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Erika Souche

Showing results (1-10 of 38) with videos related to

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BMC Bioinformatics|September 24, 2013
SynTView - an interactive multi-view genome browser for next-generation comparative microorganism genomicsPierre Lechat, Erika Souche, Ivan Moszer
Cold Spring Harbor Molecular Case Studies|July 7, 2017
<i>SPG20</i> mutation in three siblings with familial hereditary spastic paraplegiaLeila Dardour, Filip Roelens, Valerie Race, et al.
Glycoconjugate Journal|September 18, 2012
Approaches to homozygosity mapping and exome sequencing for the identification of novel types of CDGGert Matthijs, Daisy Rymen, María Beatriz Bistué Millón, et al.
Genome Medicine|October 21, 2014
NGS-Logistics: federated analysis of NGS sequence variants across multiple locationsAmin Ardeshirdavani, Erika Souche, Luc Dehaspe, et al.
Scientific Reports|January 22, 2016
The opgC gene is required for OPGs succinylation and is osmoregulated through RcsCDB and EnvZ/OmpR in the phytopathogen Dickeya dadantiiSébastien Bontemps-Gallo, Edwige Madec, Catherine Robbe-Masselot, et al.
Forensic Science International. Genetics|October 31, 2025
The first population scale compendium of complete mitochondrial genomes from Flanders, BelgiumNoah Gaens, Erika Souche, Toomas Kivisild, et al.
Genes|January 26, 2024
Gollop-Wolfgang Complex Is Associated with a Monoallelic Variation in <i>WNT11</i>Adrian Odrzywolski, Beyhan Tüysüz, Philippe Debeer, et al.
Medicina Clinica|February 15, 2018
Consensus document on the implementation of next generation sequencing in the genetic diagnosis of hereditary cancerJosé Luis Soto, Ignacio Blanco, Orland Díez, et al.
European Journal of Human Genetics : EJHG|December 20, 2017
Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathyTomas Robyns, Cuno Kuiperi, Jeroen Breckpot, et al.
Prenatal Diagnosis|July 3, 2018
Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencingMolka Kammoun, Erika Souche, Paul Brady, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
BMC Bioinformatics|September 24, 2013
SynTView - an interactive multi-view genome browser for next-generation comparative microorganism genomicsPierre Lechat, Erika Souche, Ivan Moszer
Cold Spring Harbor Molecular Case Studies|July 7, 2017
<i>SPG20</i> mutation in three siblings with familial hereditary spastic paraplegiaLeila Dardour, Filip Roelens, Valerie Race, et al.
Glycoconjugate Journal|September 18, 2012
Approaches to homozygosity mapping and exome sequencing for the identification of novel types of CDGGert Matthijs, Daisy Rymen, María Beatriz Bistué Millón, et al.
Genome Medicine|October 21, 2014
NGS-Logistics: federated analysis of NGS sequence variants across multiple locationsAmin Ardeshirdavani, Erika Souche, Luc Dehaspe, et al.
Scientific Reports|January 22, 2016
The opgC gene is required for OPGs succinylation and is osmoregulated through RcsCDB and EnvZ/OmpR in the phytopathogen Dickeya dadantiiSébastien Bontemps-Gallo, Edwige Madec, Catherine Robbe-Masselot, et al.
Forensic Science International. Genetics|October 31, 2025
The first population scale compendium of complete mitochondrial genomes from Flanders, BelgiumNoah Gaens, Erika Souche, Toomas Kivisild, et al.
Genes|January 26, 2024
Gollop-Wolfgang Complex Is Associated with a Monoallelic Variation in <i>WNT11</i>Adrian Odrzywolski, Beyhan Tüysüz, Philippe Debeer, et al.
Medicina Clinica|February 15, 2018
Consensus document on the implementation of next generation sequencing in the genetic diagnosis of hereditary cancerJosé Luis Soto, Ignacio Blanco, Orland Díez, et al.
European Journal of Human Genetics : EJHG|December 20, 2017
Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathyTomas Robyns, Cuno Kuiperi, Jeroen Breckpot, et al.
Prenatal Diagnosis|July 3, 2018
Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencingMolka Kammoun, Erika Souche, Paul Brady, et al.
Pageof 4