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Steven van Vooren

Showing results (11-20 of 22) with videos related to

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Genome Medicine|March 3, 2010
Collaboratively charting the gene-to-phenotype network of human congenital heart defectsRoland Barriot, Jeroen Breckpot, Bernard Thienpont, et al.
American Journal of Human Genetics|April 7, 2009
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesHelen V Firth, Shola M Richards, A Paul Bevan, et al.
The Journal of Molecular Diagnostics : JMD|July 7, 2024
Development, Validation, and Implementation of an Augmented Multiwell, Multitarget Quantitative PCR for the Analysis of Human Papillomavirus Genotyping through Software Automation, Data Science, and Artificial IntelligenceA Rita Pereira, Nina Redzic, Steven Van Vooren, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2005
Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosisJoris R Vermeesch, Cindy Melotte, Guy Froyen, et al.
European Journal of Medical Genetics|July 16, 2013
An update on ECARUCA, the European Cytogeneticists Association Register of Unbalanced Chromosome AberrationsAnneke T Vulto-van Silfhout, Conny M A van Ravenswaaij, Jayne Y Hehir-Kwa, et al.
The Journal of Molecular Diagnostics : JMD|December 22, 2018
Somatic Tumor Variant Filtration Strategies to Optimize Tumor-Only Molecular Profiling Using Targeted Next-Generation Sequencing PanelsMahadeo A Sukhai, Maksym Misyura, Mariam Thomas, et al.
BMC Bioinformatics|May 25, 2005
arrayCGHbase: an analysis platform for comparative genomic hybridization microarraysBjörn Menten, Filip Pattyn, Katleen De Preter, et al.
American Journal of Human Genetics|January 9, 2008
Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16Irina Balikova, Kevin Martens, Cindy Melotte, et al.
Human Mutation|May 5, 2017
Critical points for an accurate human genome analysisStefan J White, Jeroen F J Laros, Egbert Bakker, et al.
Human Mutation|August 20, 2015
Diagnostic interpretation of array data using public databases and internet sourcesNicole de Leeuw, Trijnie Dijkhuizen, Jayne Y Hehir-Kwa, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Genome Medicine|March 3, 2010
Collaboratively charting the gene-to-phenotype network of human congenital heart defectsRoland Barriot, Jeroen Breckpot, Bernard Thienpont, et al.
American Journal of Human Genetics|April 7, 2009
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesHelen V Firth, Shola M Richards, A Paul Bevan, et al.
The Journal of Molecular Diagnostics : JMD|July 7, 2024
Development, Validation, and Implementation of an Augmented Multiwell, Multitarget Quantitative PCR for the Analysis of Human Papillomavirus Genotyping through Software Automation, Data Science, and Artificial IntelligenceA Rita Pereira, Nina Redzic, Steven Van Vooren, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2005
Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosisJoris R Vermeesch, Cindy Melotte, Guy Froyen, et al.
European Journal of Medical Genetics|July 16, 2013
An update on ECARUCA, the European Cytogeneticists Association Register of Unbalanced Chromosome AberrationsAnneke T Vulto-van Silfhout, Conny M A van Ravenswaaij, Jayne Y Hehir-Kwa, et al.
The Journal of Molecular Diagnostics : JMD|December 22, 2018
Somatic Tumor Variant Filtration Strategies to Optimize Tumor-Only Molecular Profiling Using Targeted Next-Generation Sequencing PanelsMahadeo A Sukhai, Maksym Misyura, Mariam Thomas, et al.
BMC Bioinformatics|May 25, 2005
arrayCGHbase: an analysis platform for comparative genomic hybridization microarraysBjörn Menten, Filip Pattyn, Katleen De Preter, et al.
American Journal of Human Genetics|January 9, 2008
Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16Irina Balikova, Kevin Martens, Cindy Melotte, et al.
Human Mutation|May 5, 2017
Critical points for an accurate human genome analysisStefan J White, Jeroen F J Laros, Egbert Bakker, et al.
Human Mutation|August 20, 2015
Diagnostic interpretation of array data using public databases and internet sourcesNicole de Leeuw, Trijnie Dijkhuizen, Jayne Y Hehir-Kwa, et al.
Pageof 3