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Eleni Giannoulatou

Showing results (1-10 of 115) with videos related to

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NAR Genomics and Bioinformatics|August 30, 2024
Context-adjusted proportion of singletons (CAPS): a novel metric for assessing negative selection in the human genomeMikhail Gudkov, Loïc Thibaut, Eleni Giannoulatou
Biophysical Reviews|January 27, 2019
Big data: the elements of good questions, open data, and powerful softwareJoshua W K Ho, Eleni Giannoulatou
HGG Advances|January 9, 2024
Quantifying negative selection on synonymous variantsMikhail Gudkov, Loïc Thibaut, Eleni Giannoulatou
Bioinformatics (Oxford, England)|March 24, 2017
SVPV: a structural variant prediction viewer for paired-end sequencing datasetsJacob E Munro, Sally L Dunwoodie, Eleni Giannoulatou
Genomics, Proteomics & Bioinformatics|November 26, 2019
VPOT: A Customizable Variant Prioritization Ordering Tool for Annotated VariantsEddie Ip, Gavin Chapman, David Winlaw, et al.
Bioinformatics (Oxford, England)|April 18, 2019
Spliceogen: an integrative, scalable tool for the discovery of splice-altering variantsSteven Monger, Michael Troup, Eddie Ip, et al.
Bioinformatics (Oxford, England)|July 26, 2008
GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference populationEleni Giannoulatou, Christopher Yau, Stefano Colella, et al.
Nature Reviews. Cardiology|June 9, 2017
Epidemiology and treatment of pulmonary arterial hypertensionEdmund M T Lau, Eleni Giannoulatou, David S Celermajer, et al.
Briefings in Bioinformatics|November 8, 2025
Systematic evaluation of de novo mutation calling tools using whole genome sequencing dataAnushi Shah, Steven Monger, Michael Troup, et al.
Bioinformatics (Oxford, England)|April 22, 2020
dv-trio: a family-based variant calling pipeline using DeepVariantEddie K K Ip, Clinton Hadinata, Joshua W K Ho, et al.
Pageof 12

Showing results (1-10 of 115) with videos related to

Sort By:
Pageof 12
NAR Genomics and Bioinformatics|August 30, 2024
Context-adjusted proportion of singletons (CAPS): a novel metric for assessing negative selection in the human genomeMikhail Gudkov, Loïc Thibaut, Eleni Giannoulatou
Biophysical Reviews|January 27, 2019
Big data: the elements of good questions, open data, and powerful softwareJoshua W K Ho, Eleni Giannoulatou
HGG Advances|January 9, 2024
Quantifying negative selection on synonymous variantsMikhail Gudkov, Loïc Thibaut, Eleni Giannoulatou
Bioinformatics (Oxford, England)|March 24, 2017
SVPV: a structural variant prediction viewer for paired-end sequencing datasetsJacob E Munro, Sally L Dunwoodie, Eleni Giannoulatou
Genomics, Proteomics & Bioinformatics|November 26, 2019
VPOT: A Customizable Variant Prioritization Ordering Tool for Annotated VariantsEddie Ip, Gavin Chapman, David Winlaw, et al.
Bioinformatics (Oxford, England)|April 18, 2019
Spliceogen: an integrative, scalable tool for the discovery of splice-altering variantsSteven Monger, Michael Troup, Eddie Ip, et al.
Bioinformatics (Oxford, England)|July 26, 2008
GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference populationEleni Giannoulatou, Christopher Yau, Stefano Colella, et al.
Nature Reviews. Cardiology|June 9, 2017
Epidemiology and treatment of pulmonary arterial hypertensionEdmund M T Lau, Eleni Giannoulatou, David S Celermajer, et al.
Briefings in Bioinformatics|November 8, 2025
Systematic evaluation of de novo mutation calling tools using whole genome sequencing dataAnushi Shah, Steven Monger, Michael Troup, et al.
Bioinformatics (Oxford, England)|April 22, 2020
dv-trio: a family-based variant calling pipeline using DeepVariantEddie K K Ip, Clinton Hadinata, Joshua W K Ho, et al.
Pageof 12