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.
PMID: 22402612