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Non-small-cell lung cancer classification via RNA-Seq and histology imaging probability fusion

BACKGROUND: Adenocarcinoma and squamous cell carcinoma are the two most prevalent lung cancer types, and their distinction requires different screenings, such as the visual inspection of histology slides by an expert pathologist, the analysis of gene expression or computer tomography scans, among ot...

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Autores principales: Carrillo-Perez, Francisco, Morales, Juan Carlos, Castillo-Secilla, Daniel, Molina-Castro, Yésica, Guillén, Alberto, Rojas, Ignacio, Herrera, Luis Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456075/
https://www.ncbi.nlm.nih.gov/pubmed/34551733
http://dx.doi.org/10.1186/s12859-021-04376-1
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author Carrillo-Perez, Francisco
Morales, Juan Carlos
Castillo-Secilla, Daniel
Molina-Castro, Yésica
Guillén, Alberto
Rojas, Ignacio
Herrera, Luis Javier
author_facet Carrillo-Perez, Francisco
Morales, Juan Carlos
Castillo-Secilla, Daniel
Molina-Castro, Yésica
Guillén, Alberto
Rojas, Ignacio
Herrera, Luis Javier
author_sort Carrillo-Perez, Francisco
collection PubMed
description BACKGROUND: Adenocarcinoma and squamous cell carcinoma are the two most prevalent lung cancer types, and their distinction requires different screenings, such as the visual inspection of histology slides by an expert pathologist, the analysis of gene expression or computer tomography scans, among others. In recent years, there has been an increasing gathering of biological data for decision support systems in the diagnosis (e.g. histology imaging, next-generation sequencing technologies data, clinical information, etc.). Using all these sources to design integrative classification approaches may improve the final diagnosis of a patient, in the same way that doctors can use multiple types of screenings to reach a final decision on the diagnosis. In this work, we present a late fusion classification model using histology and RNA-Seq data for adenocarcinoma, squamous-cell carcinoma and healthy lung tissue. RESULTS: The classification model improves results over using each source of information separately, being able to reduce the diagnosis error rate up to a 64% over the isolate histology classifier and a 24% over the isolate gene expression classifier, reaching a mean F1-Score of 95.19% and a mean AUC of 0.991. CONCLUSIONS: These findings suggest that a classification model using a late fusion methodology can considerably help clinicians in the diagnosis between the aforementioned lung cancer cancer subtypes over using each source of information separately. This approach can also be applied to any cancer type or disease with heterogeneous sources of information. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04376-1.
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spelling pubmed-84560752021-09-22 Non-small-cell lung cancer classification via RNA-Seq and histology imaging probability fusion Carrillo-Perez, Francisco Morales, Juan Carlos Castillo-Secilla, Daniel Molina-Castro, Yésica Guillén, Alberto Rojas, Ignacio Herrera, Luis Javier BMC Bioinformatics Research BACKGROUND: Adenocarcinoma and squamous cell carcinoma are the two most prevalent lung cancer types, and their distinction requires different screenings, such as the visual inspection of histology slides by an expert pathologist, the analysis of gene expression or computer tomography scans, among others. In recent years, there has been an increasing gathering of biological data for decision support systems in the diagnosis (e.g. histology imaging, next-generation sequencing technologies data, clinical information, etc.). Using all these sources to design integrative classification approaches may improve the final diagnosis of a patient, in the same way that doctors can use multiple types of screenings to reach a final decision on the diagnosis. In this work, we present a late fusion classification model using histology and RNA-Seq data for adenocarcinoma, squamous-cell carcinoma and healthy lung tissue. RESULTS: The classification model improves results over using each source of information separately, being able to reduce the diagnosis error rate up to a 64% over the isolate histology classifier and a 24% over the isolate gene expression classifier, reaching a mean F1-Score of 95.19% and a mean AUC of 0.991. CONCLUSIONS: These findings suggest that a classification model using a late fusion methodology can considerably help clinicians in the diagnosis between the aforementioned lung cancer cancer subtypes over using each source of information separately. This approach can also be applied to any cancer type or disease with heterogeneous sources of information. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04376-1. BioMed Central 2021-09-22 /pmc/articles/PMC8456075/ /pubmed/34551733 http://dx.doi.org/10.1186/s12859-021-04376-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Carrillo-Perez, Francisco
Morales, Juan Carlos
Castillo-Secilla, Daniel
Molina-Castro, Yésica
Guillén, Alberto
Rojas, Ignacio
Herrera, Luis Javier
Non-small-cell lung cancer classification via RNA-Seq and histology imaging probability fusion
title Non-small-cell lung cancer classification via RNA-Seq and histology imaging probability fusion
title_full Non-small-cell lung cancer classification via RNA-Seq and histology imaging probability fusion
title_fullStr Non-small-cell lung cancer classification via RNA-Seq and histology imaging probability fusion
title_full_unstemmed Non-small-cell lung cancer classification via RNA-Seq and histology imaging probability fusion
title_short Non-small-cell lung cancer classification via RNA-Seq and histology imaging probability fusion
title_sort non-small-cell lung cancer classification via rna-seq and histology imaging probability fusion
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456075/
https://www.ncbi.nlm.nih.gov/pubmed/34551733
http://dx.doi.org/10.1186/s12859-021-04376-1
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