Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Biology research tools reference. Always available inside agent containers.
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설치 방법 보기설치하기 전에 에이전트에게 전달되는 지시 내용을 확인할 수 있습니다.
You are running inside a BioClaw container with the following biology tools pre-installed.
Layout: Runnable plot/PyMOL scripts live under templates/ (synced to /home/node/.claude/skills/bio-tools/templates/).
# Nucleotide BLAST
blastn -query input.fa -subject ref.fa -outfmt 6 -evalue 1e-5
# Protein BLAST
blastp -query protein.fa -subject ref_protein.fa -outfmt 6
# Translate then search
blastx -query nucleotide.fa -subject protein_db.fa -outfmt 6
# Index reference
bwa index reference.fa
# Align short reads
bwa mem reference.fa reads_R1.fq reads_R2.fq > aligned.sam
# Long reads
minimap2 -a reference.fa long_reads.fq > aligned.sam
# SAM to sorted BAM
samtools view -bS aligned.sam | samtools sort -o sorted.bam
samtools index sorted.bam
# FastQC report
fastqc reads.fq -o qc_output/
# FASTA/FASTQ stats
seqtk comp reads.fq | head
seqtk size reads.fq
# Intersect two BED files
bedtools intersect -a regions.bed -b features.bed
# Coverage
bedtools coverage -a regions.bed -b aligned.bam
# Get FASTA from BED regions
bedtools getfasta -fi reference.fa -bed regions.bed
# Read FASTA/FASTQ
from Bio import SeqIO
for record in SeqIO.parse("input.fa", "fasta"):
print(record.id, len(record.seq))
# Fetch from NCBI
from Bio import Entrez
Entrez.email = "bioclaw@example.com"
handle = Entrez.efetch(db="nucleotide", id="NM_000546", rettype="fasta")
record = SeqIO.read(handle, "fasta")
# Differential expression
from pydeseq2 import DeseqDataSet, DeseqStats
dds = DeseqDataSet(counts=count_matrix, metadata=metadata, design="~condition")
dds.deseq2()
stat_res = DeseqStats(dds, contrast=["condition", "treated", "untreated"])
stat_res.summary()
# Single-cell RNA-seq
import scanpy as sc
adata = sc.read_h5ad("data.h5ad")
sc.pp.normalize_total(adata)
sc.pp.log1p(adata)
sc.tl.pca(adata)
sc.tl.umap(adata)
sc.tl.leiden(adata)
# Molecular structures
from rdkit import Chem
from rdkit.Chem import Descriptors
mol = Chem.MolFromSmiles("CC(=O)OC1=CC=CC=C1C(=O)O") # Aspirin
print(f"MW: {Descriptors.MolWt(mol):.1f}")
print(f"LogP: {Descriptors.MolLogP(mol):.2f}")
Bio.Blast.NCBIWWW.qblast() — this sends the query over the networkSeqIO.parse() over SeqIO.read()/workspace/group/plot.png with dpi=150, bbox_inches="tight". For publication-ready figures, use cnsplots or pyGenomeTracks (see below)./workspace/group/ so the user can access themoutput/YYYY-MM-DD/ to avoid overwriting; update _latest.md with paths to newest outputsPrefer these built-in scripts when creating common BioClaw figures, instead of writing one-off plotting code from scratch.
Path:
/home/node/.claude/skills/bio-tools/templates/volcano_plot_template.py
Example:
python /home/node/.claude/skills/bio-tools/templates/volcano_plot_template.py \
--input /workspace/group/counts.csv \
--output /workspace/group/volcano_plot.png \
--title "Differential Expression Volcano Plot"
Expected columns by default: gene, log2FC, pvalue
Path:
/home/node/.claude/skills/bio-tools/templates/qc_summary_plot_template.py
Example:
python /home/node/.claude/skills/bio-tools/templates/qc_summary_plot_template.py \
--input /workspace/group/qc_metrics.csv \
--output /workspace/group/qc_summary.png \
--title "Sequencing QC Summary"
Expected sample column by default: sample
Useful metric columns: total_reads, q30_pct, gc_pct, duplication_pct
Path:
/home/node/.claude/skills/bio-tools/templates/pymol_render_template.py
Examples:
python /home/node/.claude/skills/bio-tools/templates/pymol_render_template.py \
--input 1M17 \
--output /workspace/group/1m17_render.png \
--highlight-selection "resn AQ4"
python /home/node/.claude/skills/bio-tools/templates/pymol_render_template.py \
--input /workspace/group/structure.pdb \
--output /workspace/group/structure_render.png \
--style cartoon
When the built-in scripts don't fit, use these patterns. Save to /workspace/group/<name>.png.
Heatmap (rows=genes, columns=samples):
import pandas as pd
import numpy as np
import matplotlib.pyplot as plt
import seaborn as sns
df = pd.read_csv("/workspace/group/expression.csv", index_col=0)
sns.heatmap(np.log1p(df).iloc[:50], cmap='RdBu_r', center=0)
plt.savefig("/workspace/group/heatmap.png", dpi=150, bbox_inches="tight")
PCA scatter (columns: PC1, PC2, condition):
import pandas as pd
import matplotlib.pyplot as plt
coords = pd.read_csv("/workspace/group/pca_coords.csv")
for c in coords['condition'].unique():
sub = coords[coords['condition'] == c]
plt.scatter(sub['PC1'], sub['PC2'], label=c)
plt.legend()
plt.savefig("/workspace/group/pca.png", dpi=150, bbox_inches="tight")
Bar plot (columns: gene, count):
import pandas as pd
import matplotlib.pyplot as plt
df = pd.read_csv("/workspace/group/top_genes.csv").head(20).sort_values('count', ascending=True)
plt.barh(df['gene'], df['count'])
plt.savefig("/workspace/group/barplot.png", dpi=150, bbox_inches="tight")
cnsplots provides Cell/Nature/Science journal-style figures. Use for volcano, bar, box, violin, heatmap, etc.
import cnsplots as cns
import pandas as pd
import numpy as np
# Volcano plot (columns: gene, log2FC, pvalue or padj)
df = pd.read_csv("/workspace/group/counts.csv")
df["-log10(p)"] = -np.log10(df["pvalue"].clip(lower=1e-300)) # or use padj
cns.figure(height=200, width=200)
cns.volcanoplot(data=df, x="log2FC", y="-log10(p)", symbol="gene")
cns.savefig("/workspace/group/volcano_cns.png")
# Boxplot with Mann-Whitney test
cns.figure(150, 150)
cns.boxplot(data=df, x="group", y="value", pairs="all")
cns.savefig("/workspace/group/boxplot.png")
# Heatmap from AnnData (single-cell)
import scanpy as sc
adata = sc.read_h5ad("/workspace/group/data.h5ad")
cns.figure(200, 200)
cns.heatmapplot(adata, row_cluster=True, col_cluster=True, cmap="bwr")
cns.savefig("/workspace/group/heatmap_cns.png")
See cnsplots docs for more: violin, scatter, survival, ROC, GSEA, etc.
pyGenomeTracks plots genome browser tracks (BED, BigWig, GTF, etc.). BEDTools must be installed (already in container).
# 1. Create config from your files
make_tracks_file --trackFiles /workspace/group/peaks.bed /workspace/group/coverage.bw -o /workspace/group/tracks.ini
# 2. Plot a region (chr:start-end)
pyGenomeTracks --tracks /workspace/group/tracks.ini --region chr1:1000000-4000000 -o /workspace/group/genome_tracks.png --dpi 150
Supported file types: .bed, .bw (bigwig), .gtf, .gff, .arcs, .links. Edit tracks.ini to adjust track colors, heights, titles.
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Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
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.
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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.
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