生成图文并茂的分析报告/实验报告/质检报告(固定模版)。当用户要求"生成报告/总结报告/实验报告/质检报告/QC报告",或分析流程收尾需要交付报告时使用。报告必须基于真实分析输出,包含固定章节结构、关键指标表格和真实结果图。
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Bulk-query Ensembl BioMart (and other BioMart instances) for cross-database ID mapping, gene/transcript/exon coordinates, and ortholog tables. Use when batch-converting Ensembl IDs to other namespaces (HGNC, RefSeq, UniProt, Entrez), pulling gene coordinate tables for thousands of genes, building ortholog wide-tables across species, or replacing slow Ensembl REST loops with one-shot bulk export. Encodes BioMart's XML query format, R biomaRt vs Python pybiomart trade-off, mart-vs-dataset hierarchy, and the URL endpoint that's BioMart-specific (separate from rest.ensembl.org).
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Reference examples tested with: pybiomart 0.9+, R biomaRt 2.58+ (Bioconductor); Ensembl BioMart (release 110+)
Before using code patterns, verify installed versions match. If versions differ:
pip show pybiomartpackageVersion('biomaRt')The BioMart XML query format is stable across Ensembl releases; the underlying mart names and attribute IDs can change between Ensembl releases. For published work, pin the Ensembl release via useEnsembl(version=110).
"Bulk-convert IDs / pull coordinate tables / extract ortholog wide tables" -> BioMart is the right answer for any Ensembl-rooted query producing >5,000 rows. It is a separate service from the Ensembl REST API, with separate rate behavior and a different query model (XML-based, batch-oriented). For one-off lookups (<100 records), Ensembl REST is more convenient; for bulk anything, BioMart wins.
The single most important fact: BioMart returns a flat table from a single query. There is no per-record loop, no rate-limit cascade, no async polling. One XML query in; one TSV out.
pybiomart (https://github.com/jrderuiter/pybiomart) is the lightest clientbiomaRt Bioconductor (Durinck et al. 2009 Nat Protoc 4:1184) is the canonical clientcurl against the XML endpoint works but is rarely used directlyhttps://www.ensembl.org/biomart/martview for interactive query designpip install pybiomart pandas
# R:
# BiocManager::install('biomaRt')
| Level | Examples |
|---|---|
| Mart | ENSEMBL_MART_ENSEMBL (genes), ENSEMBL_MART_SNP (variants), ENSEMBL_MART_MOUSE (mouse-specific) |
| Dataset | hsapiens_gene_ensembl, mmusculus_gene_ensembl, etc. (per species) |
| Attribute | Fields to return: ensembl_gene_id, external_gene_name, chromosome_name, etc. |
| Filter | Constraints on the query: chromosome_name = 17, biotype = protein_coding, etc. |
A query is: pick a mart, pick a dataset, list attributes to return, list filters to constrain. BioMart returns a single TSV.
Discovery:
from pybiomart import Server
server = Server(host='http://www.ensembl.org')
print(server.marts) # list marts
mart = server['ENSEMBL_MART_ENSEMBL']
print(mart.datasets) # list datasets (species)
ds = mart['hsapiens_gene_ensembl']
print(ds.attributes) # list attributes
print(ds.filters) # list filters
| Question | BioMart | Ensembl REST |
|---|---|---|
| Bulk ID mapping (>5000 IDs) | yes (1 query) | rate-limited cascade |
| Single-gene lookup | overkill | yes |
| Coordinate tables for thousands of genes | yes | rate-limited |
| Ortholog wide-table across species | yes (multi-species mart) | per-gene loop |
| VEP variant annotation | no | yes (or local VEP) |
| Sequence retrieval | partial | yes |
| Real-time | no (batch) | yes (per-record) |
| Reproducibility (version pin) | useEnsembl(version=110) | archive URL e110.rest.ensembl.org |
For >5K rows, BioMart is the right tool. For real-time per-record lookups, REST.
| Attribute | Returns |
|---|---|
ensembl_gene_id | Stable Ensembl Gene ID |
ensembl_gene_id_version | With .N version suffix |
external_gene_name | HGNC symbol (or species-equivalent) |
hgnc_id, hgnc_symbol | HGNC permanent ID and symbol |
entrezgene_id | NCBI Gene ID |
refseq_mrna, refseq_peptide | RefSeq accessions |
uniprotswissprot, uniprotsptrembl | UniProt accessions |
chromosome_name, start_position, end_position, strand | Gene coordinates |
transcript_count, exon_count | Counts |
biotype | protein_coding, lncRNA, miRNA, etc. |
description | Free-text gene description |
go_id, name_1006, namespace_1003 | GO term ID, name, namespace |
| Filter | Constraint |
|---|---|
ensembl_gene_id | List of Gene IDs |
external_gene_name | List of symbols |
entrezgene_id | List of NCBI Gene IDs |
chromosome_name | One or more chromosomes |
start / end | Coordinate range |
biotype | One or more biotypes |
with_<source> | Boolean: has cross-ref to <source> (e.g. with_hpa = has Human Protein Atlas) |
Goal: Convert 5,000 Ensembl Gene IDs to HGNC symbols, RefSeq mRNA accessions, and UniProt accessions in one query.
Approach: pybiomart query with three attributes; ID list as a filter; returns one TSV.
Reference (pybiomart 0.9+, Ensembl release 110+):
from pybiomart import Server
import pandas as pd
server = Server(host='http://www.ensembl.org')
mart = server['ENSEMBL_MART_ENSEMBL']
ds = mart['hsapiens_gene_ensembl']
ensembl_ids = ['ENSG00000139618', 'ENSG00000141510', 'ENSG00000171862'] # ...up to 5K+
df = ds.query(
attributes=['ensembl_gene_id', 'external_gene_name', 'hgnc_id',
'refseq_mrna', 'uniprotswissprot'],
filters={'ensembl_gene_id': ensembl_ids},
)
print(df.head())
# One row per (gene, cross-ref) pair; genes with multiple RefSeq mRNAs get multiple rows.
df = ds.query(
attributes=['ensembl_gene_id', 'external_gene_name', 'chromosome_name',
'start_position', 'end_position', 'strand', 'biotype'],
filters={'chromosome_name': '17', 'biotype': 'protein_coding'},
)
print(f'{len(df)} protein-coding genes on chr17')
Goal: One TSV with human Ensembl ID, mouse ortholog Ensembl ID, zebrafish ortholog Ensembl ID per row.
Approach: Ortholog attributes from the human mart query both species' orthologs.
df = ds.query(
attributes=['ensembl_gene_id', 'external_gene_name',
'mmusculus_homolog_ensembl_gene', 'mmusculus_homolog_orthology_type',
'drerio_homolog_ensembl_gene', 'drerio_homolog_orthology_type'],
filters={'chromosome_name': '17'},
)
# pybiomart columns use the mart display names, which can vary across releases.
# Resolve column names defensively rather than hardcoding strings:
mouse_type_col = next(c for c in df.columns if 'Mouse' in c and 'type' in c)
zebra_type_col = next(c for c in df.columns if 'Zebrafish' in c and 'type' in c)
df_one2one = df[(df[mouse_type_col] == 'ortholog_one2one') &
(df[zebra_type_col] == 'ortholog_one2one')]
print(f'{len(df_one2one)} 1:1 orthologs across all three species on chr17')
df = ds.query(
attributes=['ensembl_gene_id', 'external_gene_name',
'go_id', 'name_1006', 'namespace_1003'],
filters={'external_gene_name': ['TP53', 'BRCA1', 'MYC', 'EGFR']},
)
# Long format: one row per (gene, GO term) pair
# Reference: Bioconductor biomaRt 2.58+ | Verify API if version differs
library(biomaRt)
# Pin to release 110 for reproducibility
ensembl <- useEnsembl(biomart='genes', dataset='hsapiens_gene_ensembl', version=110)
# Or via host URL (for older or specific assemblies)
# ensembl <- useMart('ENSEMBL_MART_ENSEMBL',
# dataset='hsapiens_gene_ensembl',
# host='https://nov2020.archive.ensembl.org')
df <- getBM(
attributes = c('ensembl_gene_id', 'external_gene_name', 'entrezgene_id',
'uniprotswissprot', 'refseq_mrna'),
filters = 'ensembl_gene_id',
values = c('ENSG00000139618', 'ENSG00000141510'),
mart = ensembl
)
head(df)
# What attributes are available?
attrs = ds.attributes
ortho_attrs = [a for a in attrs if 'homolog' in a]
print(f'{len(ortho_attrs)} ortholog attributes; first 5: {ortho_attrs[:5]}')
# What filters?
filts = ds.filters
chrom_filts = [f for f in filts if 'chrom' in f]
useMart('ensembl', ...) without version=.useEnsembl(version=110) or archive host URL.ensembl_gene_id, refseq_mrna; a gene with 10 RefSeq mRNAs produces 10 rows.ensembl_canonical filter where available.filters={'external_gene_name': ['MARCH1']} post-2020.ensembl_gene_id or hgnc_id; these are stable.mmusculus_homolog_ensembl_gene for 30K human genes./lookup/symbol calls.ENSEMBL_MART_SNP.server.marts; pick ENSEMBL_MART_ENSEMBL for genes.| Error / symptom | Cause | Solution |
|---|---|---|
| Empty result | Wrong attribute / filter name | List with ds.attributes and ds.filters |
| Timeout on big query | No filter, too many rows | Chunk by chromosome |
| Drift between re-runs | No version pinning | useEnsembl(version=110) |
| Row count > expected | Many-to-many cross-ref joins | Filter to canonical isoform |
| Symbol filter returns nothing | HGNC rename | Filter by Ensembl ID or HGNC ID |
| Slow on ortholog wide-table | Multi-species join expensive | Chunk by chromosome |
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生成图文并茂的分析报告/实验报告/质检报告(固定模版)。当用户要求"生成报告/总结报告/实验报告/质检报告/QC报告",或分析流程收尾需要交付报告时使用。报告必须基于真实分析输出,包含固定章节结构、关键指标表格和真实结果图。
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Predicts ADMET properties using ADMETlab 3.0 (119 endpoints with uncertainty), ADMET-AI, DeepChem MolNet, and chemprop D-MPNN with explicit handling of OECD QSAR principles, applicability domain assessment, calibration, hERG/CYP/AMES gold-standard endpoints, and PAINS / Lipinski / Ro5 / Veber / BBB druglikeness filters. Use when filtering compounds for drug-likeness, prioritizing leads by predicted safety, or building an in-house ADMET QSAR model.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Trim PCR primers from aligned reads in amplicon-panel BAMs using samtools ampliconclip. Use when processing SARS-CoV-2 ARTIC, hereditary cancer panels, ctDNA hot-spot panels, or any amplicon assay where primer-derived bases would falsely confirm reference at primer footprints.
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Filter alignments by flags, mapping quality, and regions using samtools view and pysam. Use when extracting specific reads, removing low-quality alignments, or subsetting to target regions.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Create and use BAI/CSI indices for BAM/CRAM files using samtools and pysam. Use when enabling random access to alignment files or fetching specific genomic regions.
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Read, write, and convert multiple sequence alignment files using Biopython Bio.AlignIO. Supports Clustal, PHYLIP, Stockholm, FASTA, Nexus, and other alignment formats for phylogenetics and conservation analysis. Use when reading, writing, or converting alignment file formats.
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