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Bioinformatics (Oxford, England)
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June 17, 2026
Praxis-BGM: Clustering of Omics Data Using Semi-Supervised Transfer Learning for Gaussian Mixture Models via Natural-Gradient Variational Inference
Qiran Jia, Jesse A Goodrich, David V Conti
Statistics in Medicine
|
January 14, 2010
A polytomous conditional likelihood approach for combining matched and unmatched case-control studies
Mulugeta Gebregziabher, Paulo Guimaraes, Wendy Cozen, et al.
Genetic Epidemiology
|
September 14, 2012
Analysis and optimal design for association studies using next-generation sequencing with case-control pools
Wei E Liang, Duncan C Thomas, David V Conti
Genetic Epidemiology
|
April 6, 2007
Testing association between disease and multiple SNPs in a candidate gene
W James Gauderman, Cassandra Murcray, Frank Gilliland, et al.
Human Heredity
|
November 14, 2003
Bayesian modeling of complex metabolic pathways
David V Conti, Victoria Cortessis, John Molitor, et al.
Statistics in Medicine
|
June 22, 2021
Bayesian variable selection with a pleiotropic loss function in Mendelian randomization
Apostolos Gkatzionis, Stephen Burgess, David V Conti, et al.
American Journal of Human Genetics
|
December 31, 2005
A testing framework for identifying susceptibility genes in the presence of epistasis
Joshua Millstein, David V Conti, Frank D Gilliland, et al.
Journal of Data Science : JDS
|
February 28, 2022
Sign-based Shrinkage Based on an Asymmetric LASSO Penalty
Eric S Kawaguchi, Burcu F Darst, Kan Wang, et al.
BMC Genetics
|
February 3, 2006
Identifying susceptibility genes by using joint tests of association and linkage and accounting for epistasis
Joshua Millstein, Kimberly D Siegmund, David V Conti, et al.
Bioinformatics Advances
|
September 3, 2024
An extension of latent unknown clustering integrating multi-omics data (LUCID) incorporating incomplete omics data
Yinqi Zhao, Qiran Jia, Jesse Goodrich, et al.
Page
of 34
Search research articles
Search
Showing results (11-20 of 338) with videos related to
Sort By:
Page
of 34
Bioinformatics (Oxford, England)
|
June 17, 2026
Praxis-BGM: Clustering of Omics Data Using Semi-Supervised Transfer Learning for Gaussian Mixture Models via Natural-Gradient Variational Inference
Qiran Jia, Jesse A Goodrich, David V Conti
Statistics in Medicine
|
January 14, 2010
A polytomous conditional likelihood approach for combining matched and unmatched case-control studies
Mulugeta Gebregziabher, Paulo Guimaraes, Wendy Cozen, et al.
Genetic Epidemiology
|
September 14, 2012
Analysis and optimal design for association studies using next-generation sequencing with case-control pools
Wei E Liang, Duncan C Thomas, David V Conti
Genetic Epidemiology
|
April 6, 2007
Testing association between disease and multiple SNPs in a candidate gene
W James Gauderman, Cassandra Murcray, Frank Gilliland, et al.
Human Heredity
|
November 14, 2003
Bayesian modeling of complex metabolic pathways
David V Conti, Victoria Cortessis, John Molitor, et al.
Statistics in Medicine
|
June 22, 2021
Bayesian variable selection with a pleiotropic loss function in Mendelian randomization
Apostolos Gkatzionis, Stephen Burgess, David V Conti, et al.
American Journal of Human Genetics
|
December 31, 2005
A testing framework for identifying susceptibility genes in the presence of epistasis
Joshua Millstein, David V Conti, Frank D Gilliland, et al.
Journal of Data Science : JDS
|
February 28, 2022
Sign-based Shrinkage Based on an Asymmetric LASSO Penalty
Eric S Kawaguchi, Burcu F Darst, Kan Wang, et al.
BMC Genetics
|
February 3, 2006
Identifying susceptibility genes by using joint tests of association and linkage and accounting for epistasis
Joshua Millstein, Kimberly D Siegmund, David V Conti, et al.
Bioinformatics Advances
|
September 3, 2024
An extension of latent unknown clustering integrating multi-omics data (LUCID) incorporating incomplete omics data
Yinqi Zhao, Qiran Jia, Jesse Goodrich, et al.
Page
of 34