Evidence map›Paper›PMID 25823003›Full record

ArticlePloS one2015

Hierarchical gene selection and genetic fuzzy system for cancer microarray data classification.

Thanh Nguyen, Abbas Khosravi, Douglas Creighton, Saeid Nahavandi

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Thanh NguyenCentre for Intelligent Systems Research (CISR), Deakin University, Geelong Waurn Ponds Campus, Victoria, 3216, Australia.
Abbas KhosraviCentre for Intelligent Systems Research (CISR), Deakin University, Geelong Waurn Ponds Campus, Victoria, 3216, Australia.
Douglas CreightonCentre for Intelligent Systems Research (CISR), Deakin University, Geelong Waurn Ponds Campus, Victoria, 3216, Australia.
Saeid NahavandiCentre for Intelligent Systems Research (CISR), Deakin University, Geelong Waurn Ponds Campus, Victoria, 3216, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This paper introduces a novel approach to gene selection based on a substantial modification of analytic hierarchy process (AHP). The modified AHP systematically integrates outcomes of individual filter methods to select the most informative genes for microarray classification. Five individual ranking methods including t-test, entropy, receiver operating characteristic (ROC) curve, Wilcoxon and signal to noise ratio are employed to rank genes. These ranked genes are then considered as inputs for the modified AHP. Additionally, a method that uses fuzzy standard additive model (FSAM) for cancer classification based on genes selected by AHP is also proposed in this paper. Traditional FSAM learning is a hybrid process comprising unsupervised structure learning and supervised parameter tuning. Genetic algorithm (GA) is incorporated in-between unsupervised and supervised training to optimize the number of fuzzy rules. The integration of GA enables FSAM to deal with the high-dimensional-low-sample nature of microarray data and thus enhance the efficiency of the classification. Experiments are carried out on numerous microarray datasets. Results demonstrate the performance dominance of the AHP-based gene selection against the single ranking methods. Furthermore, the combination of AHP-FSAM shows a great accuracy in microarray data classification compared to various competing classifiers. The proposed approach therefore is useful for medical practitioners and clinicians as a decision support system that can be implemented in the real medical practice.

Indexed as

AlgorithmsComputational BiologyDatabases, GeneticData Interpretation, StatisticalDecision Support Systems, ClinicalDNA, NeoplasmFuzzy LogicGene Expression ProfilingHumansLeukemiaLymphoma, Large B-Cell, DiffuseModels, GeneticModels, StatisticalNeoplasmsOligonucleotide Array Sequence AnalysisROC CurveDNA, Neoplasm

Identifiers

PMID25823003
PMCPMC4378968

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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.