“…A total of 151 loci were annotated within the 2.4-Mb sequences, including three classical ( SLA-1 , SLA-2 , and SLA-3 ), and three non-classical class I genes ( SLA-6 , SLA-7 , and SLA-8 ) in the class I region, and four classical ( DRA, DRB1 , DQA , and DQB1 ), and four non-classical class II genes ( DMA , DMB , DOA , and DOB ) in the class II region as expressed SLA genes [5]. Based on the genomic and cDNA sequences in the SLA loci, many kinds of molecular-based SLA typing systems, including polymerase chain reaction (PCR) - sequence-specific primers (SSPs) [6,7], -fluorescently labeled sequence-specific oligonucleotide probes (SSOPs) [8], and -sequence-based typing (SBT) by traditional Sanger methods and/or next generation sequencing (NGS) [4,9,10,11,12] have been reported to assign SLA class I and II alleles. A systematic nomenclature for the SLA genes, alleles, and haplotypes are established by the SLA Nomenclature Committee, formed in 2002.…”