Large-scale whole-genome sequencing of the Icelandic population.
To access publisher's full text version of this article click on the hyperlink at the bottom of the page Here we describe the insights gained from sequencing the whole genomes of 2,636 Icelanders to a median depth of 20×. We found 20 million SNPs and 1.5 million insertions-deletions (indels). W...
Published in: | Nature Genetics |
---|---|
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Other Authors: | |
Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
Nature Publishing Group
2015
|
Subjects: | |
Online Access: | http://hdl.handle.net/2336/560802 https://doi.org/10.1038/ng.3247 |
id |
ftlandspitaliuni:oai:www.hirsla.lsh.is:2336/560802 |
---|---|
record_format |
openpolar |
institution |
Open Polar |
collection |
Hirsla - Landspítali University Hospital research archive |
op_collection_id |
ftlandspitaliuni |
language |
English |
topic |
Aged 80 and over Atrial Fibrillation Bulbar Palsy Progressive Female Frameshift Mutation GTP-Binding Protein alpha Subunits Gs Gene Frequency Genetic Predisposition to Disease Genome Human Genome-Wide Association Study Hearing Loss Sensorineural Humans INDEL Mutation Iceland Liver Diseases Male Middle Aged Molecular Sequence Annotation Myosin Light Chains P-Glycoproteins Phylogeography Polymorphism Single Nucleotide Receptors G-Protein-Coupled Risk Sequence Analysis DNA Thyrotropin |
spellingShingle |
Aged 80 and over Atrial Fibrillation Bulbar Palsy Progressive Female Frameshift Mutation GTP-Binding Protein alpha Subunits Gs Gene Frequency Genetic Predisposition to Disease Genome Human Genome-Wide Association Study Hearing Loss Sensorineural Humans INDEL Mutation Iceland Liver Diseases Male Middle Aged Molecular Sequence Annotation Myosin Light Chains P-Glycoproteins Phylogeography Polymorphism Single Nucleotide Receptors G-Protein-Coupled Risk Sequence Analysis DNA Thyrotropin Gudbjartsson, Daniel F Helgason, Hannes Gudjonsson, Sigurjon A Zink, Florian Oddson, Asmundur Gylfason, Arnaldur Besenbacher, Soren Magnusson, Gisli Halldorsson, Bjarni V Hjartarson, Eirikur Sigurdsson, Gunnar Th Stacey, Simon N Frigge, Michael L Holm, Hilma Saemundsdottir, Jona Helgadottir, Hafdis Th Johannsdottir, Hrefna Sigfusson, Gunnlaugur Thorgeirsson, Gudmundur Sverrisson, Jon Th Gretarsdottir, Solveig Walters, G Bragi Rafnar, Thorunn Thjodleifsson, Bjarni Bjornsson, Einar S Olafsson, Sigurdur Thorarinsdottir, Hildur Steingrimsdottir, Thora Gudmundsdottir, Thora S Theodors, Asgeir Jonasson, Jon G Sigurdsson, Asgeir Bjornsdottir, Gyda Jonsson, Jon J Thorarensen, Olafur Ludvigsson, Petur Gudbjartsson, Hakon Eyjolfsson, Gudmundur I Sigurdardottir, Olof Olafsson, Isleifur Arnar, David O Magnusson, Olafur Th Kong, Augustine Masson, Gisli Thorsteinsdottir, Unnur Helgason, Agnar Sulem, Patrick Stefansson, Kari Large-scale whole-genome sequencing of the Icelandic population. |
topic_facet |
Aged 80 and over Atrial Fibrillation Bulbar Palsy Progressive Female Frameshift Mutation GTP-Binding Protein alpha Subunits Gs Gene Frequency Genetic Predisposition to Disease Genome Human Genome-Wide Association Study Hearing Loss Sensorineural Humans INDEL Mutation Iceland Liver Diseases Male Middle Aged Molecular Sequence Annotation Myosin Light Chains P-Glycoproteins Phylogeography Polymorphism Single Nucleotide Receptors G-Protein-Coupled Risk Sequence Analysis DNA Thyrotropin |
description |
To access publisher's full text version of this article click on the hyperlink at the bottom of the page Here we describe the insights gained from sequencing the whole genomes of 2,636 Icelanders to a median depth of 20×. We found 20 million SNPs and 1.5 million insertions-deletions (indels). We describe the density and frequency spectra of sequence variants in relation to their functional annotation, gene position, pathway and conservation score. We demonstrate an excess of homozygosity and rare protein-coding variants in Iceland. We imputed these variants into 104,220 individuals down to a minor allele frequency of 0.1% and found a recessive frameshift mutation in MYL4 that causes early-onset atrial fibrillation, several mutations in ABCB4 that increase risk of liver diseases and an intronic variant in GNAS associating with increased thyroid-stimulating hormone levels when maternally inherited. These data provide a study design that can be used to determine how variation in the sequence of the human genome gives rise to human diversity. |
author2 |
1 Amgen Inc, DeCODE Genet, Reykjavik, Iceland 2 Univ Iceland, Sch Engn & Nat Sci, Reykjavik, Iceland 3 Aarhus Univ, Bioinformat Res Ctr, Aarhus, Denmark 4 Reykjavik Univ, Inst Biomed & Neural Engn, Reykjavik, Iceland 5 Mayo Clin, Div Cardiovasc Dis, Rochester, MN USA 6 Landspitali Univ Hosp, Childrens Hosp, Reykjavik, Iceland 7 Landspitali Univ Hosp, Dept Med, Reykjavik, Iceland 8 Univ Iceland, Fac Med, Reykjavik, Iceland 9 Akureyri Hosp, Dept Internal Med, Akureyri, Iceland 10 Landspitali Univ Hosp, Div Gastroenterol & Hepatol, Dept Internal Med, Reykjavik, Iceland 11 Landspitali Univ Hosp, Dept Obstet & Gynecol, Reykjavik, Iceland 12 Landspitali Univ Hosp, Dept Pathol, Reykjavik, Iceland 13 Iceland Canc Registry, Reykjavik, Iceland 14 Univ Iceland, Dept Biochem & Mol Biol, Fac Med, Reykjavik, Iceland 15 Landspitali Univ Hosp, Dept Genet & Mol Med, Reykjavik, Iceland 16 Landspitali Univ Hosp, Childrens Hosp Reykjavik, Sect Child Neurol, Dept Pediat, Reykjavik, Iceland 17 Iceland Med Ctr Laeknasetrid, Lab Mjodd RAM, Reykjavik, Iceland 18 Akureyri Hosp, Dept Clin Biochem, Akureyri, Iceland 19 Landspitali Univ Hosp, Dept Clin Biochem, Reykjavik, Iceland 20 Univ Iceland, Dept Anthropol, Reykjavik, Iceland |
format |
Article in Journal/Newspaper |
author |
Gudbjartsson, Daniel F Helgason, Hannes Gudjonsson, Sigurjon A Zink, Florian Oddson, Asmundur Gylfason, Arnaldur Besenbacher, Soren Magnusson, Gisli Halldorsson, Bjarni V Hjartarson, Eirikur Sigurdsson, Gunnar Th Stacey, Simon N Frigge, Michael L Holm, Hilma Saemundsdottir, Jona Helgadottir, Hafdis Th Johannsdottir, Hrefna Sigfusson, Gunnlaugur Thorgeirsson, Gudmundur Sverrisson, Jon Th Gretarsdottir, Solveig Walters, G Bragi Rafnar, Thorunn Thjodleifsson, Bjarni Bjornsson, Einar S Olafsson, Sigurdur Thorarinsdottir, Hildur Steingrimsdottir, Thora Gudmundsdottir, Thora S Theodors, Asgeir Jonasson, Jon G Sigurdsson, Asgeir Bjornsdottir, Gyda Jonsson, Jon J Thorarensen, Olafur Ludvigsson, Petur Gudbjartsson, Hakon Eyjolfsson, Gudmundur I Sigurdardottir, Olof Olafsson, Isleifur Arnar, David O Magnusson, Olafur Th Kong, Augustine Masson, Gisli Thorsteinsdottir, Unnur Helgason, Agnar Sulem, Patrick Stefansson, Kari |
author_facet |
Gudbjartsson, Daniel F Helgason, Hannes Gudjonsson, Sigurjon A Zink, Florian Oddson, Asmundur Gylfason, Arnaldur Besenbacher, Soren Magnusson, Gisli Halldorsson, Bjarni V Hjartarson, Eirikur Sigurdsson, Gunnar Th Stacey, Simon N Frigge, Michael L Holm, Hilma Saemundsdottir, Jona Helgadottir, Hafdis Th Johannsdottir, Hrefna Sigfusson, Gunnlaugur Thorgeirsson, Gudmundur Sverrisson, Jon Th Gretarsdottir, Solveig Walters, G Bragi Rafnar, Thorunn Thjodleifsson, Bjarni Bjornsson, Einar S Olafsson, Sigurdur Thorarinsdottir, Hildur Steingrimsdottir, Thora Gudmundsdottir, Thora S Theodors, Asgeir Jonasson, Jon G Sigurdsson, Asgeir Bjornsdottir, Gyda Jonsson, Jon J Thorarensen, Olafur Ludvigsson, Petur Gudbjartsson, Hakon Eyjolfsson, Gudmundur I Sigurdardottir, Olof Olafsson, Isleifur Arnar, David O Magnusson, Olafur Th Kong, Augustine Masson, Gisli Thorsteinsdottir, Unnur Helgason, Agnar Sulem, Patrick Stefansson, Kari |
author_sort |
Gudbjartsson, Daniel F |
title |
Large-scale whole-genome sequencing of the Icelandic population. |
title_short |
Large-scale whole-genome sequencing of the Icelandic population. |
title_full |
Large-scale whole-genome sequencing of the Icelandic population. |
title_fullStr |
Large-scale whole-genome sequencing of the Icelandic population. |
title_full_unstemmed |
Large-scale whole-genome sequencing of the Icelandic population. |
title_sort |
large-scale whole-genome sequencing of the icelandic population. |
publisher |
Nature Publishing Group |
publishDate |
2015 |
url |
http://hdl.handle.net/2336/560802 https://doi.org/10.1038/ng.3247 |
long_lat |
ENVELOPE(35.282,35.282,66.963,66.963) |
geographic |
Indel’ |
geographic_facet |
Indel’ |
genre |
Iceland |
genre_facet |
Iceland |
op_relation |
http://dx.doi.org/ 10.1038/ng.3247 http://www.nature.com/ng/journal/v47/n5/pdf/ng.3247.pdf Nat. Genet. 2015, 47 (5):435-44 1546-1718 25807286 doi:10.1038/ng.3247 http://hdl.handle.net/2336/560802 Nature genetics |
op_rights |
Archived with thanks to Nature genetics Landspitali Access - LSH-aðgangur |
op_doi |
https://doi.org/10.1038/ng.3247 |
container_title |
Nature Genetics |
container_volume |
47 |
container_issue |
5 |
container_start_page |
435 |
op_container_end_page |
444 |
_version_ |
1766038296378474496 |
spelling |
ftlandspitaliuni:oai:www.hirsla.lsh.is:2336/560802 2023-05-15T16:48:11+02:00 Large-scale whole-genome sequencing of the Icelandic population. Gudbjartsson, Daniel F Helgason, Hannes Gudjonsson, Sigurjon A Zink, Florian Oddson, Asmundur Gylfason, Arnaldur Besenbacher, Soren Magnusson, Gisli Halldorsson, Bjarni V Hjartarson, Eirikur Sigurdsson, Gunnar Th Stacey, Simon N Frigge, Michael L Holm, Hilma Saemundsdottir, Jona Helgadottir, Hafdis Th Johannsdottir, Hrefna Sigfusson, Gunnlaugur Thorgeirsson, Gudmundur Sverrisson, Jon Th Gretarsdottir, Solveig Walters, G Bragi Rafnar, Thorunn Thjodleifsson, Bjarni Bjornsson, Einar S Olafsson, Sigurdur Thorarinsdottir, Hildur Steingrimsdottir, Thora Gudmundsdottir, Thora S Theodors, Asgeir Jonasson, Jon G Sigurdsson, Asgeir Bjornsdottir, Gyda Jonsson, Jon J Thorarensen, Olafur Ludvigsson, Petur Gudbjartsson, Hakon Eyjolfsson, Gudmundur I Sigurdardottir, Olof Olafsson, Isleifur Arnar, David O Magnusson, Olafur Th Kong, Augustine Masson, Gisli Thorsteinsdottir, Unnur Helgason, Agnar Sulem, Patrick Stefansson, Kari 1 Amgen Inc, DeCODE Genet, Reykjavik, Iceland 2 Univ Iceland, Sch Engn & Nat Sci, Reykjavik, Iceland 3 Aarhus Univ, Bioinformat Res Ctr, Aarhus, Denmark 4 Reykjavik Univ, Inst Biomed & Neural Engn, Reykjavik, Iceland 5 Mayo Clin, Div Cardiovasc Dis, Rochester, MN USA 6 Landspitali Univ Hosp, Childrens Hosp, Reykjavik, Iceland 7 Landspitali Univ Hosp, Dept Med, Reykjavik, Iceland 8 Univ Iceland, Fac Med, Reykjavik, Iceland 9 Akureyri Hosp, Dept Internal Med, Akureyri, Iceland 10 Landspitali Univ Hosp, Div Gastroenterol & Hepatol, Dept Internal Med, Reykjavik, Iceland 11 Landspitali Univ Hosp, Dept Obstet & Gynecol, Reykjavik, Iceland 12 Landspitali Univ Hosp, Dept Pathol, Reykjavik, Iceland 13 Iceland Canc Registry, Reykjavik, Iceland 14 Univ Iceland, Dept Biochem & Mol Biol, Fac Med, Reykjavik, Iceland 15 Landspitali Univ Hosp, Dept Genet & Mol Med, Reykjavik, Iceland 16 Landspitali Univ Hosp, Childrens Hosp Reykjavik, Sect Child Neurol, Dept Pediat, Reykjavik, Iceland 17 Iceland Med Ctr Laeknasetrid, Lab Mjodd RAM, Reykjavik, Iceland 18 Akureyri Hosp, Dept Clin Biochem, Akureyri, Iceland 19 Landspitali Univ Hosp, Dept Clin Biochem, Reykjavik, Iceland 20 Univ Iceland, Dept Anthropol, Reykjavik, Iceland 2015 http://hdl.handle.net/2336/560802 https://doi.org/10.1038/ng.3247 en eng Nature Publishing Group http://dx.doi.org/ 10.1038/ng.3247 http://www.nature.com/ng/journal/v47/n5/pdf/ng.3247.pdf Nat. Genet. 2015, 47 (5):435-44 1546-1718 25807286 doi:10.1038/ng.3247 http://hdl.handle.net/2336/560802 Nature genetics Archived with thanks to Nature genetics Landspitali Access - LSH-aðgangur Aged 80 and over Atrial Fibrillation Bulbar Palsy Progressive Female Frameshift Mutation GTP-Binding Protein alpha Subunits Gs Gene Frequency Genetic Predisposition to Disease Genome Human Genome-Wide Association Study Hearing Loss Sensorineural Humans INDEL Mutation Iceland Liver Diseases Male Middle Aged Molecular Sequence Annotation Myosin Light Chains P-Glycoproteins Phylogeography Polymorphism Single Nucleotide Receptors G-Protein-Coupled Risk Sequence Analysis DNA Thyrotropin Article 2015 ftlandspitaliuni https://doi.org/10.1038/ng.3247 2022-05-29T08:22:05Z To access publisher's full text version of this article click on the hyperlink at the bottom of the page Here we describe the insights gained from sequencing the whole genomes of 2,636 Icelanders to a median depth of 20×. We found 20 million SNPs and 1.5 million insertions-deletions (indels). We describe the density and frequency spectra of sequence variants in relation to their functional annotation, gene position, pathway and conservation score. We demonstrate an excess of homozygosity and rare protein-coding variants in Iceland. We imputed these variants into 104,220 individuals down to a minor allele frequency of 0.1% and found a recessive frameshift mutation in MYL4 that causes early-onset atrial fibrillation, several mutations in ABCB4 that increase risk of liver diseases and an intronic variant in GNAS associating with increased thyroid-stimulating hormone levels when maternally inherited. These data provide a study design that can be used to determine how variation in the sequence of the human genome gives rise to human diversity. Article in Journal/Newspaper Iceland Hirsla - Landspítali University Hospital research archive Indel’ ENVELOPE(35.282,35.282,66.963,66.963) Nature Genetics 47 5 435 444 |