Doruk Beyter
7PUBLICATIONS
70CO-AUTHORS
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Publications (7)
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|Jul 10, 2023
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria.Ragnar P Kristjansson, Gudjon R Oskarsson, Astros Skuladottir
|Dec 09, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program.Marsha M Wheeler, Adrienne M Stilp, Shuquan Rao
|Jul 21, 2022
The sequences of 150,119 genomes in the UK Biobank.Bjarni V Halldorsson, Hannes P Eggertsson, Kristjan H S Moore
|May 11, 2021
Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits.Doruk Beyter, Helga Ingimundardottir, Asmundur Oddsson
|Nov 29, 2019
GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs.Hannes P Eggertsson, Snaedis Kristmundsdottir, Doruk Beyter
|Jul 18, 2018
Strelka2: fast and accurate calling of germline and somatic variants.Sangtae Kim, Konrad Scheffler, Aaron L Halpern
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Frequent Collaborators
5 joint publications
Bjarni V Halldorsson
4 joint publications
Daniel F Gudbjartsson
3 joint publications
Patrick Sulem
3 joint publications
Hannes P Eggertsson
3 joint publications
Hakon Jonsson
3 joint publications
Asmundur Oddsson
2 joint publications
Kari Stefansson
2 joint publications
Brynjar O Jensson
2 joint publications
Hilma Holm
2 joint publications
Gunnar Palsson
