Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits
Doruk Beyter, Helga Ingimundardóttir, Ásmundur Oddsson, Hannes P. Eggertsson, Eyþór Björnsson, Hákon Jónsson, Bjarni A. Atlason, Snædís Kristmundsdóttir, Svenja Mehringer, Marteinn T. Hardarson, Sigurjón A. Guðjónsson, Droplaug N. Magnúsdóttir, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Ragnar P. Kristjansson, Sverrir T. Sverrisson, Guillaume Holley, Gunnar Pálsson, Ólafur Andri Stefánsson, Guðmundur I. Eyjólfsson, Ísleifur Ólafsson, Ólöf Sigurðardóttir, Bjarni Torfason, Gísli Másson, Agnar Helgason, Unnur Þorsteinsdóttir, Hilma Hólm, Daníel F. Guðbjartsson, Patrick Sulem, Ólafur Þ. Magnússon, Bjarni V. Halldórsson, Kāri Stefánsson
Topics & Concepts
BiologyGeneticsAllelePhenotypePopulationGenetic associationGenome-wide association study1000 Genomes ProjectComputational biologyAllele frequencyGenotypeGeneSingle-nucleotide polymorphismDemographySociologyGenomics and Rare DiseasesGenetic Associations and EpidemiologyGenetic factors in colorectal cancer