Summary: Cancer is an extremely complex disease and each type of cancer usually has several different subtypes. Multi-omics data can provide more comprehensive biological information for identifying and discovering cancer subtypes. However, existing unsupervised cancer subtyping methods cannot effectively learn comprehensive shared and specific information of multi-omics data. Therefore, a novel method is proposed based on shared and specific representation learning. For each omics data, two autoencoders are applied to extract shared and specific information, respectively. To reduce redundancy and mutual interference, orthogonality constraint is introduced to separate shared and specific information. In addition, contrastive learning is app...
Motivation: Subtyping cancer is key to an improved and more personalized prognosis/treatment. The in...
Extensive amounts of multi-omics data and multiple cancer subtyping methods have been developed rapi...
Recent advances in experimental biology allow creation of datasets where several genome-wide data ty...
Cancer subtyping (or cancer subtypes identification) based on multi-omics data has played an importa...
Identification and prediction of cancer subtypes are important parts in the development towards pers...
Breast Cancer comprises multiple subtypes implicated in prognosis. Existing stratification methods r...
Due to the high heterogeneity and clinical characteristics of cancer, there are significant differen...
The use of genome-wide data in cancer research, for the identification of groups of patients with si...
Curs 2020-2021ancer is a complex disease caused by the abnormal behavior and interaction of differen...
Advances in high-throughput technologies allow for measurements of many types of omics data, yet the...
The identification of cancer subtypes is crucial to cancer diagnosis and treatments. A number of met...
Recent advances in high-throughput sequencing have accelerated the accumulation of omics data on the...
It is now clear that major malignancies are heterogeneous diseases associated with diverse molecular...
Increasingly, multiple omics approaches are being applied to understand the complexity of biological...
Please refer to the readme in the github link https://github.com/zhenglinyi/DL-mo. for the specific ...
Motivation: Subtyping cancer is key to an improved and more personalized prognosis/treatment. The in...
Extensive amounts of multi-omics data and multiple cancer subtyping methods have been developed rapi...
Recent advances in experimental biology allow creation of datasets where several genome-wide data ty...
Cancer subtyping (or cancer subtypes identification) based on multi-omics data has played an importa...
Identification and prediction of cancer subtypes are important parts in the development towards pers...
Breast Cancer comprises multiple subtypes implicated in prognosis. Existing stratification methods r...
Due to the high heterogeneity and clinical characteristics of cancer, there are significant differen...
The use of genome-wide data in cancer research, for the identification of groups of patients with si...
Curs 2020-2021ancer is a complex disease caused by the abnormal behavior and interaction of differen...
Advances in high-throughput technologies allow for measurements of many types of omics data, yet the...
The identification of cancer subtypes is crucial to cancer diagnosis and treatments. A number of met...
Recent advances in high-throughput sequencing have accelerated the accumulation of omics data on the...
It is now clear that major malignancies are heterogeneous diseases associated with diverse molecular...
Increasingly, multiple omics approaches are being applied to understand the complexity of biological...
Please refer to the readme in the github link https://github.com/zhenglinyi/DL-mo. for the specific ...
Motivation: Subtyping cancer is key to an improved and more personalized prognosis/treatment. The in...
Extensive amounts of multi-omics data and multiple cancer subtyping methods have been developed rapi...
Recent advances in experimental biology allow creation of datasets where several genome-wide data ty...