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Jonathon LeFaive

Showing results (1-10 of 19) with videos related to

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Bioinformatics (Oxford, England)|May 14, 2021
Sparse allele vectors and the savvy software suiteJonathon LeFaive, Albert V Smith, Hyun Min Kang, et al.
Bioinformatics (Oxford, England)|January 22, 2026
MethylModes: Computationally Efficient Detection of Multimodal Distributions in DNA Methylation DataT Sophia Luo, Jonathon LeFaive, John Dou, et al.
Nucleic Acids Research|May 6, 2024
Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation serversLukas Forer, Daniel Taliun, Jonathon LeFaive, et al.
American Journal of Human Genetics|May 4, 2022
Meta-imputation: An efficient method to combine genotype data after imputation with multiple reference panelsKetian Yu, Sayantan Das, Jonathon LeFaive, et al.
American Journal of Human Genetics|August 22, 2023
The phenotype-genotype reference map: Improving biobank data science through replicationLisa Bastarache, Sarah Delozier, Anita Pandit, et al.
Genome Biology|February 22, 2023
FixItFelix: improving genomic analysis by fixing reference errorsSairam Behera, Jonathon LeFaive, Peter Orchard, et al.
Nature Genetics|May 20, 2020
Scalable generalized linear mixed model for region-based association tests in large biobanks and cohortsWei Zhou, Zhangchen Zhao, Jonas B Nielsen, et al.
Nature Protocols|July 26, 2023
Tutorial: a statistical genetics guide to identifying HLA alleles driving complex diseaseSaori Sakaue, Saisriram Gurajala, Michelle Curtis, et al.
Plos Genetics|June 14, 2019
Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWebLars G Fritsche, Lauren J Beesley, Peter VandeHaar, et al.
Nature Genetics|August 15, 2018
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studiesWei Zhou, Jonas B Nielsen, Lars G Fritsche, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|May 14, 2021
Sparse allele vectors and the savvy software suiteJonathon LeFaive, Albert V Smith, Hyun Min Kang, et al.
Bioinformatics (Oxford, England)|January 22, 2026
MethylModes: Computationally Efficient Detection of Multimodal Distributions in DNA Methylation DataT Sophia Luo, Jonathon LeFaive, John Dou, et al.
Nucleic Acids Research|May 6, 2024
Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation serversLukas Forer, Daniel Taliun, Jonathon LeFaive, et al.
American Journal of Human Genetics|May 4, 2022
Meta-imputation: An efficient method to combine genotype data after imputation with multiple reference panelsKetian Yu, Sayantan Das, Jonathon LeFaive, et al.
American Journal of Human Genetics|August 22, 2023
The phenotype-genotype reference map: Improving biobank data science through replicationLisa Bastarache, Sarah Delozier, Anita Pandit, et al.
Genome Biology|February 22, 2023
FixItFelix: improving genomic analysis by fixing reference errorsSairam Behera, Jonathon LeFaive, Peter Orchard, et al.
Nature Genetics|May 20, 2020
Scalable generalized linear mixed model for region-based association tests in large biobanks and cohortsWei Zhou, Zhangchen Zhao, Jonas B Nielsen, et al.
Nature Protocols|July 26, 2023
Tutorial: a statistical genetics guide to identifying HLA alleles driving complex diseaseSaori Sakaue, Saisriram Gurajala, Michelle Curtis, et al.
Plos Genetics|June 14, 2019
Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWebLars G Fritsche, Lauren J Beesley, Peter VandeHaar, et al.
Nature Genetics|August 15, 2018
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studiesWei Zhou, Jonas B Nielsen, Lars G Fritsche, et al.
Pageof 2