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J Karczewski

Showing results (61-70 of 144) with videos related to

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Biorxiv : the Preprint Server for Biology|July 10, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.
Nature|January 18, 2023
Mono- and biallelic variant effects on disease at biobank scaleH O Heyne, J Karjalainen, K J Karczewski, et al.
Nature Genetics|August 18, 2016
Patterns of genic intolerance of rare copy number variation in 59,898 human exomesDouglas M Ruderfer, Tymor Hamamsy, Monkol Lek, et al.
American Journal of Human Genetics|November 24, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.
Biodata Mining|February 3, 2023
LoFTK: a framework for fully automated calculation of predicted Loss-of-Function variants and genesAbdulrahman Alasiri, Konrad J Karczewski, Brian Cole, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Mechanism of age-related accumulation of mitochondrial DNA mutations in human bloodRahul Gupta, Timothy J Durham, Grant Chau, et al.
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Nuclear genetic control of mtDNA copy number and heteroplasmy in humansRahul Gupta, Masahiro Kanai, Timothy J Durham, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Inference of elevated mutation rates and variant effects using 700k exomesPrathitha Kar, Mikhail A Moldovan, Jeremy Guez, et al.
Medrxiv : the Preprint Server for Health Sciences|October 9, 2023
Hematologic setpoints are a stable and patient-specific deep phenotypeBrody H Foy, Rachel Petherbridge, Maxwell Roth, et al.
Nature Communications|May 29, 2020
Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomesQingbo Wang, Emma Pierce-Hoffman, Beryl B Cummings, et al.
Pageof 15

Showing results (61-70 of 144) with videos related to

Sort By:
Pageof 15
Biorxiv : the Preprint Server for Biology|July 10, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.
Nature|January 18, 2023
Mono- and biallelic variant effects on disease at biobank scaleH O Heyne, J Karjalainen, K J Karczewski, et al.
Nature Genetics|August 18, 2016
Patterns of genic intolerance of rare copy number variation in 59,898 human exomesDouglas M Ruderfer, Tymor Hamamsy, Monkol Lek, et al.
American Journal of Human Genetics|November 24, 2023
CHARR efficiently estimates contamination from DNA sequencing dataWenhan Lu, Laura D Gauthier, Timothy Poterba, et al.
Biodata Mining|February 3, 2023
LoFTK: a framework for fully automated calculation of predicted Loss-of-Function variants and genesAbdulrahman Alasiri, Konrad J Karczewski, Brian Cole, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Mechanism of age-related accumulation of mitochondrial DNA mutations in human bloodRahul Gupta, Timothy J Durham, Grant Chau, et al.
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Nuclear genetic control of mtDNA copy number and heteroplasmy in humansRahul Gupta, Masahiro Kanai, Timothy J Durham, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Inference of elevated mutation rates and variant effects using 700k exomesPrathitha Kar, Mikhail A Moldovan, Jeremy Guez, et al.
Medrxiv : the Preprint Server for Health Sciences|October 9, 2023
Hematologic setpoints are a stable and patient-specific deep phenotypeBrody H Foy, Rachel Petherbridge, Maxwell Roth, et al.
Nature Communications|May 29, 2020
Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomesQingbo Wang, Emma Pierce-Hoffman, Beryl B Cummings, et al.
Pageof 15