TY - JOUR
T1 - DeepMoIC: multi-omics data integration via deep graph convolutional networks for cancer subtype classification
AU - Wu, Jiecheng
AU - Chen, Zhaoliang
AU - Xiao, Shunxin
AU - Liu, Genggeng
AU - Wu, Wenjie
AU - Wang, Shiping
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/12/18
Y1 - 2024/12/18
N2 - Background: Achieving precise cancer subtype classification is imperative for effective prognosis and treatment. Multi-omics studies, encompassing diverse data modalities, have emerged as powerful tools for unraveling the complexities of cancer. However, owing to the intricacies of biological data, multi-omics datasets generally show variations in data types, scales, and distributions. These intractable problems lead to challenges in exploring intact representations from heterogeneous data, which often result in inaccuracies in multi-omics information analysis. Results: To address the challenges of multi-omics research, our approach DeepMoIC presents a novel framework derived from deep Graph Convolutional Network (GCN). Leveraging autoencoder modules, DeepMoIC extracts compact representations from omics data and incorporates a patient similarity network through the similarity network fusion algorithm. To handle non-Euclidean data and explore high-order omics information effectively, we design a Deep GCN module with two strategies: residual connection and identity mapping. With extracted higher-order representations, our approach consistently outperforms state-of-the-art models on a pan-cancer dataset and 3 cancer subtype datasets. Conclusion: The introduction of Deep GCN shows encouraging performance in terms of supervised multi-omics feature learning, offering promising insights for precision medicine in cancer research. DeepMoIC can potentially be an important tool in the field of cancer subtype classification because of its capacity to handle complex multi-omics data and produce reliable classification findings.
AB - Background: Achieving precise cancer subtype classification is imperative for effective prognosis and treatment. Multi-omics studies, encompassing diverse data modalities, have emerged as powerful tools for unraveling the complexities of cancer. However, owing to the intricacies of biological data, multi-omics datasets generally show variations in data types, scales, and distributions. These intractable problems lead to challenges in exploring intact representations from heterogeneous data, which often result in inaccuracies in multi-omics information analysis. Results: To address the challenges of multi-omics research, our approach DeepMoIC presents a novel framework derived from deep Graph Convolutional Network (GCN). Leveraging autoencoder modules, DeepMoIC extracts compact representations from omics data and incorporates a patient similarity network through the similarity network fusion algorithm. To handle non-Euclidean data and explore high-order omics information effectively, we design a Deep GCN module with two strategies: residual connection and identity mapping. With extracted higher-order representations, our approach consistently outperforms state-of-the-art models on a pan-cancer dataset and 3 cancer subtype datasets. Conclusion: The introduction of Deep GCN shows encouraging performance in terms of supervised multi-omics feature learning, offering promising insights for precision medicine in cancer research. DeepMoIC can potentially be an important tool in the field of cancer subtype classification because of its capacity to handle complex multi-omics data and produce reliable classification findings.
KW - Cancer subtype classification
KW - Deep graph convolutional network
KW - Multi-omics
KW - Supervised learning
UR - http://www.scopus.com/inward/record.url?scp=85212776262&partnerID=8YFLogxK
U2 - 10.1186/s12864-024-11112-5
DO - 10.1186/s12864-024-11112-5
M3 - Journal article
C2 - 39695368
AN - SCOPUS:85212776262
SN - 1471-2164
VL - 25
JO - BMC Genomics
JF - BMC Genomics
IS - 1
M1 - 1209
ER -