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Releases: PathoGenOmics-Lab/snpick

First Release: Version 1.0.0 🎉

16 Nov 09:48
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We’re excited to announce the first official release of Snpick! 🚀
What's included in v1.0.0:

  • High-speed SNP extraction: Optimized for large genomic alignments, delivering exceptional performance.
  • Memory efficiency: Designed to minimize RAM usage, even with massive datasets.
  • Support for VCF generation: Extract SNPs and directly output VCF files for downstream analysis.
  • ASC-ready alignments: Ensure compatibility with tools like RAxML and IQ-TREE.
  • User-friendly CLI: Intuitive commands for seamless integration into your workflows.

This release marks the beginning of Snpick’s journey, and we’re eager to see how it helps accelerate your genomic research. Feedback and contributions are welcome to make future versions even better!

Download, explore, and let us know what you think! 😊