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Background: Mass spectrometry based screening methods have been recently introduced into clinical proteomics. This boosts the development of a new approach for early disease detection: proteomic pattern analysis. Aim: Find, analyze and compare proteomic patterns in groups of patients having different properties such as disease status or epidemio-logical parameters (e.g. sex, age) with a new pipeline to enhance sensitivity and specificity. Problems: Mass data acquired from high-throughput platforms frequently are blurred and noisy. This extremely complicates the reliable identification of peaks in general and very small peaks below noise-level in particular. Approach: Apply sophisticated signal preprocessing steps followed by statistical analyzes to purge the raw data and enable the detection of real signals while maintaining information for tracebacks. Results: A new analysis pipeline has been developed capable of finding and analyzing peak patterns discriminating different groups of patients (e.g. male/female, cancer/healthy). First steps towards distributed computing approaches have been incorporated in the design.
@InProceedings{conrad:DagSemProc.05471.12,
author = {Conrad, Tim},
title = {{New statistical algorithms for clinical proteomics}},
booktitle = {Computational Proteomics},
pages = {1--2},
series = {Dagstuhl Seminar Proceedings (DagSemProc)},
ISSN = {1862-4405},
year = {2006},
volume = {5471},
editor = {Christian G. Huber and Oliver Kohlbacher and Knut Reinert},
publisher = {Schloss Dagstuhl -- Leibniz-Zentrum f{\"u}r Informatik},
address = {Dagstuhl, Germany},
URL = {https://drops.dagstuhl.de/entities/document/10.4230/DagSemProc.05471.12},
URN = {urn:nbn:de:0030-drops-5427},
doi = {10.4230/DagSemProc.05471.12},
annote = {Keywords: MS, Mass Spectrometry, MALDI-TOF, Fingerprinting, Proteomics}
}