Evidence map›Paper›PMID 22102586›Full record

ArticleNucleic acids research2012

Enhanced analysis of real-time PCR data by using a variable efficiency model: FPK-PCR.

Antoon Lievens, S Van Aelst, M Van den Bulcke, E Goetghebeur

Abstract read
In one paragraph

Article in Nucleic acids research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Article
  2. Analysis of qPCR Data: From PCR Efficiency to Absolute Target Quantity.International journal of molecular sciences · 2025
    Review
  3. Article
  4. Viruses · 2024
    Article
  5. Introducing the fBMC bioinformatics · 2024
    Article
  6. Article
  7. Article
  8. Pharmaceuticals (Basel, Switzerland) · 2023
    Article
  9. Pharmaceuticals (Basel, Switzerland) · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Nucleic Acid Testing of SARS-CoV-2.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Affine analysis for quantitative PCR measurements.Analytical and bioanalytical chemistry · 2020
    Article
  19. Article
  20. qPCR data analysis: Better results through iconoclasm.Biomolecular detection and quantification · 2019
    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

4 authors.

Antoon LievensPlatform for Molecular Biology and Biotechnology, Scientific Institute of Public Health, J. Wytsmanstreet 14, B-1050 Brussels, Belgium. antoon.lievens@wiv-isp.be
S Van Aelst
M Van den Bulcke
E Goetghebeur

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current methodology in real-time Polymerase chain reaction (PCR) analysis performs well provided PCR efficiency remains constant over reactions. Yet, small changes in efficiency can lead to large quantification errors. Particularly in biological samples, the possible presence of inhibitors forms a challenge. We present a new approach to single reaction efficiency calculation, called Full Process Kinetics-PCR (FPK-PCR). It combines a kinetically more realistic model with flexible adaptation to the full range of data. By reconstructing the entire chain of cycle efficiencies, rather than restricting the focus on a 'window of application', one extracts additional information and loses a level of arbitrariness. The maximal efficiency estimates returned by the model are comparable in accuracy and precision to both the golden standard of serial dilution and other single reaction efficiency methods. The cycle-to-cycle changes in efficiency, as described by the FPK-PCR procedure, stay considerably closer to the data than those from other S-shaped models. The assessment of individual cycle efficiencies returns more information than other single efficiency methods. It allows in-depth interpretation of real-time PCR data and reconstruction of the fluorescence data, providing quality control. Finally, by implementing a global efficiency model, reproducibility is improved as the selection of a window of application is avoided.

Indexed as

DNA, PlantFluorescenceGlycine maxKineticsLogistic ModelsReal-Time Polymerase Chain ReactionDNA, Plant

Identifiers

PMID22102586
PMCPMC3258155

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.