Evidence map›Paper›PMID 37101254›Full record

ArticleBMC bioinformatics2023

meth-SemiCancer: a cancer subtype classification framework via semi-supervised learning utilizing DNA methylation profiles.

Joung Min Choi, Chaelin Park, Heejoon Chae

Abstract read
In one paragraph

Article in BMC bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

7 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.

Joung Min Choi *Department of Computer Science, Virginia Tech, Blacksburg, USA.
Chaelin Park *Division of Computer Science, Sookmyung Women's University, Seoul, Republic of Korea.
Heejoon ChaeDivision of Computer Science, Sookmyung Women's University, Seoul, Republic of Korea. heechae@sookmyung.ac.kr.

Funding

Bio&Medical Technology Development Program of the National Research Foundation (NRF) funded by the Korean government (MSIT) 2019M3E5D3073365National Research Foundation of Korea(NRF) grant funded by the Korea government(MSIT) 2021R1F1A1050707
6 · The paper itself

Abstract

backgroundIdentification of the cancer subtype plays a crucial role to provide an accurate diagnosis and proper treatment to improve the clinical outcomes of patients. Recent studies have shown that DNA methylation is one of the key factors for tumorigenesis and tumor growth, where the DNA methylation signatures have the potential to be utilized as cancer subtype-specific markers. However, due to the high dimensionality and the low number of DNA methylome cancer samples with the subtype information, still, to date, a cancer subtype classification method utilizing DNA methylome datasets has not been proposed.

resultsIn this paper, we present meth-SemiCancer, a semi-supervised cancer subtype classification framework based on DNA methylation profiles. The proposed model was first pre-trained based on the methylation datasets with the cancer subtype labels. After that, meth-SemiCancer generated the pseudo-subtypes for the cancer datasets without subtype information based on the model's prediction. Finally, fine-tuning was performed utilizing both the labeled and unlabeled datasets.

conclusionsFrom the performance comparison with the standard machine learning-based classifiers, meth-SemiCancer achieved the highest average F1-score and Matthews correlation coefficient, outperforming other methods. Fine-tuning the model with the unlabeled patient samples by providing the proper pseudo-subtypes, encouraged meth-SemiCancer to generalize better than the supervised neural network-based subtype classification method. meth-SemiCancer is publicly available at https://github.com/cbi-bioinfo/meth-SemiCancer .

Indexed as

DNA MethylationNeoplasmsHumansMachine LearningNeural Networks, ComputerSupervised Machine LearningCancer subtype classificationDNA methylationNeural networkSemi-supervised learning

Identifiers

PMID37101254
PMCPMC10131478

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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.