https://www.selleckchem.com/pr....oducts/i-brd9-gsk602
In the total cohort of 884 patients, RHtyper identified 38 RHD and 28 RHCE distinct alleles, including a novel RHD DAU allele, RHD* 602G, 733C, 744T 1136T. RHtyper provides comprehensive and high-throughput RH genotyping from WGS data, facilitating deconvolution of the extensive RH genetic variation among patients with SCD. We have implemented RHtyper as a cloud-based public access application in DNAnexus (https//platform.dnanexus.com/app/RHtyper), enabling clinicians and researchers to perform RH genotyping with next-generation s
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