Abstract

BackgroundOne major goal of large-scale cancer omics study is to identify molecular subtypes for more accurate cancer diagnoses and treatments. To deal with high-dimensional cancer multi-omics data, a promising strategy is to find an effective low-dimensional subspace of the original data and then cluster cancer samples in the reduced subspace. However, due to data-type diversity and big data volume, few methods can integrative and efficiently find the principal low-dimensional manifold of the high-dimensional cancer multi-omics data.ResultsIn this study, we proposed a novel low-rank approximation based integrative probabilistic model to fast find the shared principal subspace across multiple data types: the convexity of the low-rank regularized likelihood function of the probabilistic model ensures efficient and stable model fitting. Candidate molecular subtypes can be identified by unsupervised clustering hundreds of cancer samples in the reduced low-dimensional subspace. On testing datasets, our method LRAcluster (low-rank approximation based multi-omics data clustering) runs much faster with better clustering performances than the existing method. Then, we applied LRAcluster on large-scale cancer multi-omics data from TCGA. The pan-cancer analysis results show that the cancers of different tissue origins are generally grouped as independent clusters, except squamous-like carcinomas. While the single cancer type analysis suggests that the omics data have different subtyping abilities for different cancer types.ConclusionsLRAcluster is a very useful method for fast dimension reduction and unsupervised clustering of large-scale multi-omics data. LRAcluster is implemented in R and freely available via http://bioinfo.au.tsinghua.edu.cn/software/lracluster/.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-2223-8) contains supplementary material, which is available to authorized users.

Highlights

  • ResultsWe proposed a novel low-rank approximation based integrative probabilistic model to fast find the shared principal subspace across multiple data types: the convexity of the low-rank regularized likelihood function of the probabilistic model ensures efficient and stable model fitting

  • One major goal of large-scale cancer omics study is to identify molecular subtypes for more accurate cancer diagnoses and treatments

  • For somatic mutation and copy number variation data, our preliminary studies indicate that the massive passenger variations of the complete datasets deteriorated the clustering stability

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Summary

Results

LRAcluster is a computational-efficient method for fast dimension reduction and integrative clustering of largescale cancer multi-omics data. The smallest dataset containing top 100 molecular features of each data type is used to test LRAcluster and iCluster+’s clustering performances with different target dimension (from 2 to 10). A recent work reported an integrative network-based stratification (jNBS) pan-cancer clustering analysis on TCGA dataset, which incorporated multi-omics data with the information of a pre-given gene network [33]. Speaking, it reported similar results with LRAcluster: most of cancer types are separately clustered according to their tissue origin, and two types of squamous carcinomas, head/neck squamous carcinoma and lung squamous carcinoma are cluster together. For the remaining 7 cancer types, LRAcluster did not find strong molecular subtypes based on current omics data

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