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Vincent Sater

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Genes, Chromosomes & Cancer|December 12, 2022
A novel SMARCA2-CREM fusion expending the molecular spectrum of salivary gland hyalinazing clear cell carcinoma beyond the FET genesMarie-Delphine Lanic, René Guérin, Vincent Sater, et al.
Computational and Structural Biotechnology Journal|September 21, 2020
UMI-Gen: A UMI-based read simulator for variant calling evaluation in paired-end sequencing NGS librariesVincent Sater, Pierre-Julien Viailly, Thierry Lecroq, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 25, 2022
UMI-Varcal: A Low-Frequency Variant Caller for UMI-Tagged Paired-End Sequencing DataVincent Sater, Pierre-Julien Viailly, Thierry Lecroq, et al.
Histopathology|June 23, 2023
Detection of salivary gland and sinonasal fusions by a next-generation sequencing based, ligation-dependent, multiplex RT-PCR assayMarie-Delphine Lanic, René Guérin, Michel Wassef, et al.
Bioinformatics (Oxford, England)|January 28, 2020
UMI-VarCal: a new UMI-based variant caller that efficiently improves low-frequency variant detection in paired-end sequencing NGS librariesVincent Sater, Pierre-Julien Viailly, Thierry Lecroq, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|January 25, 2022
Detection of sarcoma fusions by a next-generation sequencing based-ligation-dependent multiplex RT-PCR assayMarie-Delphine Lanic, François Le Loarer, Vinciane Rainville, et al.
Hemasphere|March 4, 2024
Analysis of immunoglobulin/T-cell receptor repertoires by high-throughput RNA sequencing reveals a continuous dynamic of positive clonal selection in follicular lymphomaVictor Bobée, Mathieu Viennot, Vinciane Rainville, et al.
BMC Bioinformatics|March 13, 2021
Improving high-resolution copy number variation analysis from next generation sequencing using unique molecular identifiersPierre-Julien Viailly, Vincent Sater, Mathieu Viennot, et al.
Blood Cancer Journal|May 24, 2020
Combining gene expression profiling and machine learning to diagnose B-cell non-Hodgkin lymphomaVictor Bobée, Fanny Drieux, Vinciane Marchand, et al.
The Journal of Molecular Diagnostics : JMD|June 20, 2021
Detection of Gene Fusion Transcripts in Peripheral T-Cell Lymphoma Using a Multiplexed Targeted Sequencing AssayFanny Drieux, Philippe Ruminy, Vincent Sater, et al.
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Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Genes, Chromosomes & Cancer|December 12, 2022
A novel SMARCA2-CREM fusion expending the molecular spectrum of salivary gland hyalinazing clear cell carcinoma beyond the FET genesMarie-Delphine Lanic, René Guérin, Vincent Sater, et al.
Computational and Structural Biotechnology Journal|September 21, 2020
UMI-Gen: A UMI-based read simulator for variant calling evaluation in paired-end sequencing NGS librariesVincent Sater, Pierre-Julien Viailly, Thierry Lecroq, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 25, 2022
UMI-Varcal: A Low-Frequency Variant Caller for UMI-Tagged Paired-End Sequencing DataVincent Sater, Pierre-Julien Viailly, Thierry Lecroq, et al.
Histopathology|June 23, 2023
Detection of salivary gland and sinonasal fusions by a next-generation sequencing based, ligation-dependent, multiplex RT-PCR assayMarie-Delphine Lanic, René Guérin, Michel Wassef, et al.
Bioinformatics (Oxford, England)|January 28, 2020
UMI-VarCal: a new UMI-based variant caller that efficiently improves low-frequency variant detection in paired-end sequencing NGS librariesVincent Sater, Pierre-Julien Viailly, Thierry Lecroq, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|January 25, 2022
Detection of sarcoma fusions by a next-generation sequencing based-ligation-dependent multiplex RT-PCR assayMarie-Delphine Lanic, François Le Loarer, Vinciane Rainville, et al.
Hemasphere|March 4, 2024
Analysis of immunoglobulin/T-cell receptor repertoires by high-throughput RNA sequencing reveals a continuous dynamic of positive clonal selection in follicular lymphomaVictor Bobée, Mathieu Viennot, Vinciane Rainville, et al.
BMC Bioinformatics|March 13, 2021
Improving high-resolution copy number variation analysis from next generation sequencing using unique molecular identifiersPierre-Julien Viailly, Vincent Sater, Mathieu Viennot, et al.
Blood Cancer Journal|May 24, 2020
Combining gene expression profiling and machine learning to diagnose B-cell non-Hodgkin lymphomaVictor Bobée, Fanny Drieux, Vinciane Marchand, et al.
The Journal of Molecular Diagnostics : JMD|June 20, 2021
Detection of Gene Fusion Transcripts in Peripheral T-Cell Lymphoma Using a Multiplexed Targeted Sequencing AssayFanny Drieux, Philippe Ruminy, Vincent Sater, et al.
Pageof 1