Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Detect antimicrobial resistance genes using AMRFinderPlus, ResFinder, and CARD. Screen isolates and metagenomes for resistance determinants. Use when characterizing resistance profiles in clinical isolates, surveillance samples, or metagenomic data.
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Reference examples tested with: AMRFinderPlus 3.12+, pandas 2.2+
Before using code patterns, verify installed versions match. If versions differ:
pip show <package> then help(module.function) to check signatures<tool> --version then <tool> --help to confirm flagsIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Screen my isolates for antibiotic resistance genes" → Identify antimicrobial resistance determinants in bacterial genomes or metagenomes by searching against curated resistance gene databases.
amrfinder -n assembly.fasta --organism Escherichia (AMRFinderPlus)Identify antimicrobial resistance (AMR) genes in bacterial genomes and metagenomes.
| Tool | Database | Best For |
|---|---|---|
| AMRFinderPlus | NCBI | Comprehensive, curated |
| ResFinder | CGE | Clinical isolates |
| CARD/RGI | CARD | Detailed resistance mechanisms |
| ABRicate | Multiple | Quick screening |
conda install -c bioconda ncbi-amrfinderplus
amrfinder -u # Update database
# Assembled contigs
amrfinder -n contigs.fasta -o amr_results.tsv --threads 8
# With organism for point mutations
amrfinder -n contigs.fasta -O Escherichia -o amr_results.tsv
# Include stress/virulence genes
amrfinder -n contigs.fasta -O Salmonella --plus -o amr_results.tsv
# If you have predicted proteins
amrfinder -p proteins.faa -o amr_results.tsv
# Combined nucleotide and protein
amrfinder -n contigs.fasta -p proteins.faa -g gff_annotation.gff \
-O Escherichia -o amr_results.tsv
| Column | Description |
|---|---|
| Gene symbol | AMR gene name |
| Sequence name | Contig/protein ID |
| Element type | AMR, STRESS, VIRULENCE |
| Element subtype | Specific class |
| Class | Drug class |
| Subclass | Specific drug |
| % Coverage | Query coverage |
| % Identity | Sequence identity |
for fasta in assemblies/*.fasta; do
sample=$(basename $fasta .fasta)
amrfinder -n $fasta -O Escherichia --plus \
-o results/${sample}_amr.tsv --threads 4
done
# Combine results
head -1 results/sample1_amr.tsv > combined_amr.tsv
for f in results/*_amr.tsv; do
tail -n+2 $f >> combined_amr.tsv
done
conda install -c bioconda resfinder
# Or use web: https://cge.food.dtu.dk/services/ResFinder/
# Assembled genome
python -m resfinder -ifa contigs.fasta -o resfinder_output \
-db_res /path/to/resfinder_db -acq
# With species for point mutations
python -m resfinder -ifa contigs.fasta -o resfinder_output \
-db_res /path/to/resfinder_db \
-db_point /path/to/pointfinder_db \
-s "Escherichia coli" -acq
python -m resfinder -ifq reads_1.fq reads_2.fq -o resfinder_output \
-db_res /path/to/resfinder_db -acq
Resistance Gene Identifier with detailed mechanism annotations.
conda install -c bioconda rgi
rgi load --card_json /path/to/card.json --local
# From contigs
rgi main --input_sequence contigs.fasta --output_file rgi_output \
--input_type contig --local --clean
# From protein
rgi main --input_sequence proteins.faa --output_file rgi_output \
--input_type protein --local
# Include loose hits (more sensitive)
rgi main --input_sequence contigs.fasta --output_file rgi_output \
--input_type contig --include_loose --local
# Main results
cat rgi_output.txt
# JSON with full details
cat rgi_output.json
conda install -c bioconda abricate
abricate --setupdb # Update databases
abricate --list
# ncbi, card, resfinder, argannot, megares, ecoh, ecoli_vf, plasmidfinder, vfdb
# Default (ncbi)
abricate contigs.fasta > abricate_results.tsv
# Specific database
abricate --db resfinder contigs.fasta > resfinder_results.tsv
abricate --db card contigs.fasta > card_results.tsv
# Multiple databases
for db in ncbi card resfinder; do
abricate --db $db contigs.fasta > ${db}_results.tsv
done
# Run on multiple samples
abricate assemblies/*.fasta > all_results.tsv
# Generate summary matrix
abricate --summary all_results.tsv > summary_matrix.tsv
# Map reads to AMR markers
shortbred_quantify.py --markers amr_markers.faa \
--wgs reads_1.fq reads_2.fq \
--results amr_abundance.tsv \
--threads 8
# Index database
groot index -m card.90 -i groot_index -p 8
# Align and report
groot align -i groot_index -f reads_1.fq,reads_2.fq -p 8 | \
groot report > amr_report.tsv
Goal: Screen a bacterial assembly for antimicrobial resistance genes using multiple databases for comprehensive resistance profiling.
Approach: Run AMRFinderPlus with organism-specific point mutation detection, then ABRicate against NCBI/CARD/ResFinder databases, and summarize drug class counts.
#!/bin/bash
set -euo pipefail
ASSEMBLY=$1
ORGANISM=$2
OUTPUT_DIR=$3
mkdir -p $OUTPUT_DIR
echo "=== AMRFinderPlus ==="
amrfinder -n $ASSEMBLY -O $ORGANISM --plus \
-o $OUTPUT_DIR/amrfinder.tsv --threads 8
echo "=== ABRicate (multiple databases) ==="
for db in ncbi card resfinder; do
abricate --db $db $ASSEMBLY > $OUTPUT_DIR/abricate_${db}.tsv
done
echo "=== Summary ==="
echo "AMR genes found:"
cut -f6 $OUTPUT_DIR/amrfinder.tsv | sort | uniq -c | sort -rn | head -20
echo "=== Complete ==="
echo "Results in $OUTPUT_DIR/"
import pandas as pd
# Load AMRFinderPlus results
amr = pd.read_csv('amrfinder.tsv', sep='\t')
# Count by drug class
class_counts = amr['Class'].value_counts()
print(class_counts)
# Pivot for heatmap (multiple samples)
import glob
results = []
for f in glob.glob('results/*_amr.tsv'):
sample = f.split('/')[-1].replace('_amr.tsv', '')
df = pd.read_csv(f, sep='\t')
df['Sample'] = sample
results.append(df)
combined = pd.concat(results)
matrix = pd.crosstab(combined['Sample'], combined['Gene symbol'])
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Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
中文简介正在准备中。当前显示原文说明。
AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
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Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
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ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
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End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
中文简介正在准备中。当前显示原文说明。