RecView

RecView: Recombination Detection and Visualization Using Three-Generation Pedigree Genotype Data

RecView identifies and visualizes recombination events in whole-genome genotype datasets by analyzing grandparent-of-origin of informative alleles across offspring within three-generation pedigrees.


Key Features:

  • Recombination Inference Algorithms: Implements two algorithms: one detects shifts in the proportion of alleles with a specific grandparent-of-origin, and another evaluates continuity of alleles sharing the same grandparent-of-origin to infer recombination positions.
  • Whole-Genome Genotype Analysis: Processes genotype data across chromosomes or scaffolds and multiple offspring to localize recombination events genome-wide.
  • Base-Pair Resolution Reporting: Reports putative recombination positions in base pairs with an estimated precision metric derived from local density of informative alleles.
  • Pedigree-Based Allele Tracking: Analyzes grandparent-of-origin for all informative alleles along each chromosome to characterize genetic reshuffling across generations.

Scientific Applications:

  • Evolutionary and Population Genetics: Quantifies recombination along chromosomes to investigate genetic evolution, selection, drift, and genomic dynamics; demonstrated using genotype data from the great reed warbler (Acrocephalus arundinaceus).

Methodology:

RecView infers recombination positions by tracking grandparent-of-origin patterns of informative alleles across offspring in three-generation pedigrees, detecting proportion shifts and continuity breaks along chromosomes or scaffolds, and estimating positional precision based on local informative allele density.

Topics

Details

License:
GPL-3.0
Cost:
Free of charge
Tool Type:
library, web application
Operating Systems:
Mac, Linux, Windows
Programming Languages:
R
Added:
4/16/2024
Last Updated:
11/24/2024

Operations

Publications

Zhang H, Hansson B. RecView: an interactive R application for locating recombination positions using pedigree data. BMC Genomics. 2023;24(1). doi:10.1186/s12864-023-09807-2. PMID:38007417. PMCID:PMC10676570.

PMID: 38007417
Funding: - Vetenskapsrådet: 2016-00689