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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)
|
August 3, 2023
NCOurd: modelling length distributions of NCO events and gene conversion tracts
Marteinn T Hardarson, Gunnar Palsson, Bjarni V Halldorsson
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 29, 2008
Impact of genetics on low bone mass in adults
Gunnar Sigurdsson, Bjarni V Halldorsson, Unnur Styrkarsdottir, et al.
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.
BMC Medical Informatics and Decision Making
|
February 3, 2019
Clinical decision support system for the management of osteoporosis compared to NOGG guidelines and an osteology specialist: a validation pilot study
Haukur T Gudmundsson, Karen E Hansen, Bjarni V Halldorsson, et al.
Computational and Mathematical Methods in Medicine
|
March 28, 2015
A clinical decision support system for the diagnosis, fracture risks and treatment of osteoporosis
Bjarni V Halldorsson, Aron Hjalti Bjornsson, Haukur Tyr Gudmundsson, et al.
Computational and Mathematical Methods in Medicine
|
July 29, 2017
Corrigendum to "A Clinical Decision Support System for the Diagnosis, Fracture Risks and Treatment of Osteoporosis"
Bjarni V Halldorsson, Aron Hjalti Bjornsson, Haukur Tyr Gudmundsson, 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
|
November 29, 2019
GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs
Hannes P Eggertsson, Snaedis Kristmundsdottir, Doruk Beyter, et al.
Genome Biology
|
March 12, 2024
A comparison of methods for detecting DNA methylation from long-read sequencing of human genomes
Brynja D Sigurpalsdottir, Olafur A Stefansson, Guillaume Holley, et al.
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Search research articles
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Showing results (1-10 of 80) with videos related to
Sort By:
Page
of 8
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)
|
August 3, 2023
NCOurd: modelling length distributions of NCO events and gene conversion tracts
Marteinn T Hardarson, Gunnar Palsson, Bjarni V Halldorsson
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 29, 2008
Impact of genetics on low bone mass in adults
Gunnar Sigurdsson, Bjarni V Halldorsson, Unnur Styrkarsdottir, et al.
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.
BMC Medical Informatics and Decision Making
|
February 3, 2019
Clinical decision support system for the management of osteoporosis compared to NOGG guidelines and an osteology specialist: a validation pilot study
Haukur T Gudmundsson, Karen E Hansen, Bjarni V Halldorsson, et al.
Computational and Mathematical Methods in Medicine
|
March 28, 2015
A clinical decision support system for the diagnosis, fracture risks and treatment of osteoporosis
Bjarni V Halldorsson, Aron Hjalti Bjornsson, Haukur Tyr Gudmundsson, et al.
Computational and Mathematical Methods in Medicine
|
July 29, 2017
Corrigendum to "A Clinical Decision Support System for the Diagnosis, Fracture Risks and Treatment of Osteoporosis"
Bjarni V Halldorsson, Aron Hjalti Bjornsson, Haukur Tyr Gudmundsson, 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
|
November 29, 2019
GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs
Hannes P Eggertsson, Snaedis Kristmundsdottir, Doruk Beyter, et al.
Genome Biology
|
March 12, 2024
A comparison of methods for detecting DNA methylation from long-read sequencing of human genomes
Brynja D Sigurpalsdottir, Olafur A Stefansson, Guillaume Holley, et al.
Page
of 8