dc.contributor.author
Rudolf, Henrik
dc.contributor.author
Nuernberg, Gerd
dc.contributor.author
Koczan, Dirk
dc.contributor.author
Vanselow, Jens
dc.contributor.author
Gempe, Tanja
dc.contributor.author
Beye, Martin
dc.contributor.author
Leboulle, Gérard
dc.contributor.author
Bienefeld, Kaspar
dc.contributor.author
Reinsch, Norbert
dc.date.accessioned
2018-06-08T07:15:56Z
dc.date.available
2016-01-04T12:51:58.607Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/17522
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-21406
dc.description.abstract
Background Pooled samples are frequently used in experiments measuring gene
expression. In this method, RNA from different individuals sharing the same
experimental conditions and explanatory variables is blended and their
concentrations are jointly measured. As a matter of principle, individuals are
represented in equal shares in each pool. However, some degree of
disproportionality may arise from the limits of technical precision. As a
consequence a special kind of technical error occurs, which can be modelled by
a respective variance component. Previously published theory - allowing for
variable pool sizes - has been applied to four microarray gene expression data
sets from different species in order to assess the practical relevance of this
type of technical error in terms of significance and size of this variance
component. Results The number of transcripts with a significant variance
component due to imperfect blending was found to be 4329 (23 %) in mouse data
and 7093 (49 %) in honey bees, but only 6 in rats and none whatsoever in human
data. These results correspond to a false discovery rate of 5 % in each data
set. The number of transcripts found to be differentially expressed between
treatments was always higher when the blending error variance was neglected.
Simulations clearly indicated overly-optimistic (anti-conservative) test
results in terms of false discovery rates whenever this source of variability
was not represented in the model. Conclusions Imperfect equality of shares
when blending RNA from different individuals into joint pools of variable size
is a source of technical variation with relevance for experimental design,
practice at the laboratory bench and data analysis. Its potentially adverse
effects, incorrect identification of differentially expressed transcripts and
overly-optimistic significance tests, can be fully avoided, however, by the
sound application of recently established theory and models for data analysis.
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie
dc.title
On the relevance of technical variation due to building pools in microarray
experiments
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
BMC Genomics. - 16 (2015), Artikel Nr. 1027
dcterms.bibliographicCitation.doi
10.1186/s12864-015-2055-6
dcterms.bibliographicCitation.url
http://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-015-2055-6
refubium.affiliation
Biologie, Chemie, Pharmazie
de
refubium.mycore.fudocsId
FUDOCS_document_000000023658
refubium.note.author
Der Artikel wurde in einer Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000005807
dcterms.accessRights.openaire
open access