Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/24428
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dc.contributor.authorColonna, V-
dc.contributor.authorAyub, Q-
dc.contributor.authorChen, Y-
dc.contributor.authorPagani, L-
dc.contributor.authorLuisi, P-
dc.contributor.authorPybus, M-
dc.contributor.authorGarrison, E-
dc.contributor.authorXue, Y-
dc.contributor.authorTyler-Smith, C-
dc.contributor.authorAbecasis, GR-
dc.contributor.authorAuton, A-
dc.contributor.authorBrooks, LD-
dc.contributor.authorDepristo, MA-
dc.contributor.authorDurbin, RM-
dc.contributor.authorHandsaker, RE-
dc.contributor.authorKang, HM-
dc.contributor.authorMarth, GT-
dc.contributor.authorMcVean, G-
dc.contributor.authorAltshuler, DM-
dc.contributor.authorBentley, DR-
dc.contributor.authorChakravarti, A-
dc.contributor.authorClark, AG-
dc.contributor.authorDonnelly, P-
dc.contributor.authorEichler, EE-
dc.contributor.authorFlicek, P-
dc.contributor.authorGabriel, SB-
dc.contributor.authorGibbs, RA-
dc.contributor.authorGreen, ED-
dc.contributor.authorHurles, ME-
dc.contributor.authorKnoppers, BM-
dc.contributor.authorKorbel, JO-
dc.contributor.authorLander, ES-
dc.contributor.authorLee, C-
dc.contributor.authorLehrach, H-
dc.contributor.authorMardis, ER-
dc.contributor.authorMcVean, GA-
dc.contributor.authorNickerson, DA-
dc.contributor.authorSchmidt, JP-
dc.contributor.authorSherry, ST-
dc.contributor.authorWang, J-
dc.contributor.authorWilson, RK-
dc.contributor.authorDinh, H-
dc.contributor.authorKovar, C-
dc.contributor.authorLee, S-
dc.contributor.authorLewis, L-
dc.contributor.authorMuzny, D-
dc.contributor.authorReid, J-
dc.contributor.authorWang, M-
dc.contributor.authorFang, X-
dc.contributor.authorGuo, X-
dc.contributor.authorJian, M-
dc.contributor.authorJiang, H-
dc.contributor.authorJin, X-
dc.contributor.authorLi, G-
dc.contributor.authorLi, J-
dc.contributor.authorLi, Y-
dc.contributor.authorLi, Z-
dc.contributor.authorLiu, X-
dc.contributor.authorLu, Y-
dc.contributor.authorMa, X-
dc.contributor.authorSu, Z-
dc.contributor.authorTai, S-
dc.contributor.authorTang, M-
dc.contributor.authorWang, B-
dc.contributor.authorWang, G-
dc.contributor.authorWu, H-
dc.contributor.authorWu, R-
dc.contributor.authorYin, Y-
dc.contributor.authorZhang, W-
dc.contributor.authorZhao, J-
dc.contributor.authorZhao, M-
dc.contributor.authorZheng, X-
dc.contributor.authorZhou, Y-
dc.contributor.authorGupta, N-
dc.contributor.authorClarke, L-
dc.contributor.authorLeinonen, R-
dc.contributor.authorSmith, RE-
dc.contributor.authorZheng-Bradley, X-
dc.contributor.authorGrocock, R-
dc.contributor.authorHumphray, S-
dc.contributor.authorJames, T-
dc.contributor.authorKingsbury, Z-
dc.contributor.authorSudbrak, R-
dc.contributor.authorAlbrecht, MW-
dc.contributor.authorAmstislavskiy, VS-
dc.contributor.authorBorodina, TA-
dc.contributor.authorLienhard, M-
dc.contributor.authorMertes, F-
dc.contributor.authorSultan, M-
dc.contributor.authorTimmermann, B-
dc.contributor.authorYaspo, ML-
dc.contributor.authorFulton, L-
dc.contributor.authorFulton, R-
dc.contributor.authorWeinstock, GM-
dc.contributor.authorBalasubramaniam, S-
dc.contributor.authorBurton, J-
dc.contributor.authorDanecek, P-
dc.contributor.authorKeane, TM-
dc.contributor.authorKolb-Kokocinski, A-
dc.contributor.authorMcCarthy, S-
dc.contributor.otherThe 1000 Genomes Project Consortium-
dc.date.accessioned2022-04-11T11:13:43Z-
dc.date.available2022-04-11T11:13:43Z-
dc.date.issued2014-06-30-
dc.identifier.citationColonna, V., Ayub, Q., Chen, Y. et al. and the 1000 Genomes Project Consortium. (2014) 'Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences', Genome Biology, 15 (6), R88, pp. 1 - 14. doi: 10.1186/gb-2014-15-6-r88.en_US
dc.identifier.issn1474-7596-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/24428-
dc.descriptionData availability: The 1000 Genomes phase I integrated callset used in this study is publicly available at [The 1000 Genomes Project. http://www.1000genomes.org/]. For a list of samples used in this study, refer to Table S1 in Additional file 1. Additional files: Additional file 1: This file contains supplementary Tables ST1 to ST4 (https://static-content.springer.com/esm/art%3A10.1186%2Fgb-2014-15-6-r88/MediaObjects/13059_2014_3364_MOESM1_ESM.xlsx). Additional file 2: This file contains supplementary Figures F1 to F16 (https://static-content.springer.com/esm/art%3A10.1186%2Fgb-2014-15-6-r88/MediaObjects/13059_2014_3364_MOESM2_ESM.pdf). Additional file 3: Full list of participants and institutions in the 1000 Genomes Project (https://static-content.springer.com/esm/art%3A10.1186%2Fgb-2014-15-6-r88/MediaObjects/13059_2014_3364_MOESM3_ESM.pdf).-
dc.description.abstractCopyright © 2014 Colonna et al. Background: Population differentiation has proved to be effective for identifying loci under geographically localized positive selection, and has the potential to identify loci subject to balancing selection. We have previously investigated the pattern of genetic differentiation among human populations at 36.8 million genomic variants to identify sites in the genome showing high frequency differences. Here, we extend this dataset to include additional variants, survey sites with low levels of differentiation, and evaluate the extent to which highly differentiated sites are likely to result from selective or other processes. Results: We demonstrate that while sites with low differentiation represent sampling effects rather than balancing selection, sites showing extremely high population differentiation are enriched for positive selection events and that one half may be the result of classic selective sweeps. Among these, we rediscover known examples, where we actually identify the established functional SNP, and discover novel examples including the genes ABCA12, CALD1 and ZNF804, which we speculate may be linked to adaptations in skin, calcium metabolism and defense, respectively. Conclusions: We identify known and many novel candidate regions for geographically restricted positive selection, and suggest several directions for further research.en_US
dc.description.sponsorshipThe Wellcome Trust (098051), an Italian National Research Council (CNR) short-term mobility fellowship from the 2013 program to VC, and an EMBO Short Term Fellowship ASTF 324–2010 to VC.en_US
dc.format.extent1 - 14-
dc.format.mediumPrint-Electronic-
dc.language.isoenen_US
dc.publisherBMC Springer Natureen_US
dc.rightsCopyright © 2014 Colonna et al. Licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (https://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectselective sweepen_US
dc.subjectLevenshtein distanceen_US
dc.subjectstanding variationen_US
dc.subjectlactase persistenceen_US
dc.subjectfunctional annotation clusteren_US
dc.titleHuman genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequencesen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.1186/gb-2014-15-6-r88-
dc.relation.isPartOfGenome Biology-
pubs.issue6-
pubs.publication-statusPublished-
pubs.volume15-
dc.identifier.eissn1474-760X-
Appears in Collections:Dept of Life Sciences Research Papers

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