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biology-biopython

aiming-lab/AutoResearchClaw/.claude/skills/biology-biopython/SKILL.md

Bioinformatics with Biopython for sequence manipulation, file parsing, BLAST, and phylogenetics. Use when working with DNA/RNA/protein sequences or biological databases.

Skill15k starsChanged 6 months ago

What's in it

  1. Biopython Bioinformatics Best Practice
  2. Sequence Manipulation
  3. File Parsing (SeqIO)
  4. BLAST Operations
  5. NCBI Database Access (Entrez)
  6. Phylogenetics (Bio.Phylo)
  7. Structure Analysis (Bio.PDB)
  8. Common Pitfalls
---
name: biology-biopython
description: Bioinformatics with Biopython for sequence manipulation, file parsing, BLAST, and phylogenetics. Use when working with DNA/RNA/protein sequences or biological databases.
metadata:
  category: domain
  trigger-keywords: "sequence,FASTA,genome,protein,BLAST,phylogenetic,biopython,bioinformatics,gene,DNA,RNA"
  applicable-stages: "9,10,12"
  priority: "4"
  version: "1.0"
  author: researchclaw
  references: "adapted from K-Dense-AI/claude-scientific-skills"
---

## Biopython Bioinformatics Best Practice

### Sequence Manipulation
1. Create sequences: `from Bio.Seq import Seq; seq = Seq("ATGCGA")`
2. Complement: `seq.complement()`; Reverse complement: `seq.reverse_complement()`
3. Transcription: `seq.transcribe()` (DNA to RNA)
4. Translation: `seq.translate()` (DNA/RNA to protein)
5. GC content: `from Bio.SeqUtils import gc_fraction; gc_fraction(seq)`
6. Molecular weight: `from Bio.SeqUtils import molecular_weight`

### File Parsing (SeqIO)
1. Read FASTA: `for rec in SeqIO.parse("file.fasta", "fasta"): ...`
2. Read GenBank: `for rec in SeqIO.parse("file.gb", "genbank"): ...`
3. Read single record: `rec = SeqIO.read("file.fasta", "fasta")`
4. Write sequences: `SeqIO.write(records, "output.fasta", "fasta")`
5. Convert formats: `SeqIO.convert("input.gb", "genbank", "output.fasta", "fasta")`
6. Index large files: `idx = SeqIO.index("large.fasta", "fasta")` for random access

### BLAST Operations
1. Online BLAST: `from Bio.Blast import NCBIWWW; result = NCBIWWW.qblast("blastn", "nt", seq)`
2. Parse results: `from Bio.Blast import NCBIXML; records = NCBIXML.parse(result)`
3. Local BLAST: run via subprocess, parse XML output with NCBIXML
4. Always set `Entrez.email` before any NCBI access
5. Filter results by e-value (typically < 1e-5) and coverage

### NCBI Database Access (Entrez)
1. Always set email: `Entrez.email = "your@email.com"`
2. Search: `handle = Entrez.esearch(db="pubmed", term="query")`
3. Fetch records: `handle = Entrez.efetch(db="nucleotide", id="ID", rettype="fasta")`
4. Use API key for higher rate limits (10 req/s vs 3 req/s)
5. Respect NCBI rate limits; add delays between batch requests

### Phylogenetics (Bio.Phylo)
1. Read trees: `from Bio import Phylo; tree = Phylo.read("tree.nwk", "newick")`
2. Draw trees: `Phylo.draw(tree)` or `Phylo.draw_ascii(tree)`
3. Supported formats: newick, nexus, phyloxml
4. Traverse clades: `for clade in tree.find_clades(): ...`
5. Calculate distances: `tree.distance(clade1, clade2)`

### Structure Analysis (Bio.PDB)
1. Parse PDB: `parser = PDBParser(); structure = parser.get_structure("id", "file.pdb")`
2. Hierarchy: Structure > Model > Chain > Residue > Atom
3. Get atoms: iterate through `structure.get_atoms()`
4. Calculate distances: use atom coordinate vectors
5. For mmCIF files: use `MMCIFParser()` instead of `PDBParser()`

### Common Pitfalls
1. Always handle `SeqIO.parse` as an iterator — it exhausts after one pass
2. Check sequence alphabet compatibility before operations
3. Large files: use `SeqIO.index()` not `SeqIO.to_dict()` to avoid memory issues
4. Set proper timeout for remote BLAST queries (can take minutes)
5. Validate parsed data — missing annotations are common in public databases

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