omniCLIP: probabilistic identification of protein-RNA interactions from CLIP-seq data

Abstract CLIP-seq methods allow the generation of genome-wide maps of RNA binding protein – RNA interaction sites. However, due to differences between different CLIP-seq assays, existing computational approaches to analyze the data can only be applied to a subset of assays. Here, we present a probab...

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Main Authors: Philipp Drewe-Boss, Hans-Hermann Wessels, Uwe Ohler
Format: Article
Language:English
Published: BMC 2018-11-01
Series:Genome Biology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13059-018-1521-2
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author Philipp Drewe-Boss
Hans-Hermann Wessels
Uwe Ohler
author_facet Philipp Drewe-Boss
Hans-Hermann Wessels
Uwe Ohler
author_sort Philipp Drewe-Boss
collection DOAJ
description Abstract CLIP-seq methods allow the generation of genome-wide maps of RNA binding protein – RNA interaction sites. However, due to differences between different CLIP-seq assays, existing computational approaches to analyze the data can only be applied to a subset of assays. Here, we present a probabilistic model called omniCLIP that can detect regulatory elements in RNAs from data of all CLIP-seq assays. omniCLIP jointly models data across replicates and can integrate background information. Therefore, omniCLIP greatly simplifies the data analysis, increases the reliability of results and paves the way for integrative studies based on data from different assays.
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spelling doaj.art-fed1e40fc1db4685a5d9f0ac304a5a1a2022-12-21T18:19:03ZengBMCGenome Biology1474-760X2018-11-0119111410.1186/s13059-018-1521-2omniCLIP: probabilistic identification of protein-RNA interactions from CLIP-seq dataPhilipp Drewe-Boss0Hans-Hermann Wessels1Uwe Ohler2Berlin Institute for Medical Systems Biology, Max Delbrück Center for Molecular Medicine in the Helmholtz AssociationBerlin Institute for Medical Systems Biology, Max Delbrück Center for Molecular Medicine in the Helmholtz AssociationBerlin Institute for Medical Systems Biology, Max Delbrück Center for Molecular Medicine in the Helmholtz AssociationAbstract CLIP-seq methods allow the generation of genome-wide maps of RNA binding protein – RNA interaction sites. However, due to differences between different CLIP-seq assays, existing computational approaches to analyze the data can only be applied to a subset of assays. Here, we present a probabilistic model called omniCLIP that can detect regulatory elements in RNAs from data of all CLIP-seq assays. omniCLIP jointly models data across replicates and can integrate background information. Therefore, omniCLIP greatly simplifies the data analysis, increases the reliability of results and paves the way for integrative studies based on data from different assays.http://link.springer.com/article/10.1186/s13059-018-1521-2Machine learningBioinformaticsProtein-RNA interactionsCLIP-seqeCLIPiCLIP
spellingShingle Philipp Drewe-Boss
Hans-Hermann Wessels
Uwe Ohler
omniCLIP: probabilistic identification of protein-RNA interactions from CLIP-seq data
Genome Biology
Machine learning
Bioinformatics
Protein-RNA interactions
CLIP-seq
eCLIP
iCLIP
title omniCLIP: probabilistic identification of protein-RNA interactions from CLIP-seq data
title_full omniCLIP: probabilistic identification of protein-RNA interactions from CLIP-seq data
title_fullStr omniCLIP: probabilistic identification of protein-RNA interactions from CLIP-seq data
title_full_unstemmed omniCLIP: probabilistic identification of protein-RNA interactions from CLIP-seq data
title_short omniCLIP: probabilistic identification of protein-RNA interactions from CLIP-seq data
title_sort omniclip probabilistic identification of protein rna interactions from clip seq data
topic Machine learning
Bioinformatics
Protein-RNA interactions
CLIP-seq
eCLIP
iCLIP
url http://link.springer.com/article/10.1186/s13059-018-1521-2
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AT uweohler omniclipprobabilisticidentificationofproteinrnainteractionsfromclipseqdata