Bioinformatics Advance Access originally published online on March 9, 2006
Bioinformatics 2006 22(11):1391-1396; doi:10.1093/bioinformatics/btl085
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Progressive peak clustering in GC-MS Metabolomic experiments applied to Leishmania parasites
2,*
1 Department of Biochemistry and Molecular Biology, University of Melbourne Parkville, 3010, Australia
2 The Bio21 Molecular Science and Biotechnology Institute, University of Melbourne Parkville, 3010, Australia
*To whom correspondence should be addressed.
Motivation: A common problem in the emerging field of metabolomics is the consolidation of signal lists derived from metabolic profiling of different cell/tissue/fluid states where a number of replicate experiments was collected on each state.
Results: We describe an approach for the consolidation of peak lists based on hierarchical clustering, first within each set of replicate experiments and then between the sets of replicate experiments. The problems of finding the dendrogram tree cutoff which gives the optimal number of peak clusters and the effect of different clustering methods were addressed. When applied to gas chromatography-mass spectrometry metabolic profiling data acquired on Leishmania mexicana, this approach resulted in robust data matrices which completely separated the wild-type and two mutant parasite lines based on their metabolic profile.
Contact: vlikic{at}unimelb.edu.au
Received on January 4, 2006; revised on February 16, 2006; accepted on March 4, 2006
This article has been cited by other articles:
![]() |
A. Luedemann, K. Strassburg, A. Erban, and J. Kopka TagFinder for the quantitative analysis of gas chromatography--mass spectrometry (GC-MS)-based metabolite profiling experiments Bioinformatics, March 1, 2008; 24(5): 732 - 737. [Abstract] [Full Text] [PDF] |
||||
