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dc.contributor.authorRajeevan, Haseena
dc.contributor.authorPakstis, Andrew J.
dc.contributor.authorKidd, Kenneth K.
dc.contributor.authorBulbul, Ozlem
dc.contributor.authorSpeed, William C.
dc.contributor.authorGURKAN, Cemal
dc.contributor.authorSoundararajan, Usha
dc.date.accessioned2021-03-04T11:04:00Z
dc.date.available2021-03-04T11:04:00Z
dc.identifier.citationBulbul O., Speed W. C. , GURKAN C., Soundararajan U., Rajeevan H., Pakstis A. J. , Kidd K. K. , "Improving ancestry distinctions among Southwest Asian populations", FORENSIC SCIENCE INTERNATIONAL-GENETICS, cilt.35, ss.14-20, 2018
dc.identifier.issn1872-4973
dc.identifier.otherav_706be0ee-f086-4565-9a1c-1e44af6a6951
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/77483
dc.identifier.urihttps://doi.org/10.1016/j.fsigen.2018.03.010
dc.description.abstractThe Kidd Lab panel of 55 AISNPs can provide up to 10 statistically relevant biogeographic groupings of a global set of populations. A second-tier panel would be useful for increasing the accuracy for further differentiation of populations within a specific global grouping. Because recent advances in massively parallel sequencing (MPS) methods allow the genotyping of many more SNPs, we are now identifying additional SNPs to provide refined discrimination among regional subsets of populations; Southwest Asia and the nearby Mediterranean region (SWA) is our current target for such a "second tier" panel. We selected the potentially best SNPs from various sources: our own laboratory database ( > 4600 SNPs), AISNP panels (Kidd 55 and Seldin 128 SNP panels), and published papers reporting European and SW Asian populations. Rosenberg's Informativeness, Fst and allele frequency heatmap matrices are used to determine the best SNPs for the region. A total of 2568 individuals, from 39 different populations ranging from North-East Africa through the SW Asia and Europe to the Ural Mountains, were included in the refinement processes and analyses. Heatmap, PCA, Structure (K = 4), and ancestry inference for selected individuals with an in-lab version of FROG-kb analyses indicate that these 86 AISNPs provide the basis for building an improved, optimized panel of AISNPs that collectively provide additional information on differences among populations in that part of the world. Testing this panel with additional populations from the area and with new SNPs and/or microhaplotypes is expected to improve the panel.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTIP, YASAL
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectAdli Tıp
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.titleImproving ancestry distinctions among Southwest Asian populations
dc.typeMakale
dc.relation.journalFORENSIC SCIENCE INTERNATIONAL-GENETICS
dc.contributor.departmentYale University , ,
dc.identifier.volume35
dc.identifier.startpage14
dc.identifier.endpage20
dc.contributor.firstauthorID84442


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