Repository series · ncbi-prjeb59227
Whole‐Exome Sequencing Analyses in a Saudi Ischemic Stroke Cohort Reveal Association Signals, and shows Polygenic Risk Scores are related to modified Rankin Scale Risk
Ischemic stroke (IS) represents a significant societal burden across the globe. Rare high penetrant monogenic variants and less pathogenic common single nucleotide polymorphisms (SNPs) have been described with risk of disease. Consanguineous populations from Saudi Arabia offer a greater opportunity to detect rare high penetrant mutations enriched in tribal populations.
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
- Saudi Arabia connection indexed in BioProject metadata
- Project type
- Repository project
- Research domain
- Pathogen genomics and infectious disease
- Years
- 2023–
- Lifecycle status
- repository_recorded
- Status basis
- Registered in NCBI BioProject on 2023/01/28; operational lifecycle is not asserted.
- Status evidence date
- 2023-01-28
- 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
- European Bioinformatics Institute
- Partner organizations
- Not stated
- Organism / population
- Homo sapiens
03 / Data and access
What exists and how it can be reached.
Data types
- Other
- Sequencing
- Genome
Data access
Public repository metadata with linked data where supplied by the submitter
Identifiers
- BioProject
PRJEB59227
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