Genomics Analysis (Meta Skill)
This meta-skill coordinates a complete genomics analysis pipeline by integrating
gene database queries, sequence analysis, expression profiling, and pathway
enrichment into a unified workflow. It combines three specialized skills to
deliver comprehensive gene-level and systems-level biological insights.
Workflow
Step 1: Gene Information Retrieval
Query NCBI Entrez for comprehensive gene details including official nomenclature,
genomic coordinates, transcript variants, and functional annotations. Retrieve
orthologs across model organisms for evolutionary context. Pull known variants
from ClinVar and dbSNP, noting pathogenic or pharmacogenomic associations.
Collect linked references from PubMed for recent literature context.
Step 2: Sequence Analysis
Use BioPython to perform sequence-level analyses on retrieved gene and protein
sequences:
- Multiple sequence alignment of orthologs to identify conserved regions
- Motif discovery in promoter regions or protein domains
- Domain architecture mapping against Pfam/InterPro signatures
- Codon usage analysis for expression optimization studies
- Variant impact prediction based on conservation scores
Step 3: Expression Analysis
Apply scanpy for expression data analysis, supporting both single-cell and
bulk RNA-seq workflows:
- For single-cell: quality control, normalization, clustering, marker gene
identification, cell type annotation
- For bulk: differential expression analysis, volcano plots, heatmaps
- Cross-dataset comparison when multiple conditions are available
- Identification of co-expressed gene modules
Step 4: Pathway Enrichment and Functional Annotation
Map differentially expressed or co-expressed genes to biological pathways:
- KEGG pathway mapping for metabolic and signaling context
- Gene Ontology enrichment (biological process, molecular function, cellular component)
- Reactome pathway analysis for detailed mechanistic understanding
- Network-based enrichment to identify hub genes and regulatory modules
Step 5: Integrated Report Generation
Compile findings into a structured report with:
- Gene summary card with key identifiers and annotations
- Sequence conservation highlights and domain maps
- Expression analysis results with statistical summaries
- Enriched pathways ranked by significance
- Key findings synthesis connecting sequence, expression, and pathway data
- Publication-ready figures and supplementary tables
Integration Points
- ncbi-entrez -- Gene records, variant data, orthologs, literature links
- biopython-bio -- Sequence alignment, motif search, domain analysis, format conversion
- scanpy-singlecell -- Expression quantification, clustering, differential expression, visualization
Output Formats
- Gene card: Symbol, aliases, genomic location, function summary, disease associations
- Alignment view: Conserved regions highlighted across orthologs
- Expression summary: DE gene lists with fold change, p-values, FDR
- Pathway table: Enriched pathways with gene counts, p-values, leading-edge genes
- Figures: Heatmaps, volcano plots, UMAP embeddings, pathway diagrams
Best Practices
- Start with gene identifiers from a reliable source (NCBI Gene ID or HGNC symbol)
- Verify gene nomenclature across databases to avoid confusion from aliases
- Use appropriate normalization for the expression data type (TPM, CPM, SCTransform)
- Apply multiple testing correction (Benjamini-Hochberg) for all enrichment analyses
- Set biologically meaningful fold-change thresholds alongside statistical cutoffs
- Include both up- and down-regulated gene sets in pathway analysis
- Cross-reference pathway results with known biology to filter spurious enrichments
- Report effect sizes and confidence intervals, not just p-values
- Note species differences when translating findings from model organisms
- Archive intermediate results for reproducibility and downstream re-analysis
1---2name: genomics-analysis3description: Orchestrates a genomics analysis workflow from gene query through expression analysis to pathway enrichment. Use when investigating gene function, analyzing expression data, or performing pathway-level interpretation. NOT for pure protein structure modeling or drug-target interaction analysis.4---5
6# Genomics Analysis (Meta Skill)
7
8This meta-skill coordinates a complete genomics analysis pipeline by integrating
9gene database queries, sequence analysis, expression profiling, and pathway
10enrichment into a unified workflow. It combines three specialized skills to
11deliver comprehensive gene-level and systems-level biological insights.
12
13## Workflow
14
15### Step 1: Gene Information Retrieval
16
17Query NCBI Entrez for comprehensive gene details including official nomenclature,
18genomic coordinates, transcript variants, and functional annotations. Retrieve
19orthologs across model organisms for evolutionary context. Pull known variants
20from ClinVar and dbSNP, noting pathogenic or pharmacogenomic associations.
21Collect linked references from PubMed for recent literature context.
22
23### Step 2: Sequence Analysis
24
25Use BioPython to perform sequence-level analyses on retrieved gene and protein
26sequences:
27- Multiple sequence alignment of orthologs to identify conserved regions
28- Motif discovery in promoter regions or protein domains
29- Domain architecture mapping against Pfam/InterPro signatures
30- Codon usage analysis for expression optimization studies
31- Variant impact prediction based on conservation scores
32
33### Step 3: Expression Analysis
34
35Apply scanpy for expression data analysis, supporting both single-cell and
36bulk RNA-seq workflows:
37- For single-cell: quality control, normalization, clustering, marker gene
38 identification, cell type annotation
39- For bulk: differential expression analysis, volcano plots, heatmaps
40- Cross-dataset comparison when multiple conditions are available
41- Identification of co-expressed gene modules
42
43### Step 4: Pathway Enrichment and Functional Annotation
44
45Map differentially expressed or co-expressed genes to biological pathways:
46- KEGG pathway mapping for metabolic and signaling context
47- Gene Ontology enrichment (biological process, molecular function, cellular component)
48- Reactome pathway analysis for detailed mechanistic understanding
49- Network-based enrichment to identify hub genes and regulatory modules
50
51### Step 5: Integrated Report Generation
52
53Compile findings into a structured report with:
54- Gene summary card with key identifiers and annotations
55- Sequence conservation highlights and domain maps
56- Expression analysis results with statistical summaries
57- Enriched pathways ranked by significance
58- Key findings synthesis connecting sequence, expression, and pathway data
59- Publication-ready figures and supplementary tables
60
61## Integration Points
62
63- **ncbi-entrez** -- Gene records, variant data, orthologs, literature links
64- **biopython-bio** -- Sequence alignment, motif search, domain analysis, format conversion
65- **scanpy-singlecell** -- Expression quantification, clustering, differential expression, visualization
66
67## Output Formats
68
69- **Gene card**: Symbol, aliases, genomic location, function summary, disease associations
70- **Alignment view**: Conserved regions highlighted across orthologs
71- **Expression summary**: DE gene lists with fold change, p-values, FDR
72- **Pathway table**: Enriched pathways with gene counts, p-values, leading-edge genes
73- **Figures**: Heatmaps, volcano plots, UMAP embeddings, pathway diagrams
74
75## Best Practices
76
771. Start with gene identifiers from a reliable source (NCBI Gene ID or HGNC symbol)
782. Verify gene nomenclature across databases to avoid confusion from aliases
793. Use appropriate normalization for the expression data type (TPM, CPM, SCTransform)
804. Apply multiple testing correction (Benjamini-Hochberg) for all enrichment analyses
815. Set biologically meaningful fold-change thresholds alongside statistical cutoffs
826. Include both up- and down-regulated gene sets in pathway analysis
837. Cross-reference pathway results with known biology to filter spurious enrichments
848. Report effect sizes and confidence intervals, not just p-values
859. Note species differences when translating findings from model organisms
8610. Archive intermediate results for reproducibility and downstream re-analysis