RADseq Data Exploration, Manipulation and Visualization using R
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Updated
Nov 6, 2024 - HTML
RADseq Data Exploration, Manipulation and Visualization using R
Calculation of pairwise Linkage Disequilibrium (LD) under a probabilistic framework
command-line tools for the management of genotype likelihoods and allele counts
stackr: an R package to run stacks software pipeline
Genotype Calling with Uncertainty from Sequencing Data in Polyploids 🍌🍓🥔🍠🥝
Estimation of per-individual inbreeding coefficients under a probabilistic framework
Genotyping of segregating mobile elements insertions
A tool to calculate ploidy levels from genotype likelihoods and coverage using Hidden Markov Models
SNP genotyping in polyploids
Utilities for analyzing next generation sequencing data.
Estimation of per-individual inbreeding tracts under a probabilistic framework
Estimation of pairwise distances under a probabilistic framework
Genotype likelihood simulator for VCF/BCF files
Bioinformatics pipeline to process whole genome resequencing data and perform genotype likelihood based population genomic analyses using ANGSD and related softwares. Flexible to datasets that combine high/low coverage and historical/fresh samples.
Estimating temporally variable selection intensity from ancient DNA data with a combination of forward- and backward-in-time simulations
Estimating temporally variable selection intensity from ancient DNA data
Estimating temporally variable selection intensity from ancient DNA data with the flexibility of modelling linkage and epistasis
A pipeline to impute plink genotypes to 1000 Genomes phase 1
Perl software to cluster SNPs based on its genotype.
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