LDetect
LDetect identifies approximately independent blocks of linkage disequilibrium (LD) in the human genome to segment genomic regions for automated analysis in genome-wide association studies (GWAS).
Key Features:
- Identification of LD blocks: Systematically identifies genomic regions where alleles are non-randomly associated, defined as linkage disequilibrium blocks in the human genome.
- Genome segmentation for GWAS: Segments the genome into independent LD blocks to support automated analysis across multiple GWAS datasets.
- Approximate independence: Produces LD blocks that are approximately independent to aid statistical interpretation in association studies.
- Allele frequency analysis: Detects LD structure by analyzing allele frequency data across the genome.
Scientific Applications:
- Genome-wide association studies (GWAS): Delineates LD blocks to improve localization and interpretation of genetic associations with traits and diseases.
- Genetic mapping and marker discovery: Supports mapping of genetic variation and identification of candidate markers linked to phenotypic variation.
Methodology:
LDetect employs a computational approach that detects LD blocks by analyzing allele frequency data across the genome and defines blocks that are approximately independent.
Topics
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux
- Programming Languages:
- Python
- Added:
- 8/3/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Berisa T, Pickrell JK. Approximately independent linkage disequilibrium blocks in human populations. Bioinformatics. 2015;32(2):283-285. doi:10.1093/bioinformatics/btv546. PMID:26395773. PMCID:PMC4731402.