NovembreLab / eems-around-the-worldLinks
Repo to analyze population genetic data with many different methods
☆15Updated 6 years ago
Alternatives and similar repositories for eems-around-the-world
Users that are interested in eems-around-the-world are comparing it to the libraries listed below
Sorting:
- Sweep Inference Framework (controlling for correlation)☆29Updated last year
- Kinship (genetic relatedness) using GBS (genotyping-by-sequencing) with Depth adjustment☆21Updated 2 months ago
- ☆17Updated 10 years ago
- A series of scripts to automate sequence workflows☆19Updated 7 months ago
- Module for analysing admixture graphs☆29Updated 7 years ago
- Transposon Insertion Finder - Detection of new TE insertions in NGS data☆20Updated 7 months ago
- Runs a combination of tools to generate structural variant calls on short-read whole-genome sequencing data☆22Updated 4 years ago
- Minimal Assumption Genomic Inference of Coalescence☆14Updated 2 years ago
- detection of duplications and deletions using Python based machine learning techniques☆28Updated 6 years ago
- Guide to transcriptome assembly & analysis☆21Updated 8 years ago
- Repository for pipeline code☆26Updated last year
- Functions to compare a SV call sets against a truth set.☆30Updated 6 months ago
- intro to programming for IE2 evolution students☆12Updated last year
- ☆45Updated 9 months ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 8 months ago
- Genome-wide scan for balancing selection using beta statistic☆29Updated 2 years ago
- machine learning applications for dadi☆16Updated 11 months ago
- Demographic inference from whole genomes☆13Updated 3 years ago
- Pipeline for structural variant image curation and analysis.☆49Updated 4 years ago
- ☆11Updated 3 years ago
- ☆20Updated 5 years ago
- Work for the tree sequence inference paper.☆23Updated 5 years ago
- Two locus likelihoods and ARGs under changing population size☆14Updated last week
- Exhaustive capture of biological variation in RNA-seq data through k-mer decomposition.☆15Updated 7 years ago
- Estimation of per-individual inbreeding tracts under a probabilistic framework☆14Updated 2 years ago
- Tools for merging Tandem Repeat VCF files☆37Updated 7 months ago
- Haplotype and population structure inference using neural networks.☆27Updated last year
- Sampling and manipulating genome-wide ancestral recombination graphs (ARGs)☆57Updated 10 years ago
- Population-based detection of structural variation from High-Throughput Sequencing.☆33Updated 3 years ago
- Code and Tutorials for Running the MArginal ePIstasis Test (MAPIT)☆17Updated 3 years ago