Abstract
The HLA-DRB1 sequencing based typing strategies reported to date require separate amplifications of each sample with a series of group-specific primers followed by sequencing of any resulting polymerase chain reaction (PCR) products. Whilst this results in high resolution typing in the majority of cases, a number of unnecessary amplifications are performed Me report here a novel approach where amplification of the second exon of HLA-DRB1 is performed in a single tube for all alleles. Retrospective analysis of 642 consecutive Western Australian unrelated bone marrow registry donors has shown that this approach results in unambiguous typings in 71.1% of cases Ambiguities can be readily resolved if necessary with a single additional sequencing reaction on the original PCR product.
Original language | English |
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Pages (from-to) | 46-54 |
Journal | Tissue Antigens |
Volume | 57 |
Issue number | N/A |
DOIs | |
Publication status | Published - 2001 |