Proteomics analysis of plasma for early diagnosis of endometriosis.

Objective: To test the hypothesis that differential surface-enhanced laser desorption/ionization time-of-flight mass spectrometry protein or peptide expression in plasma can be used in infertile women with or without pelvic pain to predict the presence of laparoscopically and histologically confirmed endometriosis, especially in the subpopulation with a normal preoperative gynecologic ultrasound examination.

Methods: Surface-enhanced laser desorption/ionization time-of-flight mass spectrometry analysis was performed on 254 plasma samples obtained from 89 women without endometriosis and 165 women with endometriosis (histologically confirmed) undergoing laparoscopies for infertility with or without pelvic pain. Data were analyzed using least squares support vector machines and were divided randomly (100 times) into a training data set (70%) and a test data set (30%).

Predicting receptor-ligand pairs through kernel learning.

Background: Regulation of cellular events is, often, initiated via extracellular signaling. Extracellular signaling occurs when a circulating ligand interacts with one or more membrane-bound receptors. Identification of receptor-ligand pairs is thus an important and specific form of PPI prediction.

Candidate gene prioritization by network analysis of differential expression using machine learning approaches.

Background: Discovering novel disease genes is still challenging for diseases for which no prior knowledge--such as known disease genes or disease-related pathways--is available. Performing genetic studies frequently results in large lists of candidate genes of which only few can be followed up for further investigation. We have recently developed a computational method for constitutional genetic disorders that identifies the most promising candidate genes by replacing prior knowledge by experimental data of differential gene expression between affected and healthy individuals.

A tutorial on support vector machine-based methods for classification problems in chemometrics.

This tutorial provides a concise overview of support vector machines and different closely related techniques for pattern classification. The tutorial starts with the formulation of support vector machines for classification. The method of least squares support vector machines is explained.

A kernel-based integration of genome-wide data for clinical decision support.

Background: Although microarray technology allows the investigation of the transcriptomic make-up of a tumor in one experiment, the transcriptome does not completely reflect the underlying biology due to alternative splicing, post-translational modifications, as well as the influence of pathological conditions (for example, cancer) on transcription and translation. This increases the importance of fusing more than one source of genome-wide data, such as the genome, transcriptome, proteome, and epigenome. The current increase in the amount of available omics data emphasizes the need for a methodological integration framework.

Low rank updated LS-SVM classifiers for fast variable selection.

Least squares support vector machine (LS-SVM) classifiers are a class of kernel methods whose solution follows from a set of linear equations. In this work we present low rank modifications to the LS-SVM classifiers that are useful for fast and efficient variable selection. The inclusion or removal of a candidate variable can be represented as a low rank modification to the kernel matrix (linear kernel) of the LS-SVM classifier.

Prospective exploration of biochemical tissue composition via imaging mass spectrometry guided by principal component analysis.

MALDI-based Imaging Mass Spectrometry (IMS) is an analytical technique that provides the opportunity to study the spatial distribution of biomolecules including proteins and peptides in organic tissue. IMS measures a large collection of mass spectra spread out over an organic tissue section and retains the absolute spatial location of these measurements for analysis and imaging. The classical approach to IMS imaging, producing univariate ion images, is not well suited as a first step in a prospective study where no a priori molecular target mass can be formulated.