DE-kupl: exhaustive capture of biological variation in RNA-seq data through k-mer decomposition.
Identifieur interne : 000D47 ( PubMed/Checkpoint ); précédent : 000D46; suivant : 000D48DE-kupl: exhaustive capture of biological variation in RNA-seq data through k-mer decomposition.
Auteurs : Jérôme Audoux [France] ; Nicolas Philippe [France] ; Rayan Chikhi [France] ; Mikaël Salson [France] ; Mélina Gallopin [France] ; Marc Gabriel [France] ; Jérémy Le Coz [France] ; Emilie Drouineau [France] ; Thérèse Commes [France] ; Daniel Gautheret [France]Source :
- Genome biology [ 1474-760X ] ; 2017.
Descripteurs français
- KwdFr :
- ARN (génétique), ARN antisens, ARN long non codant (génétique), ARN messager (génétique), Allèles, Analyse de profil d'expression de gènes, Analyse de séquence d'ARN, Biologie informatique (), Humains, Logiciel, Polyadénylation, Reproductibilité des résultats, Régulation de l'expression des gènes, Séquençage nucléotidique à haut débit, Transcriptome, Variation génétique, Épissage des ARN.
- MESH :
- génétique : ARN, ARN long non codant, ARN messager.
- ARN antisens, Allèles, Analyse de profil d'expression de gènes, Analyse de séquence d'ARN, Biologie informatique, Humains, Logiciel, Polyadénylation, Reproductibilité des résultats, Régulation de l'expression des gènes, Séquençage nucléotidique à haut débit, Transcriptome, Variation génétique, Épissage des ARN.
English descriptors
- KwdEn :
- Alleles, Computational Biology (methods), Gene Expression Profiling, Gene Expression Regulation, Genetic Variation, High-Throughput Nucleotide Sequencing, Humans, Polyadenylation, RNA (genetics), RNA Splicing, RNA, Antisense, RNA, Long Noncoding (genetics), RNA, Messenger (genetics), Reproducibility of Results, Sequence Analysis, RNA, Software, Transcriptome.
- MESH :
- chemical , genetics : RNA, RNA, Long Noncoding, RNA, Messenger.
- methods : Computational Biology.
- Alleles, Gene Expression Profiling, Gene Expression Regulation, Genetic Variation, High-Throughput Nucleotide Sequencing, Humans, Polyadenylation, RNA Splicing, RNA, Antisense, Reproducibility of Results, Sequence Analysis, RNA, Software, Transcriptome.
Abstract
We introduce a k-mer-based computational protocol, DE-kupl, for capturing local RNA variation in a set of RNA-seq libraries, independently of a reference genome or transcriptome. DE-kupl extracts all k-mers with differential abundance directly from the raw data files. This enables the retrieval of virtually all variation present in an RNA-seq data set. This variation is subsequently assigned to biological events or entities such as differential long non-coding RNAs, splice and polyadenylation variants, introns, repeats, editing or mutation events, and exogenous RNA. Applying DE-kupl to human RNA-seq data sets identified multiple types of novel events, reproducibly across independent RNA-seq experiments.
DOI: 10.1186/s13059-017-1372-2
PubMed: 29284518
Affiliations:
- France
- Hauts-de-France, Languedoc-Roussillon, Nord-Pas-de-Calais, Occitanie (région administrative), Île-de-France
- Gif-sur-Yvette, Lille, Montpellier
- Université Paris-Sud
Links toward previous steps (curation, corpus...)
Links to Exploration step
pubmed:29284518Le document en format XML
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<front><div type="abstract" xml:lang="en">We introduce a k-mer-based computational protocol, DE-kupl, for capturing local RNA variation in a set of RNA-seq libraries, independently of a reference genome or transcriptome. DE-kupl extracts all k-mers with differential abundance directly from the raw data files. This enables the retrieval of virtually all variation present in an RNA-seq data set. This variation is subsequently assigned to biological events or entities such as differential long non-coding RNAs, splice and polyadenylation variants, introns, repeats, editing or mutation events, and exogenous RNA. Applying DE-kupl to human RNA-seq data sets identified multiple types of novel events, reproducibly across independent RNA-seq experiments.</div>
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<Abstract><AbstractText>We introduce a k-mer-based computational protocol, DE-kupl, for capturing local RNA variation in a set of RNA-seq libraries, independently of a reference genome or transcriptome. DE-kupl extracts all k-mers with differential abundance directly from the raw data files. This enables the retrieval of virtually all variation present in an RNA-seq data set. This variation is subsequently assigned to biological events or entities such as differential long non-coding RNAs, splice and polyadenylation variants, introns, repeats, editing or mutation events, and exogenous RNA. Applying DE-kupl to human RNA-seq data sets identified multiple types of novel events, reproducibly across independent RNA-seq experiments.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Audoux</LastName>
<ForeName>Jérôme</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>INSERM U1183 IRMB, Université de Montpellier, Hopital St Eloi, 80 avenue Augustin Fliche, Montpellier, 34295, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Philippe</LastName>
<ForeName>Nicolas</ForeName>
<Initials>N</Initials>
<AffiliationInfo><Affiliation>Institut de Biologie Computationnelle, Université Montpellier, Montpellier, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>SeqOne, IRMB, CHRU de Montpellier, Hopital St Eloi, Montpellier, France.</Affiliation>
</AffiliationInfo>
</Author>
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<ForeName>Rayan</ForeName>
<Initials>R</Initials>
<AffiliationInfo><Affiliation>Univ. Lille, CNRS, Inria, UMR 9189 - CRIStAL - F-59000, Lille, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Salson</LastName>
<ForeName>Mikaël</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Univ. Lille, CNRS, Inria, UMR 9189 - CRIStAL - F-59000, Lille, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Gallopin</LastName>
<ForeName>Mélina</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Institute for Integrative Biology of the Cell, CEA, CNRS, Université Paris-Sud, Université Paris Saclay, Gif sur Yvette, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Gabriel</LastName>
<ForeName>Marc</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Institute for Integrative Biology of the Cell, CEA, CNRS, Université Paris-Sud, Université Paris Saclay, Gif sur Yvette, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Institut de Cancérologie Gustave Roussy Cancer Campus (GRCC), AMMICA, INSERM US23/CNRS UMS3655, Villejuif, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Le Coz</LastName>
<ForeName>Jérémy</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Institute for Integrative Biology of the Cell, CEA, CNRS, Université Paris-Sud, Université Paris Saclay, Gif sur Yvette, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Drouineau</LastName>
<ForeName>Emilie</ForeName>
<Initials>E</Initials>
<AffiliationInfo><Affiliation>Institute for Integrative Biology of the Cell, CEA, CNRS, Université Paris-Sud, Université Paris Saclay, Gif sur Yvette, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Commes</LastName>
<ForeName>Thérèse</ForeName>
<Initials>T</Initials>
<AffiliationInfo><Affiliation>INSERM U1183 IRMB, Université de Montpellier, Hopital St Eloi, 80 avenue Augustin Fliche, Montpellier, 34295, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Institut de Biologie Computationnelle, Université Montpellier, Montpellier, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Gautheret</LastName>
<ForeName>Daniel</ForeName>
<Initials>D</Initials>
<Identifier Source="ORCID">0000-0002-1508-8469</Identifier>
<AffiliationInfo><Affiliation>Institute for Integrative Biology of the Cell, CEA, CNRS, Université Paris-Sud, Université Paris Saclay, Gif sur Yvette, France. daniel.gautheret@u-psud.fr.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Institut de Cancérologie Gustave Roussy Cancer Campus (GRCC), AMMICA, INSERM US23/CNRS UMS3655, Villejuif, France. daniel.gautheret@u-psud.fr.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>#bio2014-04</GrantID>
<Agency>Plan Cancer - Systems Biology</Agency>
<Country>International</Country>
</Grant>
<Grant><GrantID>ANR-10-INBS-0009 (France Génomique)</GrantID>
<Agency>ANR (France)</Agency>
<Country>International</Country>
</Grant>
</GrantList>
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<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2017</Year>
<Month>12</Month>
<Day>28</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>England</Country>
<MedlineTA>Genome Biol</MedlineTA>
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<ISSNLinking>1474-7596</ISSNLinking>
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<NameOfSubstance UI="D016372">RNA, Antisense</NameOfSubstance>
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<MeshHeading><DescriptorName UI="D005786" MajorTopicYN="N">Gene Expression Regulation</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014644" MajorTopicYN="Y">Genetic Variation</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D059014" MajorTopicYN="N">High-Throughput Nucleotide Sequencing</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D026723" MajorTopicYN="N">Polyadenylation</DescriptorName>
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<region><li>Hauts-de-France</li>
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