PSReliP

PSReliP performs population structure and relatedness analysis from genome-wide genetic variant data to support interpretation in genome-wide association studies (GWAS) and genomic selection.


Key Features:

  • Integrated workflow: Integrates analytical steps into a single workflow from data processing to result visualization.
  • Data filtering and analysis: Employs PLINK alongside custom shell scripts and Perl programs to process and analyze single nucleotide polymorphisms (SNPs) and small insertions or deletions.
  • Visualization capabilities: Provides dynamic visualization via Shiny (R), including interactive tables, plots, and charts for exploration of population structure and relatedness.

Scientific Applications:

  • Genome-Wide Association Studies (GWAS): By estimating population stratification and cryptic relatedness, it aids selection of statistical methods to mitigate false positives in GWAS.
  • Genomic Selection: In animal and plant breeding programs, it quantifies genetic relationships to improve prediction accuracy for selection.

Methodology:

PSReliP executes an ordered sequence of PLINK commands supported by custom shell scripts and Perl programs for data processing and analysis, with Shiny (R) used for interactive result visualization.

Topics

Details

License:
GPL-3.0
Cost:
Free of charge
Tool Type:
command-line tool, desktop application, workflow
Operating Systems:
Linux
Programming Languages:
R, Shell, Perl
Added:
9/4/2023
Last Updated:
11/24/2024

Operations

Publications

Solovieva E, Sakai H. PSReliP: an integrated pipeline for analysis and visualization of population structure and relatedness based on genome-wide genetic variant data. BMC Bioinformatics. 2023;24(1). doi:10.1186/s12859-023-05169-4. PMID:37020193. PMCID:PMC10074814.