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Bioinformatics (Oxford, England)
|
November 2, 2020
read_haps: using read haplotypes to detect same species contamination in DNA sequences
Hannes P Eggertsson, Bjarni V Halldorsson
Bioinformatics (Oxford, England)
|
December 6, 2019
popSTR2 enables clinical and population-scale genotyping of microsatellites
Snædis 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 assembly
Guillaume Holley, Doruk Beyter, Helga Ingimundardottir, et al.
Nature Communications
|
February 2, 2021
PopDel identifies medium-size deletions simultaneously in tens of thousands of genomes
Sebastian Niehus, Hákon Jónsson, Janina Schönberger, et al.
Nature Communications
|
November 29, 2019
GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs
Hannes P Eggertsson, Snaedis Kristmundsdottir, Doruk Beyter, et al.
Nature Genetics
|
September 26, 2017
Graphtyper enables population-scale genotyping using pangenome graphs
Hannes P Eggertsson, Hakon Jonsson, Snaedis Kristmundsdottir, et al.
Nature
|
January 22, 2025
Complete human recombination maps
Gunnar 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 map
Bjarni V Halldorsson, Gunnar Palsson, Olafur A Stefansson, et al.
Nature Genetics
|
January 8, 2021
Differences between germline genomes of monozygotic twins
Hakon Jonsson, Erna Magnusdottir, Hannes P Eggertsson, et al.
Nature Communications
|
June 29, 2023
Sequence variants affecting the genome-wide rate of germline microsatellite mutations
Snaedis Kristmundsdottir, Hakon Jonsson, Marteinn T Hardarson, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 31) with videos related to
Sort By:
Page
of 4
Bioinformatics (Oxford, England)
|
November 2, 2020
read_haps: using read haplotypes to detect same species contamination in DNA sequences
Hannes P Eggertsson, Bjarni V Halldorsson
Bioinformatics (Oxford, England)
|
December 6, 2019
popSTR2 enables clinical and population-scale genotyping of microsatellites
Snædis 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 assembly
Guillaume Holley, Doruk Beyter, Helga Ingimundardottir, et al.
Nature Communications
|
February 2, 2021
PopDel identifies medium-size deletions simultaneously in tens of thousands of genomes
Sebastian Niehus, Hákon Jónsson, Janina Schönberger, et al.
Nature Communications
|
November 29, 2019
GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs
Hannes P Eggertsson, Snaedis Kristmundsdottir, Doruk Beyter, et al.
Nature Genetics
|
September 26, 2017
Graphtyper enables population-scale genotyping using pangenome graphs
Hannes P Eggertsson, Hakon Jonsson, Snaedis Kristmundsdottir, et al.
Nature
|
January 22, 2025
Complete human recombination maps
Gunnar 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 map
Bjarni V Halldorsson, Gunnar Palsson, Olafur A Stefansson, et al.
Nature Genetics
|
January 8, 2021
Differences between germline genomes of monozygotic twins
Hakon Jonsson, Erna Magnusdottir, Hannes P Eggertsson, et al.
Nature Communications
|
June 29, 2023
Sequence variants affecting the genome-wide rate of germline microsatellite mutations
Snaedis Kristmundsdottir, Hakon Jonsson, Marteinn T Hardarson, et al.
Page
of 4