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David Atlan

Showing results (1-10 of 7) with videos related to

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Biomed Research International|July 3, 2015
DNAseq Workflow in a Diagnostic Context and an Example of a User Friendly ImplementationBeat Wolf, Pierre Kuonen, Thomas Dandekar, et al.
Genes|December 31, 2016
Non-Coding RNAs in Lung Cancer: Contribution of Bioinformatics Analysis to the Development of Non-Invasive Diagnostic ToolsMeik Kunz, Beat Wolf, Harald Schulze, et al.
Human Mutation|July 31, 2015
Cafe Variome: general-purpose software for making genotype-phenotype data discoverable in restricted or open access contextsOwen Lancaster, Tim Beck, David Atlan, et al.
Briefings in Bioinformatics|October 4, 2019
A comprehensive method protocol for annotation and integrated functional understanding of lncRNAsMeik Kunz, Beat Wolf, Maximilian Fuchs, et al.
International Journal of Molecular Sciences|September 9, 2023
Whole-Genome Sequencing Identified New Structural Variations in the <i>DMD</i> Gene That Cause Duchenne Muscular Dystrophy in Two GirlsNatalie Pluta, Arpad von Moers, Astrid Pechmann, et al.
Genes|October 27, 2022
Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular DystrophyNatalie Pluta, Sabine Hoffjan, Frederic Zimmer, et al.
BMC Bioinformatics|October 4, 2012
VarioML framework for comprehensive variation data representation and exchangeMyles Byrne, Ivo Fac Fokkema, Owen Lancaster, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Biomed Research International|July 3, 2015
DNAseq Workflow in a Diagnostic Context and an Example of a User Friendly ImplementationBeat Wolf, Pierre Kuonen, Thomas Dandekar, et al.
Genes|December 31, 2016
Non-Coding RNAs in Lung Cancer: Contribution of Bioinformatics Analysis to the Development of Non-Invasive Diagnostic ToolsMeik Kunz, Beat Wolf, Harald Schulze, et al.
Human Mutation|July 31, 2015
Cafe Variome: general-purpose software for making genotype-phenotype data discoverable in restricted or open access contextsOwen Lancaster, Tim Beck, David Atlan, et al.
Briefings in Bioinformatics|October 4, 2019
A comprehensive method protocol for annotation and integrated functional understanding of lncRNAsMeik Kunz, Beat Wolf, Maximilian Fuchs, et al.
International Journal of Molecular Sciences|September 9, 2023
Whole-Genome Sequencing Identified New Structural Variations in the <i>DMD</i> Gene That Cause Duchenne Muscular Dystrophy in Two GirlsNatalie Pluta, Arpad von Moers, Astrid Pechmann, et al.
Genes|October 27, 2022
Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular DystrophyNatalie Pluta, Sabine Hoffjan, Frederic Zimmer, et al.
BMC Bioinformatics|October 4, 2012
VarioML framework for comprehensive variation data representation and exchangeMyles Byrne, Ivo Fac Fokkema, Owen Lancaster, et al.
Pageof 1