Repository series · ncbi-prjna1475391
Detection of Low-Frequency Drug-Resistant Variants of HIV-1
Background: Highly Active Antiretroviral Therapy has transformed the management of HIV-1 infection; however, the emergence of drug-resistant variants remains a critical challenge. Whole Genome Sequencing offers comprehensive detection of resistance mutations across all viral gene regions simultaneously.Objectives: To evaluate the performance of Whole Genome HIV-1 Assay on the Ion Torrent S5 platform compared to targeted NGS and Sanger sequencing for detecting drug-resistant variants in HIV-1 positive patients at Mubarak Al Kabeer Hospital, Kuwait.
The accession and its GCC connection are verified. Registration alone does not establish that the broader research programme remains active.
01 / Project overview
What the record establishes.
- Geographic scope
- Kuwait connection indexed in BioProject metadata
- Project type
- Repository project
- Research domain
- Pathogen genomics and infectious disease
- Years
- 2026–
- Lifecycle status
- repository_recorded
- Status basis
- Registered in NCBI BioProject on 2026/06/05; operational lifecycle is not asserted.
- Status evidence date
- 2026-06-05
- Scale
- 1 BioProject accession grouped by matching submitter, date, data type and narrative.
02 / Organizations and population
Who and what the project connects.
- Lead organizations
- Ministry of Health
- Partner organizations
- Not stated
- Organism / population
- Not stated
03 / Data and access
What exists and how it can be reached.
Data types
- Raw sequence reads
- Sequencing
- Genome
Data access
Public repository metadata with linked data where supplied by the submitter
Identifiers
- BioProject
PRJNA1475391
04 / Evidence and provenance
Why the record is included.
Inclusion basis
Exact country-name match in authoritative NCBI BioProject metadata; repeated submissions are grouped into one Atlas series.
Editorial note
Repository verification confirms the accession and regional connection, not whether the broader research programme remains active.
Sources
- primary record source Verified 2026-08-15
Release v0.2.0