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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003895naa a2200469 4500
001oai:DiVA.org:umu-57417
003SwePub
008120722s2011 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:121958341
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-574172 URI
024a https://doi.org/10.1371/journal.pone.00167472 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1219583412 URI
040 a (SwePub)umud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Salmela, Elina4 aut
2451 0a Swedish population substructure revealed by genome-wide single nucleotide polymorphism data
264 c 2011-02-09
264 1b Public Library of Science (PLoS),c 2011
338 a electronic2 rdacarrier
520 a The use of genome-wide single nucleotide polymorphism (SNP) data has recently proven useful in the study of human population structure. We have studied the internal genetic structure of the Swedish population using more than 350,000 SNPs from 1525 Swedes from all over the country genotyped on the Illumina HumanHap550 array. We have also compared them to 3212 worldwide reference samples, including Finns, northern Germans, British and Russians, based on the more than 29,000 SNPs that overlap between the Illumina and Affymetrix 250K Sty arrays. The Swedes--especially southern Swedes--were genetically close to the Germans and British, while their genetic distance to Finns was substantially longer. The overall structure within Sweden appeared clinal, and the substructure in the southern and middle parts was subtle. In contrast, the northern part of Sweden, Norrland, exhibited pronounced genetic differences both within the area and relative to the rest of the country. These distinctive genetic features of Norrland probably result mainly from isolation by distance and genetic drift caused by low population density. The internal structure within Sweden (F(ST) = 0.0005 between provinces) was stronger than that in many Central European populations, although smaller than what has been observed for instance in Finland; importantly, it is of the magnitude that may hamper association studies with a moderate number of markers if cases and controls are not properly matched geographically. Overall, our results underline the potential of genome-wide data in analyzing substructure in populations that might otherwise appear relatively homogeneous, such as the Swedes.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Medicinsk genetik0 (SwePub)301072 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Medical Genetics0 (SwePub)301072 hsv//eng
700a Lappalainen, Tuuli4 aut
700a Liu, Jianjun4 aut
700a Sistonen, Pertti4 aut
700a Andersen, Peter Mu Umeå universitet,Klinisk neurovetenskap4 aut0 (Swepub:umu)pean0001
700a Schreiber, Stefan4 aut
700a Savontaus, Marja-Liisa4 aut
700a Czene, Kamilau Karolinska Institutet4 aut
700a Lahermo, Päivi4 aut
700a Hall, Peru Karolinska Institutet4 aut
700a Kere, Juhau Karolinska Institutet4 aut
710a Umeå universitetb Klinisk neurovetenskap4 org
773t PLOS ONEd : Public Library of Science (PLoS)g 6:2, s. e16747-q 6:2<e16747-x 1932-6203
856u https://umu.diva-portal.org/smash/get/diva2:541683/FULLTEXT02.pdfx primaryx Raw objecty fulltext:print
856u https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0016747&type=printable
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-57417
8564 8u https://doi.org/10.1371/journal.pone.0016747
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:121958341

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