Fastqc Report Interpreter

2. Issue Diagnosis

issues = interpreter.diagnose_issues(metrics)
for issue in issues:
    print(f"{issue.severity}: {issue.description}")
    print(f"Recommendation: {issue.recommendation}")

Common Issues:

Low Quality at Read Ends

• Cause: Phasing effects, reagent depletion
• Solution: Trim last 10-20 bases

Adapter Contamination

• Cause: Incomplete adapter removal
• Solution: Re-run cutadapt/Trimmomatic with stricter parameters

High Duplication

• Cause: PCR over-amplification, low input
• Solution: Use deduplication; consider library prep optimization

Per Base Sequence Content Bias

• Cause: Adapter dimers, non-random priming
• Solution: Check for adapter contamination; randomize primers

3. Batch Analysis

batch_results = interpreter.analyze_batch(
    fastqc_files=["sample1_fastqc.html", "sample2_fastqc.html", ...],
    output_summary="batch_summary.csv"
)

4. Recommendation Generation

recommendations = interpreter.get_recommendations(
    analysis,
    application="rna_seq",  # or "dna_seq", "chip_seq"
    quality_threshold="high"
)

Application-Specific Thresholds:

• RNA-seq: Acceptable duplication up to 40% (transcript abundance)
• DNA-seq: Strict quality requirements (variant calling)
• ChIP-seq: Moderate quality, focus on enrichment metrics

CLI Usage

# Analyze single report
python scripts/fastqc_interpreter.py --input sample_fastqc.html

# Batch analysis
python scripts/fastqc_interpreter.py --batch "*fastqc.html" --output report.pdf

# With custom thresholds
python scripts/fastqc_interpreter.py --input fastqc.html --application rna_seq

Output Interpretation

PASS (Green): Proceed with analysis WARNING (Yellow): Review but likely acceptable FAIL (Red): Requires action before downstream analysis

Troubleshooting Guide

See references/troubleshooting.md for:

• Platform-specific issues (Illumina, PacBio, Oxford Nanopore)
• Library prep problem diagnosis
• Downstream analysis impact assessment

Skill ID: 205 | Version: 1.0 | License: MIT