Repository series · ncbi-prjna330536
Genome sequencing of a consanguineous family with primary immunodeficiency
The goal of the project is to identify the genetic cause of a primary immunodeficiency characterized by recurrent infections and autoimmunity leading to death in 3 siblings from a consanguineous family from 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
- 2016–
- Lifecycle status
- repository_recorded
- Status basis
- Registered in NCBI BioProject on 2016/07/19; operational lifecycle is not asserted.
- Status evidence date
- 2016-07-19
- 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
- Boston Children's Hospital
- Partner organizations
- Not stated
- Organism / population
- Homo sapiens
03 / Data and access
What exists and how it can be reached.
Data types
- Genome sequencing and assembly
- Sequencing
- Genome
Data access
Public repository metadata with linked data where supplied by the submitter
Identifiers
- BioProject
PRJNA330536
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