RADseq workflow using STACKS
☆62Sep 24, 2026Updated this week
Alternatives and similar repositories for stacks_workflow
Users that are interested in stacks_workflow are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Genetic Map Comparison☆20Nov 10, 2022Updated 3 years ago
- eDNA metabarcoding pipeline☆49Sep 10, 2026Updated 2 weeks ago
- Population assignment analysis using R☆16Updated this week
- ☆36Jun 15, 2023Updated 3 years ago
- Transcripts annotation and GO enrichment Fisher tests☆27Apr 28, 2023Updated 3 years ago
- Deploy to Railway using AI coding agents - Free Credits Offer • AdUse Claude Code, Codex, OpenCode, and more. Autonomous software development now has the infrastructure to match with Railway.
- Genome Annotation Without Nightmares☆46Feb 2, 2026Updated 7 months ago
- Pipeline for transcriptome de novo assembly☆12Mar 1, 2018Updated 8 years ago
- ☆18Jun 30, 2023Updated 3 years ago
- Trim, Align to genome, Deduplicate, Realign WGS sequencing samples☆18Feb 23, 2026Updated 7 months ago
- RADseq Data Exploration, Manipulation and Visualization using R☆61Aug 20, 2026Updated last month
- A set of functions to visualise genotypes based on a VCF☆90Jan 28, 2022Updated 4 years ago
- strataG is a toolkit for haploid sequence and multilocus genetic data summaries, and analyses of population structure.☆26Sep 6, 2026Updated 3 weeks ago
- ☆16Jun 14, 2017Updated 9 years ago
- Fast calculation of Patterson's D (ABBA-BABA) and the f4-ratio statistics across many populations/species☆191Dec 19, 2024Updated last year
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- Tutorials on phylogenetic and phylogenomic inference☆53May 4, 2025Updated last year
- Collection of various scripts☆80Sep 2, 2026Updated 3 weeks ago
- Detects Outliers and plots genomic clines from BGC output, and extends the plotting functionality of INTROGRESS to Correlate genomic clin…☆16Oct 12, 2024Updated last year
- a bash pipeline for RAD sequencing☆56Jan 27, 2025Updated last year
- Crash course for NCBI blast tools☆48Jun 17, 2019Updated 7 years ago
- Ancestry_HMM-S is program designed to infer adaptive introgression from population genomic data☆20Sep 25, 2023Updated 3 years ago
- polysat 1.7: tools for polyploid microsatellite analysis