Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/19660
Full metadata record
DC FieldValueLanguage
dc.contributor.authorBIGIRUMURAME, Theophile-
dc.contributor.authorPERUALILA, Nolen Joy-
dc.contributor.authorSHKEDY, Ziv-
dc.contributor.authorKASIM, Adetayo-
dc.date.accessioned2015-10-05T13:32:56Z-
dc.date.available2015-10-05T13:32:56Z-
dc.date.issued2014-
dc.identifier.citationNon Clinical Statistics 2014, Brugge, Belgium, October 8-10, 2014-
dc.identifier.urihttp://hdl.handle.net/1942/19660-
dc.description.abstractNowadays, microarray technology is extensively used in biological and medical studies to monitor simultaneously the activity of thousands genes and their response to a certain treatment. In some experiment, in addition to gene expression, some responses are available and the question of interest is to identify whether or not the gene expressions can serve as biomarkers, and perhaps, as surrogate for the response. However, it is challenging to analyze the microarray data due to high dimensionality of the data and relatively small number of observations. Moreover, although the number of genes assayed is large, there may be only a small number of biomarkers that are associated with variations of the outcome. Thus, selection of genes, for which gene expression might serve as biomarker for the outcome, is needed. In our study supervised principal component analysis has been used to construct a joint biomarker. A subset of genes that are associated with the outcome is selected, and is used to build the joint biomarker.-
dc.language.isoen-
dc.subject.othersupervised principal component analysis; microarray; surrogate; leave one out ross validation-
dc.titleModeling of bioassay data and genes expression in drug discovery experiments: A supervised principal component analysis approach-
dc.typeConference Material-
local.bibliographicCitation.conferencedate2014, October 8-10-
local.bibliographicCitation.conferencenameNon Clinical Statistics 2014-
local.bibliographicCitation.conferenceplaceBrugge, Belgium-
local.bibliographicCitation.jcatC2-
dc.relation.referencesBair, E., Hastie, T., Paul, D., and Tibshirani, R. (2006). Prediction by Supervised Principal Components. Journal of the American Statistical Association, 101, 119-137 Chen, X., Wang, L., Smith, J. D., and Zhang, B. (2008). Supervised principal component analysis for gene set enrichment of microarray data with continuous or survival outcomes. Bioinformatics (Oxford, England), 24(21), 2474–81. Amaratunga, D., Cabrera, J., and Shkedy, Z.,. Exploration and Analysis of DNA Microarray and Other High-Dimensional Data, Wiley (2014).-
local.type.refereedNon-Refereed-
local.type.specifiedConference Poster-
item.fullcitationBIGIRUMURAME, Theophile; PERUALILA, Nolen Joy; SHKEDY, Ziv & KASIM, Adetayo (2014) Modeling of bioassay data and genes expression in drug discovery experiments: A supervised principal component analysis approach. In: Non Clinical Statistics 2014, Brugge, Belgium, October 8-10, 2014.-
item.contributorBIGIRUMURAME, Theophile-
item.contributorPERUALILA, Nolen Joy-
item.contributorSHKEDY, Ziv-
item.contributorKASIM, Adetayo-
item.accessRightsOpen Access-
item.fulltextWith Fulltext-
Appears in Collections:Research publications
Files in This Item:
File Description SizeFormat 
POSTER.pdfConference material210.71 kBAdobe PDFView/Open
Show simple item record

Page view(s)

24
checked on Sep 6, 2022

Download(s)

8
checked on Sep 6, 2022

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.