Coupled matrix factorization with sparse factors to identify potential biomarkers in metabolomics

TY - CONF

T1 - Coupled matrix factorization with sparse factors to identify potential biomarkers in metabolomics

AU - Evrim, Acar Ataman

AU - Gürdeniz, Gözde

AU - Rasmussen, Morten Arendt

AU - Rago, Daniela

AU - Dragsted, Lars Ove

AU - Bro, Rasmus

N1 - Conference code: 12

PY - 2012

Y1 - 2012

N2 - Metabolomics focuses on the detection of chemical substances in biological fluids such as urine and blood using a number of analytical techniques including Nuclear Magnetic Resonance (NMR) spectroscopy and Liquid Chromatography-Mass Spectroscopy (LC-MS). Among the major challenges in analysis of metabolomics data are (i) joint analysis of data from multiple platforms and (ii) capturing easily interpretable underlying patterns, which could be further utilized for biomarker discovery. In order to address these challenges, we formulate joint analysis of data from multiple platforms as a coupled matrix factorization problem with sparsity constraints on the factor matrices. We develop an all-at-once optimization algorithm, called CMF-SPOPT (Coupled Matrix Factorization with SParse OPTimization), which is a gradientbased optimization approach solving for all factor matrices simultaneously. Using numerical experiments on simulated data, we demonstrate that CMF-SPOPT can capture the underlying sparse patterns in data. Furthermore, on a real data set of blood samples collected from a group of rats, we use the proposed approach to jointly analyze metabolomic data sets and identify potential biomarkers for apple intake.

AB - Metabolomics focuses on the detection of chemical substances in biological fluids such as urine and blood using a number of analytical techniques including Nuclear Magnetic Resonance (NMR) spectroscopy and Liquid Chromatography-Mass Spectroscopy (LC-MS). Among the major challenges in analysis of metabolomics data are (i) joint analysis of data from multiple platforms and (ii) capturing easily interpretable underlying patterns, which could be further utilized for biomarker discovery. In order to address these challenges, we formulate joint analysis of data from multiple platforms as a coupled matrix factorization problem with sparsity constraints on the factor matrices. We develop an all-at-once optimization algorithm, called CMF-SPOPT (Coupled Matrix Factorization with SParse OPTimization), which is a gradientbased optimization approach solving for all factor matrices simultaneously. Using numerical experiments on simulated data, we demonstrate that CMF-SPOPT can capture the underlying sparse patterns in data. Furthermore, on a real data set of blood samples collected from a group of rats, we use the proposed approach to jointly analyze metabolomic data sets and identify potential biomarkers for apple intake.

U2 - 10.1109/icdmw.2012.17

DO - 10.1109/icdmw.2012.17

M3 - Paper

T2 - International Conference on Data Mining Workshop 2012 (IEEE)

Y2 - 10 December 2012

ER -