Clustering and variable selection evaluation of 13 unsupervised methods for multi-omics data integration

Archive ouverte

Pierre-Jean, Morgane | Deleuze, Jean-François | Le Floch, Edith | Mauger, Florence

Edité par CCSD ; Oxford University Press (OUP) -

International audience. Recent advances in NGS sequencing, microarrays and mass spectrometry for omics data production have enabled the generation and collection of different modalities of high-dimensional molecular data. The integration of multiple omics datasets is a statistical challenge, due to the limited number of individuals, the high number of variables and the heterogeneity of the datasets to integrate. Recently, a lot of tools have been developed to solve the problem of integrating omics data including canonical correlation analysis, matrix factorization and SM. These commonly used techniques aim to analyze simultaneously two or more types of omics. In this article, we compare a panel of 13 unsupervised methods based on these different approaches to integrate various types of multi-omics datasets: iClusterPlus, regularized generalized canonical correlation analysis, sparse generalized canonical correlation analysis, multiple co-inertia analysis (MCIA), integrative-NMF (intNMF), SNF, MoCluster, mixKernel, CIMLR, LRAcluster, ConsensusClustering, PINSPlus and multi-omics factor analysis (MOFA). We evaluate the ability of the methods to recover the subgroups and the variables that drive the clustering on eight benchmarks of simulation. MOFA does not provide any results on these benchmarks. For clustering, SNF, MoCluster, CIMLR, LRAcluster, ConsensusClustering and intNMF provide the best results. For variable selection, MoCluster outperforms the others. However, the performance of the methods seems to depend on the heterogeneity of the datasets (especially for MCIA, intNMF and iClusterPlus). Finally, we apply the methods on three real studies with heterogeneous data and various phenotypes. We conclude that MoCluster is the best method to analyze these omics data. Availability: An R package named CrIMMix is available on GitHub at https://github.com/CNRGH/crimmix to reproduce all the results of this article.

Suggestions

Du même auteur

PIntMF : Une méthode de factorisation matricielle pénalisée pour l'intégration de données multi-omiques

Archive ouverte | Pierre-Jean, Morgane | CCSD

International audience. The generation of multi-omics data is growing with the improvement of high-throughput technologies. The integration in the same analysis of several levels of the genome could allow a better u...

PIntMF: Penalized Integrative Matrix Factorization method for multi-omics data

Archive ouverte | Pierre-Jean, Morgane | CCSD

International audience. Motivation:It is more and more common to explore the genome at diverse levels and not only at a single omic level. Through integrative statistical methods, omics data have the power to reveal...

Comparison of commercially available whole-genome sequencing kits for variant detection in circulating cell-free DNA

Archive ouverte | Mauger, Florence | CCSD

International audience. Circulating cell-free DNA (ccfDNA) has great potential for non-invasive diagnosis, prognosis and monitoring treatment of disease. However, a sensitive and specific whole-genome sequencing (WG...

Chargement des enrichissements...