Mutually exclusive spectral biclustering and its applications in cancer subtyping

Abstract

Many soft biclustering algorithms have been developed and applied to various biological and biomedical data analyses. However, until now, few mutually exclusive (hard) biclustering algorithms have been proposed although they can be extremely useful for identify disease or molecular subtypes based on genomic or transcriptomic data. We considered the biclustering problem of expression matrices as a bipartite graph partitioning problem and developed a novel biclustering algorithm, MESBC, based on Dhillons spectral method to detect mutually exclusive biclusters. MESBC simultaneously detects relevant features (genes) and corresponding subgroups, and therefore automatically uses the signature features for each subtype to perform the clustering, improving the clustering performance. MESBC could accurately detect the pre-specified biclusters in simulations, and the identified biclusters were highly consistent with the true labels. Particularly, in setting with high noise, MESBC outperformed existing NMF and Dhillons method and provided markedly better accuracy. Analysis of two TCGA datasets (LUAD and BRAC cohorts) revealed that MESBC provided similar or more accurate prognostication (i.e., smaller p value) for overall survival in patients with breast and lung cancer, respectively, compared to the existing, gold-standard subtypes for breast (PAM50) and lung cancer (integrative clustering). In the TCGA lung cancer patients, MESBC detected two clinically relevant, rare subtypes that other biclustering or integrative clustering algorithms could not detect. These findings validated our hypothesis that MESBC could improve molecular subtyping in cancer patients and potentially facilitate better individual patient management, risk stratification, patient selection, therapeutic assignments, as well as better understanding gene signatures and molecular pathways for development of novel therapeutic agents.