YTLogos / ttplotLinks
Tao Yan's Plot Toolkit
☆12Updated 6 years ago
Alternatives and similar repositories for ttplot
Users that are interested in ttplot are comparing it to the libraries listed below
Sorting:
- ☆11Updated 3 years ago
- Code for the Brassica oleracea/rapa/napus genomic comparison☆16Updated 4 years ago
- A comprehensive collection of long inverted repeats in 424 eukaryotic genomes☆16Updated 3 years ago
- Perform GWAS with gemma in a simple pipeline☆27Updated 5 months ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 6 months ago
- https://filippob.github.io/introduction_to_gwas/☆21Updated 3 months ago
- 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
- Repository for pipeline code☆26Updated last year
- ☆13Updated 4 years ago
- ☆15Updated 5 years ago
- BayeScEnv is a Fst-based, genome-scan method that uses environmental variables to detect local adaptation.☆18Updated 8 years ago
- Automated Rice Variant calling workflow for HPC, Cloud and Desktop systems.☆13Updated last year
- ☆17Updated 5 years ago
- Experimental EIGENSOFT performance improvements.☆21Updated 10 years ago
- R package for comparing mixture solutions to similarity data, with a focus STRUCTURE like models to ChromoPainter palettes☆26Updated 6 years ago
- Integrative analysis of structural variations.☆40Updated last year
- ☆18Updated last year
- ☆31Updated 3 weeks ago
- ☆17Updated 2 years ago
- DensityMap is perl tool for the visualization of features density along chromosomes☆19Updated 3 years ago
- Module for analysing admixture graphs☆28Updated 7 years ago
- R package for binmap☆13Updated 2 years ago
- ☆44Updated 6 months ago
- ☆10Updated 5 years ago
- novoBreak: local assembly for breakpoint detection in cancer genomes☆25Updated 7 years ago
- A series of scripts to automate sequence workflows☆19Updated 4 months ago
- ☆11Updated 10 years ago
- QUILT: Low coverage whole genome sequence imputation with large reference panels☆64Updated last week
- Runs a combination of tools to generate structural variant calls on short-read whole-genome sequencing data☆22Updated 3 years ago
- ☆17Updated 9 years ago