Matches in SemOpenAlex for { <https://semopenalex.org/work/W2999697929> ?p ?o ?g. }
- W2999697929 endingPage "44" @default.
- W2999697929 startingPage "33" @default.
- W2999697929 abstract "Exposure to non-matching human platelet alloantigens (HPA) may result in alloimmunization. Antibodies to HPA can be responsible for post-transfusion purpura, refractoriness to donor platelets, and fetal and neonatal alloimmune thrombocytopenia. For the supply of compatible apheresis platelet concentrates, the HPA genotypes are determined in a routine manner.Here, we describe a novel method for genotyping twelve different HPA systems simultaneously, including HPA-1 to HPA-5, HPA-9w, HPA-10w, HPA-16w, HPA-19w, HPA-27w, and the novel HPA-34w by means of amplicon-based next-generation sequencing (NGS). Blood donor samples of 757 individuals with a migration background and 547 of Western European ancestry were genotyped in a mass-screening setup. An in-house software was developed for fast and automatic analysis. TaqMan assay and Sanger sequencing results served for validation of the NGS workflow. Finally, blood donors were divided in several groups based on their country of origin and the allele frequencies were compared.For 1,299 of 1,304 samples (99.6%) NGS was successfully performed. The concordance with TaqMan assay and Sanger sequencing results was 99.8%. Allele-calling dropouts that were observed for two samples with the TaqMan assay caused by rare single nucleotide polymorphisms were resolved by NGS. Additionally, twenty rare and two novel variants in the coding regions of the genes ITGB3, GPB1A, ITGBA2, and CD109 were detected. The determined allele frequencies were similar to those published in the gnomAD database.No significant differences were observed in the distribution of allele frequencies of HPA-1 through HPA-5 and HPA-15 throughout the analyzed groups except for a lower allele frequency for the HPA-1b allele in the group of donors with Southern Asian ancestry. In contrast, other nucleotide variants that have not yet been phenotypically characterized occurred three times more often in blood donors with a migration background. High-throughput amplicon-based NGS is a reliable method for screening HPA genotypes in a large sample cohort simultaneously. It is easily upgradeable for genotyping additional targets without changing the setup or the analysis pipeline. Mass-screening methods will help building up blood donor registries to provide matched blood products." @default.
- W2999697929 created "2020-01-23" @default.
- W2999697929 creator A5003601361 @default.
- W2999697929 creator A5011045044 @default.
- W2999697929 creator A5065538150 @default.
- W2999697929 creator A5075796454 @default.
- W2999697929 creator A5078563130 @default.
- W2999697929 creator A5079631559 @default.
- W2999697929 creator A5080667810 @default.
- W2999697929 creator A5088771221 @default.
- W2999697929 date "2020-01-01" @default.
- W2999697929 modified "2023-09-26" @default.
- W2999697929 title "High-Throughput Screening of Blood Donors for Twelve Human Platelet Antigen Systems Using Next-Generation Sequencing Reveals Detection of Rare Polymorphisms and Two Novel Protein-Changing Variants" @default.
- W2999697929 cites W1886489298 @default.
- W2999697929 cites W1970819021 @default.
- W2999697929 cites W2029523950 @default.
- W2999697929 cites W2031917485 @default.
- W2999697929 cites W2042364010 @default.
- W2999697929 cites W2074296272 @default.
- W2999697929 cites W2076209648 @default.
- W2999697929 cites W2078091763 @default.
- W2999697929 cites W2080175561 @default.
- W2999697929 cites W2087218209 @default.
- W2999697929 cites W2087663912 @default.
- W2999697929 cites W2103679307 @default.
- W2999697929 cites W2121003553 @default.
- W2999697929 cites W2132548846 @default.
- W2999697929 cites W2142052303 @default.
- W2999697929 cites W2147865091 @default.
- W2999697929 cites W2162098634 @default.
- W2999697929 cites W2256016639 @default.
- W2999697929 cites W2601763218 @default.
- W2999697929 cites W2783447594 @default.
- W2999697929 cites W2886024498 @default.
- W2999697929 cites W2906116132 @default.
- W2999697929 cites W2911613203 @default.
- W2999697929 cites W2929581362 @default.
- W2999697929 cites W3023259422 @default.
- W2999697929 cites W4250200907 @default.
- W2999697929 cites W4253718744 @default.
- W2999697929 doi "https://doi.org/10.1159/000504894" @default.
- W2999697929 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7036567" @default.
- W2999697929 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32110192" @default.
- W2999697929 hasPublicationYear "2020" @default.
- W2999697929 type Work @default.
- W2999697929 sameAs 2999697929 @default.
- W2999697929 citedByCount "11" @default.
- W2999697929 countsByYear W29996979292020 @default.
- W2999697929 countsByYear W29996979292021 @default.
- W2999697929 countsByYear W29996979292022 @default.
- W2999697929 countsByYear W29996979292023 @default.
- W2999697929 crossrefType "journal-article" @default.
- W2999697929 hasAuthorship W2999697929A5003601361 @default.
- W2999697929 hasAuthorship W2999697929A5011045044 @default.
- W2999697929 hasAuthorship W2999697929A5065538150 @default.
- W2999697929 hasAuthorship W2999697929A5075796454 @default.
- W2999697929 hasAuthorship W2999697929A5078563130 @default.
- W2999697929 hasAuthorship W2999697929A5079631559 @default.
- W2999697929 hasAuthorship W2999697929A5080667810 @default.
- W2999697929 hasAuthorship W2999697929A5088771221 @default.
- W2999697929 hasBestOaLocation W29996979291 @default.
- W2999697929 hasConcept C104317684 @default.
- W2999697929 hasConcept C135763542 @default.
- W2999697929 hasConcept C143660080 @default.
- W2999697929 hasConcept C153209595 @default.
- W2999697929 hasConcept C153911025 @default.
- W2999697929 hasConcept C172680121 @default.
- W2999697929 hasConcept C180754005 @default.
- W2999697929 hasConcept C203014093 @default.
- W2999697929 hasConcept C2779234561 @default.
- W2999697929 hasConcept C2779989375 @default.
- W2999697929 hasConcept C31467283 @default.
- W2999697929 hasConcept C37463918 @default.
- W2999697929 hasConcept C49105822 @default.
- W2999697929 hasConcept C51679486 @default.
- W2999697929 hasConcept C54355233 @default.
- W2999697929 hasConcept C76818968 @default.
- W2999697929 hasConcept C8185291 @default.
- W2999697929 hasConcept C86803240 @default.
- W2999697929 hasConceptScore W2999697929C104317684 @default.
- W2999697929 hasConceptScore W2999697929C135763542 @default.
- W2999697929 hasConceptScore W2999697929C143660080 @default.
- W2999697929 hasConceptScore W2999697929C153209595 @default.
- W2999697929 hasConceptScore W2999697929C153911025 @default.
- W2999697929 hasConceptScore W2999697929C172680121 @default.
- W2999697929 hasConceptScore W2999697929C180754005 @default.
- W2999697929 hasConceptScore W2999697929C203014093 @default.
- W2999697929 hasConceptScore W2999697929C2779234561 @default.
- W2999697929 hasConceptScore W2999697929C2779989375 @default.
- W2999697929 hasConceptScore W2999697929C31467283 @default.
- W2999697929 hasConceptScore W2999697929C37463918 @default.
- W2999697929 hasConceptScore W2999697929C49105822 @default.
- W2999697929 hasConceptScore W2999697929C51679486 @default.
- W2999697929 hasConceptScore W2999697929C54355233 @default.
- W2999697929 hasConceptScore W2999697929C76818968 @default.
- W2999697929 hasConceptScore W2999697929C8185291 @default.
- W2999697929 hasConceptScore W2999697929C86803240 @default.
- W2999697929 hasIssue "1" @default.