Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Florence Ruffle"'
Autor:
Sébastien Riquier, Marc Mathieu, Chloé Bessiere, Anthony Boureux, Florence Ruffle, Jean-Marc Lemaitre, Farida Djouad, Nicolas Gilbert, Thérèse Commes
Publikováno v:
BMC Genomics, Vol 22, Iss 1, Pp 1-23 (2021)
Abstract Background The development of RNA sequencing (RNAseq) and the corresponding emergence of public datasets have created new avenues of transcriptional marker search. The long non-coding RNAs (lncRNAs) constitute an emerging class of transcript
Externí odkaz:
https://doaj.org/article/79f676ccc29a4141b7bbf021d7f1cf0c
Autor:
Chloé Bessière, Haoliang Xue, Benoit Guibert, Anthony Boureux, Florence Rufflé, Julien Viot, Rayan Chikhi, Mikaël Salson, Camille Marchet, Thérèse Commes, Daniel Gautheret
Publikováno v:
Genome Biology, Vol 25, Iss 1, Pp 1-16 (2024)
Abstract Indexing techniques relying on k-mers have proven effective in searching for RNA sequences across thousands of RNA-seq libraries, but without enabling direct RNA quantification. We show here that arbitrary RNA sequences can be quantified in
Externí odkaz:
https://doaj.org/article/a609a092c730485c832b8c973417638f
Autor:
Raíssa Silva, Cédric Riedel, Benoit Guibert, Florence Ruffle, Anthony Boureux, Thérèse Commes
MotivationAcute Myeloid Leukemia is a highly heterogeneous disease. Although current classifications are well-known and widely adopted, many patients experience drug resistance and disease relapse. New biomarkers are needed to make classifications mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec35f0450e980f992c249acaf096d9b8
https://doi.org/10.1101/2023.01.31.23285241
https://doi.org/10.1101/2023.01.31.23285241
Autor:
Anthony Boureux, Chloé Bessière, Marc Mathieu, Farida Djouad, Nicolas Gilbert, Sébastien Riquier, Jean-Marc Lemaitre, Thérèse Commes, Florence Ruffle
Publikováno v:
BMC Genomics
BMC Genomics, BioMed Central, 2021, 22 (1), pp.412. ⟨10.1186/s12864-020-07289-0⟩
BMC Genomics, Vol 22, Iss 1, Pp 1-23 (2021)
BMC Genomics, BioMed Central, 2021, 22 (1), pp.412. ⟨10.1186/s12864-020-07289-0⟩
BMC Genomics, Vol 22, Iss 1, Pp 1-23 (2021)
Background The development of RNA sequencing (RNAseq) and the corresponding emergence of public datasets have created new avenues of transcriptional marker search. The long non-coding RNAs (lncRNAs) constitute an emerging class of transcripts with a
Autor:
Nicolas Gilbert, Thérèse Commes, Chloé Bessière, Anthony Boureux, Jérôme Audoux, Haoliang Xue, Benoit Guibert, Florence Ruffle, Sébastien Riquier, Anne-Laure Bougé, Daniel Gautheret
Publikováno v:
NAR Genomics and Bioinformatics
NAR Genomics and Bioinformatics, 2021, 3 (3), pp.lqab058. ⟨10.1093/nargab/lqab058⟩
NAR Genomics and Bioinformatics, 2021, 3 (3), pp.lqab058. ⟨10.1093/nargab/lqab058⟩
The huge body of publicly available RNA-sequencing (RNA-seq) libraries is a treasure of functional information allowing to quantify the expression of known or novel transcripts in tissues. However, transcript quantification commonly relies on alignme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c935fe62978966279f7f43f48e90b3b
https://doi.org/10.1101/2021.05.20.444982
https://doi.org/10.1101/2021.05.20.444982
Autor:
Sébastien, Riquier, Chloé, Bessiere, Benoit, Guibert, Anne-Laure, Bouge, Anthony, Boureux, Florence, Ruffle, Jérôme, Audoux, Nicolas, Gilbert, Haoliang, Xue, Daniel, Gautheret, Thérèse, Commes
Publikováno v:
NAR Genomics and Bioinformatics
The huge body of publicly available RNA-sequencing (RNA-seq) libraries is a treasure of functional information allowing to quantify the expression of known or novel transcripts in tissues. However, transcript quantification commonly relies on alignme
Autor:
Jean-Marc Lemaitre, Nicolas Gilbert, Marc Mathieu, Sébastien Riquier, Anthony Boureux, Florence Ruffle, Farida Djouad, Thérèse Commes
The development of RNA sequencing (RNAseq) and corresponding emergence of public datasets have created new avenues of transcriptional marker search. The long non-coding RNAs (lncRNAs) constitute an emerging class of transcripts with a potential for h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c48d62f082ef9774e342c75de9696b51
Autor:
Anne-Laure Bougé, Florence Ruffle, Benoit Guibert, Thérèse Commes, Sébastien Riquier, Jérôme Audoux
Publikováno v:
Chromothripsis-Methods and Protocols
Franck Pellestor. Chromothripsis-Methods and Protocols, Humana Press, New York, NY-, pp.133-156, 2018, Hardcover ISBN 978-1-4939-7779-6 ; Softcover ISBN 978-1-4939-9283-6 ; eBook ISBN 978-1-4939-7780-2. ⟨10.1007/978-1-4939-7780-2_9⟩
Methods in Molecular Biology ISBN: 9781493977796
Franck Pellestor. Chromothripsis-Methods and Protocols, Humana Press, New York, NY-, pp.133-156, 2018, Hardcover ISBN 978-1-4939-7779-6 ; Softcover ISBN 978-1-4939-9283-6 ; eBook ISBN 978-1-4939-7780-2. ⟨10.1007/978-1-4939-7780-2_9⟩
Methods in Molecular Biology ISBN: 9781493977796
International audience; RNA-Seq approach enables the detection and characterization of fusion or chimeric transcript associated to complex genome rearrangement. Until now, these events are classically identified at DNA level.Here we describe a comple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77a116eaeed173ca38564e9e0a66a7b7
https://hal.umontpellier.fr/hal-02503709
https://hal.umontpellier.fr/hal-02503709
Autor:
Anne Laure Bougé, Anthony Boureux, Sacha Beaumeunier, Sébastien Riquier, Jean-Baptiste Gaillard, Nicolas Gilbert, Jean-Marc Lemaitre, Nicolas Philippe, Jérôme Audoux, Andre Megarbane, Delphine Bacq-Daian, Ronnie Alves, Christine Chomienne, Thérèse Commes, Florence Ruffle, Elias Bou Samra, Bruno Cassinat
Publikováno v:
F1000Research
F1000Research, Faculty of 1000, 2017, 6, ⟨10.12688/f1000research.11352.2⟩
F1000Research, 2017, 6, ⟨10.12688/f1000research.11352.2⟩
F1000Research, Faculty of 1000, 2017, 6, ⟨10.12688/f1000research.11352.2⟩
F1000Research, 2017, 6, ⟨10.12688/f1000research.11352.2⟩
Background: High-throughput next generation sequencing (NGS) technologies enable the detection of biomarkers used for tumor classification, disease monitoring and cancer therapy. Whole-transcriptome analysis using RNA-seq is important, not only as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45b61a4d7351cfdf0a374c667af2da3f
https://hal.umontpellier.fr/hal-01840091/document
https://hal.umontpellier.fr/hal-01840091/document
Autor:
Ronnie Alves, Anthony Boureux, Thérèse Commes, Sacha Beaumeunier, Jérôme Audoux, Florence Ruffle, Nicolas Philippe
Publikováno v:
BioData Mining
BioData Mining, BioMed Central, 2016, 9 (1), pp.34. ⟨10.1186/s13040-016-0112-6⟩
BioData Mining, 2016, 9 (1), pp.34. ⟨10.1186/s13040-016-0112-6⟩
BioData Mining, BioMed Central, 2016, 9 (1), pp.34. ⟨10.1186/s13040-016-0112-6⟩
BioData Mining, 2016, 9 (1), pp.34. ⟨10.1186/s13040-016-0112-6⟩
Background High-throughput sequencing technology and bioinformatics have identified chimeric RNAs (chRNAs), raising the possibility of chRNAs expressing particularly in diseases can be used as potential biomarkers in both diagnosis and prognosis. Res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62379a3440186c4c24e44e1899dee7a9
https://www.hal.inserm.fr/inserm-01390470/document
https://www.hal.inserm.fr/inserm-01390470/document