scientific-genome-sequence-tools
CommunityUnified genome sequence search and annotation.
Authornahisaho
Version1.0.0
Installs0
System Documentation
What problem does it solve?
Cross-database genome data retrieval and sequence analysis across Ensembl, dbSNP, BLAST, NCBI Nucleotide, and GDC to streamline sequence search, variant annotation, and integrative genomics workflows.
Core Features & Use Cases
- Cross-database sequence retrieval from Ensembl and NCBI Nucleotide.
- Variant annotation and allele-frequency retrieval from dbSNP.
- Homology searches with BLAST and integration of cancer genomics data from GDC.
- Use Case: Researchers can fetch a gene's transcript, annotate variants, and compare across databases to build a comprehensive report.
Quick Start
Fetch Ensembl sequences and variant information across dbSNP, BLAST, NCBI Nucleotide, and GDC to initialize a cross-database genomics workflow.
Dependency Matrix
Required Modules
None requiredComponents
Standard package💻 Claude Code Installation
Recommended: Let Claude install automatically. Simply copy and paste the text below to Claude Code.
Please help me install this Skill: Name: scientific-genome-sequence-tools Download link: https://github.com/nahisaho/satori/archive/main.zip#scientific-genome-sequence-tools Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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