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Jochen Hecht

Showing results (31-40 of 87) with videos related to

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Nucleic Acids Research|December 1, 2011
The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching processVerena Heinrich, Jens Stange, Thorsten Dickhaus, et al.
BMC Genomics|January 16, 2019
GOPHER: Generator Of Probes for capture Hi-C Experiments at high ResolutionPeter Hansen, Salaheddine Ali, Hannah Blau, et al.
Development (Cambridge, England)|March 8, 2018
Genome-wide strategies identify downstream target genes of chick connective tissue-associated transcription factorsMickael Orgeur, Marvin Martens, Georgeta Leonte, et al.
Bioinformatics (Oxford, England)|February 1, 2011
Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disordersChristian Rödelsperger, Peter Krawitz, Sebastian Bauer, et al.
Plos Genetics|January 20, 2017
Genome-Wide Binding of Posterior HOXA/D Transcription Factors Reveals Subgrouping and Association with CTCFIvana Jerković, Daniel M Ibrahim, Guillaume Andrey, et al.
American Journal of Human Genetics|April 9, 2013
PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndromePeter M Krawitz, Yoshiko Murakami, Angelika Rieß, et al.
Plos Genetics|March 29, 2008
Evolution of a core gene network for skeletogenesis in chordatesJochen Hecht, Sigmar Stricker, Ulrike Wiecha, et al.
American Journal of Medical Genetics. Part A|January 23, 2016
An overlapping phenotype of Osteogenesis imperfecta and Ehlers-Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencingLuisa Mackenroth, Björn Fischer-Zirnsak, Johannes Egerer, et al.
Molecular Genetics & Genomic Medicine|October 22, 2014
Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndromePeter M Krawitz, Daniela Schiska, Ulrike Krüger, et al.
Journal of Molecular Medicine (Berlin, Germany)|December 14, 2019
Increased presence and differential molecular imprinting of transit amplifying cells in psoriasisKatrin Witte, Karsten Jürchott, Demetrios Christou, et al.
Pageof 9

Showing results (31-40 of 87) with videos related to

Sort By:
Pageof 9
Nucleic Acids Research|December 1, 2011
The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching processVerena Heinrich, Jens Stange, Thorsten Dickhaus, et al.
BMC Genomics|January 16, 2019
GOPHER: Generator Of Probes for capture Hi-C Experiments at high ResolutionPeter Hansen, Salaheddine Ali, Hannah Blau, et al.
Development (Cambridge, England)|March 8, 2018
Genome-wide strategies identify downstream target genes of chick connective tissue-associated transcription factorsMickael Orgeur, Marvin Martens, Georgeta Leonte, et al.
Bioinformatics (Oxford, England)|February 1, 2011
Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disordersChristian Rödelsperger, Peter Krawitz, Sebastian Bauer, et al.
Plos Genetics|January 20, 2017
Genome-Wide Binding of Posterior HOXA/D Transcription Factors Reveals Subgrouping and Association with CTCFIvana Jerković, Daniel M Ibrahim, Guillaume Andrey, et al.
American Journal of Human Genetics|April 9, 2013
PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndromePeter M Krawitz, Yoshiko Murakami, Angelika Rieß, et al.
Plos Genetics|March 29, 2008
Evolution of a core gene network for skeletogenesis in chordatesJochen Hecht, Sigmar Stricker, Ulrike Wiecha, et al.
American Journal of Medical Genetics. Part A|January 23, 2016
An overlapping phenotype of Osteogenesis imperfecta and Ehlers-Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencingLuisa Mackenroth, Björn Fischer-Zirnsak, Johannes Egerer, et al.
Molecular Genetics & Genomic Medicine|October 22, 2014
Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndromePeter M Krawitz, Daniela Schiska, Ulrike Krüger, et al.
Journal of Molecular Medicine (Berlin, Germany)|December 14, 2019
Increased presence and differential molecular imprinting of transit amplifying cells in psoriasisKatrin Witte, Karsten Jürchott, Demetrios Christou, et al.
Pageof 9