Evidence map›Paper›PMID 28295603›Full record

ArticleJournal of clinical laboratory analysis2018

Rapid ABO genotyping by high-speed droplet allele-specific PCR using crude samples.

Chiaki Taira, Kazuyuki Matsuda, Naoya Takeichi, Satomi Furukawa, Mitsutoshi Sugano, Takeshi Uehara, Nobuo Okumura, Takayuki Honda

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
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  3. 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 at 2 institutions in 1 country.

Chiaki TairaLaboratory of Clinical Chemistry and Immunology, Department of Biomedical Laboratory Sciences, School of Health Sciences, Shinshu University, Matsumoto, Japan.
Kazuyuki MatsudaDepartment of Laboratory Medicine, Shinshu University Hospital, Matsumoto, Japan.ORCID http://orcid.org/0000-0002-4056-7242
Naoya TakeichiDepartment of Laboratory Medicine, Shinshu University Hospital, Matsumoto, Japan.
Satomi FurukawaDepartment of Laboratory Medicine, Shinshu University Hospital, Matsumoto, Japan.
Mitsutoshi SuganoDepartment of Laboratory Medicine, Shinshu University Hospital, Matsumoto, Japan.
Takeshi UeharaDepartment of Laboratory Medicine, Shinshu University Hospital, Matsumoto, Japan.
Nobuo OkumuraLaboratory of Clinical Chemistry and Immunology, Department of Biomedical Laboratory Sciences, School of Health Sciences, Shinshu University, Matsumoto, Japan.
Takayuki HondaDepartment of Laboratory Medicine, Shinshu University Hospital, Matsumoto, Japan.
Shinshu University Hospital · JPShinshu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundABO genotyping has common tools for personal identification of forensic and transplantation field. We developed a new method based on a droplet allele-specific PCR (droplet-AS-PCR) that enabled rapid PCR amplification. We attempted rapid ABO genotyping using crude DNA isolated from dried blood and buccal cells.

methodsWe designed allele-specific primers for three SNPs (at nucleotides 261, 526, and 803) in exons 6 and 7 of the ABO gene. We pretreated dried blood and buccal cells with proteinase K, and obtained crude DNAs without DNA purification.

resultsDroplet-AS-PCR allowed specific amplification of the SNPs at the three loci using crude DNA, with results similar to those for DNA extracted from fresh peripheral blood. The sensitivity of the methods was 5%-10%. The genotyping of extracted DNA and crude DNA were completed within 8 and 9 minutes, respectively. The genotypes determined by the droplet-AS-PCR method were always consistent with those obtained by direct sequencing.

conclusionThe droplet-AS-PCR method enabled rapid and specific amplification of three SNPs of the ABO gene from crude DNA treated with proteinase K. ABO genotyping by the droplet-AS-PCR has the potential to be applied to various fields including a forensic medicine and transplantation medical care.

Indexed as

ABO Blood-Group SystemDNADried Blood Spot TestingGenotyping TechniquesHumansLimit of DetectionMouth MucosaPolymerase Chain ReactionPolymorphism, Single NucleotideTime FactorsABO Blood-Group SystemDNAABO genotypebuccal cellsdried blood spot samplesdroplet allele specific PCRsingle nucleotide polymorphism

Identifiers

PMID28295603
PMCPMC6816865
OpenAlexW2598312220

What OpenQuestion holds

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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.