Interactive scientific visualization with Plotly. Two APIs: plotly.express (px) for one-liner DataFrame plots, plotly.graph_objects (go) for trace-level control. 40+ chart types with hover, zoom, pan, animation. Exports HTML or static PNG/SVG/PDF via kaleido. Use for volcano plots with gene hover, dose-response dashboards, expression heatmaps, 3D molecular views. Use seaborn for stats; matplotlib for publication figures.
Scanned 5/29/2026
Install to Claude Code
npx -y skills add jaechang-hits/SciAgent-Skills --skill plotly-interactive-plots --agent claude-codeInstalls into .claude/skills of the current project.
Are you the author of Plotly Interactive Plots?
Add the live security badge to your README — it updates automatically with every re-scan.
[](https://www.skillsdirectory.com/skills/jaechang-hits-plotly-interactive-plots)More formats (shields.io, HTML) on the badges page.
---
name: "plotly-interactive-plots"
description: "Interactive scientific visualization with Plotly. Two APIs: plotly.express (px) for one-liner DataFrame plots, plotly.graph_objects (go) for trace-level control. 40+ chart types with hover, zoom, pan, animation. Exports HTML or static PNG/SVG/PDF via kaleido. Use for volcano plots with gene hover, dose-response dashboards, expression heatmaps, 3D molecular views. Use seaborn for stats; matplotlib for publication figures."
license: "MIT"
---
# Plotly Interactive Plots
## Overview
Plotly is a Python library for producing interactive, web-ready figures backed by HTML and JavaScript. It exposes two complementary APIs: `plotly.express` (px) provides a high-level, DataFrame-oriented interface for generating common chart types in one line, while `plotly.graph_objects` (go) offers fine-grained control over every trace, axis, and layout property. Figures are fully interactive by default — supporting hover tooltips, zoom, pan, and click events — and can be embedded in web pages, Jupyter notebooks, or built into web applications using the Dash framework.
## When to Use
- You need hover tooltips that display gene names, p-values, or sample metadata without cluttering the static figure.
- You are building a multi-panel interactive dashboard for dose-response curves, patient cohorts, or multi-condition comparisons.
- You want to share figures as self-contained HTML files that non-programmers can explore in a browser.
- You need 3D scatter or surface plots for structural biology, conformational landscapes, or PCA of high-dimensional data.
- You are creating heatmaps of gene expression or correlation matrices where users need to zoom into specific gene clusters.
- You require animation frames to show time-series or treatment-response trajectories.
- Use `seaborn` instead when you need automatic statistical aggregation (confidence intervals, regression fits) with minimal code.
- Use `matplotlib` when you need fine-grained control over every axis element for print-ready publication figures at exact journal specifications.
## Prerequisites
- **Python packages**: `plotly`, `kaleido` (static image export), `pandas`, `numpy`
- **Data requirements**: pandas DataFrames or NumPy arrays; long-form (tidy) data works best with `px`
- **Environment**: Jupyter Lab/Notebook (inline rendering), or save as HTML for browser display
```bash
pip install plotly kaleido pandas numpy
```
For Jupyter Lab inline rendering (if not automatic):
```bash
pip install "jupyterlab>=3" ipywidgets
```
## Quick Start
```python
import plotly.express as px
import pandas as pd
# Gene expression scatter with hover info
df = pd.DataFrame({
"log2FC": [-3.1, 0.2, 1.8, 2.5, -0.5, 4.1],
"neg_log10_padj": [8.2, 0.4, 2.1, 6.8, 0.1, 9.3],
"gene": ["BRCA1", "MYC", "TP53", "EGFR", "CDKN1A", "KRAS"],
"significance": ["sig", "ns", "ns", "sig", "ns", "sig"],
})
fig = px.scatter(
df, x="log2FC", y="neg_log10_padj",
color="significance", hover_name="gene",
title="Volcano Plot — Treatment vs Control",
)
fig.show()
```
## Core API
### Module 1: px Scatter and Line — Relational Plots
`px.scatter()` and `px.line()` map DataFrame columns to visual encodings (color, symbol, size) and automatically populate hover tooltips from `hover_data`.
```python
import plotly.express as px
import pandas as pd
import numpy as np
# Dose-response scatter: color by drug, symbol by cell line
np.random.seed(42)
df = pd.DataFrame({
"dose_uM": np.tile([0.01, 0.1, 1, 10, 100], 4),
"viability": np.clip(np.random.normal(
[100, 90, 70, 40, 10] * 4, 5), 0, 110),
"drug": ["DrugA"] * 5 + ["DrugA"] * 5 + ["DrugB"] * 5 + ["DrugB"] * 5,
"cell_line": ["HCT116"] * 10 + ["MCF7"] * 10,
"replicate": np.tile([1, 2, 3, 4, 5], 4),
})
fig = px.scatter(
df, x="dose_uM", y="viability",
color="drug", symbol="cell_line",
log_x=True,
hover_data={"replicate": True, "dose_uM": ":.2f"},
labels={"viability": "Cell Viability (%)", "dose_uM": "Dose (µM)"},
title="Dose-Response by Drug and Cell Line",
)
fig.show()
print(f"Figure has {len(fig.data)} traces")
```
```python
# Time-course gene expression line plot
time_df = pd.DataFrame({
"hour": list(range(0, 25, 4)) * 3,
"expression": [1.0, 1.8, 3.2, 4.5, 3.8, 2.1, 1.2,
1.0, 2.5, 5.1, 6.8, 5.5, 3.2, 1.8,
1.0, 1.1, 1.0, 1.2, 1.1, 1.0, 0.9],
"gene": ["MYC"] * 7 + ["EGFR"] * 7 + ["GAPDH"] * 7,
})
fig = px.line(
time_df, x="hour", y="expression",
color="gene", markers=True,
labels={"expression": "Relative Expression (log2)", "hour": "Time (h)"},
title="Time-Course Gene Expression",
)
fig.update_traces(line=dict(width=2.5), marker=dict(size=8))
fig.show()
```
### Module 2: px Statistical Plots — Distributions and Categories
`px.box()`, `px.violin()`, `px.histogram()`, and `px.strip()` produce publication-ready distribution summaries with built-in grouping.
```python
import plotly.express as px
import pandas as pd
import numpy as np
# Violin + strip overlay: expression by cell type
np.random.seed(7)
n = 60
cell_data = pd.DataFrame({
"expression": np.concatenate([
np.random.normal(4.2, 0.8, n),
np.random.normal(6.5, 1.2, n),
np.random.normal(2.8, 0.6, n),
]),
"cell_type": ["T cell"] * n + ["B cell"] * n + ["NK cell"] * n,
"patient_id": np.tile([f"P{i:02d}" for i in range(1, 11)], 18),
})
fig = px.violin(
cell_data, x="cell_type", y="expression",
color="cell_type", box=True, points="all",
hover_data=["patient_id"],
labels={"expression": "CD3E Expression (log2 CPM)"},
title="CD3E Expression Across Cell Types",
)
fig.update_traces(jitter=0.3, pointpos=-1.5)
fig.show()
print(f"Cells per type: {cell_data.groupby('cell_type').size().to_dict()}")
```
```python
# Histogram with rug: distribution of fold changes
fc_df = pd.DataFrame({
"log2FC": np.concatenate([
np.random.normal(0.1, 0.8, 500), # not DE genes
np.random.normal(2.5, 0.4, 50), # upregulated
np.random.normal(-2.3, 0.4, 40), # downregulated
]),
"category": ["background"] * 500 + ["up"] * 50 + ["down"] * 40,
})
fig = px.histogram(
fc_df, x="log2FC", color="category",
nbins=60, barmode="overlay", opacity=0.7,
marginal="rug",
labels={"log2FC": "log2 Fold Change", "count": "Gene Count"},
title="Distribution of Fold Changes (DESeq2 Results)",
color_discrete_map={"background": "gray", "up": "crimson", "down": "steelblue"},
)
fig.show()
```
### Module 3: px Heatmap and Matrix — Gene Expression and Correlations
`px.imshow()` renders 2D arrays or DataFrames as color-encoded matrices, ideal for expression heatmaps and correlation matrices.
```python
import plotly.express as px
import pandas as pd
import numpy as np
# Gene expression heatmap (genes × samples)
np.random.seed(12)
genes = [f"Gene_{g}" for g in ["BRCA1", "TP53", "EGFR", "MYC", "KRAS",
"CDKN1A", "RB1", "PTEN", "VHL", "APC"]]
samples = [f"S{i:02d}" for i in range(1, 9)]
expr_matrix = pd.DataFrame(
np.random.normal(0, 1.5, (10, 8)) +
np.array([2, -1, 3, -2, 1, -3, 0, 2, -1, 3]).reshape(-1, 1),
index=genes, columns=samples,
)
fig = px.imshow(
expr_matrix,
color_continuous_scale="RdBu_r",
color_continuous_midpoint=0,
aspect="auto",
labels={"color": "log2 Expression (z-score)"},
title="Gene Expression Heatmap",
)
fig.update_xaxes(side="top")
fig.update_layout(width=600, height=500)
fig.show()
print(f"Heatmap shape: {expr_matrix.shape} (genes × samples)")
```
```python
# Correlation matrix heatmap
from itertools import combinations
markers = ["IL6", "TNF", "CXCL10", "IFNg", "IL10", "IL1B", "CCL2", "IL17A"]
np.random.seed(3)
raw = np.random.multivariate_normal(
mean=np.zeros(8),
cov=np.eye(8) * 0.3 + 0.7,
size=80,
)
corr_df = pd.DataFrame(raw, columns=markers).corr()
fig = px.imshow(
corr_df,
color_continuous_scale="RdBu_r",
color_continuous_midpoint=0,
zmin=-1, zmax=1,
text_auto=".2f",
title="Cytokine Correlation Matrix (n=80 patients)",
)
fig.update_traces(textfont_size=10)
fig.show()
```
### Module 4: go Graph Objects — Full Trace Control
`plotly.graph_objects` provides fine-grained access to every trace property: marker symbols, error bars, fill areas, and multi-trace layouts. Essential when `px` lacks the flexibility you need.
```python
import plotly.graph_objects as go
import numpy as np
# Volcano plot built from scratch with go.Scatter
np.random.seed(99)
n_genes = 5000
log2fc = np.random.normal(0, 1.2, n_genes)
pval = np.random.uniform(0, 1, n_genes) ** 2 # skew toward low p-values
neg_log10_p = -np.log10(pval + 1e-300)
gene_names = [f"Gene_{i:04d}" for i in range(n_genes)]
# Classify genes
sig_mask = (np.abs(log2fc) > 1.5) & (neg_log10_p > 3)
up_mask = sig_mask & (log2fc > 0)
down_mask = sig_mask & (log2fc < 0)
ns_mask = ~sig_mask
fig = go.Figure()
# Non-significant background
fig.add_trace(go.Scatter(
x=log2fc[ns_mask], y=neg_log10_p[ns_mask],
mode="markers",
name="Not significant",
marker=dict(color="lightgray", size=4, opacity=0.5),
text=[gene_names[i] for i in np.where(ns_mask)[0]],
hovertemplate="<b>%{text}</b><br>log2FC: %{x:.2f}<br>-log10(p): %{y:.2f}<extra></extra>",
))
# Upregulated
fig.add_trace(go.Scatter(
x=log2fc[up_mask], y=neg_log10_p[up_mask],
mode="markers",
name=f"Up ({up_mask.sum()} genes)",
marker=dict(color="crimson", size=7, opacity=0.8),
text=[gene_names[i] for i in np.where(up_mask)[0]],
hovertemplate="<b>%{text}</b><br>log2FC: %{x:.2f}<br>-log10(p): %{y:.2f}<extra></extra>",
))
# Downregulated
fig.add_trace(go.Scatter(
x=log2fc[down_mask], y=neg_log10_p[down_mask],
mode="markers",
name=f"Down ({down_mask.sum()} genes)",
marker=dict(color="steelblue", size=7, opacity=0.8),
text=[gene_names[i] for i in np.where(down_mask)[0]],
hovertemplate="<b>%{text}</b><br>log2FC: %{x:.2f}<br>-log10(p): %{y:.2f}<extra></extra>",
))
# Threshold lines
fig.add_hline(y=3, line_dash="dash", line_color="black", line_width=1)
fig.add_vline(x=1.5, line_dash="dash", line_color="black", line_width=1)
fig.add_vline(x=-1.5, line_dash="dash", line_color="black", line_width=1)
fig.update_layout(
title="Volcano Plot (Treatment vs Control, n=5000 genes)",
xaxis_title="log2 Fold Change",
yaxis_title="-log10(adjusted p-value)",
legend=dict(x=0.01, y=0.99),
width=750, height=550,
)
fig.show()
print(f"Up: {up_mask.sum()}, Down: {down_mask.sum()}, NS: {ns_mask.sum()}")
```
```python
# Bar chart with error bars: mean ± SEM per treatment group
groups = ["Vehicle", "DrugA 1µM", "DrugA 10µM", "DrugB 1µM", "DrugB 10µM"]
means = [100.0, 82.3, 54.7, 91.2, 68.5]
sems = [3.2, 4.1, 3.8, 3.5, 4.7]
fig = go.Figure(go.Bar(
x=groups, y=means,
error_y=dict(type="data", array=sems, visible=True),
marker_color=["gray", "lightsalmon", "crimson", "lightblue", "steelblue"],
hovertemplate="%{x}<br>Mean: %{y:.1f}%<br>SEM: ±%{error_y.array:.1f}%<extra></extra>",
))
fig.update_layout(
title="Cell Viability by Treatment (Mean ± SEM, n=6)",
yaxis_title="Viability (%)", yaxis_range=[0, 120],
xaxis_title="Treatment Group",
showlegend=False,
)
fig.show()
```
### Module 5: 3D and Specialized Charts
Plotly supports 3D scatter, surface plots, parallel coordinates, and treemaps — chart types unavailable in seaborn or standard matplotlib.
```python
import plotly.express as px
import numpy as np
import pandas as pd
# 3D PCA scatter: cell clusters in embedding space
np.random.seed(42)
n_per_cluster = 80
cluster_centers = {"T cell": [3, 2, 1], "B cell": [-3, 1, 2], "Monocyte": [0, -3, -1]}
records = []
for ctype, center in cluster_centers.items():
coords = np.random.normal(center, 0.8, (n_per_cluster, 3))
for row in coords:
records.append({
"PC1": row[0], "PC2": row[1], "PC3": row[2],
"cell_type": ctype,
"score": np.random.uniform(0.5, 1.0),
})
pca_df = pd.DataFrame(records)
fig = px.scatter_3d(
pca_df, x="PC1", y="PC2", z="PC3",
color="cell_type", size="score", opacity=0.7,
hover_data={"score": ":.3f"},
title="3D PCA — Single-Cell Transcriptomics",
)
fig.update_traces(marker=dict(sizeref=0.04))
fig.show()
print(f"Total cells: {len(pca_df)}, clusters: {pca_df['cell_type'].nunique()}")
```
```python
import plotly.graph_objects as go
import numpy as np
import pandas as pd
# Parallel coordinates: multi-parameter drug screen
np.random.seed(5)
n_compounds = 200
drug_df = pd.DataFrame({
"MW": np.random.normal(380, 60, n_compounds),
"logP": np.random.uniform(-1, 6, n_compounds),
"HBA": np.random.randint(2, 10, n_compounds),
"HBD": np.random.randint(0, 6, n_compounds),
"IC50_nM": np.random.lognormal(4, 1.5, n_compounds),
"selectivity": np.random.uniform(1, 100, n_compounds),
})
fig = px.parallel_coordinates(
drug_df,
color="IC50_nM",
color_continuous_scale="RdYlGn_r",
dimensions=["MW", "logP", "HBA", "HBD", "IC50_nM", "selectivity"],
labels={
"MW": "MW (Da)", "logP": "logP",
"HBA": "H-Bond Acceptors", "HBD": "H-Bond Donors",
"IC50_nM": "IC50 (nM)", "selectivity": "Selectivity Index",
},
title="Drug Candidate Properties — Parallel Coordinates",
)
fig.show()
```
### Module 6: Subplots and Export
`make_subplots()` creates multi-panel layouts with shared axes, mixed chart types, and independent traces per panel. `fig.write_html()` exports interactive figures; `fig.write_image()` exports static files via kaleido.
```python
from plotly.subplots import make_subplots
import plotly.graph_objects as go
import numpy as np
# Two-panel: raw data + summary statistics
np.random.seed(77)
doses = [0.01, 0.1, 1, 10, 100]
drugs = {"DrugA": {"EC50": 1.0, "hill": 1.5}, "DrugB": {"EC50": 8.0, "hill": 0.9}}
def hill_curve(dose, ec50, hill, top=100, bottom=0):
return bottom + (top - bottom) / (1 + (ec50 / dose) ** hill)
fig = make_subplots(
rows=1, cols=2,
subplot_titles=["Dose-Response Curves", "IC50 Comparison"],
shared_yaxes=False,
)
colors = {"DrugA": "crimson", "DrugB": "steelblue"}
ic50_values = []
for drug, params in drugs.items():
# Smooth fit curve
x_fit = np.logspace(-2, 2, 200)
y_fit = hill_curve(x_fit, params["EC50"], params["hill"])
fig.add_trace(go.Scatter(
x=x_fit, y=y_fit, mode="lines",
name=f"{drug} fit", line=dict(color=colors[drug], width=2.5),
), row=1, col=1)
# Noisy data points
y_data = [hill_curve(d, params["EC50"], params["hill"]) +
np.random.normal(0, 4) for d in doses]
fig.add_trace(go.Scatter(
x=doses, y=y_data, mode="markers",
name=f"{drug} data", marker=dict(color=colors[drug], size=9),
showlegend=False,
), row=1, col=1)
ic50_values.append(params["EC50"])
# Bar chart of IC50 values
fig.add_trace(go.Bar(
x=list(drugs.keys()), y=ic50_values,
marker_color=list(colors.values()),
showlegend=False,
hovertemplate="%{x}<br>IC50: %{y:.2f} µM<extra></extra>",
), row=1, col=2)
fig.update_xaxes(type="log", title_text="Dose (µM)", row=1, col=1)
fig.update_yaxes(title_text="Viability (%)", row=1, col=1)
fig.update_xaxes(title_text="Drug", row=1, col=2)
fig.update_yaxes(title_text="IC50 (µM)", row=1, col=2)
fig.update_layout(title="Dose-Response Dashboard", height=450, width=850)
fig.show()
print(f"Subplots: {len(fig.data)} traces across 2 panels")
```
```python
# Export to HTML (interactive) and PNG (static)
# Requires: pip install kaleido
fig.write_html("dose_response_dashboard.html")
print("Saved: dose_response_dashboard.html (interactive, shareable)")
fig.write_image("dose_response_dashboard.png", width=1200, height=600, scale=2)
print("Saved: dose_response_dashboard.png (300 DPI equivalent with scale=2)")
fig.write_image("dose_response_dashboard.svg")
print("Saved: dose_response_dashboard.svg (vector, editable in Inkscape/Illustrator)")
```
## Common Workflows
### Workflow 1: Interactive Volcano Plot with Gene Annotations
**Goal**: Build a fully annotated volcano plot from DESeq2 results, with gene-name hover tooltips, threshold lines, and highlighted hit labels for sharing as HTML.
```python
import plotly.graph_objects as go
import pandas as pd
import numpy as np
# Simulate DESeq2 output (replace with pd.read_csv("deseq2_results.csv"))
np.random.seed(42)
n = 3000
df = pd.DataFrame({
"gene": [f"GENE_{i:04d}" for i in range(n)],
"log2FC": np.random.normal(0, 1.0, n),
"padj": np.clip(np.random.exponential(0.1, n), 1e-20, 1.0),
"baseMean": np.random.lognormal(5, 1.5, n),
})
# Inject some hits
df.loc[:20, "log2FC"] = np.random.uniform(2.5, 5, 21)
df.loc[:20, "padj"] = np.random.uniform(1e-15, 1e-5, 21)
df.loc[21:35, "log2FC"] = np.random.uniform(-4, -2, 15)
df.loc[21:35, "padj"] = np.random.uniform(1e-12, 1e-4, 15)
df["neg_log10_padj"] = -np.log10(df["padj"].clip(1e-300))
# Classify
FC_THRESH, P_THRESH = 1.5, 2.0 # |log2FC| > 1.5, -log10(padj) > 2
df["category"] = "NS"
df.loc[(df["log2FC"] > FC_THRESH) & (df["neg_log10_padj"] > P_THRESH), "category"] = "Up"
df.loc[(df["log2FC"] < -FC_THRESH) & (df["neg_log10_padj"] > P_THRESH), "category"] = "Down"
color_map = {"NS": "lightgray", "Up": "crimson", "Down": "steelblue"}
size_map = {"NS": 4, "Up": 7, "Down": 7}
opacity_map = {"NS": 0.4, "Up": 0.85, "Down": 0.85}
fig = go.Figure()
for cat in ["NS", "Up", "Down"]:
sub = df[df["category"] == cat]
fig.add_trace(go.Scatter(
x=sub["log2FC"], y=sub["neg_log10_padj"],
mode="markers",
name=f"{cat} (n={len(sub)})",
marker=dict(
color=color_map[cat],
size=size_map[cat],
opacity=opacity_map[cat],
),
customdata=sub[["gene", "padj", "baseMean"]].values,
hovertemplate=(
"<b>%{customdata[0]}</b><br>"
"log2FC: %{x:.3f}<br>"
"padj: %{customdata[1]:.2e}<br>"
"baseMean: %{customdata[2]:.1f}<extra></extra>"
),
))
# Threshold lines
fig.add_hline(y=P_THRESH, line_dash="dot", line_color="black", line_width=1.2,
annotation_text=f"padj=0.01", annotation_position="right")
fig.add_vline(x=FC_THRESH, line_dash="dot", line_color="black", line_width=1.2)
fig.add_vline(x=-FC_THRESH, line_dash="dot", line_color="black", line_width=1.2)
# Label top 5 upregulated hits by significance
top_up = df[df["category"] == "Up"].nlargest(5, "neg_log10_padj")
for _, row in top_up.iterrows():
fig.add_annotation(
x=row["log2FC"], y=row["neg_log10_padj"],
text=row["gene"], showarrow=True,
arrowhead=2, arrowsize=1, arrowcolor="crimson",
font=dict(size=9, color="crimson"),
xshift=8, yshift=5,
)
fig.update_layout(
title="Volcano Plot — Treatment vs Control (DESeq2)",
xaxis_title="log2 Fold Change",
yaxis_title="-log10(adjusted p-value)",
legend=dict(x=0.01, y=0.99, bordercolor="lightgray", borderwidth=1),
width=800, height=560,
plot_bgcolor="white",
)
fig.update_xaxes(showgrid=True, gridcolor="lightgray", zeroline=True, zerolinecolor="darkgray")
fig.update_yaxes(showgrid=True, gridcolor="lightgray")
fig.write_html("volcano_interactive.html")
print(f"Up: {(df.category=='Up').sum()}, Down: {(df.category=='Down').sum()}")
print("Saved: volcano_interactive.html")
```
### Workflow 2: Multi-Panel Dose-Response Dashboard with make_subplots
**Goal**: Display dose-response curves for multiple drugs across cell lines in a grid layout with a shared color scale and consistent formatting.
```python
from plotly.subplots import make_subplots
import plotly.graph_objects as go
import numpy as np
import pandas as pd
# Simulated IC50 data for 3 drugs × 3 cell lines
np.random.seed(10)
drugs = ["DrugA", "DrugB", "DrugC"]
cell_lines = ["HCT116", "MCF7", "A549"]
doses = np.logspace(-2, 2, 7) # 0.01 to 100 µM
def hill(x, ec50, hill_n, top=100, bottom=0):
return bottom + (top - bottom) / (1 + (ec50 / x) ** hill_n)
ec50_table = {
("DrugA", "HCT116"): 0.5, ("DrugA", "MCF7"): 2.0, ("DrugA", "A549"): 8.0,
("DrugB", "HCT116"): 5.0, ("DrugB", "MCF7"): 0.8, ("DrugB", "A549"): 15.0,
("DrugC", "HCT116"): 12.0, ("DrugC", "MCF7"): 6.0, ("DrugC", "A549"): 1.2,
}
palette = px_colors = ["#EF553B", "#636EFA", "#00CC96", "#AB63FA", "#FFA15A",
"#19D3F3", "#FF6692", "#B6E880", "#FF97FF"]
fig = make_subplots(
rows=len(drugs), cols=len(cell_lines),
subplot_titles=[f"{d} / {c}" for d in drugs for c in cell_lines],
shared_xaxes=True, shared_yaxes=True,
vertical_spacing=0.08, horizontal_spacing=0.04,
)
for r, drug in enumerate(drugs, start=1):
for c, cell_line in enumerate(cell_lines, start=1):
ec50 = ec50_table[(drug, cell_line)]
x_fit = np.logspace(-2, 2, 200)
y_fit = hill(x_fit, ec50, hill_n=1.5)
# Noisy replicate data
y_data = np.array([hill(d, ec50, 1.5) + np.random.normal(0, 5) for d in doses])
color = palette[(r - 1) * len(cell_lines) + (c - 1)]
show_legend = (c == 1 and r == 1)
fig.add_trace(go.Scatter(
x=x_fit, y=y_fit, mode="lines",
line=dict(color=color, width=2),
name=f"{drug}/{cell_line}",
showlegend=False,
hovertemplate=f"{drug} in {cell_line}<br>Dose: %{{x:.2f}} µM<br>Viability: %{{y:.1f}}%<extra></extra>",
), row=r, col=c)
fig.add_trace(go.Scatter(
x=doses, y=np.clip(y_data, 0, 110), mode="markers",
marker=dict(color=color, size=7, opacity=0.8),
showlegend=False,
hovertemplate=f"Measured<br>Dose: %{{x:.2f}} µM<br>Viability: %{{y:.1f}}%<extra></extra>",
), row=r, col=c)
# IC50 annotation
fig.add_annotation(
x=np.log10(ec50), y=50,
text=f"IC50={ec50:.1f}µM",
font=dict(size=8), showarrow=False,
xref=f"x{(r-1)*len(cell_lines)+c if (r-1)*len(cell_lines)+c > 1 else ''}",
yref=f"y{(r-1)*len(cell_lines)+c if (r-1)*len(cell_lines)+c > 1 else ''}",
)
# Apply log scale to all x-axes
for i in range(1, len(drugs) * len(cell_lines) + 1):
axis_key = f"xaxis{i if i > 1 else ''}"
fig.layout[axis_key].update(type="log", title_text="Dose (µM)" if i > 6 else "")
for i in range(1, len(drugs) * len(cell_lines) + 1):
axis_key = f"yaxis{i if i > 1 else ''}"
fig.layout[axis_key].update(range=[-5, 115],
title_text="Viability (%)" if i in [1, 4, 7] else "")
fig.update_layout(
title="Dose-Response Dashboard — 3 Drugs × 3 Cell Lines",
height=700, width=900,
)
fig.write_html("dose_response_dashboard.html")
print("Saved: dose_response_dashboard.html")
print(f"Grid: {len(drugs)} drugs × {len(cell_lines)} cell lines = {len(drugs)*len(cell_lines)} panels")
```
## Key Parameters
| Parameter | Module / Function | Default | Range / Options | Effect |
|-----------|------------------|---------|-----------------|--------|
| `color` | `px.*` | `None` | Column name | Maps a DataFrame column to trace color; auto-assigns palette |
| `hover_data` | `px.*` | `{}` | Dict or list of column names | Extra columns shown in hover tooltip |
| `log_x` / `log_y` | `px.*` | `False` | `True`, `False` | Apply log10 scale to x or y axis |
| `facet_col` / `facet_row` | `px.*` | `None` | Column name | Split into subplot grid by a categorical variable |
| `color_continuous_scale` | `px.imshow`, `px.scatter` | `"plasma"` | `"RdBu_r"`, `"Viridis"`, `"Hot"`, etc. | Colormap for continuous color mapping |
| `color_continuous_midpoint` | `px.imshow` | `None` | Any numeric | Centers the diverging colormap at this value (use `0` for z-scores) |
| `barmode` | `px.histogram`, `px.bar` | `"relative"` | `"relative"`, `"overlay"`, `"group"` | How multiple bar traces are displayed |
| `opacity` | `go.Scatter`, `px.*` | `1.0` | `0.0`–`1.0` | Point/bar transparency |
| `size` / `sizeref` | `go.Scatter` | `6` / auto | Positive numeric | Marker size; `sizeref` normalizes sizes across traces |
| `line_dash` | `fig.add_hline`, `go.Scatter` | `"solid"` | `"solid"`, `"dash"`, `"dot"`, `"dashdot"` | Line style for reference lines and traces |
| `shared_xaxes` / `shared_yaxes` | `make_subplots` | `False` | `True`, `False`, `"rows"`, `"cols"` | Link axes across subplot panels |
| `scale` | `fig.write_image` | `1` | `1`–`4` | Resolution multiplier for PNG export (use `2` for ~150 DPI) |
## Best Practices
1. **Prefer `px` for DataFrame data, fall back to `go` for multi-trace composition.** Use `px.scatter()` and its siblings for 80% of plots. Switch to `go` when you need traces with different types in the same figure (e.g., scatter + filled area) or need fine-grained per-trace control.
```python
# Correct: px for simple grouped plots
fig = px.box(df, x="treatment", y="expression", color="genotype")
# Correct: go when px cannot express the structure
fig = go.Figure()
fig.add_trace(go.Scatter(x=x, y=y_upper, fill="tonexty", ...))
fig.add_trace(go.Scatter(x=x, y=y_lower, ...))
```
2. **Always include `hovertemplate` for scientific figures.** The default tooltip shows raw coordinates without units or gene names. A custom template with `customdata` provides full biological context.
```python
fig.add_trace(go.Scatter(
customdata=df[["gene", "padj"]].values,
hovertemplate="<b>%{customdata[0]}</b><br>padj: %{customdata[1]:.2e}<extra></extra>",
))
```
3. **Export HTML for sharing, PNG/SVG for journals.** `fig.write_html()` produces a self-contained file with no external dependencies. Use `scale=2` or higher with `write_image()` to achieve sufficient resolution for print.
4. **Don't use `fig.show()` in batch scripts.** In non-interactive contexts (CI, HPC, cron jobs), `fig.show()` may open a browser window or fail. Use `write_html()` or `write_image()` exclusively.
5. **Use `color_continuous_midpoint=0` for diverging palettes on z-score data.** Without it, the midpoint color defaults to the data midpoint, not zero, misrepresenting symmetric fold changes or correlations.
```python
fig = px.imshow(corr_matrix, color_continuous_scale="RdBu_r",
color_continuous_midpoint=0, zmin=-1, zmax=1)
```
6. **Set `plot_bgcolor="white"` for publication figures.** Plotly defaults to a light-gray grid background. White background with subtle gridlines is cleaner for most scientific contexts.
```python
fig.update_layout(plot_bgcolor="white")
fig.update_xaxes(showgrid=True, gridcolor="lightgray")
fig.update_yaxes(showgrid=True, gridcolor="lightgray")
```
## Common Recipes
### Recipe: Dropdown Menu to Toggle Between Conditions
When to use: Overlay multiple conditions in one figure with a dropdown button to show/hide individual traces cleanly.
```python
import plotly.graph_objects as go
import numpy as np
conditions = ["Untreated", "DrugA", "DrugB"]
colors = ["gray", "crimson", "steelblue"]
np.random.seed(1)
x = np.linspace(0, 24, 49)
fig = go.Figure()
for i, (cond, color) in enumerate(zip(conditions, colors)):
y = np.sin(x / 4 + i * 0.5) * (1 - i * 0.2) + np.random.normal(0, 0.05, len(x))
fig.add_trace(go.Scatter(
x=x, y=y, mode="lines+markers",
name=cond, line=dict(color=color, width=2),
visible=(i == 0), # only first trace visible initially
))
# One button per condition (shows only that trace)
buttons = []
for i, cond in enumerate(conditions):
visibility = [j == i for j in range(len(conditions))]
buttons.append(dict(label=cond, method="update",
args=[{"visible": visibility}, {"title": f"Gene Expression — {cond}"}]))
# "Show All" button
buttons.append(dict(label="Show All", method="update",
args=[{"visible": [True] * len(conditions)}, {"title": "Gene Expression — All Conditions"}]))
fig.update_layout(
updatemenus=[dict(type="dropdown", x=0.01, y=1.15, showactive=True, buttons=buttons)],
title="Gene Expression — Untreated",
xaxis_title="Time (h)", yaxis_title="Relative Expression",
)
fig.show()
```
### Recipe: Annotating Specific Hits with Arrows
When to use: Label outliers, drug hits, or significant genes directly on the figure without cluttering non-annotated points.
```python
import plotly.graph_objects as go
import numpy as np
import pandas as pd
np.random.seed(33)
df = pd.DataFrame({
"x": np.random.normal(0, 1.5, 300),
"y": np.random.normal(0, 1.5, 300),
"gene": [f"G{i:03d}" for i in range(300)],
})
# Inject top hits
hits = pd.DataFrame({
"x": [3.2, -2.8, 2.5, -3.5],
"y": [4.1, 3.8, -3.2, -2.9],
"gene": ["BRCA1", "TP53", "EGFR", "KRAS"],
})
fig = go.Figure()
fig.add_trace(go.Scatter(
x=df["x"], y=df["y"], mode="markers",
marker=dict(color="lightgray", size=5, opacity=0.6),
text=df["gene"],
hovertemplate="<b>%{text}</b><br>x: %{x:.2f}, y: %{y:.2f}<extra></extra>",
name="Background",
))
fig.add_trace(go.Scatter(
x=hits["x"], y=hits["y"], mode="markers",
marker=dict(color="crimson", size=10, symbol="diamond"),
text=hits["gene"],
hovertemplate="<b>%{text}</b> [HIT]<br>x: %{x:.2f}, y: %{y:.2f}<extra></extra>",
name="Hits",
))
for _, row in hits.iterrows():
fig.add_annotation(
x=row["x"], y=row["y"],
text=f"<b>{row['gene']}</b>",
showarrow=True, arrowhead=2, arrowwidth=1.5,
arrowcolor="crimson", font=dict(size=11, color="crimson"),
ax=25, ay=-30, # arrow offset in pixels
bgcolor="rgba(255,255,255,0.7)", bordercolor="crimson", borderwidth=1,
)
fig.update_layout(
title="Hit Identification with Arrow Annotations",
xaxis_title="Score A", yaxis_title="Score B",
plot_bgcolor="white",
)
fig.show()
```
## Troubleshooting
| Problem | Cause | Solution |
|---------|-------|----------|
| `ValueError: kaleido is required for static image export` | `kaleido` not installed | `pip install kaleido`; verify with `import kaleido` |
| Blank figure in Jupyter Notebook | Renderer not configured | Run `import plotly.io as pio; pio.renderers.default = "notebook"` or upgrade JupyterLab to ≥3 |
| `fig.show()` opens blank browser tab | No data in figure or offline renderer issue | Check `len(fig.data) > 0`; use `pio.renderers.default = "browser"` |
| Hover tooltips show wrong values | `customdata` index mismatch in `hovertemplate` | Verify `customdata` column order matches `%{customdata[N]}` indices in template |
| Colors not assigned consistently across traces | `px` re-orders palette when category counts differ | Use `color_discrete_map={"Cat1": "#color1", ...}` to pin colors explicitly |
| `write_image` produces blurry PNG | Default `scale=1` is too low for print | Use `fig.write_image("fig.png", scale=2)` for 150 DPI or `scale=4` for 300 DPI |
| Subplots x-axes not all log-scaled after `shared_xaxes=True` | Shared axis only synchronizes range, not type | Iterate over all `xaxis` keys in `fig.layout` and set `type="log"` explicitly |
| Large datasets slow to render in browser | Too many individual points in a single scatter trace | Downsample background noise points; keep labeled hits as a separate, smaller trace |
| `fig.update_layout` does not apply to subplot axes | Multi-panel figures use indexed axes (`xaxis2`, `xaxis3`) | Use `fig.update_xaxes()` (applies to all) or target `fig.layout["xaxis2"]` explicitly |
## Related Skills
- **seaborn-statistical-plots** — use for statistical aggregation (confidence intervals, regression), publication-quality static figures with minimal code, and when matplotlib-level output is required
- **matplotlib-scientific-plotting** — use for full control over every figure element, custom layouts, embedded text rendering, and journal-specification figure preparation
- **pydeseq2-differential-expression** — volcano plot outputs from DESeq2 results are a primary input for the interactive volcano workflow above
- **scanpy-scrna-seq** — Scanpy's UMAP embeddings can be visualized interactively in 3D with `px.scatter_3d`
## References
- [Plotly Python Documentation](https://plotly.com/python/) — official API reference, examples gallery, and getting-started guides
- [Plotly Express API Reference](https://plotly.com/python-api-reference/plotly.express.html) — complete `px` function signatures and parameters
- [Plotly Graph Objects Reference](https://plotly.com/python/graph-objects/) — full `go` trace and layout attribute reference
- [Plotly GitHub Repository](https://github.com/plotly/plotly.py) — source code, issue tracker, changelog
- [Kaleido Static Image Export](https://github.com/plotly/Kaleido) — dependency for `write_image()` PNG/SVG/PDF export
Is this your skill, or is something wrong with this listing? Request removal or report an issue. Author removals are honored within 72 hours.
No comments yet. Be the first to comment!