Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Karczewski

Showing results (51-60 of 144) with videos related to

Pageof 15
Sort By:
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.
Inorganic Chemistry|February 28, 2020
Nano Tin/Tin Oxide Attached onto Graphene Oxide Skeleton as a Fluorine Free Anode Material for Lithium-Ion BatteriesAndrzej P Nowak, K Trzciński, M Szkoda, et al.
Blood Advances|October 26, 2020
Human mutational constraint as a tool to understand biology of rare and emerging bone marrow failure syndromesJoseph H Oved, Daria V Babushok, Michele P Lambert, 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|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.
Genome Research|June 3, 2018
Base-specific mutational intolerance near splice sites clarifies the role of nonessential splice nucleotidesSidi Zhang, Kaitlin E Samocha, Manuel A Rivas, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 17, 2011
Interpretome: a freely available, modular, and secure personal genome interpretation engineKonrad J Karczewski, Robert P Tirrell, Pablo Cordero, et al.
G3 (Bethesda, Md.)|November 4, 2016
Small RNA Sequencing in Cells and Exosomes Identifies eQTLs and 14q32 as a Region of Active ExportEmily K Tsang, Nathan S Abell, Xin Li, et al.
American Journal of Human Genetics|September 6, 2014
Transcriptome sequencing of a large human family identifies the impact of rare noncoding variantsXin Li, Alexis Battle, Konrad J Karczewski, et al.
Pageof 15

Showing results (51-60 of 144) with videos related to

Sort By:
Pageof 15
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.
Inorganic Chemistry|February 28, 2020
Nano Tin/Tin Oxide Attached onto Graphene Oxide Skeleton as a Fluorine Free Anode Material for Lithium-Ion BatteriesAndrzej P Nowak, K Trzciński, M Szkoda, et al.
Blood Advances|October 26, 2020
Human mutational constraint as a tool to understand biology of rare and emerging bone marrow failure syndromesJoseph H Oved, Daria V Babushok, Michele P Lambert, 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|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.
Genome Research|June 3, 2018
Base-specific mutational intolerance near splice sites clarifies the role of nonessential splice nucleotidesSidi Zhang, Kaitlin E Samocha, Manuel A Rivas, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 17, 2011
Interpretome: a freely available, modular, and secure personal genome interpretation engineKonrad J Karczewski, Robert P Tirrell, Pablo Cordero, et al.
G3 (Bethesda, Md.)|November 4, 2016
Small RNA Sequencing in Cells and Exosomes Identifies eQTLs and 14q32 as a Region of Active ExportEmily K Tsang, Nathan S Abell, Xin Li, et al.
American Journal of Human Genetics|September 6, 2014
Transcriptome sequencing of a large human family identifies the impact of rare noncoding variantsXin Li, Alexis Battle, Konrad J Karczewski, et al.
Pageof 15