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Ira M Hall

Showing results (31-40 of 54) with videos related to

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Science (New York, N.Y.)|November 2, 2013
Mosaic copy number variation in human neuronsMichael J McConnell, Michael R Lindberg, Kristen J Brennand, et al.
Nature Genetics|April 4, 2017
The impact of structural variation on human gene expressionColby Chiang, Alexandra J Scott, Joe R Davis, et al.
Neuron|March 8, 2016
The Complete Genome Sequences, Unique Mutational Spectra, and Developmental Potency of Adult Neurons Revealed by CloningJennifer L Hazen, Gregory G Faust, Alberto R Rodriguez, et al.
Nature|October 13, 2017
The impact of rare variation on gene expression across tissuesXin Li, Yungil Kim, Emily K Tsang, et al.
Molecular Psychiatry|February 2, 2021
Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variantsElmo Christian Saarentaus, Aki Samuli Havulinna, Nina Mars, et al.
Cell|September 2, 2022
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 triosMarta Byrska-Bishop, Uday S Evani, Xuefang Zhao, et al.
Nature Communications|October 4, 2018
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projectsAllison A Regier, Yossi Farjoun, David E Larson, et al.
Nature|May 28, 2020
Mapping and characterization of structural variation in 17,795 human genomesHaley J Abel, David E Larson, Allison A Regier, et al.
Human Genomics|June 8, 2021
Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differencesLiron Ganel, Lei Chen, Ryan Christ, et al.
Briefings in Bioinformatics|March 27, 2026
Comparison of variant callers using 60 532 multi-ancestry whole genome sequencesHufeng Zhou, Zilin Li, Derek Shyr, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
Science (New York, N.Y.)|November 2, 2013
Mosaic copy number variation in human neuronsMichael J McConnell, Michael R Lindberg, Kristen J Brennand, et al.
Nature Genetics|April 4, 2017
The impact of structural variation on human gene expressionColby Chiang, Alexandra J Scott, Joe R Davis, et al.
Neuron|March 8, 2016
The Complete Genome Sequences, Unique Mutational Spectra, and Developmental Potency of Adult Neurons Revealed by CloningJennifer L Hazen, Gregory G Faust, Alberto R Rodriguez, et al.
Nature|October 13, 2017
The impact of rare variation on gene expression across tissuesXin Li, Yungil Kim, Emily K Tsang, et al.
Molecular Psychiatry|February 2, 2021
Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variantsElmo Christian Saarentaus, Aki Samuli Havulinna, Nina Mars, et al.
Cell|September 2, 2022
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 triosMarta Byrska-Bishop, Uday S Evani, Xuefang Zhao, et al.
Nature Communications|October 4, 2018
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projectsAllison A Regier, Yossi Farjoun, David E Larson, et al.
Nature|May 28, 2020
Mapping and characterization of structural variation in 17,795 human genomesHaley J Abel, David E Larson, Allison A Regier, et al.
Human Genomics|June 8, 2021
Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differencesLiron Ganel, Lei Chen, Ryan Christ, et al.
Briefings in Bioinformatics|March 27, 2026
Comparison of variant callers using 60 532 multi-ancestry whole genome sequencesHufeng Zhou, Zilin Li, Derek Shyr, et al.
Pageof 6