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Sebastian Zöllner

Showing results (1-10 of 103) with videos related to

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Bioinformatics (Oxford, England)|October 8, 2010
CopyMap: localization and calling of copy number variation by joint analysis of hybridization data from multiple individualsSebastian Zöllner
European Journal of Human Genetics : EJHG|April 19, 2012
Sampling strategies for rare variant tests in case-control studiesSebastian Zöllner
Biorxiv : the Preprint Server for Biology|March 30, 2023
Inferring CpG methylation signatures accumulated along human history from genetic variation catalogsYichen Si, Sebastian Zöllner
Medrxiv : the Preprint Server for Health Sciences|March 4, 2024
A Stacking Framework for Polygenic Risk Prediction in Admixed IndividualsKevin Liao, Sebastian Zöllner
Genetic Epidemiology|May 14, 2015
Robust and Powerful Affected Sibpair Test for Rare Variant AssociationKeng-Han Lin, Sebastian Zöllner
Genetics|October 19, 2004
Coalescent-based association mapping and fine mapping of complex trait lociSebastian Zöllner, Jonathan K Pritchard
Bioinformatics (Oxford, England)|March 24, 2012
FTEC: a coalescent simulator for modeling faster than exponential growthMark Reppell, Michael Boehnke, Sebastian Zöllner
G3 (Bethesda, Md.)|February 9, 2023
The effect of mutation subtypes on the allele frequency spectrum and population genetics inferenceKevin Liao, Jedidiah Carlson, Sebastian Zöllner
Genetics|March 9, 2021
Why are rare variants hard to impute? Coalescent models reveal theoretical limits in existing algorithmsYichen Si, Brett Vanderwerff, Sebastian Zöllner
Genetics|January 2, 2014
The impact of accelerating faster than exponential population growth on genetic variationMark Reppell, Michael Boehnke, Sebastian Zöllner
Pageof 11

Showing results (1-10 of 103) with videos related to

Sort By:
Pageof 11
Bioinformatics (Oxford, England)|October 8, 2010
CopyMap: localization and calling of copy number variation by joint analysis of hybridization data from multiple individualsSebastian Zöllner
European Journal of Human Genetics : EJHG|April 19, 2012
Sampling strategies for rare variant tests in case-control studiesSebastian Zöllner
Biorxiv : the Preprint Server for Biology|March 30, 2023
Inferring CpG methylation signatures accumulated along human history from genetic variation catalogsYichen Si, Sebastian Zöllner
Medrxiv : the Preprint Server for Health Sciences|March 4, 2024
A Stacking Framework for Polygenic Risk Prediction in Admixed IndividualsKevin Liao, Sebastian Zöllner
Genetic Epidemiology|May 14, 2015
Robust and Powerful Affected Sibpair Test for Rare Variant AssociationKeng-Han Lin, Sebastian Zöllner
Genetics|October 19, 2004
Coalescent-based association mapping and fine mapping of complex trait lociSebastian Zöllner, Jonathan K Pritchard
Bioinformatics (Oxford, England)|March 24, 2012
FTEC: a coalescent simulator for modeling faster than exponential growthMark Reppell, Michael Boehnke, Sebastian Zöllner
G3 (Bethesda, Md.)|February 9, 2023
The effect of mutation subtypes on the allele frequency spectrum and population genetics inferenceKevin Liao, Jedidiah Carlson, Sebastian Zöllner
Genetics|March 9, 2021
Why are rare variants hard to impute? Coalescent models reveal theoretical limits in existing algorithmsYichen Si, Brett Vanderwerff, Sebastian Zöllner
Genetics|January 2, 2014
The impact of accelerating faster than exponential population growth on genetic variationMark Reppell, Michael Boehnke, Sebastian Zöllner
Pageof 11