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biopython

Biopython is a comprehensive set of freely available Python tools for biological computation. It provides functionality for sequence manipulation, file I/O, database access, structural bioinformatics, phylogenetics, and many other bioinformatics tasks.

Documentation

Biopython: Computational Molecular Biology in Python

Overview

Biopython is a comprehensive set of freely available Python tools for biological computation. It provides functionality for sequence manipulation, file I/O, database access, structural bioinformatics, phylogenetics, and many other bioinformatics tasks. The current version is Biopython 1.85 (released January 2025), which supports Python 3 and requires NumPy.

When to Use This Skill

Use this skill when:

  • Working with biological sequences (DNA, RNA, or protein)
  • Reading, writing, or converting biological file formats (FASTA, GenBank, FASTQ, PDB, mmCIF, etc.)
  • Accessing NCBI databases (GenBank, PubMed, Protein, Gene, etc.) via Entrez
  • Running BLAST searches or parsing BLAST results
  • Performing sequence alignments (pairwise or multiple sequence alignments)
  • Analyzing protein structures from PDB files
  • Creating, manipulating, or visualizing phylogenetic trees
  • Finding sequence motifs or analyzing motif patterns
  • Calculating sequence statistics (GC content, molecular weight, melting temperature, etc.)
  • Performing structural bioinformatics tasks
  • Working with population genetics data
  • Any other computational molecular biology task

Core Capabilities

Biopython is organized into modular sub-packages, each addressing specific bioinformatics domains:

  1. Sequence Handling - Bio.Seq and Bio.SeqIO for sequence manipulation and file I/O
  2. Alignment Analysis - Bio.Align and Bio.AlignIO for pairwise and multiple sequence alignments
  3. Database Access - Bio.Entrez for programmatic access to NCBI databases
  4. BLAST Operations - Bio.Blast for running and parsing BLAST searches
  5. Structural Bioinformatics - Bio.PDB for working with 3D protein structures
  6. Phylogenetics - Bio.Phylo for phylogenetic tree manipulation and visualization
  7. Advanced Features - Motifs, population genetics, sequence utilities, and more

Installation and Setup

Install Biopython using pip (requires Python 3 and NumPy):

uv pip install biopython

For NCBI database access, always set your email address (required by NCBI):

from Bio import Entrez
Entrez.email = "your.email@example.com"

# Optional: API key for higher rate limits (10 req/s instead of 3 req/s)
Entrez.api_key = "your_api_key_here"

Using This Skill

This skill provides comprehensive documentation organized by functionality area. When working on a task, consult the relevant reference documentation:

1. Sequence Handling (Bio.Seq & Bio.SeqIO)

Reference: references/sequence_io.md

Use for:

  • Creating and manipulating biological sequences
  • Reading and writing sequence files (FASTA, GenBank, FASTQ, etc.)
  • Converting between file formats
  • Extracting sequences from large files
  • Sequence translation, transcription, and reverse complement
  • Working with SeqRecord objects

Quick example:

from Bio import SeqIO

# Read sequences from FASTA file
for record in SeqIO.parse("sequences.fasta", "fasta"):
    print(f"{record.id}: {len(record.seq)} bp")

# Convert GenBank to FASTA
SeqIO.convert("input.gb", "genbank", "output.fasta", "fasta")

2. Alignment Analysis (Bio.Align & Bio.AlignIO)

Reference: references/alignment.md

Use for:

  • Pairwise sequence alignment (global and local)
  • Reading and writing multiple sequence alignments
  • Using substitution matrices (BLOSUM, PAM)
  • Calculating alignment statistics
  • Customizing alignment parameters

Quick example:

from Bio import Align

# Pairwise alignment
aligner = Align.PairwiseAligner()
aligner.mode = 'global'
alignments = aligner.align("ACCGGT", "ACGGT")
print(alignments[0])

3. Database Access (Bio.Entrez)

Reference: references/databases.md

Use for:

  • Searching NCBI databases (PubMed, GenBank, Protein, Gene, etc.)
  • Downloading sequences and records
  • Fetching publication information
  • Finding related records across databases
  • Batch downloading with proper rate limiting

Quick example:

from Bio import Entrez
Entrez.email = "your.email@example.com"

# Search PubMed
handle = Entrez.esearch(db="pubmed", term="biopython", retmax=10)
results = Entrez.read(handle)
handle.close()
print(f"Found {results['Count']} results")

4. BLAST Operations (Bio.Blast)

Reference: references/blast.md

Use for:

  • Running BLAST searches via NCBI web services
  • Running local BLAST searches
  • Parsing BLAST XML output
  • Filtering results by E-value or identity
  • Extracting hit sequences

Quick example:

from Bio.Blast import NCBIWWW, NCBIXML

# Run BLAST search
result_handle = NCBIWWW.qblast("blastn", "nt", "ATCGATCGATCG")
blast_record = NCBIXML.read(result_handle)

# Display top hits
for alignment in blast_record.alignments[:5]:
    print(f"{alignment.title}: E-value={alignment.hsps[0].expect}")

5. Structural Bioinformatics (Bio.PDB)

Reference: references/structure.md

Use for:

  • Parsing PDB and mmC

Use Cases

  • Working with biological sequences (DNA, RNA, or protein)
  • Reading, writing, or converting biological file formats (FASTA, GenBank, FASTQ, PDB, mmCIF, etc.)
  • Accessing NCBI databases (GenBank, PubMed, Protein, Gene, etc.) via Entrez
  • Running BLAST searches or parsing BLAST results
  • Performing sequence alignments (pairwise or multiple sequence alignments)