Evidence map›Paper›PMID 35304543›Full record

ArticleScientific reports2022

A high-throughput real-time PCR tissue-of-origin test to distinguish blood from lymphoblastoid cell line DNA for (epi)genomic studies.

Lise M Hardy, Yosra Bouyacoub, Antoine Daunay, Mourad Sahbatou, Laura G Baudrin, Laetitia Gressin, Mathilde Touvier, Hélène Blanché, Jean-François Deleuze, Alexandre How-Kit

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. 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
0.3field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  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

10 authors at 3 institutions in 1 country.

Lise M HardyLaboratory for Genomics, Foundation Jean Dausset-CEPH, 75010, Paris, France.
Yosra BouyacoubLaboratory for Genomics, Foundation Jean Dausset-CEPH, 75010, Paris, France.
Antoine DaunayLaboratory for Genomics, Foundation Jean Dausset-CEPH, 75010, Paris, France.
Mourad SahbatouLaboratory for Genomics, Foundation Jean Dausset-CEPH, 75010, Paris, France.
Laura G BaudrinLaboratory for Genomics, Foundation Jean Dausset-CEPH, 75010, Paris, France.
Laetitia GressinCentre de Ressources Biologiques, CEPH Biobank, Foundation Jean Dausset-CEPH, Paris, France.
Mathilde TouvierSorbonne Paris Nord University, Nutritional Epidemiology Research Team (EREN), Epidemiology and Statistics Research Center Inserm U1153, Inrae U1125, Cnam, University of Paris (CRESS), Bobigny, France.
Hélène BlanchéLaboratory of Excellence GenMed, Paris, France.
Jean-François DeleuzeLaboratory for Genomics, Foundation Jean Dausset-CEPH, 75010, Paris, France.
Alexandre How-KitLaboratory for Genomics, Foundation Jean Dausset-CEPH, 75010, Paris, France. alexandre.how-kit@fjd-ceph.org.
Fondation Jean Dausset-CEPH · FRDirection de la Recherche Fondamentale · FRUniversité Sorbonne Paris Nord · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymphoblastoid cell lines (LCLs) derive from blood infected in vitro by Epstein-Barr virus and were used in several genetic, transcriptomic and epigenomic studies. Although few changes were shown between LCL and blood genotypes (SNPs) validating their use in genetics, more were highlighted for other genomic features and/or in their transcriptome and epigenome. This could render them less appropriate for these studies, notably when blood DNA could still be available. Here we developed a simple, high-throughput and cost-effective real-time PCR approach allowing to distinguish blood from LCL DNA samples based on the presence of EBV relative load and rearranged T-cell receptors γ and β. Our approach was able to achieve 98.5% sensitivity and 100% specificity on DNA of known origin (458 blood and 316 LCL DNA). It was further applied to 1957 DNA samples from the CEPH Aging cohort comprising DNA of uncertain origin, identifying 784 blood and 1016 LCL DNA. A subset of these DNA was further analyzed with an epigenetic clock indicating that DNA extracted from blood should be preferred to LCL for DNA methylation-based age prediction analysis. Our approach could thereby be a powerful tool to ascertain the origin of DNA in old collections prior to (epi)genomic studies.

Indexed as

Epstein-Barr Virus InfectionsHerpesvirus 4, HumanCell LineDNAEpigenomicsHumansReal-Time Polymerase Chain ReactionDNA

Identifiers

PMID35304543
PMCPMC8933453
OpenAlexW4220853077

What Socratic holds

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Registered trials

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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 Socratic graph.