AGENT SKILL

plotly-interactive-plots

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 许可
MIT
所属仓库
bg-szy/TOP-SKILLS
最近更新
2026-11-15
Stars
★ 6
Forks
0

01 前言 Front Matter

name
plotly-interactive-plots
license
MIT
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.

03 SKILL.md 正文

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
pip install plotly kaleido pandas numpy

For Jupyter Lab inline rendering (if not automatic):

pip install "jupyterlab>=3" ipywidgets

Quick Start

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.

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")
# 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.

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()}")
# 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.

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)")
# 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.

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()}")
# 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.

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()}")
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.

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")
# 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.

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.

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.

    # 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.

    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.

    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.

    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.

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.

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

04 同仓库更多 Skills

bg-szy
bg-szy/TOP-SKILLS

serpmaven

Scrape Google search results (SERP) to JSON with SERP Maven (serpmaven) - a real Chrome browser on a residential proxy with sticky sessions. Run it as a CLI, a Python library, a local HTTP search API (`serve`), an MCP server or a Docker image; set the proxy login, workers, pages and cost tracking. Use when the user wants Google results, rank tracking, a self-hosted SERP API, or live Google search for an AI agent.

★ 6
bg-szy
bg-szy/TOP-SKILLS

revnu-landing-page-audit

Find out why a landing page isn't turning visitors into signups, demos or sales. Audits one page against what the ad, post or search that sends people there promised, then checks the first screen, proof, call to action, friction and mobile. Returns at most 7 prioritized fixes, plus what is fine and what could not be checked; rewrites specific lines and fixes the page in the repo when asked. Never promises a conversion lift. Works without a Revnu account. Use when the user says or asks: "audit my landing page", "why isn't this page converting", "review my homepage", "my ads get clicks but no signups", "people bounce from the pricing page", "CRO review", "improve conversion rate", "is my hero section clear", "roast my landing page", "rewrite my headline", "what's wrong with this page", "landing page feedback", "make the signup page convert better". Not for SEO or AI-search audits, page speed engineering on its own, or building a new page from scratch.

★ 6
bg-szy
bg-szy/TOP-SKILLS

revnu-growth-context

Write down once who buys, what they're stuck on, what it costs, what proof you have and what you've already tried, so every growth task starts from facts instead of a questionnaire. Creates or updates .agents/revnu-growth.md from the repo, the live site and the user, and imports an existing product-marketing.md. Use when the user says "set up our marketing context", "who is our ideal customer", "write our ICP", "describe the product for marketing", "positioning doc", "what's our brand voice", "remember this about our customers", "log what we tried", "what have we learned from marketing", "we changed pricing, update the context", "update our growth notes", "summarize the business for the agent", "import my product-marketing.md", "start a growth doc", or before a first marketing, SEO, outreach or launch task when no context file exists. Works without a Revnu account.

★ 6
bg-szy
bg-szy/TOP-SKILLS

revnu-get-listed

Get onto the third-party pages AI answers and search cite when buyers ask for the best tool in your category: "best X" roundups, directories, review sites, GitHub awesome lists, community threads and comparison pages. Finds which ones are cited, ranks them by fit and effort, and drafts each submission, PR or pitch by the target's own rules. Use when the user says "get us listed", "which directories should we submit to", "how do we get into best-of lists", "why does ChatGPT recommend competitors and not us", "get mentioned in AI answers", "submit to awesome lists", "get on G2", "where are our competitors listed", "pitch listicle authors", "find backlink opportunities", "launch directories", "get into roundups", "Product Hunt alternatives", "where should we be listed", "get cited by Perplexity". Never submits, pays or posts without a yes. Works without a Revnu account.

★ 6
bg-szy
bg-szy/TOP-SKILLS

revnu-ai-readiness-audit

Audit whether your website gives ChatGPT, Perplexity, Claude, Gemini and Google's AI Overviews something worth quoting, and fix the pages that don't. Use when the user says or asks "is my site ready for AI search", "audit my site for AI answers", "AEO audit", "GEO audit", "why doesn't ChatGPT quote our pricing", "make our pages citable by AI", "do I need llms.txt", "does schema help with ChatGPT", "check our structured data", "is our content visible without JavaScript", "AI SEO audit", "optimize our homepage for AI answers", "LLM SEO check", "why does AI get our product wrong", "fix our site for AI Overviews". Checks fetchability and indexability, answers in the raw HTML, entity facts, schema (including JS-injected markup), headings, dates and llms.txt, then gives at most 10 prioritised fixes and edits the repo when asked. Works without a Revnu account.

★ 6
bg-szy
bg-szy/TOP-SKILLS

proxy-troubleshooting

Diagnose residential proxy failures, with NodeMaven's gateway as the reference - 407 with correct credentials, 406, 410, 500, a connection that hangs, ERR_TUNNEL_CONNECTION_FAILED in a browser, Playwright or Puppeteer ignoring proxy credentials, a sticky session that changes IP, geo-targeting that is silently ignored, passwords with special characters, and unexpected traffic from headless Chrome. Use when a proxy connection fails, returns the wrong location, or costs more traffic than expected.

★ 6