Development of mass spectrometry‐based genotyping method for simultaneous detection of 35 <scp>HPA</scp> systems, 5 <scp>HNA</scp> systems and the <scp>CD36</scp> antigen

We successfully developed an MS panel capable of detecting all currently known HPAs, HNAs, and the CD36 antigen, overcoming limitations of previous methods related to non-specific HNA-1 amplification. This method also demonstrated its efficacy in establishing a large-scale platelet donor database, and rare allele data support precise transfusion matching for special patients.