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Freerk van Dijk

Showing results (1-10 of 28) with videos related to

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BMC Research Notes|August 20, 2015
Molgenis-impute: imputation pipeline in a boxAlexandros Kanterakis, Patrick Deelen, Freerk van Dijk, et al.
Circulation|February 21, 2018
Genetics, Lifestyle, and Low-Density Lipoprotein Cholesterol in Young and Apparently Healthy WomenJan-Willem Balder, Antoine Rimbert, Xiang Zhang, et al.
Scientific Reports|May 20, 2021
Feasibility of predicting allele specific expression from DNA sequencing using machine learningZhenhua Zhang, Freerk van Dijk, Niek de Klein, et al.
BMC Bioinformatics|December 19, 2018
NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testingLennart F Johansson, Hendrik A de Weerd, Eddy N de Boer, et al.
Blood Neoplasia|June 23, 2025
T-cell lymphoblastic lymphoma compared with T-cell acute lymphoblastic leukemia: similar subtypes and different fusionsEmma Kroeze, Michelle M Kleisman, Rico Hagelaar, et al.
Advanced Genetics (Hoboken, N.J.)|January 9, 2023
A pipeline-friendly software tool for genome diagnostics to prioritize genes by matching patient symptoms to literatureK Joeri van der Velde, Sander van den Hoek, Freerk van Dijk, et al.
International Journal of Epidemiology|December 16, 2014
Cohort Profile: LifeLines, a three-generation cohort study and biobankSalome Scholtens, Nynke Smidt, Morris A Swertz, et al.
British Journal of Haematology|August 2, 2021
Minimal residual disease (MRD) detection in acute lymphoblastic leukaemia based on fusion genes and genomic deletions: towards MRD for allRoland P Kuiper, Patricia G Hoogeveen, Reno Bladergroen, et al.
Plos Genetics|March 8, 2013
Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequencyAdam Kiezun, Sara L Pulit, Laurent C Francioli, et al.
Human Mutation|February 12, 2016
CoNVaDING: Single Exon Variation Detection in Targeted NGS DataLennart F Johansson, Freerk van Dijk, Eddy N de Boer, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
BMC Research Notes|August 20, 2015
Molgenis-impute: imputation pipeline in a boxAlexandros Kanterakis, Patrick Deelen, Freerk van Dijk, et al.
Circulation|February 21, 2018
Genetics, Lifestyle, and Low-Density Lipoprotein Cholesterol in Young and Apparently Healthy WomenJan-Willem Balder, Antoine Rimbert, Xiang Zhang, et al.
Scientific Reports|May 20, 2021
Feasibility of predicting allele specific expression from DNA sequencing using machine learningZhenhua Zhang, Freerk van Dijk, Niek de Klein, et al.
BMC Bioinformatics|December 19, 2018
NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testingLennart F Johansson, Hendrik A de Weerd, Eddy N de Boer, et al.
Blood Neoplasia|June 23, 2025
T-cell lymphoblastic lymphoma compared with T-cell acute lymphoblastic leukemia: similar subtypes and different fusionsEmma Kroeze, Michelle M Kleisman, Rico Hagelaar, et al.
Advanced Genetics (Hoboken, N.J.)|January 9, 2023
A pipeline-friendly software tool for genome diagnostics to prioritize genes by matching patient symptoms to literatureK Joeri van der Velde, Sander van den Hoek, Freerk van Dijk, et al.
International Journal of Epidemiology|December 16, 2014
Cohort Profile: LifeLines, a three-generation cohort study and biobankSalome Scholtens, Nynke Smidt, Morris A Swertz, et al.
British Journal of Haematology|August 2, 2021
Minimal residual disease (MRD) detection in acute lymphoblastic leukaemia based on fusion genes and genomic deletions: towards MRD for allRoland P Kuiper, Patricia G Hoogeveen, Reno Bladergroen, et al.
Plos Genetics|March 8, 2013
Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequencyAdam Kiezun, Sara L Pulit, Laurent C Francioli, et al.
Human Mutation|February 12, 2016
CoNVaDING: Single Exon Variation Detection in Targeted NGS DataLennart F Johansson, Freerk van Dijk, Eddy N de Boer, et al.
Pageof 3