Abstract
Background: Identification of biomarkers among thousands of genes arrayed for disease classification has been the subject of considerable research in recent years. These studies have focused on disease classification, comparing experimental groups of effected to normal patients. Related experiments can be done to identify tissue-restricted biomarkers, genes with a high level of expression in one tissue compared to other tissue types in the body. Results: In this study, cartilage was compared with ten other body tissues using a two color array experimental design. Thirty-seven probe sets were identified as cartilage biomarkers. Of these, 13 (35%) have existing annotation associated with cartilage including several well-established cartilage biomarkers. These genes comprise a useful database from which novel targets for cartilage biology research can be selected. We determined cartilage specific Z-scores based on the observed M to classify genes with Z-scores ≥ 1.96 in all ten cartilage/tissue comparisons as cartilage-specific genes. Conclusion: Quantile regression is a promising method for the analysis of two color array experiments that compare multiple samples in the absence of biological replicates, thereby limiting quantifiable error. We used a nonparametric approach to reveal the relationship between percentiles of M and A, where M is log2(R/G) and A is 0.5 log2(RG) with R representing the gene expression level in cartilage and G representing the gene expression level in one of the other 10 tissues. Then we performed linear quantile regression to identify genes with a cartilage-restricted pattern of expression.
Original language | English |
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Article number | 300 |
Journal | BMC Bioinformatics |
Volume | 9 |
DOIs | |
State | Published - Jul 2 2008 |
Bibliographical note
Funding Information:This work was supported by Gluck Equine Research Foundation, the Geoffrey C. Hughes Foundation, IC Post Doctorial Research Fellowship, NGIA HM1582-06-1-2016 (CPS), National Science Foundation Grant DMS-0604920 (MZ, ACB) and NIH KBRIN P20 RR16481 (LH, CPS, AJS). We also wish to thank Michael Mienaltowski, Department of Veterinary Science for his help with the microarray experiments.
Funding
This work was supported by Gluck Equine Research Foundation, the Geoffrey C. Hughes Foundation, IC Post Doctorial Research Fellowship, NGIA HM1582-06-1-2016 (CPS), National Science Foundation Grant DMS-0604920 (MZ, ACB) and NIH KBRIN P20 RR16481 (LH, CPS, AJS). We also wish to thank Michael Mienaltowski, Department of Veterinary Science for his help with the microarray experiments.
Funders | Funder number |
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University of Kentucky Gluck Equine Research Foundation | NGIA HM1582-06-1-2016 |
National Science Foundation Arctic Social Science Program | DMS-0604920 |
National Institutes of Health (NIH) | |
National Center for Research Resources | P20RR016481 |
ASJC Scopus subject areas
- Structural Biology
- Biochemistry
- Molecular Biology
- Computer Science Applications
- Applied Mathematics