seaborn-statistical-plots
Seaborn provides statistical visualization functions built on matplotlib with native pandas DataFrame support, automatically handling grouping, confidence intervals, and aggregation across distribution, categorical, relational, regression, and matrix plot types. Use it for rapid exploratory analysis and publication-ready statistical summaries when comparing groups, visualizing correlations, or faceting plots across sample subsets; choose matplotlib for fine pixel-level control or plotly for interactive HTML output.
git clone --depth 1 https://github.com/jaechang-hits/SciAgent-Skills /tmp/seaborn-statistical-plots && cp -r /tmp/seaborn-statistical-plots/skills/data-visualization/seaborn-statistical-plots ~/.claude/skills/seaborn-statistical-plotsSKILL.md
# Seaborn — Statistical Plots
## Overview
Seaborn is a Python library for statistical data visualization built on top of matplotlib. It works directly with pandas DataFrames, automatically handles grouping by categorical variables, computes confidence intervals and kernel density estimates, and produces attractive publication-ready figures with minimal configuration. Seaborn separates axes-level functions (embeddable in custom layouts) from figure-level functions (with built-in faceting), enabling both quick exploratory analysis and structured multi-panel figures.
## When to Use
- Comparing gene expression, protein abundance, or measurement distributions across experimental conditions (treatment vs. control, cell lines, time points)
- Generating grouped box plots, violin plots, or strip plots to show both summary statistics and individual data points simultaneously
- Visualizing pairwise correlations in multi-gene or multi-feature datasets as annotated heatmaps
- Plotting regression fits with confidence bands between continuous variables (e.g., cell viability vs. drug concentration)
- Faceting a single plot type across multiple sample subsets, tissue types, or experimental batches in one call
- Rapid exploratory analysis of a new dataset using `pairplot` to survey all pairwise relationships at once
- Use `matplotlib` directly when you need pixel-level control over figure elements, complex mixed-type layouts, or non-statistical custom plots
- Use `plotly` when the output must be interactive (hover tooltips, zoom, pan) or embedded in a web application
## Prerequisites
- **Python packages**: `seaborn>=0.13`, `matplotlib`, `pandas`, `numpy`
- **Data requirements**: Pandas DataFrame in long-form (tidy) format; each observation is a row, each variable is a column
- **Environment**: Standard Python environment; no GPU or special hardware required
```bash
pip install "seaborn>=0.13" matplotlib pandas numpy scipy
```
## Quick Start
```python
import seaborn as sns
import matplotlib.pyplot as plt
import pandas as pd
import numpy as np
# Simulate gene expression across conditions
rng = np.random.default_rng(42)
df = pd.DataFrame({
"gene": ["BRCA1"] * 60 + ["TP53"] * 60,
"condition": ["control", "treated"] * 60,
"log2_expr": np.concatenate([
rng.normal(5.2, 0.8, 60),
rng.normal(6.1, 0.9, 60),
])
})
sns.set_theme(style="ticks", context="notebook")
sns.boxplot(data=df, x="gene", y="log2_expr", hue="condition", palette="Set2")
plt.ylabel("log2 Expression")
plt.title("Gene Expression by Condition")
plt.tight_layout()
plt.savefig("quickstart_boxplot.png", dpi=150)
print("Saved quickstart_boxplot.png")
```
## Core API
### 1. Distribution Plots
Visualize univariate distributions and compare them across groups. `histplot` bins data; `kdeplot` fits a smooth density estimate; `displot` is the figure-level wrapper that adds faceting.
```python
import seaborn as sns
import matplotlib.pyplot as plt
import numpy as np
import pandas as pd
rng = np.random.default_rng(0)
n = 200
df = pd.DataFrame({
"log2_tpm": np.concatenate([rng.normal(4.5, 1.1, n), rng.normal(6.0, 1.3, n)]),
"sample": ["tumor"] * n + ["normal"] * n,
})
fig, axes = plt.subplots(1, 3, figsize=(15, 4))
# Histogram with density normalization and stacked hue groups
sns.histplot(data=df, x="log2_tpm", hue="sample", stat="density",
multiple="stack", bins=30, ax=axes[0])
axes[0].set_title("Histogram (stacked)")
# KDE with fill — bandwidth controlled by bw_adjust
sns.kdeplot(data=df, x="log2_tpm", hue="sample", fill=True,
bw_adjust=0.8, alpha=0.4, ax=axes[1])
axes[1].set_title("KDE (filled)")
# ECDF — useful for comparing cumulative distributions
sns.ecdfplot(data=df, x="log2_tpm", hue="sample", ax=axes[2])
axes[2].set_title("ECDF")
plt.tight_layout()
plt.savefig("distributions.png", dpi=150)
print("Saved distributions.png")
```
```python
# Bivariate KDE: joint distribution of two continuous variables
rng = np.random.default_rng(1)
df2 = pd.DataFrame({
"log2_rna": rng.normal(5.5, 1.2, 300),
"log2_prot": rng.normal(4.8, 1.0, 300) + 0.6 * rng.normal(5.5, 1.2, 300),
})
sns.kdeplot(data=df2, x="log2_rna", y="log2_prot",
fill=True, levels=8, thresh=0.05, cmap="Blues")
plt.xlabel("log2 RNA (TPM)")
plt.ylabel("log2 Protein (iBAQ)")
plt.title("RNA–Protein Correlation Density")
plt.tight_layout()
plt.savefig("bivariate_kde.png", dpi=150)
print("Saved bivariate_kde.png")
```
### 2. Categorical Plots
Compare distributions or aggregated statistics across categorical groups. Axes-level functions (`boxplot`, `violinplot`, `stripplot`, `swarmplot`, `barplot`) accept an `ax=` parameter for embedding in custom layouts.
```python
import seaborn as sns
import matplotlib.pyplot as plt
import numpy as np
import pandas as pd
rng = np.random.default_rng(2)
conditions = ["DMSO", "Drug A 1uM", "Drug A 10uM", "Drug B 1uM", "Drug B 10uM"]
df = pd.DataFrame({
"condition": np.repeat(conditions, 30),
"viability": np.concatenate([
rng.normal(100, 5, 30),
rng.normal(92, 7, 30),
rng.normal(65, 10, 30),
rng.normal(88, 8, 30),
rng.normal(45, 12, 30),
])
})
fig, axes = plt.subplots(1, 3, figsize=(18, 5))
# Box plot — shows quartiles and outliers
sns.boxplot(data=df, x="condition", y="viability",
palette="husl", width=0.5, ax=axes[0])
axes[0].set_xticklabels(axes[0].get_xticklabels(), rotation=30, ha="right")
axes[0].set_title("Box Plot")
# Violin — KDE shape + inner quartile lines
sns.violinplot(data=df, x="condition", y="viability",
inner="quart", palette="muted", ax=axes[1])
axes[1].set_xticklabels(axes[1].get_xticklabels(), rotation=30, ha="right")
axes[1].set_title("Violin Plot")
# Strip plot overlaid on box — shows all individual points
sns.boxplot(data=df, x="condition", y="viability",
palette="pastel", width=0.5, ax=axes[2])
sns.stripplot(data=df, x="condition", y="viabilitAnnotated matrices for single-cell genomics. Stores X with obs/var metadata, layers, embeddings (obsm/varm), graphs (obsp/varp), uns. Use for .h5ad/.zarr I/O, concatenation, scverse integration. For analysis use scanpy; for probabilistic models use scvi-tools.
GRN inference from expression via GRNBoost2 (gradient boosting) or GENIE3 (Random Forest). Load matrix, filter by TFs, infer TF-target-importance links, save network. Dask-parallelized to single-cell scale. Core SCENIC component.
Query ARCHS4 REST API for uniformly processed RNA-seq expression, tissue patterns, co-expression across 1M+ human/mouse samples. Retrieve z-scores, co-expressed genes, samples by metadata, HDF5 matrices. For variant population genetics use gnomad-database; for pathway enrichment use gget-genomic-databases (Enrichr).
Annotate bacterial and archaeal genomes and plasmids with Bakta's Prodigal/HMM/diamond pipeline. Identifies CDS, ncRNA, tRNA, rRNA, tmRNA, sORFs, CRISPR arrays, oriC/oriV/oriT, and gaps against a curated UniRef-derived database. Produces NCBI-compatible GFF3, GenBank, EMBL, JSON, FASTA, TSV, and a circular genome plot. Use Prokka for legacy pipelines or non-bacterial kingdoms; PGAP for NCBI GenBank submission.
CLI for VCF/BCF: filter, merge, annotate, query, normalize, compute stats. Core post-variant-calling: quality filtering, multi-sample merging, rsID annotation, genotype extraction. Samtools companion in HTSlib. Use GATK for complex indel realignment during calling; use VCFtools for population genetics stats.
Genomic interval ops on BED/BAM/GFF/VCF. Find overlaps, merge intervals, compute coverage, extract FASTA, find nearest features. Core for ChIP-seq peak annotation, region filtering, genome arithmetic. Use tabix for indexed single-region queries; use deeptools for normalized bigWig coverage.
Molecular biology toolkit: sequence manipulation, FASTA/GenBank/PDB I/O, NCBI Entrez, BLAST automation, pairwise/MSA alignment, Bio.PDB, phylogenetic trees. Use for batch processing, custom pipelines, format conversion, PubMed/GenBank queries. For quick gene lookups use gget; for multi-service REST APIs use bioservices.
Biopython sequence analysis: parse FASTA/FASTQ/GenBank/GFF (SeqIO), NCBI Entrez (esearch/efetch/elink), remote/local BLAST, pairwise/MSA alignment (PairwiseAligner, MUSCLE/ClustalW), phylogenetic trees (Phylo). Use for gene family studies, phylogenomics, comparative genomics, NCBI pipelines. For PCR/restriction/cloning use biopython-molecular-biology; for SAM/BAM use pysam.