PAMOGK: A Pathway Graph Kernel based Multi-Omics Clustering Approach for Discovering Cancer Patient Subgroups
Tepeli, Y. I.; Unal, A. B.; Akdemir, F. M.; Tastan, O.
Show abstract
Accurate classification of patients into molecular subgroups is critical for the development of effective therapeutics and for deciphering what drives these subgroups to cancer. The availability of multi-omics data cat-alogs for large cohorts of cancer patients provides multiple views into the molecular biology of the tumors with unprecedented resolution. We develop PAMOGK (Pathway based Multi Omic Graph Kernel clustering) that not only integrates multi-omics patient data with existing biological knowledge on pathways. We develop a novel graph kernel that evaluates patient similarities based on a single molecular alteration type in the context of a pathway. To corroborate multiple views of patients evaluated by hundreds of pathways and molecular alteration combinations, we use multi-view kernel clustering. Applying PAMOGK to kidney renal clear cell carcinoma (KIRC) patients results in four clusters with significantly different survival times (p-value = 1.24e-11). When we compare PAMOGK to eight other state-of-the-art multi-omics clustering methods, PAMOGK consistently outperforms these in terms of its ability to partition KIRC patients into groups with different survival distributions. The discovered patient subgroups also differ with respect to other clinical parameters such as tumor stage and grade, and primary tumor and metastasis tumor spreads. The pathways identified as important are highly relevant to KIRC. PAMOGK is available at github.com/tastanlab/pamogk
Matching journals
The top 3 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- Multi-omics subtyping of hepatocellular carcinoma patients using a Bayesian network mixture model 96%
- A Generalized Higher-order Correlation Analysis Framework for Multi-Omics Network Inference 96%
- Biological networks and GWAS: comparing and combining network methods to understand the genetics of familial breast cancer susceptibility in the GENESIS study 95%
Similar papers in this journal
- Species-Agnostic Transfer Learning for Cross-species Transcriptomics Data Integration without Gene Orthology 95%
- Graph Contrastive Learning as a Versatile Foundation for Advanced scRNA-seq Data Analysis 95%
- Novel multi-omics deconfounding variational autoencoders can obtain meaningful disease subtyping 95%
Similar papers in this journal
- DriveWays: A Method for Identifying Possibly Overlapping Driver Pathways in Cancer 96%
- DeepInsight-3D for precision oncology: an improved anti-cancer drug response prediction from high-dimensional multi-omics data with convolutional neural networks 96%
- Finding disease modules for cancer and COVID-19 in gene co-expression networks with the Core&Peel method 95%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.