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Hannes P Eggertsson

Showing results (1-10 of 31) with videos related to

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Bioinformatics (Oxford, England)|November 2, 2020
read_haps: using read haplotypes to detect same species contamination in DNA sequencesHannes P Eggertsson, Bjarni V Halldorsson
Bioinformatics (Oxford, England)|December 6, 2019
popSTR2 enables clinical and population-scale genotyping of microsatellitesSnædis Kristmundsdottir, Hannes P Eggertsson, Gudny A Arnadottir, et al.
Genome Biology|January 9, 2021
Ratatosk: hybrid error correction of long reads enables accurate variant calling and assemblyGuillaume Holley, Doruk Beyter, Helga Ingimundardottir, et al.
Nature Communications|February 2, 2021
PopDel identifies medium-size deletions simultaneously in tens of thousands of genomesSebastian Niehus, Hákon Jónsson, Janina Schönberger, et al.
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 26, 2017
Graphtyper enables population-scale genotyping using pangenome graphsHannes P Eggertsson, Hakon Jonsson, Snaedis Kristmundsdottir, 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 Genetics|January 8, 2021
Differences between germline genomes of monozygotic twinsHakon Jonsson, Erna Magnusdottir, Hannes P Eggertsson, 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.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Bioinformatics (Oxford, England)|November 2, 2020
read_haps: using read haplotypes to detect same species contamination in DNA sequencesHannes P Eggertsson, Bjarni V Halldorsson
Bioinformatics (Oxford, England)|December 6, 2019
popSTR2 enables clinical and population-scale genotyping of microsatellitesSnædis Kristmundsdottir, Hannes P Eggertsson, Gudny A Arnadottir, et al.
Genome Biology|January 9, 2021
Ratatosk: hybrid error correction of long reads enables accurate variant calling and assemblyGuillaume Holley, Doruk Beyter, Helga Ingimundardottir, et al.
Nature Communications|February 2, 2021
PopDel identifies medium-size deletions simultaneously in tens of thousands of genomesSebastian Niehus, Hákon Jónsson, Janina Schönberger, et al.
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 26, 2017
Graphtyper enables population-scale genotyping using pangenome graphsHannes P Eggertsson, Hakon Jonsson, Snaedis Kristmundsdottir, 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 Genetics|January 8, 2021
Differences between germline genomes of monozygotic twinsHakon Jonsson, Erna Magnusdottir, Hannes P Eggertsson, 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.
Pageof 4