JaeYoonKim72 / GMStoolLinks
☆17Updated 4 years ago
Alternatives and similar repositories for GMStool
Users that are interested in GMStool are comparing it to the libraries listed below
Sorting:
- ☆10Updated 4 years ago
- Integrative analysis of structural variations.☆40Updated last year
- ☆43Updated 5 months ago
- Pipeline to take VCF through to Selection Analysis.☆58Updated 2 years ago
- ☆30Updated this week
- A set of workflows written in Nextflow for Genome Annotation.☆45Updated last year
- Transposable element polymorphism identification☆34Updated 5 years ago
- Evolutionary Transcriptomics with R☆45Updated this week
- ☆11Updated 3 years ago
- Pipeline for structural variant image curation and analysis.☆48Updated 3 years ago
- Code for the Brassica oleracea/rapa/napus genomic comparison☆16Updated 4 years ago
- A program for the Maximum-likelihood analysis of population genomic data.☆29Updated 4 years ago
- R package for comparing mixture solutions to similarity data, with a focus STRUCTURE like models to ChromoPainter palettes☆25Updated 5 years ago
- QUILT: Low coverage whole genome sequence imputation with large reference panels☆65Updated last month
- Splice junction analysis and filtering from BAM files☆40Updated 3 years ago
- BayeScEnv is a Fst-based, genome-scan method that uses environmental variables to detect local adaptation.☆18Updated 8 years ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 4 months ago
- Perform GWAS using the FarmCPU model.☆23Updated 8 months ago
- An Efficient Swiss Army Knife for Population Genomic Analyses in R☆37Updated last year
- Repository created to host the R package OneMap: software for constructing genetic maps in experimental crosses: full-sib, RILs, F2 and b…☆38Updated last year
- A series of scripts to automate sequence workflows☆19Updated 3 months ago
- Module for analysing admixture graphs☆28Updated 7 years ago
- Pipeline for structural variation detection in cohorts☆49Updated 3 years ago
- Runs a combination of tools to generate structural variant calls on short-read whole-genome sequencing data☆22Updated 3 years ago
- A tool to extract LOH blocks from VCF, BAM and FASTA data☆23Updated last year
- Flexible Genotyping of Polyploids using Next Generation Sequencing Data☆29Updated 10 months ago
- Perform GWAS with gemma in a simple pipeline☆26Updated 4 months ago
- Genome Annotation Without Nightmares☆46Updated 7 months ago
- Upscaling SV detection to a multi-population level.☆22Updated last month
- Make Pseudo-Reference Genome from VCF/BCF☆14Updated 4 years ago