Evidence map›Paper›PMID 38066817›Full record

ArticleDiagnostics (Basel, Switzerland)2023

Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy Termination.

Carole Goumy, Zangbéwendé Guy Ouedraogo, Elodie Bellemonte, Eleonore Eymard-Pierre, Gwendoline Soler, Isabelle Perthus, Céline Pebrel-Richard, Laetitia Gouas, Gaëlle Salaun, Lauren Véronèse and 3 more

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2023. 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
–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

0 citing papers in PubMed.

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

13 authors.

Carole GoumyCytogénétique Médicale, Centre Hospitalier Universitaire de Clermont-Ferrand, CHU Estaing, 63000 Clermont-Ferrand, France.
Zangbéwendé Guy OuedraogoCytogénétique Médicale, Centre Hospitalier Universitaire de Clermont-Ferrand, CHU Estaing, 63000 Clermont-Ferrand, France.ORCID 0000-0002-1142-8788
Elodie BellemonteUMR 1095 INRAE/UCA Génétique, Diversité et Ecophysiologie des Céréales (GDEC), Genotyping and Sequencing Plateform Gentyane, 63000 Clermont-Ferrand, France.
Eleonore Eymard-PierreCytogénétique Médicale, Centre Hospitalier Universitaire de Clermont-Ferrand, CHU Estaing, 63000 Clermont-Ferrand, France.
Gwendoline SolerCytogénétique Médicale, Centre Hospitalier Universitaire de Clermont-Ferrand, CHU Estaing, 63000 Clermont-Ferrand, France.
Isabelle PerthusService de Génétique Médicale, CHU Clermont-Ferrand, CHU Estaing, 63000 Clermont-Ferrand, France.ORCID 0000-0002-3845-6180
Céline Pebrel-RichardCytogénétique Médicale, Centre Hospitalier Universitaire de Clermont-Ferrand, CHU Estaing, 63000 Clermont-Ferrand, France.
Laetitia GouasCytogénétique Médicale, Centre Hospitalier Universitaire de Clermont-Ferrand, CHU Estaing, 63000 Clermont-Ferrand, France.
Gaëlle SalaunCytogénétique Médicale, Centre Hospitalier Universitaire de Clermont-Ferrand, CHU Estaing, 63000 Clermont-Ferrand, France.
Lauren VéronèseCytogénétique Médicale, Centre Hospitalier Universitaire de Clermont-Ferrand, CHU Estaing, 63000 Clermont-Ferrand, France.
Hélène LaurichesseService d'Anatomie et de Cytologie Pathologique, Centre Hospitalier Universitaire de Clermont-Ferrand, CHU Estaing, 63000 Clermont-Ferrand, France.
Claude DarchaService d'Anatomie et de Cytologie Pathologique, Centre Hospitalier Universitaire de Clermont-Ferrand, CHU Estaing, 63000 Clermont-Ferrand, France.ORCID 0000-0003-3811-9683
Andrei TchirkovCytogénétique Médicale, Centre Hospitalier Universitaire de Clermont-Ferrand, CHU Estaing, 63000 Clermont-Ferrand, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Optical genome mapping (OGM) is an alternative to classical cytogenetic techniques to improve the detection rate of clinically significant genomic abnormalities. The isolation of high-molecular-weight (HMW) DNA is critical for a successful OGM analysis. HMW DNA quality depends on tissue type, sample size, and storage conditions. We assessed the feasibility of OGM analysis of DNA from nine umbilical cord (UC) and six chorionic villus (CV) samples collected after the spontaneous or therapeutic termination of pregnancy. We analyzed quality control metrics provided by the Saphyr system (Bionano Genomics) and assessed the length of extracted DNA molecules using pulsed-field capillary electrophoresis. OMG data were successfully analyzed for all six CV samples. Five of the UC samples did not meet the Saphyr quality criteria, mainly due to poor DNA quality. In this regard, we found that DNA quality assessment with pulsed-field capillary electrophoresis can predict a successful OGM analysis. OGM data were fully concordant with the results of standard cytogenetic methods. Moreover, OGM detected an average of 14 additional structural variants involving OMIM genes per sample. On the basis of our results, we established the optimal conditions for sample storage and preparation required for a successful OGM analysis. We recommend checking DNA quality before analysis with pulsed-field capillary electrophoresis if the storage conditions were not ideal or if the quality of the sample is poor. OGM can therefore be performed on fetal tissue harvested after the termination of pregnancy, which opens up the perspective for improved diagnostic yield.

Indexed as

birth defectchorionic villioptical genome mappingtermination of pregnancyumbilical cord biopsies

Identifiers

PMID38066817
PMCPMC10706391

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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 OpenQuestion graph.