Evidence map›Paper›PMID 37454173›Full record

ArticleScientific reports2023

Reverse transcription-quantitative PCR (RT-qPCR) without the need for prior removal of DNA.

Damir Đermić, Sven Ljubić, Maja Matulić, Alfredo Procino, Maria Chiara Feliciello, Đurđica Ugarković, Isidoro Feliciello

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Downregulation of Gene Expression by Alpha Satellite Transcripts.International journal of molecular sciences · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Alpha Satellite DNA in Targeted Drug Therapy for Prostate Cancer.International journal of molecular sciences · 2023
    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

7 authors at 4 institutions in 2 countries.

Damir ĐermićDivision of Molecular Biology, Ruder Boskovic Institute, 10000, Zagreb, Croatia.
Sven LjubićDivision of Molecular Biology, Ruder Boskovic Institute, 10000, Zagreb, Croatia.
Maja MatulićDivision of Molecular Biology, Department of Biology, Faculty of Science, University of Zagreb, 10000, Zagreb, Croatia.
Alfredo ProcinoDivision of Molecular Biology, Ruder Boskovic Institute, 10000, Zagreb, Croatia.
Maria Chiara FelicielloDepartment of Statistical Science, Alma Mater Studiorum, University of Bologna, 40126, Bologna, Italy.
Đurđica UgarkovićDivision of Molecular Biology, Ruder Boskovic Institute, 10000, Zagreb, Croatia. ugarkov@irb.hr.
Isidoro FelicielloDepartment of Clinical Medicine and Surgery, University of Naples Federico II, 80135, Naples, Italy. isidoro.feliciello@unina.it.
Rudjer Boskovic Institute · HRUniversity of Bologna · ITUniversity of Naples Federico II · ITUniversity of Zagreb · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The procedure illustrated in this paper represents a new method for transcriptome analysis by PCR (Polymerase Chain Reaction), which circumvents the need for elimination of potential DNA contamination. Compared to the existing methodologies, our method is more precise, simpler and more reproducible because it preserves the RNA's integrity, does not require materials and/or reagents that are used for elimination of DNA and it also reduces the number of samples that should be set up as negative controls. This novel procedure involves the use of a specifically modified primer during reverse transcription step, which contains mismatched bases, thus producing cDNA molecules that differ from genomic DNA. By using the same modified primer in PCR amplification, only cDNA template is amplified since genomic DNA template is partially heterologous to the primer. In this way, amplification by PCR is unaffected by any potential DNA contamination since it is specific only for the cDNA template. Furthermore, it accurately reflects the initial RNA concentration of the sample, which is prone to changes due to various physical or enzymatic treatments commonly used by the current methodologies for DNA elimination. The method is particularly suitable for quantification of highly repetitive DNA transcripts, such as satellite DNA.

Indexed as

DNAReverse TranscriptionDNA, ComplementaryPolymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionRNADNADNA, ComplementaryRNA

Identifiers

PMID37454173
PMCPMC10349872
OpenAlexW4384408082

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.