Version Compatibility

Reference examples tested with: pandas 2.2+

Before using code patterns, verify installed versions match. If versions differ:

• Python:

  pip show <package>

  then

  help(module.function)

  to check signatures
• CLI:

  <tool> --version

  then

  <tool> --help

  to confirm flags

If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.

Quality Reports

Generate quality reports for FASTQ files using FastQC and aggregate multiple reports with MultiQC.

"Run quality control on FASTQ files" → Generate per-base quality, adapter content, and duplication plots, then aggregate across samples.

• CLI:

  fastqc *.fastq.gz

  then

  multiqc .

FastQC - Single Sample Reports

Basic Usage

# Single file
fastqc sample.fastq.gz

# Multiple files
fastqc *.fastq.gz

# Specify output directory
fastqc -o qc_reports/ sample_R1.fastq.gz sample_R2.fastq.gz

# Set threads
fastqc -t 4 *.fastq.gz

Output Files

FastQC produces two files per input:

• sample_fastqc.html

  - Interactive HTML report

• sample_fastqc.zip

  - Data files and images

Key Modules

Module	What It Shows	Warning Signs
Per base sequence quality	Quality scores across read	Drop below Q20 at 3' end
Per sequence quality	Quality score distribution	Bimodal distribution
Per base sequence content	Nucleotide composition	Imbalance at start (normal)
Per sequence GC content	GC distribution	Secondary peak (contamination)
Per base N content	Unknown bases	High N content
Sequence length distribution	Read lengths	Unexpected variation
Sequence duplication	Duplicate reads	High duplication (PCR)
Overrepresented sequences	Common sequences	Adapter contamination
Adapter content	Adapter sequences	Visible adapter curves

Extract Data from ZIP

# Unzip to access raw data
unzip sample_fastqc.zip

# View summary
cat sample_fastqc/summary.txt

# Get per-base quality
cat sample_fastqc/fastqc_data.txt | grep -A 50 ">>Per base sequence quality"

MultiQC - Aggregate Reports

Basic Usage

# Aggregate all FastQC reports in current directory
multiqc .

# Specify input and output
multiqc qc_reports/ -o multiqc_output/

# Custom report name
multiqc . -n my_project_qc

# Force overwrite
multiqc . -f

Common Options

# Flat directory (no sample subdirs)
multiqc --flat .

# Export data as TSV
multiqc . --export

# Only specific modules
multiqc . -m fastqc

# Exclude patterns
multiqc . --ignore '*_trimmed*'

# Include patterns
multiqc . --ignore-samples '*negative*'

Output Files

• multiqc_report.html

  - Interactive HTML report

• multiqc_data/

  - Directory with data tables

  • multiqc_fastqc.txt

    - FastQC metrics

  • multiqc_general_stats.txt

    - Summary statistics

  • multiqc_sources.txt

    - Source files used

Extract Data Programmatically

import pandas as pd

general_stats = pd.read_csv('multiqc_data/multiqc_general_stats.txt', sep='\t')
print(general_stats.columns)

fastqc_data = pd.read_csv('multiqc_data/multiqc_fastqc.txt', sep='\t')

Batch Processing

Process Multiple Samples

# All FASTQ files in parallel
fastqc -t 8 -o qc_reports/ raw_data/*.fastq.gz

# Then aggregate
multiqc qc_reports/ -o multiqc_output/

Before and After Trimming

# Create separate directories
mkdir -p qc_reports/raw qc_reports/trimmed

# QC raw reads
fastqc -o qc_reports/raw/ raw_data/*.fastq.gz

# After trimming (using fastp, cutadapt, etc.)
fastqc -o qc_reports/trimmed/ trimmed_data/*.fastq.gz

# Compare with MultiQC
multiqc qc_reports/ -o qc_comparison/

Interpretation Guide

Quality Scores

Phred Score	Error Rate	Interpretation
Q40	0.0001	Excellent
Q30	0.001	Good (Illumina target)
Q20	0.01	Acceptable
Q10	0.1	Poor

Common Issues

Issue	Likely Cause	Action
Low quality at 3' end	Normal degradation	Trim 3' end
Adapter contamination	Short inserts	Trim adapters
GC bias	Library prep	Consider correction
High duplication	Low complexity, PCR	Mark/remove duplicates
Overrepresented seqs	Adapters, primers	Check sequences

Configuration

Custom Adapters

Create

~/.fastqc/Configuration/adapter_list.txt

:

Custom_Adapter_Name    ACGTACGTACGT

Custom Limits

Create

~/.fastqc/Configuration/limits.txt

to customize thresholds:

# Warn if mean quality below 25
quality_sequence    warn    25
quality_sequence    error   20

Related Skills

• adapter-trimming - Remove adapters detected by FastQC
• fastp-workflow - All-in-one QC and trimming
• sequence-io/read-sequences - FASTQ file reading/writing