2021
DOI: 10.3390/biomedicines9111733
|View full text |Cite
|
Sign up to set email alerts
|

Deep Learning for Human Disease Detection, Subtype Classification, and Treatment Response Prediction Using Epigenomic Data

Abstract: Deep learning (DL) is a distinct class of machine learning that has achieved first-class performance in many fields of study. For epigenomics, the application of DL to assist physicians and scientists in human disease-relevant prediction tasks has been relatively unexplored until very recently. In this article, we critically review published studies that employed DL models to predict disease detection, subtype classification, and treatment responses, using epigenomic data. A comprehensive search on PubMed, Sco… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
7
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
4
2
1

Relationship

0
7

Authors

Journals

citations
Cited by 10 publications
(7 citation statements)
references
References 90 publications
(273 reference statements)
0
7
0
Order By: Relevance
“…Several N-glycan signatures, such as sialylation, fucosylation, bisecting GlcNAcylation, and branching, are regulated by various glycosyltransferase activities, and their synthetic pathways could influence each other. Although discriminating three or more diseases by discriminant analysis using N-glycan signatures has been limited, an ML approach combined with omics data has been used for early detection of diseases, including cancer [16][17][18][19] and seems to be suitable for extraction of disease-specific N-glycan features and precise discrimination between benign and malignant conditions.…”
Section: Discussionmentioning
confidence: 99%
See 2 more Smart Citations
“…Several N-glycan signatures, such as sialylation, fucosylation, bisecting GlcNAcylation, and branching, are regulated by various glycosyltransferase activities, and their synthetic pathways could influence each other. Although discriminating three or more diseases by discriminant analysis using N-glycan signatures has been limited, an ML approach combined with omics data has been used for early detection of diseases, including cancer [16][17][18][19] and seems to be suitable for extraction of disease-specific N-glycan features and precise discrimination between benign and malignant conditions.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, ML approaches could be an important tool for these analyses. [16][17][18][19] We aimed to simultaneously detect nine urological diseases including five cancers (RCC, BCa, UTUC, PC, and GCT) and three benign diseases (BPH, US, and UTI) using a diagnostic modeling ML approach with Ig N-glycan signature data. Thirty-seven patients were excluded because the presence or absence of disease could not be determined from medical records.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…RNN are a subclass of neural networks that introduce recurrent connections between the neuron units, which furnish the network with a memory capability: past observations can be employed to understand the current observation or predict future observations in an input sequence. These characteristics provide RNN with sequential dynamic behavior, making them suitable for processing sequential data and identifying inner relationships and variation tendencies [101,102]. Sahin et al [103] developed an RNN framework to model a stability mechanism for robust feature selection of microarray datasets.…”
Section: Multi-layer Perceptron (Mlp) Neural Networkmentioning
confidence: 99%
“…Most of these methods are based on networks (34,35). These computational methods have been widely used in the discovery of diseaserelated genes (33,(35)(36)(37)(38)(39), genetic mechanism (40,41), gene expression (37,40), protein function (42,43), metabolic association (44,45), and drug target (46,47). Therefore, in this paper, we developed a novel method named "DBN-GTN" to identify gastric cancer-related genes in a large scale.…”
Section: Introductionmentioning
confidence: 99%