Evidence map›Paper›PMID 40564908›Full record

ArticleInternational journal of molecular sciences2025

Characterisation of the ABO Blood Group Phenotypes Using Third-Generation Sequencing.

Fredrick M Mobegi, Samuel Bruce, Naser El-Lagta, Felipe Ayora, Benedict M Matern, Mathijs Groeneweg, Lloyd J D'Orsogna, Dianne De Santis

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Fredrick M MobegiDepartment of Clinical Immunology, PathWest Laboratory Medicine WA, Fiona Stanley Hospital Network, Murdoch, WA 6150, Australia.ORCID 0000-0003-0554-9919
Samuel BruceDepartment of Clinical Immunology, PathWest Laboratory Medicine WA, Fiona Stanley Hospital Network, Murdoch, WA 6150, Australia.
Naser El-LagtaDepartment of Clinical Immunology, PathWest Laboratory Medicine WA, Fiona Stanley Hospital Network, Murdoch, WA 6150, Australia.
Felipe AyoraResearch and Advanced Computing, BizData Pty Limited, Melbourne, VIC 3000, Australia.ORCID 0000-0003-3540-3371
Benedict M MaternThe Transplant Immunology Department, Maastricht University Medical Centre, 6229 HX Maastricht, The Netherlands.
Mathijs GroenewegThe Transplant Immunology Department, Maastricht University Medical Centre, 6229 HX Maastricht, The Netherlands.
Lloyd J D'OrsognaDepartment of Clinical Immunology, PathWest Laboratory Medicine WA, Fiona Stanley Hospital Network, Murdoch, WA 6150, Australia.ORCID 0000-0002-6824-4189
Dianne De SantisDepartment of Clinical Immunology, PathWest Laboratory Medicine WA, Fiona Stanley Hospital Network, Murdoch, WA 6150, Australia.

Funding

PATHWEST TRANSLATIONAL RESEARCH & AUDIT FUND 2024/2025
6 · The paper itself

Abstract

Third-generation sequencing (TGS), also known as long-read sequencing, has become a promising tool in clinical and research laboratories because it delivers high-resolution results with unmatched throughput. Specialised immunohematology laboratories currently employ sequencing-based methods to characterise rare ABO blood group phenotypes that cannot be identified through serology and genotyping methods. However, routine clinical application of these methods remains elusive due to the absence of validated laboratory protocols and bioinformatics tools. In this study, we have developed and validated a TGS-based workflow for comprehensive determination of the clinically relevant ABO phenotypes from DNA isolated from buccal swabs or whole blood. The region spanning exons 2 to 7 of the

Indexed as

ABO Blood-Group SystemHigh-Throughput Nucleotide SequencingAllelesExonsGenotypeHumansPhenotypePolymorphism, Single NucleotideABO Blood-Group SystemABO blood typesABO genotypingABO phenotypingABO subtypessingle-nucleotide variantsthird-generation sequencing

Identifiers

PMID40564908
PMCPMC12192586

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.