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Combining globally search for a regular expression and print matching lines with bibliographic monitoring of genomic database improves diagnosis.

Authors :
Tran Mau-Them F
Overs A
Bruel AL
Duquet R
Thareau M
Denommé-Pichon AS
Vitobello A
Sorlin A
Safraou H
Nambot S
Delanne J
Moutton S
Racine C
Engel C
De Giraud d'Agay M
Lehalle D
Goldenberg A
Willems M
Coubes C
Genevieve D
Verloes A
Capri Y
Perrin L
Jacquemont ML
Lambert L
Lacaze E
Thevenon J
Hana N
Van-Gils J
Dubucs C
Bizaoui V
Gerard-Blanluet M
Lespinasse J
Mercier S
Guerrot AM
Maystadt I
Tisserant E
Faivre L
Philippe C
Duffourd Y
Thauvin-Robinet C
Source :
Frontiers in genetics [Front Genet] 2023 Apr 20; Vol. 14, pp. 1122985. Date of Electronic Publication: 2023 Apr 20 (Print Publication: 2023).
Publication Year :
2023

Abstract

Introduction: Exome sequencing has a diagnostic yield ranging from 25% to 70% in rare diseases and regularly implicates genes in novel disorders. Retrospective data reanalysis has demonstrated strong efficacy in improving diagnosis, but poses organizational difficulties for clinical laboratories. Patients and methods: We applied a reanalysis strategy based on intensive prospective bibliographic monitoring along with direct application of the GREP command-line tool (to "globally search for a regular expression and print matching lines") in a large ES database. For 18 months, we submitted the same five keywords of interest [( intellectual disability , ( neuro ) developmental delay , and ( neuro ) developmental disorder )] to PubMed on a daily basis to identify recently published novel disease-gene associations or new phenotypes in genes already implicated in human pathology. We used the Linux GREP tool and an in-house script to collect all variants of these genes from our 5,459 exome database. Results: After GREP queries and variant filtration, we identified 128 genes of interest and collected 56 candidate variants from 53 individuals. We confirmed causal diagnosis for 19/128 genes (15%) in 21 individuals and identified variants of unknown significance for 19/128 genes (15%) in 23 individuals. Altogether, GREP queries for only 128 genes over a period of 18 months permitted a causal diagnosis to be established in 21/2875 undiagnosed affected probands (0.7%). Conclusion: The GREP query strategy is efficient and less tedious than complete periodic reanalysis. It is an interesting reanalysis strategy to improve diagnosis.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2023 Tran Mau-Them, Overs, Bruel, Duquet, Thareau, Denommé-Pichon, Vitobello, Sorlin, Safraou, Nambot, Delanne, Moutton, Racine, Engel, De Giraud d’Agay, Lehalle, Goldenberg, Willems, Coubes, Genevieve, Verloes, Capri, Perrin, Jacquemont, Lambert, Lacaze, Thevenon, Hana, Van-Gils, Dubucs, Bizaoui, Gerard-Blanluet, Lespinasse, Mercier, Guerrot, Maystadt, Tisserant, Faivre, Philippe, Duffourd and Thauvin-Robinet.)

Details

Language :
English
ISSN :
1664-8021
Volume :
14
Database :
MEDLINE
Journal :
Frontiers in genetics
Publication Type :
Academic Journal
Accession number :
37152996
Full Text :
https://doi.org/10.3389/fgene.2023.1122985