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bio-workflows-fastq-to-variants

maintained by GPTomics

star 299 account_tree 51 verified_user MIT License
bolt View GitHub
Overview Implementation Examples History

End-to-end DNA sequencing workflow from FASTQ files to variant calls. Covers QC, alignment with BWA, BAM processing, and variant calling with bcftools or GATK HaplotypeCaller.

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Skill Details

GitHub Stars 299
GitHub Forks 51
Created Jan 2026
Last Updated 5个月前
tools tools bioinformatics

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