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PIntMF: Penalized Integrative Matrix Factorization method for multi-omics data.
Pierre-Jean, Morgane; Mauger, Florence; Deleuze, Jean-François; Le Floch, Edith.
Afiliação
  • Pierre-Jean M; Centre National de Recherche en Génomique Humaine, CEA, Université de Paris-Saclay, Evry, France.
  • Mauger F; Centre National de Recherche en Génomique Humaine, CEA, Université de Paris-Saclay, Evry, France.
  • Deleuze JF; Centre National de Recherche en Génomique Humaine, CEA, Université de Paris-Saclay, Evry, France.
  • Le Floch E; Centre National de Recherche en Génomique Humaine, CEA, Université de Paris-Saclay, Evry, France.
Bioinformatics ; 38(4): 900-907, 2022 01 27.
Article em En | MEDLINE | ID: mdl-34849583
MOTIVATION: It is more and more common to perform multi-omics analyses to explore the genome at diverse levels and not only at a single level. Through integrative statistical methods, multi-omics data have the power to reveal new biological processes, potential biomarkers and subgroups in a cohort. Matrix factorization (MF) is an unsupervised statistical method that allows a clustering of individuals, but also reveals relevant omics variables from the various blocks. RESULTS: Here, we present PIntMF (Penalized Integrative Matrix Factorization), an MF model with sparsity, positivity and equality constraints. To induce sparsity in the model, we used a classical Lasso penalization on variable and individual matrices. For the matrix of samples, sparsity helps in the clustering, while normalization (matching an equality constraint) of inferred coefficients is added to improve interpretation. Moreover, we added an automatic tuning of the sparsity parameters using the famous glmnet package. We also proposed three criteria to help the user to choose the number of latent variables. PIntMF was compared with other state-of-the-art integrative methods including feature selection techniques in both synthetic and real data. PIntMF succeeds in finding relevant clusters as well as variables in two types of simulated data (correlated and uncorrelated). Next, PIntMF was applied to two real datasets (Diet and cancer), and it revealed interpretable clusters linked to available clinical data. Our method outperforms the existing ones on two criteria (clustering and variable selection). We show that PIntMF is an easy, fast and powerful tool to extract patterns and cluster samples from multi-omics data. AVAILABILITY AND IMPLEMENTATION: An R package is available at https://github.com/mpierrejean/pintmf. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Multiômica / Neoplasias Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Multiômica / Neoplasias Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article