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Benjamin M Neale

Showing results (51-60 of 293) with videos related to

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Bioinformatics (Oxford, England)|December 24, 2024
The scalable variant call representation: enabling genetic analysis beyond one million genomesTimothy Poterba, Christopher Vittal, Daniel King, et al.
Molecular Autism|March 22, 2013
Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorderSamira Bahl, Colby Chiang, Roberta L Beauchamp, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2024
The Scalable Variant Call Representation: Enabling Genetic Analysis Beyond One Million GenomesTimothy Poterba, Christopher Vittal, Daniel King, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|February 28, 2017
The Weighting is the Hardest Part: On the Behavior of the Likelihood Ratio Test and the Score Test Under a Data-Driven Weighting Scheme in Sequenced SamplesCamelia C Minică, Giulio Genovese, Christina M Hultman, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2025
Polygenic Scores for Schizophrenia and Educational Attainment Predict Global Functioning Across Psychiatric Hospitalization Among People with SchizophreniaEvan J Giangrande, Anders Kämpe, Jaana Suvisaari, et al.
Nature Genetics|September 22, 2022
SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association testsWei Zhou, Wenjian Bi, Zhangchen Zhao, et al.
Nature Genetics|November 30, 2023
Improving fine-mapping by modeling infinitesimal effectsRan Cui, Roy A Elzur, Masahiro Kanai, et al.
Nature Genetics|October 18, 2022
Publisher Correction: SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association testsWei Zhou, Wenjian Bi, Zhangchen Zhao, et al.
Nature|February 9, 2023
Polygenic architecture of rare coding variation across 394,783 exomesDaniel J Weiner, Ajay Nadig, Karthik A Jagadeesh, et al.
Genome Research|May 30, 2023
Discordant calls across genotype discovery approaches elucidate variants with systematic errorsElizabeth G Atkinson, Mykyta Artomov, Alexander A Loboda, et al.
Pageof 30

Showing results (51-60 of 293) with videos related to

Sort By:
Pageof 30
Bioinformatics (Oxford, England)|December 24, 2024
The scalable variant call representation: enabling genetic analysis beyond one million genomesTimothy Poterba, Christopher Vittal, Daniel King, et al.
Molecular Autism|March 22, 2013
Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorderSamira Bahl, Colby Chiang, Roberta L Beauchamp, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2024
The Scalable Variant Call Representation: Enabling Genetic Analysis Beyond One Million GenomesTimothy Poterba, Christopher Vittal, Daniel King, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|February 28, 2017
The Weighting is the Hardest Part: On the Behavior of the Likelihood Ratio Test and the Score Test Under a Data-Driven Weighting Scheme in Sequenced SamplesCamelia C Minică, Giulio Genovese, Christina M Hultman, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2025
Polygenic Scores for Schizophrenia and Educational Attainment Predict Global Functioning Across Psychiatric Hospitalization Among People with SchizophreniaEvan J Giangrande, Anders Kämpe, Jaana Suvisaari, et al.
Nature Genetics|September 22, 2022
SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association testsWei Zhou, Wenjian Bi, Zhangchen Zhao, et al.
Nature Genetics|November 30, 2023
Improving fine-mapping by modeling infinitesimal effectsRan Cui, Roy A Elzur, Masahiro Kanai, et al.
Nature Genetics|October 18, 2022
Publisher Correction: SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association testsWei Zhou, Wenjian Bi, Zhangchen Zhao, et al.
Nature|February 9, 2023
Polygenic architecture of rare coding variation across 394,783 exomesDaniel J Weiner, Ajay Nadig, Karthik A Jagadeesh, et al.
Genome Research|May 30, 2023
Discordant calls across genotype discovery approaches elucidate variants with systematic errorsElizabeth G Atkinson, Mykyta Artomov, Alexander A Loboda, et al.
Pageof 30