Geometrical method for non-negative source separation : Application to dynamic PET imaging and mass spectrometry

This thesis addresses the problem of non-negative blind source separation (i.e. positive or zero quantities). The situation of linear instantaneous mixtures of non-negative sources occurs in many problems of signal and image processing, such as decompositions of signals measured by a spectrometer (mass spectra, Raman spectra, infrared spectra), decomposition of images (medical, multi-spectral and hyperspectral) or estimating of the activity of a radionuclide. In these problems, the sources are inherently non-negative and this property should be preserved during their estimation, in order to get physical meaning components. Most of existing non-negative blind source separation methods require ``strong" assumptions on sources (such as mutual independence, local dominance or total additivity), which are not always satisfied in practice. In this work, we propose a new geometrical method for separating non-negative sources. The mixing matrix and the sources are estimated by finding the minimum aperture simplicial cone containing the scatter plot of mixed data. The proposed method does not require the mutual independence of the sources, neither their decorrelation, nor their local dominance, or their total additivity. One condition is necessary and sufficient: the positive orthant must be the unique minimum aperture simplicial cone cone containing the scatter plot of the sources. The proposed algorithm is successfully evaluated in two different problems of non-negative sources separation. In the first situation, we perform the separation of mass spectra measured at the output of a liquid chromatograph to identify and quantify the different metabolites (small molecules) present in the urine of rats treated with phenobarbital . In the second situation, we estimate the different pharmacokinetics compartments of the radiotracer [18F]-FDG in human brain, from a set of 3D PET images of this organ, without blood sampling. Among these pharmacokinetics, arterial input function is of great interest to evaluate the effectiveness of anti-cancer treatment in oncology.

Data and Resources

Additional Info

Field Value
Source https://theses.hal.science/tel-00859690
Author Ouedraogo, Wendyam, S. B.
Maintainer CCSD
Last Updated May 9, 2026, 19:53 (UTC)
Created May 9, 2026, 19:53 (UTC)
Identifier NNT: 2012GRENT098
Language fr
Rights https://about.hal.science/hal-authorisation-v1/
contributor Grenoble Images Parole Signal Automatique (GIPSA-lab) ; Université Pierre Mendès France - Grenoble 2 (UPMF)-Université Stendhal - Grenoble 3-Université Joseph Fourier - Grenoble 1 (UJF)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP)-Centre National de la Recherche Scientifique (CNRS)
creator Ouedraogo, Wendyam, S. B.
date 2012-11-28T00:00:00
harvest_object_id 6ec21414-4e1d-4792-9238-3afead61a4c6
harvest_source_id 3374d638-d20b-4672-ba96-a23232d55657
harvest_source_title test moissonnage SELUNE
metadata_modified 2026-03-31T00:00:00
set_spec type:THESE