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Logo of bmcsysbioBioMed Centralsearchsubmit a manuscriptregisterthis articleBMC Systems Biology
 
BMC Syst Biol. 2012; 6: 63.
Published online Jun 12, 2012. doi:  10.1186/1752-0509-6-63
PMCID: PMC3441531
Network methods for describing sample relationships in genomic datasets: application to Huntington’s disease
Michael C Oldham,corresponding author1 Peter Langfelder,2 and Steve Horvathcorresponding author2,3
1Department of Neurology, The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, USA
2Department of Human Genetics, University of California, Los Angeles, USA
3Department of Biostatistics, University of California, Los Angeles, CA, USA
corresponding authorCorresponding author.
Michael C Oldham: oldhamm/at/stemcell.ucsf.edu; Peter Langfelder: peter.langfelder/at/gmail.com; Steve Horvath: shorvath/at/mednet.ucla.edu
Received March 1, 2012; Accepted May 3, 2012.
Abstract
Background
Genomic datasets generated by new technologies are increasingly prevalent in disparate areas of biological research. While many studies have sought to characterize relationships among genomic features, commensurate efforts to characterize relationships among biological samples have been less common. Consequently, the full extent of sample variation in genomic studies is often under-appreciated, complicating downstream analytical tasks such as gene co-expression network analysis.
Results
Here we demonstrate the use of network methods for characterizing sample relationships in microarray data generated from human brain tissue. We describe an approach for identifying outlying samples that does not depend on the choice or use of clustering algorithms. We introduce a battery of measures for quantifying the consistency and integrity of sample relationships, which can be compared across disparate studies, technology platforms, and biological systems. Among these measures, we provide evidence that the correlation between the connectivity and the clustering coefficient (two important network concepts) is a sensitive indicator of homogeneity among biological samples. We also show that this measure, which we refer to as cor(K,C), can distinguish biologically meaningful relationships among subgroups of samples. Specifically, we find that cor(K,C) reveals the profound effect of Huntington’s disease on samples from the caudate nucleus relative to other brain regions. Furthermore, we find that this effect is concentrated in specific modules of genes that are naturally co-expressed in human caudate nucleus, highlighting a new strategy for exploring the effects of disease on sets of genes.
Conclusions
These results underscore the importance of systematically exploring sample relationships in large genomic datasets before seeking to analyze genomic feature activity. We introduce a standardized platform for this purpose using freely available R software that has been designed to enable iterative and interactive exploration of sample networks.
Keywords: Sample networks, Sample network analysis, Huntington’s disease, Clustering coefficient, cor(K,C), Standardized C(k) curve, Data pre-processing, Microarrays, Gene expression
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