Calling Chromosome Alterations, DNA Methylation Statuses, and Mutations in Tumors by Simple Targeted Next-Generation Sequencing: A Solution for Transferring Integrated Pangenomic Studies into Routine Practice?

Garinet, Simon; Néou, Mario; de La Villéon, Bruno; Faillot, Simon; Sakat, Julien; Da Fonseca, Juliana P; Jouinot, Anne; Le Tourneau, Christophe; Kamal, Maud; Luscap-Rondof, Windy; Boeva, Valentina; Gaujoux, Sebastien; Vidaud, Michel; Pasmant, Eric; Letourneur, Franck; Bertherat, Jérôme; Assié, Guillaume

Garinet, Simon; Néou, Mario; de La Villéon, Bruno; Faillot, Simon; Sakat, Julien; Da Fonseca, Juliana P; Jouinot, Anne; Le Tourneau, Christophe; Kamal, Maud; Luscap-Rondof, Windy; Boeva, Valentina; Gaujoux, Sebastien; Vidaud, Michel; Pasmant, Eric; Letourneur, Franck; Bertherat, Jérôme; Assié, Guillaume.

Affiliation

Garinet S; Institut Cochin, INSERMU1016, Centre National de la Recherche Scientifique UMR_8104, Paris, France.
Néou M; Institut Cochin, INSERMU1016, Centre National de la Recherche Scientifique UMR_8104, Paris, France.
de La Villéon B; Institut Cochin, INSERMU1016, Centre National de la Recherche Scientifique UMR_8104, Paris, France.
Faillot S; Institut Cochin, INSERMU1016, Centre National de la Recherche Scientifique UMR_8104, Paris, France.
Sakat J; Institut Cochin, INSERMU1016, Centre National de la Recherche Scientifique UMR_8104, Paris, France; Department of Digestive and Endocrine Surgery, Reference Center for Rare Adrenal Diseases, Reference Center for Rare Adrenal Cancer Network COMETE, Cochin Hospital, Assistance Publique-Hôpitaux de Par
Da Fonseca JP; Institut Cochin, INSERMU1016, Centre National de la Recherche Scientifique UMR_8104, Paris, France.
Jouinot A; Institut Cochin, INSERMU1016, Centre National de la Recherche Scientifique UMR_8104, Paris, France.
Le Tourneau C; Department of Medical Oncology, Institut Curie, Paris and Saint-Cloud, France.
Kamal M; Department of Medical Oncology, Institut Curie, Paris and Saint-Cloud, France.
Luscap-Rondof W; Institut Curie, Paris Sciences et Lettres Research University, Mines Paris Tech, INSERM, U900, F-75005, Paris, France.
Boeva V; Institut Cochin, INSERMU1016, Centre National de la Recherche Scientifique UMR_8104, Paris, France.
Gaujoux S; Institut Cochin, INSERMU1016, Centre National de la Recherche Scientifique UMR_8104, Paris, France; Department of Digestive and Endocrine Surgery, Reference Center for Rare Adrenal Diseases, Reference Center for Rare Adrenal Cancer Network COMETE, Cochin Hospital, Assistance Publique-Hôpitaux de Par
Vidaud M; Department of Molecular Genetics, Reference Center for Rare Adrenal Diseases, Reference Center for Rare Adrenal Cancer Network COMETE, Cochin Hospital, Assistance Publique-Hôpitaux de Paris, Paris; University of Pharmaceutic and Biologic Sciences, INSERM UMR_S745 and EA7331, Paris Descartes Universi
Pasmant E; Department of Molecular Genetics, Reference Center for Rare Adrenal Diseases, Reference Center for Rare Adrenal Cancer Network COMETE, Cochin Hospital, Assistance Publique-Hôpitaux de Paris, Paris; University of Pharmaceutic and Biologic Sciences, INSERM UMR_S745 and EA7331, Paris Descartes Universi
Letourneur F; Institut Cochin, INSERMU1016, Centre National de la Recherche Scientifique UMR_8104, Paris, France.
Bertherat J; Institut Cochin, INSERMU1016, Centre National de la Recherche Scientifique UMR_8104, Paris, France; Department of Endocrinology, Reference Center for Rare Adrenal Diseases, Reference Center for Rare Adrenal Cancer Network COMETE, Cochin Hospital, Assistance Publique-Hôpitaux de Paris, Paris.
Assié G; Institut Cochin, INSERMU1016, Centre National de la Recherche Scientifique UMR_8104, Paris, France; Department of Endocrinology, Reference Center for Rare Adrenal Diseases, Reference Center for Rare Adrenal Cancer Network COMETE, Cochin Hospital, Assistance Publique-Hôpitaux de Paris, Paris. Electro

J Mol Diagn ; 19(5): 776-787, 2017 09.

Article in En | MEDLINE | ID: mdl-28826610

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers, Tumor / Chromosome Aberrations / DNA Methylation / High-Throughput Nucleotide Sequencing / Mutation / Neoplasms Type of study: Guideline / Prognostic_studies Limits: Humans Language: En Journal: J Mol Diagn Journal subject: BIOLOGIA MOLECULAR Year: 2017 Document type: Article Affiliation country: Francia Country of publication: Estados Unidos

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