Molecular signatures that can be transferred across different omics platforms
Autor: | Jörg Reinders, Michael Altenbuchinger, Neus Masqué-Soler, Peter J. Oefner, Wolfram Klapper, Wolfram Gronwald, Thorsten Rehberg, Christian W. Kohler, Rainer Spang, Monika Szczepanowski, Philipp Schwarzfischer, Julia Richter |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Statistics and Probability Matching (statistics) Proteome Computer science Proteomics computer.software_genre Biochemistry Transcriptome 03 medical and health sciences 0302 clinical medicine Formaldehyde Freezing Humans Molecular Biology Models Statistical Paraffin Embedding Computational Biology Transmed Omics Burkitt Lymphoma Ismb/Eccb 2017: The 25th Annual Conference Intelligent Systems for Molecular Biology Held Jointly with the 16th Annual European Conference on Computational Biology Prague Czech Republic July 21–25 2017 Computer Science Applications Human tumor Computational Mathematics 030104 developmental biology Computational Theory and Mathematics Feature (computer vision) 030220 oncology & carcinogenesis Lymphoma Large B-Cell Diffuse Tissue Preservation Data mining Erratum DNA microarray computer Algorithms Software |
Zdroj: | Bioinformatics |
ISSN: | 1367-4811 |
Popis: | Motivation Molecular signatures for treatment recommendations are well researched. Still it is challenging to apply them to data generated by different protocols or technical platforms. Results We analyzed paired data for the same tumors (Burkitt lymphoma, diffuse large B-cell lymphoma) and features that had been generated by different experimental protocols and analytical platforms including the nanoString nCounter and Affymetrix Gene Chip transcriptomics as well as the SWATH and SRM proteomics platforms. A statistical model that assumes independent sample and feature effects accounted for 69–94% of technical variability. We analyzed how variability is propagated through linear signatures possibly affecting predictions and treatment recommendations. Linear signatures with feature weights adding to zero were substantially more robust than unbalanced signatures. They yielded consistent predictions across data from different platforms, both for transcriptomics and proteomics data. Similarly stable were their predictions across data from fresh frozen and matching formalin-fixed paraffin-embedded human tumor tissue. Availability and Implementation The R-package ‘zeroSum’ can be downloaded at https://github.com/rehbergT/zeroSum. Complete data and R codes necessary to reproduce all our results can be received from the authors upon request. |
Databáze: | OpenAIRE |
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