Rehh

Rehh detects genomic regions showing signatures of selection by analyzing haplotype homozygosity in SNP haplotype datasets.


Key Features:

  • Haplotype homozygosity analysis: Implements analysis of haplotype homozygosity to identify regions with elevated local homozygosity relative to neutral expectations.
  • Genome-wide scans: Performs genome-wide scans of long-range haplotypes across whole genomes using SNP haplotype datasets.
  • Detection of recent and ongoing selection: Detects footprints of both recent and ongoing selection events.
  • Graphical functions: Provides graphical functions for visualization of haplotype homozygosity and scan results.
  • Support for model and non-model species: Operates on SNP haplotype data from both model and non-model species, including datasets generated by next-generation sequencing and genotyping.

Scientific Applications:

  • Detection of selection signals: Identification of genomic regions and candidate genes under natural or artificial selection by detecting elevated haplotype homozygosity.
  • Evolutionary and population genetics: Study of recent adaptive evolution and population genetic patterns using long-range haplotype information.
  • Conservation genomics: Prioritization of loci relevant to conservation biology by detecting adaptive variation.
  • Functional genomics: Linking selection footprints to putative functional or phenotypic effects for downstream functional studies.

Methodology:

Computes haplotype homozygosity and performs genome-wide scans of long-range haplotypes in SNP haplotype datasets to identify regions with unusually high local homozygosity compared to neutral expectations, and produces graphical visualizations of results.

Topics

Details

Tool Type:
command-line tool
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
12/18/2017
Last Updated:
11/25/2024

Operations

Publications

Gautier M, Vitalis R. <i>rehh</i>: an R package to detect footprints of selection in genome-wide SNP data from haplotype structure. Bioinformatics. 2012;28(8):1176-1177. doi:10.1093/bioinformatics/bts115. PMID:22402612.

Documentation

Links