2020
DOI: 10.1186/s12859-020-03544-z
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Uncovering the prognostic gene signatures for the improvement of risk stratification in cancers by using deep learning algorithm coupled with wavelet transform

Abstract: Background: The aim of gene expression-based clinical modelling in tumorigenesis is not only to accurately predict the clinical endpoints, but also to reveal the genome characteristics for downstream analysis for the purpose of understanding the mechanisms of cancers. Most of the conventional machine learning methods involved a gene filtering step, in which tens of thousands of genes were firstly filtered based on the gene expression levels by a statistical method with an arbitrary cutoff. Although gene filter… Show more

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Cited by 4 publications
(2 citation statements)
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“…Compared with the traditional LASSO method and the latest method SWT-CNN, the predictive ability of the proposed deep learning method is significantly higher than that of LASSO [18] and SWT-CNN [19].…”
Section: Methodsmentioning
confidence: 92%
“…Compared with the traditional LASSO method and the latest method SWT-CNN, the predictive ability of the proposed deep learning method is significantly higher than that of LASSO [18] and SWT-CNN [19].…”
Section: Methodsmentioning
confidence: 92%
“…In breast cancer research, there are several gene expression panels to classify and/or predict subtypes, outcomes, or patient survival such as PAM50, which used mRNA expression values of 50 preselected genes ( 15 ), while MammaPrint using 70-gene signatures ( 16 ), BluePrint using 80-gene signatures ( 17 ), and Oncotype DX using 21-gene signatures ( 18 ). Recently, there is a growing number of literatures regarding the applications of machine learning and deep learning to predict the mRNA gene expression values using hematoxylin and eosin staining ( 19 ) or (synthetic) gene signature prediction using RNA sequencing and clinical information ( 20 ). The capacity in predicting gene expression signature taxonomy is extremely important due to the high correlation between these gene panels and patient outcomes or subtypes.…”
Section: Introductionmentioning
confidence: 99%