CBC-UCONN / Structural-AnnotationLinks
☆12Updated 2 years ago
Alternatives and similar repositories for Structural-Annotation
Users that are interested in Structural-Annotation are comparing it to the libraries listed below
Sorting:
- ☆15Updated last year
- Automated Rice Variant calling workflow for HPC, Cloud and Desktop systems.☆13Updated last year
- Pipeline for eukaryotic genome annotation based on external evidences☆13Updated 2 years ago
- MODAS: Multi-Omics Data Association Study toolkit☆21Updated 7 months ago
- Scripts for Hill et al. (2022) doi:10.1093/molbev/msac085 🟣☆11Updated 2 years ago
- The Vertebrate Genomes Project Mitogenome Assembly Pipeline☆18Updated 2 years ago
- ☆10Updated last year
- ☆9Updated 7 months ago
- Small and simple scripts useful for various bioinformatics purposes e.g. extract sequences from fasta files☆21Updated 2 years ago
- ☆14Updated 4 months ago
- a tree splitting and pruning algorithm for retrieving single-copy orthologs from gene family trees☆26Updated 5 months ago
- This is a basic repository with all the scripts necessary to reconstruct the data analysis from our work on the 200 Genomes☆11Updated 6 years ago
- ☆25Updated 2 years ago
- I often use some of the self-written programs.☆16Updated 3 months ago
- Scripts for NGS processing☆17Updated 7 years ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 3 months ago
- A software suite for accurate identification, annotation, translation, and feature characterization of annotate transcripts.☆19Updated 3 years ago
- A series of scripts to automate sequence workflows☆19Updated last month
- Scripts to do haplotype analysis on pan genomes.☆21Updated 4 years ago
- ☆10Updated 3 years ago
- Assemble and following pipeline used in wisent genome paper.☆17Updated 8 years ago
- ☆13Updated 2 years ago
- Scripts to convert between file formats for various analyses☆16Updated 2 months ago
- GWAS analysis process based on EMMAX software☆12Updated last year
- Common scripts☆13Updated this week
- Long Read Based SV Calling Tools Analysis☆14Updated last year
- 基因组组装注释流程及脚本☆16Updated 2 years ago
- Bash scripts and data used in pantranscriptomic paper☆22Updated 2 years ago
- ☆24Updated 2 months ago
- This is used to achieve haplotype-resolved assembly of tetraploid genomes using gamete sequencings☆12Updated 3 years ago