A method for detecting long non-coding RNAs with tiled RNA expression microarrays.

Long non-coding ribonucleic acids (lncRNAs) have been proposed as biomarkers in prostate cancer. This paper proposes a selection method which uses data from tiled microarrays to identify relatively long regions of moderate expression independent of the microarray platform and probe design. The metho...

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Main Authors: Sigrun Helga Lund, Daniel Fannar Gudbjartsson, Thorunn Rafnar, Asgeir Sigurdsson, Sigurjon Axel Gudjonsson, Julius Gudmundsson, Kari Stefansson, Gunnar Stefansson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24937006/?tool=EBI
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spelling doaj-bb755d99fe6e462c9c016cdb49384e6c2021-03-04T11:50:15ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0196e9989910.1371/journal.pone.0099899A method for detecting long non-coding RNAs with tiled RNA expression microarrays.Sigrun Helga LundDaniel Fannar GudbjartssonThorunn RafnarAsgeir SigurdssonSigurjon Axel GudjonssonJulius GudmundssonKari StefanssonGunnar StefanssonLong non-coding ribonucleic acids (lncRNAs) have been proposed as biomarkers in prostate cancer. This paper proposes a selection method which uses data from tiled microarrays to identify relatively long regions of moderate expression independent of the microarray platform and probe design. The method is used to search for candidate long non-coding ribonucleic acids (lncRNAs) at locus 8q24 and is run on three independent experiments which all use samples from prostate cancer patients. The robustness of the method is tested by utilizing repeated copies of tiled probes. The method shows high consistency between experiments that used the same samples, but different probe layout. There also is statistically significant consistency when comparing experiments with different samples. The method selected the long non-coding ribonucleic acid PCNCR1 in all three experiments.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24937006/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Sigrun Helga Lund
Daniel Fannar Gudbjartsson
Thorunn Rafnar
Asgeir Sigurdsson
Sigurjon Axel Gudjonsson
Julius Gudmundsson
Kari Stefansson
Gunnar Stefansson
spellingShingle Sigrun Helga Lund
Daniel Fannar Gudbjartsson
Thorunn Rafnar
Asgeir Sigurdsson
Sigurjon Axel Gudjonsson
Julius Gudmundsson
Kari Stefansson
Gunnar Stefansson
A method for detecting long non-coding RNAs with tiled RNA expression microarrays.
PLoS ONE
author_facet Sigrun Helga Lund
Daniel Fannar Gudbjartsson
Thorunn Rafnar
Asgeir Sigurdsson
Sigurjon Axel Gudjonsson
Julius Gudmundsson
Kari Stefansson
Gunnar Stefansson
author_sort Sigrun Helga Lund
title A method for detecting long non-coding RNAs with tiled RNA expression microarrays.
title_short A method for detecting long non-coding RNAs with tiled RNA expression microarrays.
title_full A method for detecting long non-coding RNAs with tiled RNA expression microarrays.
title_fullStr A method for detecting long non-coding RNAs with tiled RNA expression microarrays.
title_full_unstemmed A method for detecting long non-coding RNAs with tiled RNA expression microarrays.
title_sort method for detecting long non-coding rnas with tiled rna expression microarrays.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Long non-coding ribonucleic acids (lncRNAs) have been proposed as biomarkers in prostate cancer. This paper proposes a selection method which uses data from tiled microarrays to identify relatively long regions of moderate expression independent of the microarray platform and probe design. The method is used to search for candidate long non-coding ribonucleic acids (lncRNAs) at locus 8q24 and is run on three independent experiments which all use samples from prostate cancer patients. The robustness of the method is tested by utilizing repeated copies of tiled probes. The method shows high consistency between experiments that used the same samples, but different probe layout. There also is statistically significant consistency when comparing experiments with different samples. The method selected the long non-coding ribonucleic acid PCNCR1 in all three experiments.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24937006/?tool=EBI
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