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Benjamin M Neale

Showing results (61-70 of 293) with videos related to

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Genome Research|June 3, 2018
Base-specific mutational intolerance near splice sites clarifies the role of nonessential splice nucleotidesSidi Zhang, Kaitlin E Samocha, Manuel A Rivas, et al.
Nature Genetics|June 29, 2010
Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independentSoumya Raychaudhuri, Stephan Ripke, Mingyao Li, et al.
Nature Genetics|February 3, 2015
LD Score regression distinguishes confounding from polygenicity in genome-wide association studiesBrendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 21, 2014
Searching for missing heritability: designing rare variant association studiesOr Zuk, Stephen F Schaffner, Kaitlin Samocha, et al.
American Journal of Human Genetics|October 2, 2020
Human Demographic History Impacts Genetic Risk Prediction across Diverse PopulationsAlicia R Martin, Christopher R Gignoux, Raymond K Walters, et al.
American Journal of Human Genetics|November 24, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.
American Journal of Human Genetics|April 4, 2017
Human Demographic History Impacts Genetic Risk Prediction across Diverse PopulationsAlicia R Martin, Christopher R Gignoux, Raymond K Walters, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.
Plos Genetics|March 17, 2011
Testing for an unusual distribution of rare variantsBenjamin M Neale, Manuel A Rivas, Benjamin F Voight, et al.
Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK BiobankFrederik H Lassen, Samvida S Venkatesh, Nikolas Baya, et al.
Pageof 30

Showing results (61-70 of 293) with videos related to

Sort By:
Pageof 30
Genome Research|June 3, 2018
Base-specific mutational intolerance near splice sites clarifies the role of nonessential splice nucleotidesSidi Zhang, Kaitlin E Samocha, Manuel A Rivas, et al.
Nature Genetics|June 29, 2010
Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independentSoumya Raychaudhuri, Stephan Ripke, Mingyao Li, et al.
Nature Genetics|February 3, 2015
LD Score regression distinguishes confounding from polygenicity in genome-wide association studiesBrendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 21, 2014
Searching for missing heritability: designing rare variant association studiesOr Zuk, Stephen F Schaffner, Kaitlin Samocha, et al.
American Journal of Human Genetics|October 2, 2020
Human Demographic History Impacts Genetic Risk Prediction across Diverse PopulationsAlicia R Martin, Christopher R Gignoux, Raymond K Walters, et al.
American Journal of Human Genetics|November 24, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.
American Journal of Human Genetics|April 4, 2017
Human Demographic History Impacts Genetic Risk Prediction across Diverse PopulationsAlicia R Martin, Christopher R Gignoux, Raymond K Walters, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.
Plos Genetics|March 17, 2011
Testing for an unusual distribution of rare variantsBenjamin M Neale, Manuel A Rivas, Benjamin F Voight, et al.
Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK BiobankFrederik H Lassen, Samvida S Venkatesh, Nikolas Baya, et al.
Pageof 30