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Cross-domain directory aggregating tools, AI models, datasets, and research resources from bio.tools, Bioconductor, HuggingFace, curated GitHub awesome-lists, and more.

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samtools/bcftools are a suite of tools for manipulating NGS data and can be used to call variants.

A polymorphic bayesian genotyping model with wide applicability.

Variant Discovery in High-Throughput Sequencing Data.

Bayesian haplotype-based polymorphism discovery and genotyping.

Deep learning-based variant caller