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Vincent Meyer

Showing results (21-30 of 55) with videos related to

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European Journal of Medical Genetics|July 15, 2018
LARP7 variants and further delineation of the Alazami syndrome phenotypic spectrum among primordial dwarfisms: 2 sistersMarion Imbert-Bouteille, Frédéric Tran Mau Them, Julien Thevenon, et al.
Plos One|April 6, 2018
Performance comparison of three DNA extraction kits on human whole-exome data from formalin-fixed paraffin-embedded normal and tumor samplesEric Bonnet, Marie-Laure Moutet, Céline Baulard, et al.
Plos Genetics|March 31, 2025
Parental germline mosaicism in genome-wide phased de novo variants: Recurrence risk assessment and implications for precision genetic counsellingFrançois Lecoquierre, Nathalie Drouot, Sophie Coutant, et al.
Nature Communications|November 5, 2017
Mutational signatures reveal the dynamic interplay of risk factors and cellular processes during liver tumorigenesisEric Letouzé, Jayendra Shinde, Victor Renault, et al.
Human Genetics|April 19, 2023
High diagnostic potential of short and long read genome sequencing with transcriptome analysis in exome-negative developmental disordersFrançois Lecoquierre, Olivier Quenez, Steeve Fourneaux, et al.
Journal of Medical Genetics|July 26, 2023
Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disordersKevin Riquin, Bertrand Isidor, Sandra Mercier, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|May 30, 2025
Nationwide analysis on the role of neoadjuvant radiotherapy and watch and wait in rectal cancerDavid M Mens, Robert R J Coebergh van den Braak, Denise E Hilling, et al.
Neurology|April 5, 2015
GRID2 mutations span from congenital to mild adult-onset cerebellar ataxiaMarie Coutelier, Lydie Burglen, Emeline Mundwiller, et al.
Bioinformatics (Oxford, England)|January 18, 2018
QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstructionPaul Deveau, Leo Colmet Daage, Derek Oldridge, et al.
Nature Communications|April 30, 2024
Positive selection in the genomes of two Papua New Guinean populations at distinct altitude levelsMathilde André, Nicolas Brucato, Georgi Hudjasov, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
European Journal of Medical Genetics|July 15, 2018
LARP7 variants and further delineation of the Alazami syndrome phenotypic spectrum among primordial dwarfisms: 2 sistersMarion Imbert-Bouteille, Frédéric Tran Mau Them, Julien Thevenon, et al.
Plos One|April 6, 2018
Performance comparison of three DNA extraction kits on human whole-exome data from formalin-fixed paraffin-embedded normal and tumor samplesEric Bonnet, Marie-Laure Moutet, Céline Baulard, et al.
Plos Genetics|March 31, 2025
Parental germline mosaicism in genome-wide phased de novo variants: Recurrence risk assessment and implications for precision genetic counsellingFrançois Lecoquierre, Nathalie Drouot, Sophie Coutant, et al.
Nature Communications|November 5, 2017
Mutational signatures reveal the dynamic interplay of risk factors and cellular processes during liver tumorigenesisEric Letouzé, Jayendra Shinde, Victor Renault, et al.
Human Genetics|April 19, 2023
High diagnostic potential of short and long read genome sequencing with transcriptome analysis in exome-negative developmental disordersFrançois Lecoquierre, Olivier Quenez, Steeve Fourneaux, et al.
Journal of Medical Genetics|July 26, 2023
Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disordersKevin Riquin, Bertrand Isidor, Sandra Mercier, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|May 30, 2025
Nationwide analysis on the role of neoadjuvant radiotherapy and watch and wait in rectal cancerDavid M Mens, Robert R J Coebergh van den Braak, Denise E Hilling, et al.
Neurology|April 5, 2015
GRID2 mutations span from congenital to mild adult-onset cerebellar ataxiaMarie Coutelier, Lydie Burglen, Emeline Mundwiller, et al.
Bioinformatics (Oxford, England)|January 18, 2018
QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstructionPaul Deveau, Leo Colmet Daage, Derek Oldridge, et al.
Nature Communications|April 30, 2024
Positive selection in the genomes of two Papua New Guinean populations at distinct altitude levelsMathilde André, Nicolas Brucato, Georgi Hudjasov, et al.
Pageof 6