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Impact of whole-genome duplications on structural variant evolution in Cochlearia

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10.1038/s41467-024-49679-y
Hämälä, Tuomas; Moore, Christopher; Cowan, Laura; Carlile, Matthew; Gopaulchan, David; Brandrud, Mar...
Nature communications2024

Exploring the optimal strategy of imputation from SNP array to whole-genome sequencing data in farm animals

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10.3389/fgene.2022.963654
Jiang, Yifan; Song, Hailiang; Gao, Hongding; Zhang, Qin; Ding, Xiangdong
Frontiers in Genetics2022

Genetic Drift Dominates Genome-Wide Regulatory Evolution Following an Ancient Whole-Genome Duplication in Atlantic Salmon

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10.1093/gbe/evab059
Verta, Jukka-Pekka; Barton, Henry Juho; Pritchard, Victoria; Primmer, Craig
Genome Biology and Evolution2021

Whole Genome Sequencing Indicates Heterogeneity of Hyperostotic Disorders in Dogs

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10.3390/genes11020163
Letko, Anna; Leuthard, Fabienne; Jagannathan, Vidhya; Corlazzoli, Daniele; Matiasek, Kaspar; Schweiz...
Genes2020

Candidate Predisposition Variants in Kaposi Sarcoma as Detected by Whole-Genome Sequencing

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10.1093/ofid/ofz337
Rinne, Sanni J.; Sipilä, Lauri J.; Sulo, Päivi; Jouanguy, Emmanuelle; Beziat, Vivien; Abel, Laurent;...
Open forum infectious diseases2019

Simulating the Genetics Clinic of the Future - whether undergoing whole-genome sequencing shapes professional attitudes

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10.1007/s12687-021-00561-0
Brunfeldt, Minna; Teare, Harriet; Schuurbiers, Daan; Steinberger, Daniela; Gerrits, Elianne; Vornane...
Journal of community genetics2022

Evaluation of Sparse Proximal Multi-Task Learning for Genome-Wide Prediction

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10.1109/ACCESS.2024.3386093
Fan, Yuhua; Launonen, Ilkka; Sillanpää, Mikko J.; Waldmann, Patrik
IEEE access2024

Whole-Genome Sequencing in Epidemiology of Campylobacter jejuni Infections

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10.1128/JCM.00017-17
Llarena, Ann-Katrin; Taboada, Eduardo; Rossi, Mirko
Journal of Clinical Microbiology2017

Tabular deep learning: a comparative study applied to multi-task genome-wide prediction

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10.1186/s12859-024-05940-1
Fan, Yuhua; Waldmann, Patrik
Bmc bioinformatics2024

Clinical characterization, genetic mapping and whole-genome sequence analysis of a novel autosomal recessive intellectual disability syndrome

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10.1016/j.ejmg.2014.07.002
Kaasinen, Eevi; Rahikkala, Elisa; Koivunen, Peppi; Miettinen, Sirpa; Wamelink, Mirjam M. C.; Aavikko...
European journal of medical genetics2014

Impact of whole-genome duplications on structural variant evolution in Cochlearia

Referentgranskad
Öppen tillgång
DOI
10.1038/s41467-024-49679-y
2024

Exploring the optimal strategy of imputation from SNP array to whole-genome sequencing data in farm animals

Referentgranskad
Öppen tillgång
DOI
10.3389/fgene.2022.963654
2022

Genetic Drift Dominates Genome-Wide Regulatory Evolution Following an Ancient Whole-Genome Duplication in Atlantic Salmon

Referentgranskad
Öppen tillgång
DOI
10.1093/gbe/evab059
2021

Whole Genome Sequencing Indicates Heterogeneity of Hyperostotic Disorders in Dogs

Referentgranskad
Öppen tillgång
DOI
10.3390/genes11020163
2020

Candidate Predisposition Variants in Kaposi Sarcoma as Detected by Whole-Genome Sequencing

Referentgranskad
Öppen tillgång
DOI
10.1093/ofid/ofz337
2019

Simulating the Genetics Clinic of the Future - whether undergoing whole-genome sequencing shapes professional attitudes

Referentgranskad
Öppen tillgång
DOI
10.1007/s12687-021-00561-0
2022

Evaluation of Sparse Proximal Multi-Task Learning for Genome-Wide Prediction

Referentgranskad
Öppen tillgång
DOI
10.1109/ACCESS.2024.3386093
2024

Whole-Genome Sequencing in Epidemiology of Campylobacter jejuni Infections

Referentgranskad
Öppen tillgång
DOI
10.1128/JCM.00017-17
2017

Tabular deep learning: a comparative study applied to multi-task genome-wide prediction

Referentgranskad
Öppen tillgång
DOI
10.1186/s12859-024-05940-1
2024

Clinical characterization, genetic mapping and whole-genome sequence analysis of a novel autosomal recessive intellectual disability syndrome

Referentgranskad
DOI
10.1016/j.ejmg.2014.07.002
2014