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.

Documentation

Links