specifically on case-control studies with rule-based supervised classification algorithms that build a model able to discriminate cases from controls. State of the art algorithms compute a single classification model that contains few features (genes). On the contrary, our goal is to elicit a higher amount of knowledge by computing many classification models, and therefore to identify most of the genes related to the predicted class. We propose CAMUR, a new method that extracts multiple and equivalent classification models. CAMUR iteratively computes a rule-based classification model, calculates the power set of the genes present in the rules, iteratively eliminates those combinations from the data set, and performs again the classification procedure until a stopping criterion is verified. CAMUR includes an ad-hoc knowledge repository (database) and a querying tool.We analyze three different types of RNA-seq data sets (Breast, Head and Neck, and Stomach Cancer) from The Cancer Genome Atlas (TCGA) and we validate CAMUR and its models also on non-TCGA data. Our experimental results show the efficacy of CAMUR: we obtain several reliable equivalent classification models, from which the most frequent genes, their relationships, and the relation with a particular cancer are deduced. dmb.iasi.cnr.it/camur.php emanuel@iasi.cnr.it Supplementary data are available at Bioinformatics online.
Medical subject headings
- Neoplasms