| Literature DB >> 30990192 |
Abstract
In the age of personalized medicine, there is a great need to classify cancer (from the same organ site) into homogeneous subtypes. Recent technology advancements in genome-wide molecular profiling have made it possible to profiling multiple molecular datasets to characterize the genomic changes in various cancer types. How to take full advantage of the availability of these omics data? And how to integrate these molecular data with patient clinical data to do a more systematic subtyping of cancer are the focuses of the paper. We proposed a new method called Molecular and Clinical Networks Fusion (MCNF) to classify cancer into homogeneous subtypes. Our method has two highlights: one is that it can integrate both numerical and non-numerical data into the fused network; the next highlight is that it is unsupervised, which means it can automatically determine the optimal number of clusters.Entities:
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Year: 2019 PMID: 30990192 DOI: 10.1109/TCBB.2019.2910515
Source DB: PubMed Journal: IEEE/ACM Trans Comput Biol Bioinform ISSN: 1545-5963 Impact factor: 3.710