☆12Apr 10, 2021Updated 5 years ago
Alternatives and similar repositories for maizeG2P
Users that are interested in maizeG2P are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ☆31Apr 16, 2023Updated 3 years ago
- ☆22Sep 22, 2022Updated 4 years ago
- Simple and fast algorithm for selecting core subset applied to large genotype dataset☆10Jun 3, 2019Updated 7 years ago
- Scripts to do haplotype analysis on pan genomes.☆20Sep 24, 2020Updated 6 years ago
- The GitHub repository for the A. thaliana pan-NLR'ome project.☆18Jun 6, 2019Updated 7 years ago
- 1-Click AI Models by DigitalOcean Gradient • AdDeploy popular AI models on DigitalOcean Gradient GPU virtual machines with just a single click. Zero configuration with optimized deployments.
- scripts for the project of seven thaliana genomes assembly☆42May 22, 2021Updated 5 years ago
- Design gene specific KASP and CAPS/dCAPS primers for any species☆19Sep 19, 2022Updated 4 years ago
- QTLseqr is an R package for QTL mapping using NGS Bulk Segregant Analysis☆85Jan 20, 2020Updated 6 years ago
- R语言代谢组学数据分析☆12Feb 29, 2016Updated 10 years ago
- scripts used for processing and analyzing data in the article.☆13Oct 31, 2019Updated 7 years ago
- An interactive web portal for exploring SNPs among 1,007 rapeseed germplasm accessions☆15Mar 4, 2025Updated last year
- This is a basic repository with all the scripts necessary to reconstruct the data analysis from our work on the 200 Genomes☆12Aug 31, 2018Updated 8 years ago
- Influence of algorithms, parameter choice, and feature selection on genomic prediction accuracy☆13Apr 2, 2018Updated 8 years ago
- Scripts for NGS processing☆16Sep 6, 2017Updated 9 years ago
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- Guide through code for a Minimmap2 genome alignment and a seq-seq-pan pan-genome alignment with visualizations in R. The tutorial present…☆19May 16, 2025Updated last year
- Long Read Based SV Calling Tools Analysis☆16Mar 22, 2024Updated 2 years ago
- scripts for sequence and feature conversion, annotation, analysis ...☆28Mar 17, 2025Updated last year
- Genome-Phenome Wide Association Study☆15Feb 7, 2023Updated 3 years ago
- A tool to plot significant regions of GWAS☆31Jan 27, 2023Updated 3 years ago
- ☆20May 27, 2026Updated 5 months ago
- ☆14Jul 27, 2019Updated 7 years ago
- ☆27Jul 28, 2025Updated last year
- The code used in the manuscript titled "Gene duplication and evolution in recurring polyploidization-diploidization cycles in plants".☆29Mar 19, 2021Updated 5 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.
- a Semi-automated pipeline for assembling T2T genome☆30Oct 16, 2025Updated last year
- Tool set for processing fasta/fastq/table formated data. Usually they are perl scripts.☆56Oct 20, 2026Updated 2 weeks ago
- Gene Prediction using MAKER, CEGMA, SNAP, GENEMARK & AUGUSTUS☆10Jul 20, 2017Updated 9 years ago
- Compare different genome alignment tools using a wide range of genomes with different complexities.☆14Dec 3, 2022Updated 3 years ago
- Core Hunter 3: a flexible core subset selection tool☆10Sep 11, 2025Updated last year
- Customized codes used in Tibetan wheat sequencing project.☆13Oct 18, 2022Updated 4 years ago
- Working on cotton resequencing☆11Jun 2, 2020Updated 6 years ago
- Bulked-Segregant Analysis using vcf file with or without parents☆34Apr 1, 2026Updated 7 months ago
- Detailed bioinformatics scripts and methods used in the Maize-Pan-genome paper.☆17Oct 8, 2025Updated 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.
- my commonly used perl script☆20Aug 28, 2020Updated 6 years ago
- QTL-seq pipeline to identify causative mutations responsible for a phenotype☆69Mar 21, 2026Updated 7 months ago
- A machine learning model for the prediction of lncRNAs (Singh et. al NAR 2017)☆11Jan 19, 2022Updated 4 years ago
- De novo lncRNA discovery pipeline, re-write of PLAR in shell and awk☆10Oct 13, 2026Updated 3 weeks ago
- ☆13Oct 30, 2019Updated 7 years ago
- Add multiple thread function for genome comparison☆17Sep 29, 2021Updated 5 years ago
- ☆22Apr 2, 2015Updated 11 years ago