CAMUR: Knowledge extraction from RNA-seq cancer data through equivalent classification rules.

Bioinformatics

Institute of Systems Analysis and Computer Science - National Research Council, 00185, Rome, Italy, Department of Engineering - Uninettuno International University, Corso Vittorio Emanuele II, 39 - 00186 Rome, Italy.

Published: March 2016


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Article Abstract

Motivation: 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.

Results: 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.

Availability And Implementation: dmb.iasi.cnr.it/camur.php

Contact: emanuel@iasi.cnr.it

Supplementary Information: Supplementary data are available at Bioinformatics online.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795614PMC
http://dx.doi.org/10.1093/bioinformatics/btv635DOI Listing

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