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Network methods for describing sample relationships in genomic datasets: application to Huntington’s disease
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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3441531/ https://www.ncbi.nlm.nih.gov/pubmed/22691535 http://dx.doi.org/10.1186/1752-0509-6-63 |
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author | Oldham, Michael C Langfelder, Peter Horvath, Steve |
author_facet | Oldham, Michael C Langfelder, Peter Horvath, Steve |
author_sort | Oldham, Michael C |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3441531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34415312012-09-18 Network methods for describing sample relationships in genomic datasets: application to Huntington’s disease Oldham, Michael C Langfelder, Peter Horvath, Steve BMC Syst Biol Methodology Article 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. BioMed Central 2012-06-12 /pmc/articles/PMC3441531/ /pubmed/22691535 http://dx.doi.org/10.1186/1752-0509-6-63 Text en Copyright ©2012 Oldham et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Oldham, Michael C Langfelder, Peter Horvath, Steve Network methods for describing sample relationships in genomic datasets: application to Huntington’s disease |
title | Network methods for describing sample relationships in genomic datasets: application to Huntington’s disease |
title_full | Network methods for describing sample relationships in genomic datasets: application to Huntington’s disease |
title_fullStr | Network methods for describing sample relationships in genomic datasets: application to Huntington’s disease |
title_full_unstemmed | Network methods for describing sample relationships in genomic datasets: application to Huntington’s disease |
title_short | Network methods for describing sample relationships in genomic datasets: application to Huntington’s disease |
title_sort | network methods for describing sample relationships in genomic datasets: application to huntington’s disease |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3441531/ https://www.ncbi.nlm.nih.gov/pubmed/22691535 http://dx.doi.org/10.1186/1752-0509-6-63 |
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