Evidence map›Paper›PMID 26519501›Full record

ArticleBioinformatics (Oxford, England)2016

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

Valerio Cestarelli, Giulia Fiscon, Giovanni Felici, Paola Bertolazzi, Emanuel Weitschek

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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.

2 · The registry

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3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

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  5. Knowledge Generation with Rule Induction in Cancer Omics.International journal of molecular sciences · 2019
    Review
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Valerio CestarelliInstitute of Systems Analysis and Computer Science - National Research Council, 00185, Rome, Italy.
Giulia FisconInstitute of Systems Analysis and Computer Science - National Research Council, 00185, Rome, Italy, Department of Computer, Control, and Management Engineering - Sapienza University, 00185, Rome, Italy and.
Giovanni FeliciInstitute of Systems Analysis and Computer Science - National Research Council, 00185, Rome, Italy.
Paola BertolazziInstitute of Systems Analysis and Computer Science - National Research Council, 00185, Rome, Italy.
Emanuel WeitschekInstitute 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.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationNowadays, 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.

resultsWe 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.

Indexed as

NeoplasmsAlgorithmsHigh-Throughput Nucleotide SequencingHumansRNASequence Analysis, RNARNA

Identifiers

PMID26519501
PMCPMC4795614

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.