tooluniverse-variant-analysis

name

tooluniverse-variant-analysis

description

Production-ready VCF processing, variant annotation, mutation analysis, and structural variant (SV/CNV) interpretation for bioinformatics questions. Parses VCF files (streaming, large files), classifies mutation types (missense, nonsense, synonymous, frameshift, splice, intronic, intergenic) and structural variants (deletions, duplications, inversions, translocations), applies VAF/depth/quality/consequence filters, annotates with ClinVar/dbSNP/gnomAD/CADD via ToolUniverse, interprets SV/CNV clinical significance using ClinGen dosage sensitivity scores, computes variant statistics, and generates reports. Solves questions like "What fraction of variants with VAF < 0.3 are missense?", "How many non-reference variants remain after filtering intronic/intergenic?", "What is the pathogenicity of this deletion affecting BRCA1?", or "Which dosage-sensitive genes overlap this CNV?". Use when processing VCF files, annotating variants, filtering by VAF/depth/consequence, classifying mutations, interpreting structural variants, assessing CNV pathogenicity, comparing cohorts, or answering variant analysis questions.

Variant Analysis and Annotation

Production-ready VCF processing and variant annotation skill combining local bioinformatics computation with ToolUniverse database integration. Designed to answer bioinformatics analysis questions about VCF data, mutation classification, variant filtering, and clinical annotation.

When to Use This Skill

Triggers:

• User provides a VCF file (SNV/indel or SV) and asks questions about its contents
• Questions about variant allele frequency (VAF) filtering
• Mutation type classification queries (missense, nonsense, synonymous, etc.)
• Structural variant interpretation requests (deletions, duplications, CNVs)
• Variant annotation requests (ClinVar, gnomAD, CADD, dbSNP)
• CNV pathogenicity assessment using ClinGen dosage sensitivity
• Cohort comparison questions
• Population frequency filtering (SNVs or SVs)
• Intronic/intergenic variant filtering
• Gene dosage sensitivity queries

Example Questions:

• "What fraction of variants with VAF < 0.3 are annotated as missense mutations?"
• "After filtering intronic/intergenic variants, how many non-reference variants remain?"
• "What is the clinical significance of this deletion affecting BRCA1?"
• "Which dosage-sensitive genes overlap this 500kb duplication on chr17?"
• "How many variants have clinical significance annotations?"
• "Compare variant counts between samples"

---

Core Capabilities

Capability	Description
VCF Parsing	Pure Python + cyvcf2 parsers. VCF 4.x, gzipped, multi-sample, SNV/indel/SV
Mutation Classification	Maps SO terms, SnpEff ANN, VEP CSQ, GATK Funcotator to standard types
VAF Extraction	Handles AF, AD, AO/RO, NR/NV, INFO AF formats
Filtering	VAF, depth, quality, PASS, variant type, mutation type, consequence, chromosome, SV size
Statistics	Ti/Tv ratio, per-sample VAF/depth stats, mutation type distribution, SV size distribution
Annotation	MyVariant.info (aggregates ClinVar, dbSNP, gnomAD, CADD, SIFT, PolyPhen)
SV/CNV Analysis	gnomAD SV population frequencies, DGVa/dbVar known SVs, ClinGen dosage sensitivity
Clinical Interpretation	ACMG/ClinGen CNV pathogenicity classification using haploinsufficiency/triplosensitivity scores
DataFrame	Convert to pandas for advanced analytics
Reporting	Markdown reports with tables and statistics, SV clinical reports

---

Workflow Overview

Input VCF File (SNVs/indels or SVs)
    |
    v
Phase 1: Parse VCF
    |-- Pure Python parser (any VCF 4.x)
    |-- cyvcf2 parser (faster, C-based)
    |-- Extract: CHROM, POS, REF, ALT, QUAL, FILTER, INFO, FORMAT, samples
    |-- Extract per-sample: GT, VAF, depth
    |-- Extract annotations from INFO (ANN, CSQ, FUNCOTATION)
    |-- Detect variant class: SNV/indel vs SV/CNV
    |
    v
Phase 2: Classify Variants
    |-- Variant type: SNV, INS, DEL, MNV, COMPLEX, SV
    |-- Mutation type: missense, nonsense, synonymous, frameshift, splice, etc.
    |-- Impact: HIGH, MODERATE, LOW, MODIFIER
    |-- SV type: DEL, DUP, INV, BND, CNV (if structural variant)
    |
    v
Phase 3: Apply Filters
    |-- VAF range (min/max)
    |-- Read depth minimum
    |-- Quality threshold
    |-- PASS only
    |-- Variant/mutation type inclusion/exclusion
    |-- Consequence exclusion (intronic, intergenic)
    |-- Population frequency range
    |-- Chromosome selection
    |-- SV size range (for structural variants)
    |
    v
Phase 4: Compute Statistics
    |-- Variant type distribution
    |-- Mutation type distribution
    |-- Impact distribution
    |-- Chromosome distribution
    |-- Ti/Tv ratio (for SNVs)
    |-- Per-sample VAF/depth stats
    |-- Gene mutation counts
    |-- SV size distribution (for structural variants)
    |
    v
Phase 5: Annotate with ToolUniverse (optional)
    |-- MyVariant.info: ClinVar, dbSNP, gnomAD, CADD, SIFT, PolyPhen
    |-- dbSNP: Population frequencies, gene associations
    |-- gnomAD: Population allele frequencies
    |-- Ensembl VEP: Consequence prediction
    |
    v
Phase 6: Generate Report / Answer Question
    |-- Markdown report with tables
    |-- Direct answer to specific question
    |-- DataFrame for downstream analysis
    |
    v
Phase 7: Structural Variant & CNV Analysis (if SV/CNV detected)
    |-- Annotate with gnomAD SV population frequencies
    |-- Query DGVa/dbVar for known SVs (Ensembl)
    |-- Identify affected genes
    |-- Query ClinGen dosage sensitivity (HI/TS scores)
    |-- Classify pathogenicity (Pathogenic/Likely Pathogenic/VUS/Benign)
    |-- Generate SV clinical report with ACMG/ClinGen guidelines

---

Phase Summaries

Phase 1: VCF Parsing

Use pandas for:

• Reading VCF as structured data
• Quick exploratory analysis
• When you need to manipulate columns and rows

Use python_implementation tools for:

• Production parsing with annotation extraction
• Multi-sample VCF handling
• VAF extraction from FORMAT fields
• Large file streaming

Key functions:

vcf_data = parse_vcf("input.vcf")           # Pure Python (always works)
vcf_data = parse_vcf_cyvcf2("input.vcf")    # Fast C-based (if installed)
df = variants_to_dataframe(vcf_data.variants, sample="TUMOR")  # For pandas

Phase 2: Variant Classification

Automatic classification from annotations:

• SnpEff ANN field
• VEP CSQ field
• GATK Funcotator FUNCOTATION field
• Standard INFO keys: EFFECT, EFF, TYPE

Mutation types supported: missense, nonsense, synonymous, frameshift, splice_site, splice_region, inframe_insertion, inframe_deletion, intronic, intergenic, UTR_5, UTR_3, upstream, downstream, stop_lost, start_lost

See references/mutation_classification_guide.md for full details

Phase 3: Filtering

Common filtering patterns:

# Somatic-like variants
criteria = FilterCriteria(
    min_vaf=0.05, max_vaf=0.95,
    min_depth=20, pass_only=True,
    exclude_consequences=["intronic", "intergenic", "upstream", "downstream"]
)

# High-confidence germline
criteria = FilterCriteria(
    min_vaf=0.25, min_depth=30, pass_only=True,
    chromosomes=["1", "2", ..., "22", "X", "Y"]
)

# Rare pathogenic candidates
criteria = FilterCriteria(
    min_depth=20, pass_only=True,
    mutation_types=["missense", "nonsense", "frameshift"]
)

See references/vcf_filtering.md for all filter options

Phase 4: Statistics

Use pandas for:

• Complex aggregations (groupby, pivot tables)
• Custom statistical tests
• Data exploration

Use python_implementation for:

• Standard variant statistics (Ti/Tv, type distribution)
• Per-sample VAF/depth summary
• Quick mutation type counts

Phase 5: ToolUniverse Annotation

When to use ToolUniverse annotation tools:

1. ClinVar clinical significance: Use MyVariant.info or dbSNP tools
2. Population frequencies: Use MyVariant.info (aggregates gnomAD, ExAC, 1000G)
3. Pathogenicity scores: Use MyVariant.info (aggregates CADD, SIFT, PolyPhen)
4. Consequence prediction: Use Ensembl VEP tools

Best practices:

• Annotate variants with rsIDs first (most reliable)
• Use MyVariant.info for batch annotation (aggregates multiple sources)
• Limit to top variants (max_annotate=50-100) to respect rate limits
• Query dbSNP/gnomAD directly for specific use cases

Key tools:

• MyVariant_query_variants: Batch annotation (ClinVar, dbSNP, gnomAD, CADD)
• dbsnp_get_variant_by_rsid: Population frequencies
• gnomad_get_variant: Basic variant metadata
• EnsemblVEP_annotate_rsid: Consequence prediction

See references/annotation_guide.md for detailed examples

Phase 6: Report Generation

Report includes:

1. Summary Statistics (total variants, type counts, Ti/Tv)
2. Mutation Type Distribution (table with counts and percentages)
3. Impact Distribution
4. Chromosome Distribution
5. VAF Distribution (per-sample)
6. Clinical Significance
7. Top Mutated Genes
8. Variant Annotations (ClinVar-annotated variants)

Phase 7: Structural Variant & CNV Analysis

When VCF contains SV calls (SVTYPE=DEL/DUP/INV/BND):

1. Identify affected genes (from VCF annotation or coordinate overlap)
2. Query ClinGen dosage sensitivity:

   clingen = ClinGen_dosage_by_gene(gene_symbol="BRCA1")
   # Returns: haploinsufficiency_score, triplosensitivity_score
   

3. Check population frequency:

   gnomad_sv = gnomad_get_sv_by_gene(gene_symbol="BRCA1")
   # Returns: SVs with AF, AC, AN
   

4. Classify pathogenicity:
   • Pathogenic: Deletion + HI score = 3, AF < 0.0001
   • Likely Pathogenic: Deletion + HI score = 2, AF < 0.001
   • VUS: HI/TS score = 0-1, AF 0.001-0.01
   • Benign: AF > 0.01

ClinGen dosage score interpretation:

• 3: Sufficient evidence for dosage pathogenicity (HIGH impact)
• 2: Some evidence (MODERATE impact)
• 1: Little evidence (LOW impact)
• 0: No evidence (MINIMAL impact)
• 40: Dosage sensitivity unlikely

See references/sv_cnv_analysis.md for full SV workflow

---

Answering BixBench Questions

Pattern 1: VAF + Mutation Type Fraction

Question: "What fraction of variants with VAF < X are annotated as Y mutations?"

result = answer_vaf_mutation_fraction(
    vcf_path="input.vcf",
    max_vaf=0.3,
    mutation_type="missense",
    sample="TUMOR"
)
# Returns: fraction, total_below_vaf, matching_mutation_type

Pattern 2: Cohort Comparison

Question: "What is the difference in mutation frequency between cohorts?"

result = answer_cohort_comparison(
    vcf_paths=["cohort1.vcf", "cohort2.vcf"],
    mutation_type="missense",
    cohort_names=["Treatment", "Control"]
)
# Returns: cohorts, frequency_difference

Pattern 3: Filter and Count

Question: "After filtering X, how many Y remain?"

result = answer_non_reference_after_filter(
    vcf_path="input.vcf",
    exclude_intronic_intergenic=True
)
# Returns: total_input, non_reference, remaining

---

ToolUniverse Tools Reference

SNV/Indel Annotation

Tool	When to Use	Parameters	Response
MyVariant_query_variants	Batch annotation	query (rsID/HGVS)	ClinVar, dbSNP, gnomAD, CADD
dbsnp_get_variant_by_rsid	Population frequencies	rsid	Frequencies, clinical significance
gnomad_get_variant	gnomAD metadata	variant_id (CHR-POS-REF-ALT)	Basic variant info
EnsemblVEP_annotate_rsid	Consequence prediction	variant_id (rsID)	Transcript impact

Structural Variant Annotation

Tool	When to Use	Parameters	Response
gnomad_get_sv_by_gene	SV population frequency	gene_symbol	SVs with AF, AC, AN
gnomad_get_sv_by_region	Regional SV search	chrom, start, end	SVs in region
ClinGen_dosage_by_gene	Dosage sensitivity	gene_symbol	HI/TS scores, disease
ClinGen_dosage_region_search	Dosage-sensitive genes in region	chromosome, start, end	All genes with HI/TS scores
ensembl_get_structural_variants	Known SVs from DGVa/dbVar	chrom, start, end, species	Clinical significance

See references/annotation_guide.md for detailed tool usage examples

---

Common Use Patterns

Pattern 1: Quick VCF Summary

Parse VCF, compute statistics, generate report.

report = variant_analysis_pipeline("input.vcf", output_file="report.md")

Pattern 2: Filtered Analysis

Parse VCF, apply multi-criteria filter, compute statistics on filtered set.

report = variant_analysis_pipeline(
    vcf_path="input.vcf",
    filters=FilterCriteria(min_vaf=0.1, min_depth=20, pass_only=True),
    output_file="filtered_report.md"
)

Pattern 3: Annotated Report

Parse VCF, annotate top variants with ClinVar/gnomAD/CADD, generate clinical report.

report = variant_analysis_pipeline(
    vcf_path="input.vcf",
    annotate=True,
    max_annotate=50,
    output_file="annotated_report.md"
)

Pattern 4: BixBench Question Answering

Parse VCF, apply specific filters, compute targeted statistics to answer precise questions.

result = answer_vaf_mutation_fraction(
    vcf_path="input.vcf",
    max_vaf=0.3,
    mutation_type="missense"
)

Pattern 5: Cohort Comparison

Parse multiple VCFs, compare mutation frequencies across cohorts.

result = answer_cohort_comparison(
    vcf_paths=["cohort1.vcf", "cohort2.vcf"],
    mutation_type="missense"
)

---

When to Use pandas vs python_implementation

Use pandas when:

• You need to read VCF as a flat table
• You want to do custom aggregations (groupby, pivot)
• You need to join with other data
• You're doing exploratory data analysis
• You want to export to CSV/Excel

Use python_implementation when:

• You need production-grade VCF parsing
• You need to extract INFO annotations (ANN, CSQ)
• You need per-sample VAF/depth extraction
• You need to classify mutation types
• You need standard variant statistics (Ti/Tv)
• You need to integrate with ToolUniverse annotation

Best approach: Use python_implementation for parsing/classification, then convert to DataFrame for custom analysis:

# Parse and classify
vcf_data = parse_vcf("input.vcf")
passing, failing = filter_variants(vcf_data.variants, criteria)

# Convert to DataFrame for custom analysis
df = variants_to_dataframe(passing, sample="TUMOR")

# Now use pandas
missense_high_vaf = df[(df['mutation_type'] == 'missense') & (df['vaf'] >= 0.3)]

---

Limitations

• VCF annotation required for mutation classification: If VCF has no ANN/CSQ/FUNCOTATION in INFO, mutation types will be "unknown" until ToolUniverse annotation is applied
• Multi-allelic variants: Parser takes first ALT allele for type classification
• ToolUniverse annotation rate: API-based, limited to ~100 variants per batch by default to respect rate limits
• gnomAD tool: Returns basic metadata only (not full allele frequencies); use MyVariant.info for gnomAD AF
• Large VCFs: Pure Python parser streams line-by-line; cyvcf2 is recommended for files with >100K variants

---

Reference Documentation

• references/vcf_filtering.md: Complete filter options and examples
• references/mutation_classification_guide.md: Detailed mutation type classification rules
• references/annotation_guide.md: ToolUniverse annotation workflows with examples
• references/sv_cnv_analysis.md: Complete SV/CNV interpretation workflow

---

Utility Scripts

• scripts/parse_vcf.py: Standalone VCF parsing script
• scripts/filter_variants.py: Command-line variant filtering
• scripts/annotate_variants.py: Batch variant annotation

---

Quick Start

See QUICK_START.md for:

• Python SDK examples (pipeline, question functions, individual tools)
• MCP conversational examples
• Common recipes (somatic analysis, clinical screening, population frequency)
• Expected output formats
• Troubleshooting guide