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Eric Banks

Showing results (21-30 of 54) with videos related to

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Nature Communications|February 28, 2025
Pan-cancer multi-omic model of LINE-1 activity reveals locus heterogeneity of retrotransposition efficiencyAlexander Solovyov, Julie M Behr, David Hoyos, et al.
JCO Precision Oncology|January 18, 2024
Detection of Copy-Number Variation in Circulating Cell-Free DNA in Patients With Uveal MelanomaTakuto Sato, Kamaneh Montazeri, Evangelos S Gragoudas, et al.
Nature Genetics|January 24, 2024
Author Correction: GATK-gCNV enables the discovery of rare copy number variants from exome sequencing dataMehrtash Babadi, Jack M Fu, Samuel K Lee, et al.
Nature Genetics|August 21, 2023
GATK-gCNV enables the discovery of rare copy number variants from exome sequencing dataMehrtash Babadi, Jack M Fu, Samuel K Lee, et al.
Genome Research|January 25, 2022
Mitochondrial DNA variation across 56,434 individuals in gnomADKristen M Laricchia, Nicole J Lake, Nicholas A Watts, et al.
American Journal of Human Genetics|October 9, 2012
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depthMenachem Fromer, Jennifer L Moran, Kimberly Chambert, et al.
Nature Biotechnology|June 8, 2023
High-throughput RNA isoform sequencing using programmed cDNA concatenationAziz M Al'Khafaji, Jonathan T Smith, Kiran V Garimella, et al.
Nature Genetics|April 12, 2011
A framework for variation discovery and genotyping using next-generation DNA sequencing dataMark A DePristo, Eric Banks, Ryan Poplin, 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.
Journal of the American Medical Informatics Association : JAMIA|August 13, 2024
Empowering the biomedical research community: Innovative SAS deployment on the All of Us Researcher WorkbenchIzabelle Humes, Cathy Shyr, Moira Dillon, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Nature Communications|February 28, 2025
Pan-cancer multi-omic model of LINE-1 activity reveals locus heterogeneity of retrotransposition efficiencyAlexander Solovyov, Julie M Behr, David Hoyos, et al.
JCO Precision Oncology|January 18, 2024
Detection of Copy-Number Variation in Circulating Cell-Free DNA in Patients With Uveal MelanomaTakuto Sato, Kamaneh Montazeri, Evangelos S Gragoudas, et al.
Nature Genetics|January 24, 2024
Author Correction: GATK-gCNV enables the discovery of rare copy number variants from exome sequencing dataMehrtash Babadi, Jack M Fu, Samuel K Lee, et al.
Nature Genetics|August 21, 2023
GATK-gCNV enables the discovery of rare copy number variants from exome sequencing dataMehrtash Babadi, Jack M Fu, Samuel K Lee, et al.
Genome Research|January 25, 2022
Mitochondrial DNA variation across 56,434 individuals in gnomADKristen M Laricchia, Nicole J Lake, Nicholas A Watts, et al.
American Journal of Human Genetics|October 9, 2012
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depthMenachem Fromer, Jennifer L Moran, Kimberly Chambert, et al.
Nature Biotechnology|June 8, 2023
High-throughput RNA isoform sequencing using programmed cDNA concatenationAziz M Al'Khafaji, Jonathan T Smith, Kiran V Garimella, et al.
Nature Genetics|April 12, 2011
A framework for variation discovery and genotyping using next-generation DNA sequencing dataMark A DePristo, Eric Banks, Ryan Poplin, 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.
Journal of the American Medical Informatics Association : JAMIA|August 13, 2024
Empowering the biomedical research community: Innovative SAS deployment on the All of Us Researcher WorkbenchIzabelle Humes, Cathy Shyr, Moira Dillon, et al.
Pageof 6