Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Verena Heinrich

Showing results (1-10 of 25) with videos related to

Pageof 3
Sort By:
Bioinformatics (Oxford, England)|August 28, 2016
A likelihood ratio-based method to predict exact pedigrees for complex families from next-generation sequencing dataVerena Heinrich, Tom Kamphans, Stefan Mundlos, et al.
Development (Cambridge, England)|November 22, 2013
Efficient CRISPR/Cas9 genome editing with low off-target effects in zebrafishAlexander Hruscha, Peter Krawitz, Alexandra Rechenberg, et al.
Bioinformatics (Oxford, England)|August 8, 2015
Strategies to improve the performance of rare variant association studies by optimizing the selection of controlsNa Zhu, Verena Heinrich, Thorsten Dickhaus, et al.
Genome Medicine|August 2, 2013
Estimating exome genotyping accuracy by comparing to data from large scale sequencing projectsVerena Heinrich, Tom Kamphans, Jens Stange, et al.
Plos One|August 14, 2013
Filtering for compound heterozygous sequence variants in non-consanguineous pedigreesTom Kamphans, Peggy Sabri, Na Zhu, et al.
Skin Pharmacology and Physiology|January 24, 2015
Non-invasive spectroscopic determination of the antioxidative status of gravidae and neonatesHanne Lademann, Bernd Gerber, Dirk M Olbertz, et al.
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.
Genome Research|December 8, 2016
Characterization of hundreds of regulatory landscapes in developing limbs reveals two regimes of chromatin foldingGuillaume Andrey, Robert Schöpflin, Ivana Jerković, 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.
Nature Cell Biology|February 12, 2019
Serial genomic inversions induce tissue-specific architectural stripes, gene misexpression and congenital malformationsKaterina Kraft, Andreas Magg, Verena Heinrich, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Bioinformatics (Oxford, England)|August 28, 2016
A likelihood ratio-based method to predict exact pedigrees for complex families from next-generation sequencing dataVerena Heinrich, Tom Kamphans, Stefan Mundlos, et al.
Development (Cambridge, England)|November 22, 2013
Efficient CRISPR/Cas9 genome editing with low off-target effects in zebrafishAlexander Hruscha, Peter Krawitz, Alexandra Rechenberg, et al.
Bioinformatics (Oxford, England)|August 8, 2015
Strategies to improve the performance of rare variant association studies by optimizing the selection of controlsNa Zhu, Verena Heinrich, Thorsten Dickhaus, et al.
Genome Medicine|August 2, 2013
Estimating exome genotyping accuracy by comparing to data from large scale sequencing projectsVerena Heinrich, Tom Kamphans, Jens Stange, et al.
Plos One|August 14, 2013
Filtering for compound heterozygous sequence variants in non-consanguineous pedigreesTom Kamphans, Peggy Sabri, Na Zhu, et al.
Skin Pharmacology and Physiology|January 24, 2015
Non-invasive spectroscopic determination of the antioxidative status of gravidae and neonatesHanne Lademann, Bernd Gerber, Dirk M Olbertz, et al.
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.
Genome Research|December 8, 2016
Characterization of hundreds of regulatory landscapes in developing limbs reveals two regimes of chromatin foldingGuillaume Andrey, Robert Schöpflin, Ivana Jerković, 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.
Nature Cell Biology|February 12, 2019
Serial genomic inversions induce tissue-specific architectural stripes, gene misexpression and congenital malformationsKaterina Kraft, Andreas Magg, Verena Heinrich, et al.
Pageof 3