Evidence map›Paper›PMID 25986937›Full record

ArticleBMC bioinformatics2015

Multi-class BCGA-ELM based classifier that identifies biomarkers associated with hallmarks of cancer.

Vasily Sachnev, Saras Saraswathi, Rashid Niaz, Andrzej Kloczkowski, Sundaram Suresh

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 33% of its field
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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
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

5 authors at 4 institutions in 4 countries.

Vasily SachnevDepartment of Information, Communication and Electronics Engineering, Catholic University of Korea, Bucheon, Republic of Korea. bassvasys@hotmail.com.
Saras SaraswathiBattelle Center for Mathematical Medicine at The Research Institute at Nationwide Children's Hospital; currently at Sidra, Medical and Research Center, Doha, Qatar. ssundararajan@sidra.org.
Rashid NiazDepartment of Medical Informatics, Sidra Medical and Research Center, Doha, Qatar. rniaz@sidra.org.
Andrzej KloczkowskiBattelle Center for Mathematical Medicine at The Research Institute at Nationwide Children's Hospital; Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, USA. andrzej.kloczkowski@nationwidechildrens.org.
Sundaram SureshSchool of Computer Science, Nanyang Technological University, Nanyang, Singapore. ssundaram@ntu.edu.sg.
Nationwide Children's Hospital · USCatholic University of Korea · KRNanyang Technological University · SGSidra Medical and Research Center · QA

Funding

Coarse-Grained Models of ProteinsR01GM072014 · NIGMS · IOWA STATE UNIVERSITY · PI JERNIGAN, ROBERT L · 2004 to 2012
$2.3M
NIGMS NIH HHS 2R01GM072014-05A1NIGMS NIH HHS R01 GM072014
6 · The paper itself

Abstract

backgroundTraditional cancer treatments have centered on cytotoxic drugs and general purpose chemotherapy that may not be tailored to treat specific cancers. Identification of molecular markers that are related to different types of cancers might lead to discovery of drugs that are patient and disease specific. This study aims to use microarray gene expression cancer data to identify biomarkers that are indicative of different types of cancers. Our aim is to provide a multi-class cancer classifier that can simultaneously differentiate between cancers and identify type-specific biomarkers, through the application of the Binary Coded Genetic Algorithm (BCGA) and a neural network based Extreme Learning Machine (ELM) algorithm.

resultsBCGA and ELM are combined and used to select a subset of genes that are present in the Global Cancer Mapping (GCM) data set. This set of candidate genes contains over 52 biomarkers that are related to multiple cancers, according to the literature. They include APOA1, VEGFC, YWHAZ, B2M, EIF2S1, CCR9 and many other genes that have been associated with the hallmarks of cancer. BCGA-ELM is tested on several cancer data sets and the results are compared to other classification methods. BCGA-ELM compares or exceeds other algorithms in terms of accuracy. We were also able to show that over 50% of genes selected by BCGA-ELM on GCM data are cancer related biomarkers.

conclusionsWe were able to simultaneously differentiate between 14 different types of cancers, using only 92 genes, to achieve a multi-class classification accuracy of 95.4% which is between 21.6% and 38% higher than other results in the literature for multi-class cancer classification. Our findings suggest that computational algorithms such as BCGA-ELM can facilitate biomarker-driven integrated cancer research that can lead to a detailed understanding of the complexities of cancer.

Indexed as

AlgorithmsArtificial IntelligenceNeural Networks, ComputerBiomarkers, TumorGene Expression Regulation, NeoplasticHumansNeoplasmsOligonucleotide Array Sequence AnalysisPattern Recognition, AutomatedBiomarkers, Tumor

Identifiers

PMID25986937
PMCPMC4448565
OpenAlexW2170615026

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.