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Niels Morling

Showing results (91-100 of 194) with videos related to

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Forensic Science International. Genetics|December 17, 2008
Comparison of five DNA quantification methodsKarsten Nielsen, Helle Smidt Mogensen, Johannes Hedman, et al.
Forensic Science International. Genetics|August 22, 2017
Analysis of ancestry informative markers in three main ethnic groups from Ecuador supports a trihybrid origin of EcuadoriansRoberta Santangelo, Fabricio González-Andrade, Claus Børsting, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 28, 2014
A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classificationChristin L Hertz, Laura Ferrero-Miliani, Rune Frank-Hansen, et al.
Forensic Science International. Genetics|May 22, 2012
Sequence variants of allele 22 and 23 of DYS635 causing different stutter ratesJill Olofsson, Mikkel Meyer Andersen, Helle Smidt Mogensen, et al.
Plos One|March 29, 2023
Comparison of whole transcriptome sequencing of fresh, frozen, and formalin-fixed, paraffin-embedded cardiac tissueStine Bøttcher Jacobsen, Jacob Tfelt-Hansen, Morten Holdgaard Smerup, et al.
Plos One|May 15, 2025
RNA degradation patterns in cardiac tissues kept at different time intervals and temperatures before RNA sequencingStine Bøttcher Jacobsen, Jacob Tfelt-Hansen, Morten Holdgaard Smerup, et al.
Forensic Science International. Genetics|August 3, 2018
Modelling allelic drop-outs in STR sequencing data generated by MPSSøren B Vilsen, Torben Tvedebrink, Poul S Eriksen, et al.
Annals of Human Genetics|December 22, 2006
Carrier frequency of a nonsense mutation in the adenosine deaminase (ADA) gene implies a high incidence of ADA-deficient severe combined immunodeficiency (SCID) in Somalia and a single, common haplotype indicates common ancestryJuan J Sanchez, Gemma Monaghan, Claus Børsting, et al.
Scientific Reports|October 12, 2022
SNP allele calling of Illumina Infinium Omni5-4 data using the butterfly methodMikkel Meyer Andersen, Steffan Noe Christiansen, Jeppe Dyrberg Andersen, et al.
BMC Genetics|January 1, 2010
Genetic determinants of hair and eye colours in the Scottish and Danish populationsJonas Mengel-From, Terence H Wong, Niels Morling, et al.
Pageof 20

Showing results (91-100 of 194) with videos related to

Sort By:
Pageof 20
Forensic Science International. Genetics|December 17, 2008
Comparison of five DNA quantification methodsKarsten Nielsen, Helle Smidt Mogensen, Johannes Hedman, et al.
Forensic Science International. Genetics|August 22, 2017
Analysis of ancestry informative markers in three main ethnic groups from Ecuador supports a trihybrid origin of EcuadoriansRoberta Santangelo, Fabricio González-Andrade, Claus Børsting, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 28, 2014
A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classificationChristin L Hertz, Laura Ferrero-Miliani, Rune Frank-Hansen, et al.
Forensic Science International. Genetics|May 22, 2012
Sequence variants of allele 22 and 23 of DYS635 causing different stutter ratesJill Olofsson, Mikkel Meyer Andersen, Helle Smidt Mogensen, et al.
Plos One|March 29, 2023
Comparison of whole transcriptome sequencing of fresh, frozen, and formalin-fixed, paraffin-embedded cardiac tissueStine Bøttcher Jacobsen, Jacob Tfelt-Hansen, Morten Holdgaard Smerup, et al.
Plos One|May 15, 2025
RNA degradation patterns in cardiac tissues kept at different time intervals and temperatures before RNA sequencingStine Bøttcher Jacobsen, Jacob Tfelt-Hansen, Morten Holdgaard Smerup, et al.
Forensic Science International. Genetics|August 3, 2018
Modelling allelic drop-outs in STR sequencing data generated by MPSSøren B Vilsen, Torben Tvedebrink, Poul S Eriksen, et al.
Annals of Human Genetics|December 22, 2006
Carrier frequency of a nonsense mutation in the adenosine deaminase (ADA) gene implies a high incidence of ADA-deficient severe combined immunodeficiency (SCID) in Somalia and a single, common haplotype indicates common ancestryJuan J Sanchez, Gemma Monaghan, Claus Børsting, et al.
Scientific Reports|October 12, 2022
SNP allele calling of Illumina Infinium Omni5-4 data using the butterfly methodMikkel Meyer Andersen, Steffan Noe Christiansen, Jeppe Dyrberg Andersen, et al.
BMC Genetics|January 1, 2010
Genetic determinants of hair and eye colours in the Scottish and Danish populationsJonas Mengel-From, Terence H Wong, Niels Morling, et al.
Pageof 20