Doruk Beyter
Doruk Beyter
Research Scientist, deCODE genetics
Bestätigte E-Mail-Adresse bei
Zitiert von
Zitiert von
Strelka2: fast and accurate calling of germline and somatic variants
S Kim, K Scheffler, AL Halpern, MA Bekritsky, E Noh, M Källberg, X Chen, ...
Nature methods 15 (8), 591-594, 2018
Extrachromosomal oncogene amplification drives tumour evolution and genetic heterogeneity
KM Turner, V Deshpande, D Beyter, T Koga, J Rusert, C Lee, B Li, ...
Nature 543 (7643), 122-125, 2017
The sequences of 150,119 genomes in the UK Biobank
BV Halldorsson, HP Eggertsson, KHS Moore, H Hauswedell, O Eiriksson, ...
Nature 607 (7920), 732-740, 2022
Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits
D Beyter, H Ingimundardottir, A Oddsson, HP Eggertsson, E Bjornsson, ...
Nature genetics 53 (6), 779-786, 2021
GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs
HP Eggertsson, S Kristmundsdottir, D Beyter, H Jonsson, A Skuladottir, ...
Nature communications 10 (1), 5402, 2019
Differences between germline genomes of monozygotic twins
H Jonsson, E Magnusdottir, HP Eggertsson, OA Stefansson, GA Arnadottir, ...
Nature Genetics 53 (1), 27-34, 2021
Diversity, productivity, and stability of an industrial microbial ecosystem
D Beyter, PZ Tang, S Becker, T Hoang, D Bilgin, YW Lim, TC Peterson, ...
Applied and environmental microbiology 82 (8), 2494-2505, 2016
Ratatosk: hybrid error correction of long reads enables accurate variant calling and assembly
G Holley, D Beyter, H Ingimundardottir, PL Møller, S Kristmundsdottir, ...
Genome Biology 22 (1), 28, 2021
Proteostorm: An ultrafast metaproteomics database search framework
D Beyter, MS Lin, Y Yu, R Pieper, V Bafna
Cell systems 7 (4), 463-467. e6, 2018
PopDel identifies medium-size deletions simultaneously in tens of thousands of genomes
S Niehus, H Jónsson, J Schönberger, E Björnsson, D Beyter, ...
Nature communications 12 (1), 730, 2021
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura
G Bjornsdottir, MA Chalmer, L Stefansdottir, AT Skuladottir, G Einarsson, ...
Nature Genetics 55 (11), 1843-1853, 2023
Sequence variants affecting the genome-wide rate of germline microsatellite mutations
S Kristmundsdottir, H Jonsson, MT Hardarson, G Palsson, D Beyter, ...
Nature Communications 14 (1), 3855, 2023
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
A Oddsson, P Sulem, G Sveinbjornsson, GA Arnadottir, V Steinthorsdottir, ...
nature communications 14 (1), 3453, 2023
Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program
MM Wheeler, AM Stilp, S Rao, BV Halldórsson, D Beyter, J Wen, ...
Medrxiv, 2021.12. 16.21267871, 2021
Benchmarking small variant detection with ONT reveals high performance in challenging regions
PL Møller, G Holley, D Beyter, M Nyegaard, BV Halldórsson
bioRxiv, 2020.10. 22.350009, 2020
Methods of diagnosing and treating cancer targeting extrachromosomal DNA
P Mischel, P Mali, V Bafna, K Turner, V Deshpande, D Beyter
US Patent 11,193,164, 2021
Variants at the Interleukin 1 gene locus and pericarditis
RB Thorolfsdottir, AB Jonsdottir, G Sveinbjornsson, HM Aegisdottir, ...
JAMA cardiology 9 (2), 165-172, 2024
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria
RP Kristjansson, GR Oskarsson, A Skuladottir, A Oddsson, ...
Communications Biology 6 (1), 703, 2023
A comparison of methods for detecting DNA methylation from long-read sequencing of human genomes
BD Sigurpalsdottir, OA Stefansson, G Holley, D Beyter, F Zink, ...
Genome Biology 25 (1), 69, 2024
Homozygosity for R47H in TREM2 and the Risk of Alzheimer’s Disease
H Stefansson, GB Walters, G Sveinbjornsson, V Tragante, G Einarsson, ...
New England Journal of Medicine 390 (23), 2217-2219, 2024
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