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Manuel A Rivas

Showing results (1-10 of 104) with videos related to

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Biorxiv : the Preprint Server for Biology|February 3, 2025
Unified meta regression models for rare variant association studiesLarissa Lauer, Manuel A Rivas
Bioinformatics (Oxford, England)|February 11, 2025
Efficient storage and regression computation for population-scale genome sequencing studiesManuel A Rivas, Christopher Chang
Biorxiv : the Preprint Server for Biology|April 25, 2024
Efficient storage and regression computation for population-scale genome sequencing studiesManuel A Rivas, Christopher Chang
Human Molecular Genetics|August 1, 2019
Rare and common variant discovery in complex disease: the IBD case studyGuhan R Venkataraman, Manuel A Rivas
American Journal of Human Genetics|July 30, 2019
Phenome-wide Burden of Copy-Number Variation in the UK BiobankMatthew Aguirre, Manuel A Rivas, James Priest
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
A unified meta-regression model identifies genes associated with epilepsyOscar Aguilar, Mijail Rivas, Manuel A Rivas
Biorxiv : the Preprint Server for Biology|April 25, 2024
Integrative machine learning approaches for predicting disease risk using multi-omics data from the UK BiobankOscar Aguilar, Cheng Chang, Elsa Bismuth, et al.
Plos Genetics|August 23, 2013
A flexible approach for the analysis of rare variants allowing for a mixture of effects on binary or quantitative traitsGeraldine M Clarke, Manuel A Rivas, Andrew P Morris
NPJ Genomic Medicine|December 22, 2017
Mosaic mutations in blood DNA sequence are associated with solid tumor cancersMykyta Artomov, Manuel A Rivas, Giulio Genovese, et al.
Nature Communications|January 14, 2021
Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanksDavid Amar, Nasa Sinnott-Armstrong, Euan A Ashley, et al.
Pageof 11

Showing results (1-10 of 104) with videos related to

Sort By:
Pageof 11
Biorxiv : the Preprint Server for Biology|February 3, 2025
Unified meta regression models for rare variant association studiesLarissa Lauer, Manuel A Rivas
Bioinformatics (Oxford, England)|February 11, 2025
Efficient storage and regression computation for population-scale genome sequencing studiesManuel A Rivas, Christopher Chang
Biorxiv : the Preprint Server for Biology|April 25, 2024
Efficient storage and regression computation for population-scale genome sequencing studiesManuel A Rivas, Christopher Chang
Human Molecular Genetics|August 1, 2019
Rare and common variant discovery in complex disease: the IBD case studyGuhan R Venkataraman, Manuel A Rivas
American Journal of Human Genetics|July 30, 2019
Phenome-wide Burden of Copy-Number Variation in the UK BiobankMatthew Aguirre, Manuel A Rivas, James Priest
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
A unified meta-regression model identifies genes associated with epilepsyOscar Aguilar, Mijail Rivas, Manuel A Rivas
Biorxiv : the Preprint Server for Biology|April 25, 2024
Integrative machine learning approaches for predicting disease risk using multi-omics data from the UK BiobankOscar Aguilar, Cheng Chang, Elsa Bismuth, et al.
Plos Genetics|August 23, 2013
A flexible approach for the analysis of rare variants allowing for a mixture of effects on binary or quantitative traitsGeraldine M Clarke, Manuel A Rivas, Andrew P Morris
NPJ Genomic Medicine|December 22, 2017
Mosaic mutations in blood DNA sequence are associated with solid tumor cancersMykyta Artomov, Manuel A Rivas, Giulio Genovese, et al.
Nature Communications|January 14, 2021
Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanksDavid Amar, Nasa Sinnott-Armstrong, Euan A Ashley, et al.
Pageof 11