Evidence map›Paper›PMID 35547719›Full record

ArticleRSC advances2018

Unlocked nucleic acid modified primer-based enzymatic polymerization assay: towards allele-specific genotype detection of human platelet antigens.

Bao T Le, Quintin Hughes, Shilpa Rakesh, Ross Baker, Per T Jørgensen, Jesper Wengel, Rakesh N Veedu

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 46% of its field
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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 2 institutions in 4 countries.

Bao T LeCentre for Comparative Genomics, Murdoch University Perth Australia-6150.ORCID https://orcid.org/0000-0003-1881-8153
Quintin HughesPerth Blood Institute Nedlands Perth WA Australia.
Shilpa RakeshPerth Blood Institute Nedlands Perth WA Australia.
Ross BakerPerth Blood Institute Nedlands Perth WA Australia.
Per T JørgensenBioNEC, Department of Physics, Chemistry and Pharmacy, University of Southern Denmark Odense M 5231 Denmark R.Veedu@murdoch.edu.au jwe@sdu.dk.ORCID https://orcid.org/0000-0003-3932-5921
Jesper WengelBioNEC, Department of Physics, Chemistry and Pharmacy, University of Southern Denmark Odense M 5231 Denmark R.Veedu@murdoch.edu.au jwe@sdu.dk.ORCID https://orcid.org/0000-0001-9835-1009
Rakesh N VeeduCentre for Comparative Genomics, Murdoch University Perth Australia-6150.ORCID https://orcid.org/0000-0003-2192-9532
Murdoch University · AUUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate detection of single nucleotide polymorphisms (SNPs) is paramount for the appropriate therapeutic intervention of debilitating diseases associated with SNPs. However, in some cases current nucleic acid probes fail to detect allele-specific mutations, for example, human platelet antigens, HPA-15a (TCC) and HPA-15b (TAC) alleles associated with neonatal alloimmune thrombocytopenia. Towards this, it is necessary to develop a novel assay for detection of allele-specific mutations. In this study, we investigated the potential of unlocked nucleic acid (UNA)-modified primers in SNP detection utilising an enzymatic polymerisation-based approach. Our results of primer extension and asymmetric polymerase chain reaction by KOD XL DNA polymerase revealed that UNA-modified primers achieved excellent allele-specificity in discriminating the human platelet antigen DNA template, whereas the DNA control primers were not able to differentiate between the normal and mutant alleles, demonstrating the scope of this novel UNA-based enzymatic approach as a robust methodology for efficient detection of allele-specific mismatches. Although further evaluation is required for other disease conditions, we firmly believe that our findings offer a great promise for the diagnosis of neonatal alloimmune thrombocytopenia and other SNP-related diseases.

Identifiers

PMID35547719
PMCPMC9086379
OpenAlexW2891284455

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.