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10.1155/2017/9130879

http://scihub22266oqcxt.onion/10.1155/2017/9130879
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C5329668!5329668!28286782
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suck abstract from ncbi


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pmid28286782      J+Immunol+Res 2017 ; 2017 (ä): ä
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  • Computational Approaches to Facilitate Epitope-Based HLA Matching in Solid Organ Transplantation #MMPMID28286782
  • Geneugelijk K; Wissing J; Koppenaal D; Niemann M; Spierings E
  • J Immunol Res 2017[]; 2017 (ä): ä PMID28286782show ga
  • Epitope-based HLA matching has been emerged over the last few years as an improved method for HLA matching in solid organ transplantation. The epitope-based matching concept has been incorporated in both the PIRCHE-II and the HLAMatchmaker algorithm to find the most suitable donor for a recipient. For these algorithms, high-resolution HLA genotype data of both donor and recipient is required. Since high-resolution HLA genotype data is often not available, we developed a computational method which allows epitope-based HLA matching from serological split level HLA typing relying on HLA haplotype frequencies. To validate this method, we simulated a donor-recipient population for which PIRCHE-II and eplet values were calculated when using both high-resolution HLA genotype data and serological split level HLA typing. The majority of the serological split level HLA-determined ln(PIRCHE-II)/ln(eplet) values did not or only slightly deviate from the reference group of high-resolution HLA-determined ln(PIRCHE-II)/ln(eplet) values. This deviation was slightly increased when HLA-C or HLA-DQ was omitted from the input and was substantially decreased when using two-field resolution HLA genotype data of the recipient and serological split level HLA typing of the donor. Thus, our data suggest that our computational approach is a powerful tool to estimate PIRCHE-II/eplet values when high-resolution HLA genotype data is not available.
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