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Editorially curated · om-dengue-2022-23-genomic-epidemiology

Oman 2022–23 Dengue Genomic Epidemiology Study

OmanPathogen genomics and infectious diseaseCompleted / retained

Near-complete dengue virus genomes generated from 162 positive samples using long-read amplicon-based sequencing; DENV-2 genotype II-F1.1 predominated, with DENV-1 and DENV-3 also detected.

01 / Project overview

What the record establishes.

Geographic scope
Oman; Sultan Qaboos University Hospital cohort
Project type
outbreak genomic epidemiology study
Research domain
dengue whole-genome sequencing and genomic epidemiology
Years
2022–2023
Lifecycle status
Published study
Status basis
Peer-reviewed article available online 9 May 2026; journal volume 170 is assigned to September 2026.
Status evidence date
2026-05-09
Scale
162 DENV-positive patient samples; near-complete viral genomes generated by long-read amplicon-based sequencing.

02 / Organizations and population

Who and what the project connects.

Lead organizations
Sultan Qaboos University Hospital / University Medical City
Partner organizations
King Abdullah University of Science and Technology
Organism / population
162 DENV-positive patient samples from Sultan Qaboos University Hospital, Oman

03 / Data and access

What exists and how it can be reached.

Data types

  • whole-genome sequencing
  • long-read amplicon sequencing
  • phylogenetic analysis

Data access

Open-access peer-reviewed article; no durable public sequence accession was verified as of 2026-08-22. Sequence-level public access remains unverified.

Identifiers

  • DOI10.1016/j.ijid.2026.108748
  • PMID42114647

04 / Evidence and provenance

Why the record is included.

Inclusion basis

Distinct Oman-focused dengue genomic epidemiology study. Exact DOI, PMID, title and DENV-specific title fragments were absent from the frozen 951-record v0.2 preview.

Editorial note

Public metadata confirms 162 DENV-positive samples and long-read near-complete genomes. Repository/accession searches on 22 August 2026 did not verify a durable sequence accession, so Atlas must not claim public sequence-level data access. The publication includes KAUST-affiliated coauthors; this record is public-source curation only and does not authorize outreach.

Sources

  1. peer-reviewed publication Verified 2026-09-05
  2. peer-reviewed publication Verified 2026-09-05
  3. institutional publication record Verified 2026-09-05

Release v0.3.0

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