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

Marteinn T Hardarson

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Bioinformatics (Oxford, England)|August 3, 2023
NCOurd: modelling length distributions of NCO events and gene conversion tractsMarteinn T Hardarson, Gunnar Palsson, Bjarni V Halldorsson
Nature Communications|November 29, 2019
GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphsHannes P Eggertsson, Snaedis Kristmundsdottir, Doruk Beyter, et al.
Nature Genetics|September 22, 2018
Author Correction: The rate of meiotic gene conversion varies by sex and ageBjarni V Halldorsson, Marteinn T Hardarson, Birte Kehr, et al.
Nature Genetics|September 20, 2016
The rate of meiotic gene conversion varies by sex and ageBjarni V Halldorsson, Marteinn T Hardarson, Birte Kehr, et al.
Nature|January 22, 2025
Complete human recombination mapsGunnar Palsson, Marteinn T Hardarson, Hakon Jonsson, et al.
Science (New York, N.Y.)|January 26, 2019
Characterizing mutagenic effects of recombination through a sequence-level genetic mapBjarni V Halldorsson, Gunnar Palsson, Olafur A Stefansson, et al.
Nature Communications|June 29, 2023
Sequence variants affecting the genome-wide rate of germline microsatellite mutationsSnaedis Kristmundsdottir, Hakon Jonsson, Marteinn T Hardarson, et al.
Nature|September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from IcelandHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Scientific Data|September 22, 2017
Whole genome characterization of sequence diversity of 15,220 IcelandersHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Nature Genetics|May 11, 2021
Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traitsDoruk Beyter, Helga Ingimundardottir, Asmundur Oddsson, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|August 3, 2023
NCOurd: modelling length distributions of NCO events and gene conversion tractsMarteinn T Hardarson, Gunnar Palsson, Bjarni V Halldorsson
Nature Communications|November 29, 2019
GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphsHannes P Eggertsson, Snaedis Kristmundsdottir, Doruk Beyter, et al.
Nature Genetics|September 22, 2018
Author Correction: The rate of meiotic gene conversion varies by sex and ageBjarni V Halldorsson, Marteinn T Hardarson, Birte Kehr, et al.
Nature Genetics|September 20, 2016
The rate of meiotic gene conversion varies by sex and ageBjarni V Halldorsson, Marteinn T Hardarson, Birte Kehr, et al.
Nature|January 22, 2025
Complete human recombination mapsGunnar Palsson, Marteinn T Hardarson, Hakon Jonsson, et al.
Science (New York, N.Y.)|January 26, 2019
Characterizing mutagenic effects of recombination through a sequence-level genetic mapBjarni V Halldorsson, Gunnar Palsson, Olafur A Stefansson, et al.
Nature Communications|June 29, 2023
Sequence variants affecting the genome-wide rate of germline microsatellite mutationsSnaedis Kristmundsdottir, Hakon Jonsson, Marteinn T Hardarson, et al.
Nature|September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from IcelandHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Scientific Data|September 22, 2017
Whole genome characterization of sequence diversity of 15,220 IcelandersHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Nature Genetics|May 11, 2021
Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traitsDoruk Beyter, Helga Ingimundardottir, Asmundur Oddsson, et al.
Pageof 2