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Virginie Saillour

Showing results (1-10 of 14) with videos related to

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BMC Bioinformatics|June 6, 2013
Joint genotype inference with germline and somatic mutationsEric Bareke, Virginie Saillour, Jean-François Spinella, et al.
BMC Cancer|July 24, 2015
Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genesJean-François Spinella, Jasmine Healy, Virginie Saillour, et al.
BMC Genomics|November 16, 2016
SNooPer: a machine learning-based method for somatic variant identification from low-pass next-generation sequencingJean-François Spinella, Pamela Mehanna, Ramon Vidal, et al.
Neurology. Genetics|November 8, 2021
Adult Cerebellar Ataxia, Axonal Neuropathy, and Sensory Impairments Caused by Biallelic <i>SCO2</i> VariantsBenoit Rucheton, Claire Ewenczyk, Pauline Gaignard, et al.
BMC Cancer|September 9, 2015
A novel somatic mutation in ACD induces telomere lengthening and apoptosis resistance in leukemia cellsJean-François Spinella, Pauline Cassart, Nicolas Garnier, et al.
Cancer Research|June 1, 2013
Integration of high-resolution methylome and transcriptome analyses to dissect epigenomic changes in childhood acute lymphoblastic leukemiaStephan Busche, Bing Ge, Ramon Vidal, et al.
Oncotarget|September 8, 2016
Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutationsJean-François Spinella, Pauline Cassart, Chantal Richer, et al.
European Journal of Human Genetics : EJHG|November 8, 2019
A variant of neonatal progeroid syndrome, or Wiedemann-Rautenstrauch syndrome, is associated with a nonsense variant in POLR3GLEliane Beauregard-Lacroix, Smrithi Salian, Hyunyun Kim, et al.
Blood|January 11, 2017
KMT2E-ASNS: a novel relapse-specific fusion gene in early T-cell precursor acute lymphoblastic leukemiaFida Khater, Mathieu Lajoie, Sylvie Langlois, et al.
American Journal of Hematology|January 18, 2021
VPS4A mutation in syndromic congenital hemolytic anemia without obvious signs of dyserythropoiesisAriane Lunati, Arnaud Petit, Hélène Lapillonne, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
BMC Bioinformatics|June 6, 2013
Joint genotype inference with germline and somatic mutationsEric Bareke, Virginie Saillour, Jean-François Spinella, et al.
BMC Cancer|July 24, 2015
Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genesJean-François Spinella, Jasmine Healy, Virginie Saillour, et al.
BMC Genomics|November 16, 2016
SNooPer: a machine learning-based method for somatic variant identification from low-pass next-generation sequencingJean-François Spinella, Pamela Mehanna, Ramon Vidal, et al.
Neurology. Genetics|November 8, 2021
Adult Cerebellar Ataxia, Axonal Neuropathy, and Sensory Impairments Caused by Biallelic <i>SCO2</i> VariantsBenoit Rucheton, Claire Ewenczyk, Pauline Gaignard, et al.
BMC Cancer|September 9, 2015
A novel somatic mutation in ACD induces telomere lengthening and apoptosis resistance in leukemia cellsJean-François Spinella, Pauline Cassart, Nicolas Garnier, et al.
Cancer Research|June 1, 2013
Integration of high-resolution methylome and transcriptome analyses to dissect epigenomic changes in childhood acute lymphoblastic leukemiaStephan Busche, Bing Ge, Ramon Vidal, et al.
Oncotarget|September 8, 2016
Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutationsJean-François Spinella, Pauline Cassart, Chantal Richer, et al.
European Journal of Human Genetics : EJHG|November 8, 2019
A variant of neonatal progeroid syndrome, or Wiedemann-Rautenstrauch syndrome, is associated with a nonsense variant in POLR3GLEliane Beauregard-Lacroix, Smrithi Salian, Hyunyun Kim, et al.
Blood|January 11, 2017
KMT2E-ASNS: a novel relapse-specific fusion gene in early T-cell precursor acute lymphoblastic leukemiaFida Khater, Mathieu Lajoie, Sylvie Langlois, et al.
American Journal of Hematology|January 18, 2021
VPS4A mutation in syndromic congenital hemolytic anemia without obvious signs of dyserythropoiesisAriane Lunati, Arnaud Petit, Hélène Lapillonne, et al.
Pageof 2