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Genetic Epidemiology
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September 24, 2015
SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations
Xiaowei Zhan, Dajiang J Liu
European Journal of Human Genetics : EJHG
|
December 15, 2011
A flexible likelihood framework for detecting associations with secondary phenotypes in genetic studies using selected samples: application to sequence data
Dajiang J Liu, Suzanne M Leal
Human Heredity
|
May 5, 2012
A unified framework for detecting rare variant quantitative trait associations in pedigree and unrelated individuals via sequence data
Dajiang J Liu, Suzanne M Leal
Plos Genetics
|
November 21, 2012
A unified method for detecting secondary trait associations with rare variants: application to sequence data
Dajiang J Liu, Suzanne M Leal
American Journal of Human Genetics
|
December 7, 2010
Replication strategies for rare variant complex trait association studies via next-generation sequencing
Dajiang J Liu, Suzanne M Leal
Plos Genetics
|
October 27, 2010
A novel adaptive method for the analysis of next-generation sequencing data to detect complex trait associations with rare variants due to gene main effects and interactions
Dajiang J Liu, Suzanne M Leal
Bioinformatics (Oxford, England)
|
May 5, 2012
SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations
Dajiang J Liu, Suzanne M Leal
American Journal of Human Genetics
|
October 2, 2012
Estimating genetic effects and quantifying missing heritability explained by identified rare-variant associations
Dajiang J Liu, Suzanne M Leal
Current Protocols in Human Genetics
|
July 16, 2013
Identifying rare variants associated with complex traits via sequencing
Bingshan Li, Dajiang J Liu, Suzanne M Leal
Behavior Genetics
|
April 28, 2026
Insights into the Cross-Population Transferability of Polygenic Scores for Substance Use
Gretchen R B Saunders, Scott Vrieze, Dajiang J Liu
Page
of 8
Search research articles
Search
Showing results (1-10 of 76) with videos related to
Sort By:
Page
of 8
Genetic Epidemiology
|
September 24, 2015
SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations
Xiaowei Zhan, Dajiang J Liu
European Journal of Human Genetics : EJHG
|
December 15, 2011
A flexible likelihood framework for detecting associations with secondary phenotypes in genetic studies using selected samples: application to sequence data
Dajiang J Liu, Suzanne M Leal
Human Heredity
|
May 5, 2012
A unified framework for detecting rare variant quantitative trait associations in pedigree and unrelated individuals via sequence data
Dajiang J Liu, Suzanne M Leal
Plos Genetics
|
November 21, 2012
A unified method for detecting secondary trait associations with rare variants: application to sequence data
Dajiang J Liu, Suzanne M Leal
American Journal of Human Genetics
|
December 7, 2010
Replication strategies for rare variant complex trait association studies via next-generation sequencing
Dajiang J Liu, Suzanne M Leal
Plos Genetics
|
October 27, 2010
A novel adaptive method for the analysis of next-generation sequencing data to detect complex trait associations with rare variants due to gene main effects and interactions
Dajiang J Liu, Suzanne M Leal
Bioinformatics (Oxford, England)
|
May 5, 2012
SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations
Dajiang J Liu, Suzanne M Leal
American Journal of Human Genetics
|
October 2, 2012
Estimating genetic effects and quantifying missing heritability explained by identified rare-variant associations
Dajiang J Liu, Suzanne M Leal
Current Protocols in Human Genetics
|
July 16, 2013
Identifying rare variants associated with complex traits via sequencing
Bingshan Li, Dajiang J Liu, Suzanne M Leal
Behavior Genetics
|
April 28, 2026
Insights into the Cross-Population Transferability of Polygenic Scores for Substance Use
Gretchen R B Saunders, Scott Vrieze, Dajiang J Liu
Page
of 8