A flexible, scalable, and reproducible pipeline to automate variant calling from raw sequence reads, with lots of bells and whistles - for sampled individuals, and for pool sequencing.
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Updated
Jun 24, 2025 - Python
A flexible, scalable, and reproducible pipeline to automate variant calling from raw sequence reads, with lots of bells and whistles - for sampled individuals, and for pool sequencing.
🔧 Simple script in python to convert CSV files to VCF
Bioinformatics on GCP, AWS or Azure
Intersect multiple VCF files with haplotype awareness
🐍 DRAGEN Tumor/Normal workflow post-processing
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