tiledbvcf

Community

Genomic variant data storage and retrieval.

AuthorRowtion
Version1.0.0
Installs0

System Documentation

What problem does it solve?

This Skill addresses the challenge of efficiently storing, querying, and analyzing large-scale genomic variant data, which is often cumbersome with traditional VCF/BCF formats.

Core Features & Use Cases

  • Scalable Storage: Ingest and store VCF/BCF data using TileDB's sparse array technology for efficient access.
  • Efficient Querying: Perform rapid queries across genomic regions and samples, ideal for population genomics.
  • Incremental Updates: Add new samples to existing datasets without costly re-processing.
  • Use Case: Researchers can quickly query allele frequencies for specific genes across thousands of samples or export subsets of variant data for downstream analysis.

Quick Start

Use the tiledbvcf skill to create a new dataset and ingest samples from 'sample1.vcf.gz' and 'sample2.vcf.gz'.

Dependency Matrix

Required Modules

tiledb-pytiledbvcf-pypandaspyarrownumpy

Components

scriptsreferences

💻 Claude Code Installation

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Please help me install this Skill:
Name: tiledbvcf
Download link: https://github.com/Rowtion/Bioclaw/archive/main.zip#tiledbvcf

Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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