This project contains the workflow, results, and reports from NGS analysis of BYMV (SRA ID: SRX7118692), performed on Galaxy.eu.
- FastQC, Trim Galore, MultiQC
- BWA-MEM2, SAMtools
- LoFreq for SNP calling
- Velvet, SPAdes for assembly
- IGV for visualization
- Initial mapping rate: 26.98%
- Post-duplicate removal: 37.59%
- SNPs identified via LoFreq
- De novo assembly validated with QUAST and BLAST
results/: Contains reports and summary filesplots/: Visuals like FastQC plots or IGV screenshotsscripts/: Command lines or workflow stepsreferences/: Reference genome links or notes
Analysis was performed using the Galaxy.eu platform.