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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 individuals
Sebastian Zöllner
European Journal of Human Genetics : EJHG
|
April 19, 2012
Sampling strategies for rare variant tests in case-control studies
Sebastian Zöllner
Biorxiv : the Preprint Server for Biology
|
March 30, 2023
Inferring CpG methylation signatures accumulated along human history from genetic variation catalogs
Yichen Si, Sebastian Zöllner
Medrxiv : the Preprint Server for Health Sciences
|
March 4, 2024
A Stacking Framework for Polygenic Risk Prediction in Admixed Individuals
Kevin Liao, Sebastian Zöllner
Genetic Epidemiology
|
May 14, 2015
Robust and Powerful Affected Sibpair Test for Rare Variant Association
Keng-Han Lin, Sebastian Zöllner
Genetics
|
October 19, 2004
Coalescent-based association mapping and fine mapping of complex trait loci
Sebastian Zöllner, Jonathan K Pritchard
Bioinformatics (Oxford, England)
|
March 24, 2012
FTEC: a coalescent simulator for modeling faster than exponential growth
Mark Reppell, Michael Boehnke, Sebastian Zöllner
G3 (Bethesda, Md.)
|
February 9, 2023
The effect of mutation subtypes on the allele frequency spectrum and population genetics inference
Kevin Liao, Jedidiah Carlson, Sebastian Zöllner
Genetics
|
March 9, 2021
Why are rare variants hard to impute? Coalescent models reveal theoretical limits in existing algorithms
Yichen Si, Brett Vanderwerff, Sebastian Zöllner
Genetics
|
January 2, 2014
The impact of accelerating faster than exponential population growth on genetic variation
Mark Reppell, Michael Boehnke, Sebastian Zöllner
Page
of 11
Search research articles
Search
Showing results (1-10 of 103) with videos related to
Sort By:
Page
of 11
Bioinformatics (Oxford, England)
|
October 8, 2010
CopyMap: localization and calling of copy number variation by joint analysis of hybridization data from multiple individuals
Sebastian Zöllner
European Journal of Human Genetics : EJHG
|
April 19, 2012
Sampling strategies for rare variant tests in case-control studies
Sebastian Zöllner
Biorxiv : the Preprint Server for Biology
|
March 30, 2023
Inferring CpG methylation signatures accumulated along human history from genetic variation catalogs
Yichen Si, Sebastian Zöllner
Medrxiv : the Preprint Server for Health Sciences
|
March 4, 2024
A Stacking Framework for Polygenic Risk Prediction in Admixed Individuals
Kevin Liao, Sebastian Zöllner
Genetic Epidemiology
|
May 14, 2015
Robust and Powerful Affected Sibpair Test for Rare Variant Association
Keng-Han Lin, Sebastian Zöllner
Genetics
|
October 19, 2004
Coalescent-based association mapping and fine mapping of complex trait loci
Sebastian Zöllner, Jonathan K Pritchard
Bioinformatics (Oxford, England)
|
March 24, 2012
FTEC: a coalescent simulator for modeling faster than exponential growth
Mark Reppell, Michael Boehnke, Sebastian Zöllner
G3 (Bethesda, Md.)
|
February 9, 2023
The effect of mutation subtypes on the allele frequency spectrum and population genetics inference
Kevin Liao, Jedidiah Carlson, Sebastian Zöllner
Genetics
|
March 9, 2021
Why are rare variants hard to impute? Coalescent models reveal theoretical limits in existing algorithms
Yichen Si, Brett Vanderwerff, Sebastian Zöllner
Genetics
|
January 2, 2014
The impact of accelerating faster than exponential population growth on genetic variation
Mark Reppell, Michael Boehnke, Sebastian Zöllner
Page
of 11