Tools to work with variant call format files
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Updated
Jun 8, 2026 - R
Tools to work with variant call format files
Recombination Landscape Estimation using Recurrent Neural Networks
Calculation of pairwise Linkage Disequilibrium (LD) under a probabilistic framework
An Efficient Swiss Army Knife for Population Genomic Analyses in R
rhierbaps: R implementation of hierBAPS
Population-wide Deletion Calling
Genome-wide scan for balancing selection using beta statistic
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.
the hierfstat package
Estimation of population genetic parameters using deep learning
strataG is a toolkit for haploid sequence and multilocus genetic data summaries, and analyses of population structure.
Some script and skills in Population Genetic analyzes
A tool to visualize the haplotype pattern and various information in excel.
PyPop: Python for Population Genomics
Upscaling SV detection to a multi-population level.
Estimation of per-individual inbreeding coefficients under a probabilistic framework
Python package for detecting positive selective sweeps using time-series genomics sampling data.
The fastest VCF/BCF parser in R https://doi.org/10.1093/bioinformatics/btae049
Automated and Distributed Population Genetic Model Inference from Allele Frequency Spectra
Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data
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