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MLW-gcForest: a multi-weighted gcForest model towards the staging of lung adenocarcinoma based on multi-modal genetic data

BACKGROUND: Lung cancer is one of the most common types of cancer, among which lung adenocarcinoma accounts for the largest proportion. Currently, accurate staging is a prerequisite for effective diagnosis and treatment of lung adenocarcinoma. Previous research has used mainly single-modal data, suc...

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Autores principales: Dong, Yunyun, Yang, Wenkai, Wang, Jiawen, Zhao, Juanjuan, Qiang, Yan, Zhao, Zijuan, Kazihise, Ntikurako Guy Fernand, Cui, Yanfen, Yang, Xiaotong, Liu, Siyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857238/
https://www.ncbi.nlm.nih.gov/pubmed/31726986
http://dx.doi.org/10.1186/s12859-019-3172-z
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author Dong, Yunyun
Yang, Wenkai
Wang, Jiawen
Zhao, Juanjuan
Qiang, Yan
Zhao, Zijuan
Kazihise, Ntikurako Guy Fernand
Cui, Yanfen
Yang, Xiaotong
Liu, Siyuan
author_facet Dong, Yunyun
Yang, Wenkai
Wang, Jiawen
Zhao, Juanjuan
Qiang, Yan
Zhao, Zijuan
Kazihise, Ntikurako Guy Fernand
Cui, Yanfen
Yang, Xiaotong
Liu, Siyuan
author_sort Dong, Yunyun
collection PubMed
description BACKGROUND: Lung cancer is one of the most common types of cancer, among which lung adenocarcinoma accounts for the largest proportion. Currently, accurate staging is a prerequisite for effective diagnosis and treatment of lung adenocarcinoma. Previous research has used mainly single-modal data, such as gene expression data, for classification and prediction. Integrating multi-modal genetic data (gene expression RNA-seq, methylation data and copy number variation) from the same patient provides the possibility of using multi-modal genetic data for cancer prediction. A new machine learning method called gcForest has recently been proposed. This method has been proven to be suitable for classification in some fields. However, the model may face challenges when applied to small samples and high-dimensional genetic data. RESULTS: In this paper, we propose a multi-weighted gcForest algorithm (MLW-gcForest) to construct a lung adenocarcinoma staging model using multi-modal genetic data. The new algorithm is based on the standard gcForest algorithm. First, different weights are assigned to different random forests according to the classification performance of these forests in the standard gcForest model. Second, because the feature vectors generated under different scanning granularities have a diverse influence on the final classification result, the feature vectors are given weights according to the proposed sorting optimization algorithm. Then, we train three MLW-gcForest models based on three single-modal datasets (gene expression RNA-seq, methylation data, and copy number variation) and then perform decision fusion to stage lung adenocarcinoma. Experimental results suggest that the MLW-gcForest model is superior to the standard gcForest model in constructing a staging model of lung adenocarcinoma and is better than the traditional classification methods. The accuracy, precision, recall, and AUC reached 0.908, 0.896, 0.882, and 0.96, respectively. CONCLUSIONS: The MLW-gcForest model has great potential in lung adenocarcinoma staging, which is helpful for the diagnosis and personalized treatment of lung adenocarcinoma. The results suggest that the MLW-gcForest algorithm is effective on multi-modal genetic data, which consist of small samples and are high dimensional.
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spelling pubmed-68572382019-12-05 MLW-gcForest: a multi-weighted gcForest model towards the staging of lung adenocarcinoma based on multi-modal genetic data Dong, Yunyun Yang, Wenkai Wang, Jiawen Zhao, Juanjuan Qiang, Yan Zhao, Zijuan Kazihise, Ntikurako Guy Fernand Cui, Yanfen Yang, Xiaotong Liu, Siyuan BMC Bioinformatics Research Article BACKGROUND: Lung cancer is one of the most common types of cancer, among which lung adenocarcinoma accounts for the largest proportion. Currently, accurate staging is a prerequisite for effective diagnosis and treatment of lung adenocarcinoma. Previous research has used mainly single-modal data, such as gene expression data, for classification and prediction. Integrating multi-modal genetic data (gene expression RNA-seq, methylation data and copy number variation) from the same patient provides the possibility of using multi-modal genetic data for cancer prediction. A new machine learning method called gcForest has recently been proposed. This method has been proven to be suitable for classification in some fields. However, the model may face challenges when applied to small samples and high-dimensional genetic data. RESULTS: In this paper, we propose a multi-weighted gcForest algorithm (MLW-gcForest) to construct a lung adenocarcinoma staging model using multi-modal genetic data. The new algorithm is based on the standard gcForest algorithm. First, different weights are assigned to different random forests according to the classification performance of these forests in the standard gcForest model. Second, because the feature vectors generated under different scanning granularities have a diverse influence on the final classification result, the feature vectors are given weights according to the proposed sorting optimization algorithm. Then, we train three MLW-gcForest models based on three single-modal datasets (gene expression RNA-seq, methylation data, and copy number variation) and then perform decision fusion to stage lung adenocarcinoma. Experimental results suggest that the MLW-gcForest model is superior to the standard gcForest model in constructing a staging model of lung adenocarcinoma and is better than the traditional classification methods. The accuracy, precision, recall, and AUC reached 0.908, 0.896, 0.882, and 0.96, respectively. CONCLUSIONS: The MLW-gcForest model has great potential in lung adenocarcinoma staging, which is helpful for the diagnosis and personalized treatment of lung adenocarcinoma. The results suggest that the MLW-gcForest algorithm is effective on multi-modal genetic data, which consist of small samples and are high dimensional. BioMed Central 2019-11-14 /pmc/articles/PMC6857238/ /pubmed/31726986 http://dx.doi.org/10.1186/s12859-019-3172-z Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Dong, Yunyun
Yang, Wenkai
Wang, Jiawen
Zhao, Juanjuan
Qiang, Yan
Zhao, Zijuan
Kazihise, Ntikurako Guy Fernand
Cui, Yanfen
Yang, Xiaotong
Liu, Siyuan
MLW-gcForest: a multi-weighted gcForest model towards the staging of lung adenocarcinoma based on multi-modal genetic data
title MLW-gcForest: a multi-weighted gcForest model towards the staging of lung adenocarcinoma based on multi-modal genetic data
title_full MLW-gcForest: a multi-weighted gcForest model towards the staging of lung adenocarcinoma based on multi-modal genetic data
title_fullStr MLW-gcForest: a multi-weighted gcForest model towards the staging of lung adenocarcinoma based on multi-modal genetic data
title_full_unstemmed MLW-gcForest: a multi-weighted gcForest model towards the staging of lung adenocarcinoma based on multi-modal genetic data
title_short MLW-gcForest: a multi-weighted gcForest model towards the staging of lung adenocarcinoma based on multi-modal genetic data
title_sort mlw-gcforest: a multi-weighted gcforest model towards the staging of lung adenocarcinoma based on multi-modal genetic data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857238/
https://www.ncbi.nlm.nih.gov/pubmed/31726986
http://dx.doi.org/10.1186/s12859-019-3172-z
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