A scatter plot displaying high-dimensional data projected into 2D space using non-linear dimensionality reduction techniques such as t-SNE or UMAP. Points are colored by cluster or class label, revealing groupings and latent structure in the data. This is a standard visualization in machine learning for exploring embeddings, single-cell RNA-seq data, and NLP document clustering, helping practitioners verify that learned representations capture meaningful distinctions.

""" anyplot.ai
scatter-embedding: t-SNE and UMAP Embedding Visualization
Library: letsplot 4.11.0 | Python 3.13.14
Quality: 94/100 | Updated: 2026-08-11
"""
import os
import shutil
import numpy as np
import pandas as pd
from lets_plot import *
from sklearn.datasets import make_blobs
from sklearn.manifold import TSNE
LetsPlot.setup_html()
# Theme tokens
THEME = os.getenv("ANYPLOT_THEME", "light")
PAGE_BG = "#FAF8F1" if THEME == "light" else "#1A1A17"
ELEVATED_BG = "#FFFDF6" if THEME == "light" else "#242420"
INK = "#1A1A17" if THEME == "light" else "#F0EFE8"
INK_SOFT = "#4A4A44" if THEME == "light" else "#B8B7B0"
# Imprint palette — first series always #009E73
IMPRINT = ["#009E73", "#C475FD", "#4467A3", "#BD8233", "#AE3030", "#2ABCCD"]
# Data — simulate single-cell RNA-seq gene expression then embed via t-SNE
np.random.seed(42)
X, y = make_blobs(n_samples=1500, centers=6, n_features=20, cluster_std=2.8)
cell_types = ["T-cell", "B-cell", "NK-cell", "Monocyte", "Dendritic", "Neutrophil"]
labels = [cell_types[i] for i in y]
tsne = TSNE(n_components=2, perplexity=30, random_state=42, max_iter=1000)
coords = tsne.fit_transform(X)
df = pd.DataFrame({"tsne_1": coords[:, 0], "tsne_2": coords[:, 1], "cell_type": labels})
centroids = df.groupby("cell_type", as_index=False)[["tsne_1", "tsne_2"]].mean()
# Theme — sized for the 3200x1800 canvas (ggsize(800, 450) x scale=4)
anyplot_theme = theme(
plot_background=element_rect(fill=PAGE_BG, color=PAGE_BG),
panel_background=element_rect(fill=PAGE_BG, color=PAGE_BG),
panel_grid_major=element_blank(),
panel_grid_minor=element_blank(),
panel_border=element_blank(),
axis_title=element_text(color=INK, size=12),
axis_text=element_blank(),
axis_ticks=element_blank(),
axis_line=element_blank(),
plot_title=element_text(color=INK, size=16),
plot_subtitle=element_text(color=INK_SOFT, size=13),
legend_background=element_rect(fill=ELEVATED_BG, color=INK_SOFT),
legend_text=element_text(color=INK_SOFT, size=10),
legend_title=element_text(color=INK, size=11),
)
# Plot — points carry a tooltip (cell type + coordinates); centroids get a
# boxed label so clusters are identifiable even with the legend collapsed.
plot = (
ggplot(df, aes(x="tsne_1", y="tsne_2", color="cell_type"))
+ geom_density2d(size=0.4, alpha=0.5, bins=4, show_legend=False)
+ geom_point(
size=2.1,
alpha=0.5,
tooltips=layer_tooltips().line("Cell type|@cell_type").line("t-SNE 1|@tsne_1").line("t-SNE 2|@tsne_2"),
)
+ geom_label(
aes(x="tsne_1", y="tsne_2", label="cell_type"),
data=centroids,
color=INK,
fill=ELEVATED_BG,
size=4,
fontface="bold",
label_padding=0.3,
show_legend=False,
)
+ scale_color_manual(values=IMPRINT)
+ labs(
x="t-SNE 1",
y="t-SNE 2",
color="Cell Type",
title="scatter-embedding · python · letsplot · anyplot.ai",
subtitle="t-SNE (perplexity=30) · Single-cell RNA-seq Cell Type Clusters",
)
+ ggsize(800, 450)
+ anyplot_theme
)
# Save
ggsave(plot, f"plot-{THEME}.png", scale=4, path=".")
ggsave(plot, f"plot-{THEME}.html", path=".")
if os.path.exists("lets-plot-images"):
shutil.rmtree("lets-plot-images")
Part of t-SNE and UMAP Embedding Visualization on anyplot.ai.