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Lude Franke

Showing results (81-90 of 265) with videos related to

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Genome Biology|January 18, 2017
GAVIN: Gene-Aware Variant INterpretation for medical sequencingK Joeri van der Velde, Eddy N de Boer, Cleo C van Diemen, et al.
Nature Communications|July 1, 2018
Reply to 'Misestimation of heritability and prediction accuracy of male-pattern baldness'Nicola Pirastu, Peter K Joshi, Paul S de Vries, et al.
Nature Genetics|June 30, 2019
High-throughput identification of human SNPs affecting regulatory element activityJoris van Arensbergen, Ludo Pagie, Vincent D FitzPatrick, et al.
BMC Biology|June 26, 2019
RNA-Seq in 296 phased trios provides a high-resolution map of genomic imprintingBharati Jadhav, Ramin Monajemi, Kristina K Gagalova, et al.
Plos Genetics|January 24, 2013
Human disease-associated genetic variation impacts large intergenic non-coding RNA expressionVinod Kumar, Harm-Jan Westra, Juha Karjalainen, et al.
Genome Biology|January 15, 2022
Functional genomics analysis identifies T and NK cell activation as a driver of epigenetic clock progressionThomas H Jonkman, Koen F Dekkers, Roderick C Slieker, et al.
The Lancet. Neurology|March 4, 2008
Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screenHylke M Blauw, Jan H Veldink, Michael A van Es, et al.
NAR Genomics and Bioinformatics|February 13, 2026
Accelerating rare disease diagnostics by linking DNA and RNA through an explainable and interactive RNA-guided workflowWillem T K Maassen, Charlotte C E T Pape, Carlos G Urzua-Traslavina, et al.
BMJ Open|August 31, 2015
Cohort profile: LifeLines DEEP, a prospective, general population cohort study in the northern Netherlands: study design and baseline characteristicsEttje F Tigchelaar, Alexandra Zhernakova, Jackie A M Dekens, et al.
Nature|August 12, 2021
Phantom epistasis between unlinked lociGibran Hemani, Joseph E Powell, Huanwei Wang, et al.
Pageof 27

Showing results (81-90 of 265) with videos related to

Sort By:
Pageof 27
Genome Biology|January 18, 2017
GAVIN: Gene-Aware Variant INterpretation for medical sequencingK Joeri van der Velde, Eddy N de Boer, Cleo C van Diemen, et al.
Nature Communications|July 1, 2018
Reply to 'Misestimation of heritability and prediction accuracy of male-pattern baldness'Nicola Pirastu, Peter K Joshi, Paul S de Vries, et al.
Nature Genetics|June 30, 2019
High-throughput identification of human SNPs affecting regulatory element activityJoris van Arensbergen, Ludo Pagie, Vincent D FitzPatrick, et al.
BMC Biology|June 26, 2019
RNA-Seq in 296 phased trios provides a high-resolution map of genomic imprintingBharati Jadhav, Ramin Monajemi, Kristina K Gagalova, et al.
Plos Genetics|January 24, 2013
Human disease-associated genetic variation impacts large intergenic non-coding RNA expressionVinod Kumar, Harm-Jan Westra, Juha Karjalainen, et al.
Genome Biology|January 15, 2022
Functional genomics analysis identifies T and NK cell activation as a driver of epigenetic clock progressionThomas H Jonkman, Koen F Dekkers, Roderick C Slieker, et al.
The Lancet. Neurology|March 4, 2008
Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screenHylke M Blauw, Jan H Veldink, Michael A van Es, et al.
NAR Genomics and Bioinformatics|February 13, 2026
Accelerating rare disease diagnostics by linking DNA and RNA through an explainable and interactive RNA-guided workflowWillem T K Maassen, Charlotte C E T Pape, Carlos G Urzua-Traslavina, et al.
BMJ Open|August 31, 2015
Cohort profile: LifeLines DEEP, a prospective, general population cohort study in the northern Netherlands: study design and baseline characteristicsEttje F Tigchelaar, Alexandra Zhernakova, Jackie A M Dekens, et al.
Nature|August 12, 2021
Phantom epistasis between unlinked lociGibran Hemani, Joseph E Powell, Huanwei Wang, et al.
Pageof 27