Evidence map›Paper›PMID 36550951›Full record

ReviewBioengineering (Basel, Switzerland)2022

Enhancing Molecular Testing for Effective Delivery of Actionable Gene Diagnostics.

Árpád Ferenc Kovács, Zaránd Némethi, Tünde Abonyi, György Fekete, Gábor T Kovács

Open access · goldAbstract readReview
In one paragraph

Review in Bioengineering (Basel, Switzerland), 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
0.1field-weighted citation impact, top 62% 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, 1 citations in OpenAlex.

  1. Review
  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

5 authors at 1 institution in 1 country.

Árpád Ferenc Kovács2nd Department of Paediatrics, Semmelweis University, Üllői út 26, 1085 Budapest, Hungary.ORCID 0000-0002-7742-160X
Zaránd Némethi2nd Department of Paediatrics, Semmelweis University, Üllői út 26, 1085 Budapest, Hungary.
Tünde Abonyi2nd Department of Paediatrics, Semmelweis University, Üllői út 26, 1085 Budapest, Hungary.
György Fekete2nd Department of Paediatrics, Semmelweis University, Üllői út 26, 1085 Budapest, Hungary.
Gábor T Kovács2nd Department of Paediatrics, Semmelweis University, Üllői út 26, 1085 Budapest, Hungary.
Semmelweis University · HU

Funding

Hungarian Academy of Sciences PC-2022-9/2022Hungarian National Research, Development and Innovation Office - NKFIH OTKA PD_21 138521
6 · The paper itself

Abstract

There is a deep need to navigate within our genomic data to find, understand and pave the way for disease-specific treatments, as the clinical diagnostic journey provides only limited guidance. The human genome is enclosed in every nucleated cell, and yet at the single-cell resolution many unanswered questions remain, as most of the sequencing techniques use a bulk approach. Therefore, heterogeneity, mosaicism and many complex structural variants remain partially uncovered. As a conceptual approach, nanopore-based sequencing holds the promise of being a single-molecule-based, long-read and high-resolution technique, with the ability of uncovering the nucleic acid sequence and methylation almost in real time. A key limiting factor of current clinical genetics is the deciphering of key disease-causing genomic sequences. As the technological revolution is expanding regarding genetic data, the interpretation of genotype-phenotype correlations should be made with fine caution, as more and more evidence points toward the presence of more than one pathogenic variant acting together as a result of intergenic interplay in the background of a certain phenotype observed in a patient. This is in conjunction with the observation that many inheritable disorders manifest in a phenotypic spectrum, even in an intra-familial way. In the present review, we summarized the relevant data on nanopore sequencing regarding clinical genomics as well as highlighted the importance and content of pre-test and post-test genetic counselling, yielding a complex approach to phenotype-driven molecular diagnosis. This should significantly lower the time-to-right diagnosis as well lower the time required to complete a currently incomplete genotype-phenotype axis, which will boost the chance of establishing a new actionable diagnosis followed by therapeutical approach.

Indexed as

actionable genetic diagnosiscomplex structural variantsgenetic counsellinglong-read sequencingnanopore sequencingsingle cells

Identifiers

PMID36550951
PMCPMC9774983
OpenAlexW4311050761

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.