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

Klaudia Walter

Showing results (1-10 of 63) with videos related to

Pageof 7
Sort By:
Methods in Molecular Biology (Clifton, N.J.)|June 8, 2018
Quality Control of Common and Rare VariantsKalliope Panoutsopoulou, Klaudia Walter
Genome Biology|April 29, 2017
The impact of rare and low-frequency genetic variants in common diseaseLorenzo Bomba, Klaudia Walter, Nicole Soranzo
Trends in Genetics : TIG|June 28, 2005
Striking nucleotide frequency pattern at the borders of highly conserved vertebrate non-coding sequencesKlaudia Walter, Irina Abnizova, Greg Elgar, et al.
BMC Bioinformatics|April 29, 2005
Some statistical properties of regulatory DNA sequences, and their use in predicting regulatory regions in the Drosophila genome: the fluffy-tail testIrina Abnizova, Rene te Boekhorst, Klaudia Walter, et al.
Genome Biology|February 6, 2007
Parallel evolution of conserved non-coding elements that target a common set of developmental regulatory genes from worms to humansTanya Vavouri, Klaudia Walter, Walter R Gilks, et al.
Genetic Epidemiology|March 29, 2014
Estimating genome-wide significance for whole-genome sequencing studiesChangJiang Xu, Ioanna Tachmazidou, Klaudia Walter, et al.
Genetic Epidemiology|September 15, 2019
Population-wide copy number variation calling using variant call format files from 6,898 individualsGrace Png, Daniel Suveges, Young-Chan Park, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United KingdomHimanshu Chheda, Priit Palta, Matti Pirinen, et al.
Nature Genetics|January 30, 2019
GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signalsValentina Iotchkova, Graham R S Ritchie, Matthias Geihs, et al.
Bioinformatics (Oxford, England)|August 29, 2015
An interactive genome browser of association results from the UK10K cohorts projectMatthias Geihs, Ying Yan, Klaudia Walter, et al.
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
Methods in Molecular Biology (Clifton, N.J.)|June 8, 2018
Quality Control of Common and Rare VariantsKalliope Panoutsopoulou, Klaudia Walter
Genome Biology|April 29, 2017
The impact of rare and low-frequency genetic variants in common diseaseLorenzo Bomba, Klaudia Walter, Nicole Soranzo
Trends in Genetics : TIG|June 28, 2005
Striking nucleotide frequency pattern at the borders of highly conserved vertebrate non-coding sequencesKlaudia Walter, Irina Abnizova, Greg Elgar, et al.
BMC Bioinformatics|April 29, 2005
Some statistical properties of regulatory DNA sequences, and their use in predicting regulatory regions in the Drosophila genome: the fluffy-tail testIrina Abnizova, Rene te Boekhorst, Klaudia Walter, et al.
Genome Biology|February 6, 2007
Parallel evolution of conserved non-coding elements that target a common set of developmental regulatory genes from worms to humansTanya Vavouri, Klaudia Walter, Walter R Gilks, et al.
Genetic Epidemiology|March 29, 2014
Estimating genome-wide significance for whole-genome sequencing studiesChangJiang Xu, Ioanna Tachmazidou, Klaudia Walter, et al.
Genetic Epidemiology|September 15, 2019
Population-wide copy number variation calling using variant call format files from 6,898 individualsGrace Png, Daniel Suveges, Young-Chan Park, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United KingdomHimanshu Chheda, Priit Palta, Matti Pirinen, et al.
Nature Genetics|January 30, 2019
GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signalsValentina Iotchkova, Graham R S Ritchie, Matthias Geihs, et al.
Bioinformatics (Oxford, England)|August 29, 2015
An interactive genome browser of association results from the UK10K cohorts projectMatthias Geihs, Ying Yan, Klaudia Walter, et al.
Pageof 7