The sequences of 150,119 genomes in the UK Biobank

Autor: Bjarni V, Halldorsson, Hannes P, Eggertsson, Kristjan H S, Moore, Hannes, Hauswedell, Ogmundur, Eiriksson, Magnus O, Ulfarsson, Gunnar, Palsson, Marteinn T, Hardarson, Asmundur, Oddsson, Brynjar O, Jensson, Snaedis, Kristmundsdottir, Brynja D, Sigurpalsdottir, Olafur A, Stefansson, Doruk, Beyter, Guillaume, Holley, Vinicius, Tragante, Arnaldur, Gylfason, Pall I, Olason, Florian, Zink, Margret, Asgeirsdottir, Sverrir T, Sverrisson, Brynjar, Sigurdsson, Sigurjon A, Gudjonsson, Gunnar T, Sigurdsson, Gisli H, Halldorsson, Gardar, Sveinbjornsson, Kristjan, Norland, Unnur, Styrkarsdottir, Droplaug N, Magnusdottir, Steinunn, Snorradottir, Kari, Kristinsson, Emilia, Sobech, Helgi, Jonsson, Arni J, Geirsson, Isleifur, Olafsson, Palmi, Jonsson, Ole Birger, Pedersen, Christian, Erikstrup, Søren, Brunak, Sisse Rye, Ostrowski, Gudmar, Thorleifsson, Frosti, Jonsson, Pall, Melsted, Ingileif, Jonsdottir, Thorunn, Rafnar, Hilma, Holm, Hreinn, Stefansson, Jona, Saemundsdottir, Daniel F, Gudbjartsson, Olafur T, Magnusson, Gisli, Masson, Unnur, Thorsteinsdottir, Agnar, Helgason, Hakon, Jonsson, Patrick, Sulem, Thomas, Werge
Rok vydání: 2021
Předmět:
Zdroj: Nature. 607(7920)
ISSN: 1476-4687
Popis: Detailed knowledge of how diversity in the sequence of the human genome affects phenotypic diversity depends on a comprehensive and reliable characterization of both sequences and phenotypic variation. Over the past decade, insights into this relationship have been obtained from whole-exome sequencing or whole-genome sequencing of large cohorts with rich phenotypic data
Databáze: OpenAIRE