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

被引:20
作者
Carrillo-Perez, Francisco [1 ]
Morales, Juan Carlos [1 ]
Castillo-Secilla, Daniel [1 ]
Molina-Castro, Yesica [1 ]
Guillen, Alberto [1 ]
Rojas, Ignacio [1 ]
Herrera, Luis Javier [1 ]
机构
[1] Univ Granada, CITIC, Dept Comp Architecture & Technol, Periodista Rafael Gomez Montero 2, Granada 18014, Spain
关键词
Deep learning; Gene expression; Late fusion; Whole slide imaging; NSCLC; FEATURE-SELECTION; NEURAL-NETWORKS; IDENTIFICATION;
D O I
10.1186/s12859-021-04376-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页数:19
相关论文
共 70 条
[1]   End-to-end lung cancer screening with three-dimensional deep learning on low-dose chest computed tomography [J].
Ardila, Diego ;
Kiraly, Atilla P. ;
Bharadwaj, Sujeeth ;
Choi, Bokyung ;
Reicher, Joshua J. ;
Peng, Lily ;
Tse, Daniel ;
Etemadi, Mozziyar ;
Ye, Wenxing ;
Corrado, Greg ;
Naidich, David P. ;
Shetty, Shravya .
NATURE MEDICINE, 2019, 25 (06) :954-+
[2]  
Bernard PS, 2002, CLIN CHEM, V48, P1178
[3]  
Bishop C. M., 2006, Pattern recognition and machine learning
[4]   Open Targets Platform: new developments and updates two years on [J].
Carvalho-Silva, Denise ;
Pierleoni, Andrea ;
Pignatelli, Miguel ;
Ong, ChuangKee ;
Fumis, Luca ;
Karamanis, Nikiforos ;
Carmona, Miguel ;
Faulconbridge, Adam ;
Hercules, Andrew ;
McAuley, Elaine ;
Miranda, Alfredo ;
Peat, Gareth ;
Spitzer, Michaela ;
Barrett, Jeffrey ;
Hulcoop, David G. ;
Papa, Eliseo ;
Koscielny, Gautier ;
Dunham, Ian .
NUCLEIC ACIDS RESEARCH, 2019, 47 (D1) :D1056-D1065
[5]   Leukemia multiclass assessment and classification from Microarray and RNA-seq technologies integration at gene expression level [J].
Castillo, Daniel ;
Manuel Galvez, Juan ;
Herrera, Luis J. ;
Rojas, Fernando ;
Valenzuela, Olga ;
Caba, Octavio ;
Prados, Jose ;
Rojas, Ignacio .
PLOS ONE, 2019, 14 (02)
[6]   Integration of RNA-Seq data with heterogeneous microarray data for breast cancer profiling [J].
Castillo, Daniel ;
Manuel Galvez, Juan ;
Javier Herrera, Luis ;
San Roman, Belen ;
Rojas, Fernando ;
Rojas, Ignacio .
BMC BIOINFORMATICS, 2017, 18
[7]  
Castillo-Secilla D, 2020, KNOWSEQ R PACKAGE EX
[8]   Deep learning with multimodal representation for pancancer prognosis prediction [J].
Cheerla, Anika ;
Gevaert, Olivier .
BIOINFORMATICS, 2019, 35 (14) :I446-I454
[9]  
Chen R., 2019, ARXIV PREPRINT ARXIV
[10]  
Cho K., 2014, P SSST 8 8 WORKSHOP, P103, DOI DOI 10.3115/V1/W14-4012