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Next-generation HLA typing of 382 International Histocompatibility Working Group reference B-Lymphoblastoid cell lines: report from the 17th International HLA and Immunogenetics Workshop

机译:382个国际组织相容性工作组参考的B淋巴母细胞系的下一代HLA分型:第17届国际HLA和免疫遗传学研讨会的报告

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摘要

Extended molecular characterization of HLA genes in the IHWG reference B-lymphoblastoid cell lines (B-LCLs) was one of the major goals for the 17th International HLA and Immunogenetics Workshop (IHIW). Although reference B-LCLs have been examined extensively in previous workshops complete high-resolution typing was not completed for all the classical class I and class II HLA genes. To address this, we conducted a single-blind study where select panels of B-LCL genomic DNA samples were distributed to multiple laboratories for HLA genotyping by next-generation sequencing methods. Identical cell panels comprised of 24 and 346 samples were distributed and typed by at least four laboratories in order to derive accurate consensus HLA genotypes. Overall concordance rates calculated at both 2- and 4-field allele-level resolutions ranged from 90.4% to 100%. Concordance for the class I genes ranged from 91.7 to 100%, whereas concordance for class II genes was variable; the lowest observed at HLA-DRB3 (84.2%). At the maximum allele-resolution 78 B-LCLs were defined as homozygous for all 11 loci. We identified 11 novel exon polymorphisms in the entire cell panel. A comparison of the B-LCLs NGS HLA genotypes with the HLA genotypes catalogued in the IPD-IMGT/HLA Database Cell Repository, revealed an overall allele match at 68.4%. Typing discrepancies between the two datasets were mostly due to the lower-resolution historical typing methods resulting in incomplete HLA genotypes for some samples listed in the IPD-IMGT/HLA Database Cell Repository. Our approach of multiple-laboratory NGS HLA typing of the B-LCLs has provided accurate genotyping data. The data generated by the tremendous collaborative efforts of the 17th IHIW participants is useful for updating the current cell and sequence databases and will be a valuable resource for future studies.
机译:在IHWG参考B淋巴母细胞系(B-LCLs)中扩展HLA基因的分子特性是第17届国际HLA和免疫遗传学研讨会(IHIW)的主要目标之一。尽管参考B-LCL在先前的研讨会中已得到广泛检查,但对于所有经典的I类和II类HLA基因而言,尚未完成完整的高分辨率分型。为了解决这个问题,我们进行了单盲研究,其中选择的B-LCL基因组DNA样本小组通过下一代测序方法分配给多个实验室进行HLA基因分型。为了获得准确的共有HLA基因型,由至少四个实验室分配并分类了由24个样品和346个样品组成的相同细胞板。在2场和4场等位基因水平分辨率下计算的总体一致性比率范围为90.4%至100%。 I类基因的一致性从91.7到100%不等,而II类基因的一致性则是可变的。在HLA-DRB3处观察到的最低值(84.2%)。在最大的等位基因分辨率下,所有11个基因座均被定义为纯合的78个B-LCL。我们在整个细胞组中鉴定出11种新颖的外显子多态性。将B-LCLs NGS HLA基因型与IPD-IMGT / HLA数据库细胞存储库中分类的HLA基因型进行比较,发现总体等位基因匹配率为68.4%。这两个数据集之间的打字差异主要是由于较低分辨率的历史打字方法导致IPD-IMGT / HLA数据库单元存储库中列出的某些样本的HLA基因型不完整。我们的B-LCL多实验室NGS HLA分型方法提供了准确的基因分型数据。第17届IHIW参加者的巨大协作努力所产生的数据对于更新当前的细胞和序列数据库很有用,并且将为将来的研究提供宝贵的资源。

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