Evidence map›Paper›PMID 28122525›Full record

ArticleBMC cancer2017

An approach to forecast human cancer by profiling microRNA expressions from NGS data.

A Salim, R Amjesh, S S Vinod Chandra

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Article in BMC cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

A SalimDepartment of Computer Science, College of Engineering Trivandrum, Sreekaryam, Thiruvananthapuram, India. salim.mangad@gmail.com.ORCID 0000-0003-2953-0972
R AmjeshDepartment of Computational Biology and BioInformatics, University of Kerala, Karyavattom, Thiruvananthapuram, India.
S S Vinod ChandraDepartment of Computational Biology and BioInformatics, University of Kerala, Karyavattom, Thiruvananthapuram, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundmicroRNAs are single-stranded non-coding RNA sequences of 18 - 24 nucleotides in length. They play an important role in post-transcriptional regulation of gene expression. Evidences of microRNA acting as promoter/suppressor of several diseases including cancer are being unveiled. Recent studies have shown that microRNAs are differentially expressed in disease states when compared with that of normal states. Profiling of microRNA is a good measure to estimate the differences in expression levels, which can be further utilized to understand the progression of any associated disease.

methodsMachine learning techniques, when applied to microRNA expression values obtained from NGS data, could be utilized for the development of effective disease prediction system. This paper discusses an approach for microRNA expression profiling, its normalization and a Support Vector based machine learning technique to develop a Cancer Prediction System. Presently, the system has been trained with data samples of hepatocellular carcinoma, carcinomas of the bladder and lung cancer. microRNAs related to specific types of cancer were used to build the classifier.

resultsWhen the system is trained and tested with 10 fold cross validation, the prediction accuracy obtained is 97.56% for lung cancer, 97.82% for hepatocellular carcinoma and 95.0% for carcinomas of the bladder. The system is further validated with separate test sets, which show accuracies higher than 90%. A ranking based on differential expression marks the relative significance of each microRNA in the prediction process.

conclusionsResults from experiments proved that microRNA expression profiling is an effective mechanism for disease identification, provided sufficiently large database is available.

Indexed as

PrognosisGene Expression ProfilingGene Expression Regulation, NeoplasticHigh-Throughput Nucleotide SequencingHumansMicroRNAsNeoplasmsMicroRNAsExpression profilingMicroRNASequence mappingSVM classifiers

Identifiers

PMID28122525
PMCPMC5267436

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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.