Detection theory in identification of RNA-DNA sequence differences using RNA-sequencing.

Advances in sequencing technology have allowed for detailed analyses of the transcriptome at single-nucleotide resolution, facilitating the study of RNA editing or sequence differences between RNA and DNA genome-wide. In humans, two types of post-transcriptional RNA editing processes are known to oc...

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Main Authors: Jonathan M Toung, Nicholas Lahens, John B Hogenesch, Gregory Grant
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4232354?pdf=render
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author Jonathan M Toung
Nicholas Lahens
John B Hogenesch
Gregory Grant
author_facet Jonathan M Toung
Nicholas Lahens
John B Hogenesch
Gregory Grant
author_sort Jonathan M Toung
collection DOAJ
description Advances in sequencing technology have allowed for detailed analyses of the transcriptome at single-nucleotide resolution, facilitating the study of RNA editing or sequence differences between RNA and DNA genome-wide. In humans, two types of post-transcriptional RNA editing processes are known to occur: A-to-I deamination by ADAR and C-to-U deamination by APOBEC1. In addition to these sequence differences, researchers have reported the existence of all 12 types of RNA-DNA sequence differences (RDDs); however, the validity of these claims is debated, as many studies claim that technical artifacts account for the majority of these non-canonical sequence differences. In this study, we used a detection theory approach to evaluate the performance of RNA-Sequencing (RNA-Seq) and associated aligners in accurately identifying RNA-DNA sequence differences. By generating simulated RNA-Seq datasets containing RDDs, we assessed the effect of alignment artifacts and sequencing error on the sensitivity and false discovery rate of RDD detection. Overall, we found that even in the presence of sequencing errors, false negative and false discovery rates of RDD detection can be contained below 10% with relatively lenient thresholds. We also assessed the ability of various filters to target false positive RDDs and found them to be effective in discriminating between true and false positives. Lastly, we used the optimal thresholds we identified from our simulated analyses to identify RDDs in a human lymphoblastoid cell line. We found approximately 6,000 RDDs, the majority of which are A-to-G edits and likely to be mediated by ADAR. Moreover, we found the majority of non A-to-G RDDs to be associated with poorer alignments and conclude from these results that the evidence for widespread non-canonical RDDs in humans is weak. Overall, we found RNA-Seq to be a powerful technique for surveying RDDs genome-wide when coupled with the appropriate thresholds and filters.
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spelling doaj.art-635848d3879d4cebae4e6153c080d1862022-12-22T00:13:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01911e11204010.1371/journal.pone.0112040Detection theory in identification of RNA-DNA sequence differences using RNA-sequencing.Jonathan M ToungNicholas LahensJohn B HogeneschGregory GrantAdvances in sequencing technology have allowed for detailed analyses of the transcriptome at single-nucleotide resolution, facilitating the study of RNA editing or sequence differences between RNA and DNA genome-wide. In humans, two types of post-transcriptional RNA editing processes are known to occur: A-to-I deamination by ADAR and C-to-U deamination by APOBEC1. In addition to these sequence differences, researchers have reported the existence of all 12 types of RNA-DNA sequence differences (RDDs); however, the validity of these claims is debated, as many studies claim that technical artifacts account for the majority of these non-canonical sequence differences. In this study, we used a detection theory approach to evaluate the performance of RNA-Sequencing (RNA-Seq) and associated aligners in accurately identifying RNA-DNA sequence differences. By generating simulated RNA-Seq datasets containing RDDs, we assessed the effect of alignment artifacts and sequencing error on the sensitivity and false discovery rate of RDD detection. Overall, we found that even in the presence of sequencing errors, false negative and false discovery rates of RDD detection can be contained below 10% with relatively lenient thresholds. We also assessed the ability of various filters to target false positive RDDs and found them to be effective in discriminating between true and false positives. Lastly, we used the optimal thresholds we identified from our simulated analyses to identify RDDs in a human lymphoblastoid cell line. We found approximately 6,000 RDDs, the majority of which are A-to-G edits and likely to be mediated by ADAR. Moreover, we found the majority of non A-to-G RDDs to be associated with poorer alignments and conclude from these results that the evidence for widespread non-canonical RDDs in humans is weak. Overall, we found RNA-Seq to be a powerful technique for surveying RDDs genome-wide when coupled with the appropriate thresholds and filters.http://europepmc.org/articles/PMC4232354?pdf=render
spellingShingle Jonathan M Toung
Nicholas Lahens
John B Hogenesch
Gregory Grant
Detection theory in identification of RNA-DNA sequence differences using RNA-sequencing.
PLoS ONE
title Detection theory in identification of RNA-DNA sequence differences using RNA-sequencing.
title_full Detection theory in identification of RNA-DNA sequence differences using RNA-sequencing.
title_fullStr Detection theory in identification of RNA-DNA sequence differences using RNA-sequencing.
title_full_unstemmed Detection theory in identification of RNA-DNA sequence differences using RNA-sequencing.
title_short Detection theory in identification of RNA-DNA sequence differences using RNA-sequencing.
title_sort detection theory in identification of rna dna sequence differences using rna sequencing
url http://europepmc.org/articles/PMC4232354?pdf=render
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