Abstract
Acute cardiac allograft rejection is a serious complication of heart transplantation. Investigating molecular processes in whole blood via microarrays is a promising avenue of research in transplantation, particularly due to the non-invasive nature of blood sampling. However, whole blood is a complex tissue and the consequent heterogeneity in composition amongst samples is ignored in traditional microarray analysis. This complicates the biological interpretation of microarray data. Here we have applied a statistical deconvolution approach, cell-specific Significance analysis of microarrays (csSAM), to whole blood samples from subjects either undergoing acute heart allograft rejection (AR) or not (NR). We identified eight differentially expressed probe-sets signifcantly correlated to monocytes (mapping to 6 genes, all down-regulated in ARs versus NRs) at a false discovery rate (FDR) ≤ 15%. None of the genes identified are present in a biomarker panel of acute heart rejection previously published by our group and discovered in the same data. © the author(s), publisher and licensee Libertas Academica Ltd.
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Shannon, C. P., Hollander, Z., Wilson-McManus, J., Balshaw, R., Ng, R. T., McMaster, R., … Tebbutt, S. J. (2012). White blood cell differentials enrich whole blood expression data in the context of acute cardiac allograft rejection. Bioinformatics and Biology Insights, 6, 49–58. https://doi.org/10.4137/BBI.S9197
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