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Article: A bootstrap-based regression method for comprehensive discovery of differential gene expressions: An application to the osteoporosis study
Title | A bootstrap-based regression method for comprehensive discovery of differential gene expressions: An application to the osteoporosis study |
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Authors | |
Keywords | Bootstrap Microarray Osteoporosis Regression |
Issue Date | 2011 |
Publisher | Elsevier France, Editions Scientifiques et Medicales. The Journal's web site is located at http://www.elsevier.com/locate/ejmg |
Citation | European Journal Of Medical Genetics, 2011, v. 54 n. 6, p. e560-e564 How to Cite? |
Abstract | A common purpose of microarray experiments is to study the variation in gene expression across the categories of an experimental factor such as tissue types and drug treatments. However, it is not uncommon that the studied experimental factor is a quantitative variable rather than categorical variable. Loss of information would occur by comparing gene-expression levels between groups that are factitiously defined according to the quantitative threshold values of an experimental factor. Additionally, lack of control for some sensitive clinical factors may bring serious false positive or negative findings.In the present study, we described a bootstrap-based regression method for analyzing gene-expression data from the non-categorical microarray experiments. To illustrate the utility of this method, we applied it to our recent gene-expression study of circulating monocytes in subjects with a wide range of variations in bone mineral density (BMD). This method allows a comprehensive discovery of gene expressions associated with osteoporosis-related traits while controlling other common confounding factors such as height, weight and age. Several genes identified in our study are involved in osteoblast and osteoclast functions and bone remodeling and/or menopause-associated estrogen-dependent pathways, which provide important clues to understand the etiology of osteoporosis. Availability: SAS code is available from the authors upon request. © 2011 Elsevier Masson SAS. |
Persistent Identifier | http://hdl.handle.net/10722/140927 |
ISSN | 2023 Impact Factor: 1.6 2023 SCImago Journal Rankings: 0.666 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Lu, Y | en_HK |
dc.contributor.author | Liu, YZ | en_HK |
dc.contributor.author | Liu, PY | en_HK |
dc.contributor.author | Dvornyk, V | en_HK |
dc.contributor.author | Deng, HW | en_HK |
dc.date.accessioned | 2011-09-23T06:21:30Z | - |
dc.date.available | 2011-09-23T06:21:30Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | European Journal Of Medical Genetics, 2011, v. 54 n. 6, p. e560-e564 | en_HK |
dc.identifier.issn | 1769-7212 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/140927 | - |
dc.description.abstract | A common purpose of microarray experiments is to study the variation in gene expression across the categories of an experimental factor such as tissue types and drug treatments. However, it is not uncommon that the studied experimental factor is a quantitative variable rather than categorical variable. Loss of information would occur by comparing gene-expression levels between groups that are factitiously defined according to the quantitative threshold values of an experimental factor. Additionally, lack of control for some sensitive clinical factors may bring serious false positive or negative findings.In the present study, we described a bootstrap-based regression method for analyzing gene-expression data from the non-categorical microarray experiments. To illustrate the utility of this method, we applied it to our recent gene-expression study of circulating monocytes in subjects with a wide range of variations in bone mineral density (BMD). This method allows a comprehensive discovery of gene expressions associated with osteoporosis-related traits while controlling other common confounding factors such as height, weight and age. Several genes identified in our study are involved in osteoblast and osteoclast functions and bone remodeling and/or menopause-associated estrogen-dependent pathways, which provide important clues to understand the etiology of osteoporosis. Availability: SAS code is available from the authors upon request. © 2011 Elsevier Masson SAS. | en_HK |
dc.language | eng | en_US |
dc.publisher | Elsevier France, Editions Scientifiques et Medicales. The Journal's web site is located at http://www.elsevier.com/locate/ejmg | en_HK |
dc.relation.ispartof | European Journal of Medical Genetics | en_HK |
dc.rights | NOTICE: this is the author’s version of a work that was accepted for publication in European Journal of Medical Genetics. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in European Journal of Medical Genetics, 2011, v. 54 n. 6, p. e560-e564. DOI: 10.1016/j.ejmg.2011.07.002 | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Bootstrap | en_HK |
dc.subject | Microarray | en_HK |
dc.subject | Osteoporosis | en_HK |
dc.subject | Regression | en_HK |
dc.subject.mesh | Bone Density - genetics | - |
dc.subject.mesh | Bone Remodeling - genetics | - |
dc.subject.mesh | Gene Expression Profiling - methods - statistics and numerical data | - |
dc.subject.mesh | Menopause - genetics - metabolism | - |
dc.subject.mesh | Osteoporosis - genetics - metabolism | - |
dc.title | A bootstrap-based regression method for comprehensive discovery of differential gene expressions: An application to the osteoporosis study | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Dvornyk, V: dvornyk@hku.hk | en_HK |
dc.identifier.authority | Dvornyk, V=rp00693 | en_HK |
dc.description.nature | postprint | - |
dc.identifier.doi | 10.1016/j.ejmg.2011.07.002 | en_HK |
dc.identifier.pmid | 21843665 | - |
dc.identifier.scopus | eid_2-s2.0-80052287771 | en_HK |
dc.identifier.hkuros | 195105 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-80052287771&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 54 | en_HK |
dc.identifier.issue | 6 | en_HK |
dc.identifier.spage | e560 | en_HK |
dc.identifier.epage | e564 | en_HK |
dc.identifier.isi | WOS:000307537100006 | - |
dc.publisher.place | France | en_HK |
dc.identifier.scopusauthorid | Lu, Y=36019236400 | en_HK |
dc.identifier.scopusauthorid | Liu, YZ=36007508500 | en_HK |
dc.identifier.scopusauthorid | Liu, PY=7404618030 | en_HK |
dc.identifier.scopusauthorid | Dvornyk, V=6701789786 | en_HK |
dc.identifier.scopusauthorid | Deng, HW=7401775190 | en_HK |
dc.identifier.issnl | 1769-7212 | - |