dc.contributor.author | AL ABDULKAREEM, I. | |
dc.contributor.author | Uyar, Fatma Aytül | |
dc.contributor.author | AL JUMAH, M. | |
dc.contributor.author | ALHAIDAN, Y. | |
dc.contributor.author | ALABDULRAHMAN, A. | |
dc.contributor.author | Hajeer, A. H. | |
dc.contributor.author | AL BALWI, M. A. | |
dc.date.accessioned | 2021-03-05T12:20:38Z | |
dc.date.available | 2021-03-05T12:20:38Z | |
dc.date.issued | 2013 | |
dc.identifier.citation | Hajeer A. H. , AL BALWI M. A. , Uyar F. A. , ALHAIDAN Y., ALABDULRAHMAN A., AL ABDULKAREEM I., AL JUMAH M., "HLA-A, -B, -C,-DRB1 and-DQB1 allele and haplotype frequencies in Saudis using next generation sequencing technique", TISSUE ANTIGENS, cilt.82, ss.252-258, 2013 | |
dc.identifier.issn | 0001-2815 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_acaf43dd-afdb-4c66-bbf0-7da48e416ec3 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/115244 | |
dc.identifier.uri | https://doi.org/10.1111/tan.12200 | |
dc.description.abstract | Next generation sequencing (NGS) is a promising technique that can reveal the entire gene sequences and to the highest possible resolution without any phase ambiguities. We have used this technique to investigate the frequencies of HLA-A, -B, -C, -DRB1 and -DQB1 in a Saudi cohort of healthy individuals. We used NGS using the 454 genome sequence (GS) FLX System and Conexio assign atf 454 software to human leukocyte antigen (HLA) genotype eight class I and class II loci. A total of 158 healthy Saudi adults were analyzed. The most frequently observed allele for HLA-A was HLA-A*02:01:01:01 (13.6%); for HLA-B, HLA-B*50:01:01 (15.8%); for HLA-C, HLA-C*06:02:01:01 (18.7%); for HLA-DRB1, HLA-DRB1*07:01:01:01 (26.6%); and for HLA-DQB1, HLA-DQB1*02:01:01 (20.3%). The most common four loci haplotypes in the Saudi population were HLA-A*24:02:01:01-B*08:01:01-C*07:02:01:01-DRB1*03:01:01:01 and HLA-A*23:01:01-B*50:01:01-C*06:02:01:01-DRB1*07:01:01:01.. We have used a highly informative technique for HLA typing of a Saudi healthy cohort to establish allele and haplotype frequencies. These results should prove useful for population studies, disease associations and future planning of the unrelated bone marrow donor registry. | |
dc.language.iso | eng | |
dc.subject | Temel Tıp Bilimleri | |
dc.subject | Biyokimya | |
dc.subject | Histoloji-Embriyoloji | |
dc.subject | Cerrahi Tıp Bilimleri | |
dc.subject | Patoloji | |
dc.subject | Yaşam Bilimleri | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | Temel Bilimler | |
dc.subject | Biyoloji ve Biyokimya | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | PATOLOJİ | |
dc.subject | İmmünoloji | |
dc.subject | Yaşam Bilimleri (LIFE) | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | HÜCRE BİYOLOJİSİ | |
dc.title | HLA-A, -B, -C,-DRB1 and-DQB1 allele and haplotype frequencies in Saudis using next generation sequencing technique | |
dc.type | Makale | |
dc.relation.journal | TISSUE ANTIGENS | |
dc.contributor.department | King Saud Bin Abdulaziz University for Health Sciences , , | |
dc.identifier.volume | 82 | |
dc.identifier.issue | 4 | |
dc.identifier.startpage | 252 | |
dc.identifier.endpage | 258 | |
dc.contributor.firstauthorID | 43658 | |