bio-expression-matrix-gene-id-mapping
SkillDev toolsLets your agent map gene IDs across bioexpression matrix datasets.
Available today. Use it from your connected AI after setup.
No other account needed.
Connect ahel once, and every AI you use reads what you have installed.
Then ask your AI: use the bio-expression-matrix-gene-id-mapping skill
About this capability
The largest open-source medical AI skills library for OpenClaw🦞.
What this skill tells your AI
The instructions your AI receives, as published by freedomintelligence/openclaw-medical-skills in skills/bio-expression-matrix-gene-id-mapping/SKILL.md and read by ahel’s review.
name: bio-expression-matrix-gene-id-mapping description: Convert between gene identifier systems including Ensembl, Entrez, HGNC symbols, and UniProt. Use when mapping IDs for pathway analysis or matching different data sources. tool_type: mixed primary_tool: biomaRt measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools:
- read_file
- run_shell_command
Gene ID Mapping
Python: mygene
import mygene
import pandas as pd
mg = mygene.MyGeneInfo()
# Ensembl to Symbol
ensembl_ids = ['ENSG00000141510', 'ENSG00000012048', 'ENSG00000141736']
results = mg.querymany(ensembl_ids, scopes='ensembl.gene', fields='symbol', species='human')
mapping = {r['query']: r.get('symbol', None) for r in results}
# {'ENSG00000141510': 'TP53', 'ENSG00000012048': 'BRCA1', 'ENSG00000141736': 'ERBB2'}
# Symbol to Entrez
symbols = ['TP53', 'BRCA1', 'ERBB2']
results = mg.querymany(symbols, scopes='symbol', fields='entrezgene', species='human')
mapping = {r['query']: r.get('entrezgene', None) for r in results}
# Ensembl to multiple fields
results = mg.querymany(ensembl_ids, scopes='ensembl.gene',
fields=['symbol', 'entrezgene', 'uniprot'], species='human')
Python: pyensembl
from pyensembl import EnsemblRelease
# Load Ensembl release (downloads automatically first time)
ensembl = EnsemblRelease(110, species='human') # or 'mouse'
# Gene ID to symbol
gene = ensembl.gene_by_id('ENSG00000141510')
print(gene.gene_name) # TP53
# Symbol to gene ID
gene = ensembl.genes_by_name('TP53')[0]
print(gene.gene_id) # ENSG00000141510
# Batch conversion
def ensembl_to_symbol(ensembl_ids, release=110):
ens = EnsemblRelease(release, species='human')
mapping = {}
for eid in ensembl_ids:
try:
gene = ens.gene_by_id(eid.split('.')[0]) # Remove version
mapping[eid] = gene.gene_name
except ValueError:
mapping[eid] = None
return mapping
Python: gseapy
import gseapy as gp
# Ensembl to Symbol using Enrichr
gene_list = ['ENSG00000141510', 'ENSG00000012048']
converted = gp.biomart.ensembl2name(gene_list, organism='hsapiens')
R: biomaRt
library(biomaRt)
# Connect to Ensembl
ensembl <- useEnsembl(biomart='genes', dataset='hsapiens_gene_ensembl')
# Ensembl to Symbol
ensembl_ids <- c('ENSG00000141510', 'ENSG00000012048', 'ENSG00000141736')
results <- getBM(
attributes=c('ensembl_gene_id', 'hgnc_symbol', 'entrezgene_id'),
filters='ensembl_gene_id',
values=ensembl_ids,
mart=ensembl
)
# Symbol to Ensembl
symbols <- c('TP53', 'BRCA1', 'ERBB2')
results <- getBM(
attributes=c('hgnc_symbol', 'ensembl_gene_id'),
filters='hgnc_symbol',
values=symbols,
mart=ensembl
)
# All available attributes
listAttributes(ensembl)
R: org.db Packages
library(org.Hs.eg.db) # Human
library(AnnotationDbi)
# Ensembl to Symbol
ensembl_ids <- c('ENSG00000141510', 'ENSG00000012048')
symbols <- mapIds(org.Hs.eg.db, keys=ensembl_ids, keytype='ENSEMBL', column='SYMBOL')
# Symbol to Entrez
symbols <- c('TP53', 'BRCA1')
entrez <- mapIds(org.Hs.eg.db, keys=symbols, keytype='SYMBOL', column='ENTREZID')
# Available keytypes
keytypes(org.Hs.eg.db)
# ENSEMBL, ENSEMBLPROT, ENSEMBLTRANS, ENTREZID, SYMBOL, UNIPROT, etc.
Apply Mapping to Count Matrix
import pandas as pd
import mygene
def map_count_matrix_ids(counts, from_type='ensembl.gene', to_type='symbol', species='human'):
'''Map gene IDs in count matrix index.'''
mg = mygene.MyGeneInfo()
# Remove version numbers from Ensembl IDs
clean_ids = [g.split('.')[0] for g in counts.index]
# Query mygene
results = mg.querymany(clean_ids, scopes=from_type, fields=to_type, species=species)
# Build mapping
mapping = {}
for r in results:
if to_type in r:
mapping[r['query']] = r[to_type]
# Apply mapping
new_index = [mapping.get(g.split('.')[0], g) for g in counts.index]
counts_mapped = counts.copy()
counts_mapped.index = new_index
# Handle duplicates (sum)
counts_mapped = counts_mapped.groupby(counts_mapped.index).sum()
return counts_mapped
# Usage
counts_symbols = map_count_matrix_ids(counts, 'ensembl.gene', 'symbol')
R Equivalent
library(biomaRt)
map_count_matrix_ids <- function(counts, from_type='ensembl_gene_id', to_type='hgnc_symbol') {
ensembl <- useEnsembl(biomart='genes', dataset='hsapiens_gene_ensembl')
# Remove version numbers
clean_ids <- gsub('\\..*', '', rownames(counts))
# Get mapping
mapping <- getBM(
attributes=c(from_type, to_type),
filters=from_type,
values=clean_ids,
mart=ensembl
)
# Merge and aggregate duplicates
counts$gene_id <- clean_ids
merged <- merge(counts, mapping, by.x='gene_id', by.y=from_type, all.x=TRUE)
merged$gene_id <- NULL
# Use symbol as rowname, sum duplicates
rownames(merged) <- merged[[to_type]]
merged[[to_type]] <- NULL
counts_mapped <- aggregate(. ~ rownames(merged), data=merged, FUN=sum)
rownames(counts_mapped) <- counts_mapped[,1]
counts_mapped <- counts_mapped[,-1]
return(counts_mapped)
}
Handle Unmapped IDs
def robust_id_mapping(gene_ids, from_type, to_type, species='human'):
'''Map IDs with fallback for unmapped genes.'''
import mygene
mg = mygene.MyGeneInfo()
clean_ids = [g.split('.')[0] for g in gene_ids]
results = mg.querymany(clean_ids, scopes=from_type, fields=to_type, species=species)
mapping = {}
unmapped = []
for r in results:
original = gene_ids[clean_ids.index(r['query'])]
if to_type in r:
mapping[original] = r[to_type]
else:
mapping[original] = original # Keep original if unmapped
unmapped.append(original)
print(f'Mapped: {len(gene_ids) - len(unmapped)}/{len(gene_ids)}')
print(f'Unmapped: {len(unmapped)}')
return mapping, unmapped
Common ID Types
| Type | Example | Use Case |
|---|---|---|
| Ensembl Gene | ENSG00000141510 | RNA-seq, GTF files |
| Ensembl Transcript | ENST00000269305 | Transcript-level analysis |
| Entrez Gene | 7157 | NCBI databases, KEGG |
| HGNC Symbol | TP53 | Human readable |
| UniProt | P04637 | Protein databases |
| RefSeq | NM_000546 | NCBI RefSeq |
Related Skills
- expression-matrix/counts-ingest - Load count data
- expression-matrix/metadata-joins - Add annotations
- pathway-analysis/go-enrichment - Requires Entrez IDs
- pathway-analysis/kegg-pathways - Requires Entrez IDs
Signals
- GitHub stars
- 3k
- Forks
- 407
- Last commit
- Jul 2026
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bio-expression-matrix-gene-id-mapping- Source
- github.com/freedomintelligence/openclaw-medical-skills