Evidence map›Paper›PMID 41960320›Full record

ArticleResearch square2026

Consensus-based Detection of Aetiologic Copy Number Variants For Syndromic Orofacial Clefts Utilising Whole Exome Sequencing of Case Parent Trios.

Samuel Kanor Quaynor, Gideon Okyere Mensah, Tamara Busch, Bruce Tsri, Solomon Obiri-Yeboah, Daniel Kwesi Sabbah, Pius Agbenorku, Peter Donkor, Azeez Butali, Lord Jephthah Joojo Gowans

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Article in Research square, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Samuel Kanor QuaynorKwame Nkrumah University of Science and Technology (KNUST).
Gideon Okyere MensahKwame Nkrumah University of Science and Technology (KNUST).
Tamara BuschUniversity of Iowa.
Bruce TsriKwame Nkrumah University of Science and Technology (KNUST).
Solomon Obiri-YeboahKwame Nkrumah University of Science and Technology.
Daniel Kwesi SabbahKwame Nkrumah University of Science and Technology.
Pius AgbenorkuKwame Nkrumah University of Science and Technology.
Peter DonkorKwame Nkrumah University of Science and Technology.
Azeez ButaliUniversity of Iowa.
Lord Jephthah Joojo GowansKwame Nkrumah University of Science and Technology (KNUST).

Funding

Whole Genome Sequencing for Orofacial Clefts, Incidental Findings and Role of Community GatekeepersR01DE028300 · NIDCR · UNIVERSITY OF IOWA · PI BUTALI, AZEEZ · 2020 to 2024
$3.9M
Elucidating Cleft Etiology Employing Multiplex and Twin Families (ElCEEMuTF)K43DE029427 · NIDCR · KWAME NKRUMAH UNIVERSITY/SCIENCE/TECH · PI GOWANS, LORD JEPHTHAH JOOJO · 2019 to 2023
$529k
NIDCR NIH HHS K43 DE029427NIDCR NIH HHS R01 DE028300
6 · The paper itself

Abstract

Background: Orofacial clefts (OFCs) are the most common craniofacial congenital anomalies, with complex aetiology involving both genetic and environmental factors. Most genetic studies on the condition have focused on the contribution of single nucleotide variants (SNVs) and small insertions and deletions (indels). However, the contribution of copy number variants (CNVs), especially in African populations, remains underexplored despite their known contribution to congenital anomalies. This study aimed to identify high-confidence CNVs contributing to the aetiology of syndromic OFCs in Ghanaian case parent trios using whole exome sequencing (WES) datasets. Methods: WES data from Ghanaian case parent trios were processed through a comprehensive five-phase pipeline. Following stringent quality control and preprocessing, CNVs were called using four independent tools, namely, cn.MOPS, CODEX, ExomeDepth, and GATK-gCNV. The called CNVs were merged through a consensus-based approach using BEDtools, requiring support from at least two tools to classify them as true CNVs. AnnotSV was used to annotate and classify CNVs, while VarElect was employed to prioritise CNVs based on clinical phenotypes. High-confidence CNVs were mapped to patient phenotypes and further interrogated for pathogenic potential using databases such as DECIPHER, ClinVar, Mouse Genome Informatics (MGI), and the Alliance of Genome Resources. Gene expression patterns utilized MGI, Zebrahub and CELLxGENE Discover. Finally, pathway enrichment and interaction analyses were performed using g:Profiler, the STRING database, and Cytoscape. Results: Several Conclusion: This study highlights the value of CNV analysis in studies on the genetic aetiology of OFCs and supports broader inclusion of African genomic data to identify population-specific aetiologic variants, thereby enhancing understanding of pathophysiology and clinical care.

Indexed as

Copy Number VariantsGenetic syndromesOrofacial CleftsRead DepthSub-Saharan AfricansWhole Exome Sequencing

Identifiers

PMID41960320
PMCPMC13060495

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