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141bacd | 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 159 160 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 197 198 199 200 201 202 203 204 205 206 207 208 209 210 211 212 213 214 215 216 217 218 219 220 221 222 223 224 225 226 227 228 229 230 231 232 233 234 235 236 237 238 239 240 241 242 243 244 245 246 247 248 249 250 251 252 253 254 255 256 | """main-text figures for PAPER.tex — cv per-class F1 bars, dahlin heatmap, veres stage stack.
Uses shared canonical palette (scripts/figures/palette.py) so the same class
gets the same color in every figure.
"""
from __future__ import annotations
from pathlib import Path
import warnings, json, sys
warnings.filterwarnings("ignore")
import numpy as np, pandas as pd
import matplotlib
matplotlib.use("Agg")
import matplotlib.pyplot as plt
from pathlib import Path as _P_root
ROOT = _P_root(__file__).resolve().parents[2]
ROOT_STR = str(ROOT)
FIG = Path(f"{ROOT_STR}/figures")
FIG.mkdir(exist_ok=True)
# shared canonical palette + style
sys.path.insert(0, str(_P_root(__file__).resolve().parent))
from palette import color_for, apply_style, CLASS_COLORS
apply_style()
# ---- shared style constants (user style spec) ----
SUPTITLE_FS = 15 # figure suptitles
TITLE_FS = 14 # panel / axes titles
LABEL_FS = 12 # axis labels
TICK_FS = 11 # tick labels
LEGEND_FS = 10 # legend text
LEGEND_TITLE_FS = 11 # legend titles
ANNOT_FS = 11 # in-plot annotations
CBAR_LABEL_FS = 12 # colorbar labels
PANEL_FS = 13 # panel letters (a)/(b)/(c)
# override rc defaults from apply_style() so implicit sizes also conform
plt.rcParams.update({
"axes.titlesize": TITLE_FS,
"axes.labelsize": LABEL_FS,
"xtick.labelsize": TICK_FS,
"ytick.labelsize": TICK_FS,
"legend.fontsize": LEGEND_FS,
"legend.title_fontsize": LEGEND_TITLE_FS,
"figure.titlesize": SUPTITLE_FS,
})
def _panel_letter(ax, letter, x=-0.14, y=1.06, fontsize=PANEL_FS):
ax.text(x, y, f"({letter})", transform=ax.transAxes,
fontsize=fontsize, fontweight="bold", va="bottom", ha="left")
def fig1_perclass_f1():
"""per-class F1 bars from 5-fold CV JSONs, one axis per system, class-colored."""
panels = [
("Pan-skin", f"{ROOT_STR}/discovery/pan_skin/marker/cv_5fold.json"),
("Pan-hematopoiesis", f"{ROOT_STR}/discovery/hematopoiesis/marker/cv_5fold.json"),
("Pan-pancreas", f"{ROOT_STR}/discovery/pancreas/marker/cv_5fold.json"),
]
fig, axes = plt.subplots(1, 3, figsize=(18, 6), constrained_layout=True)
for i, (ax, (title, path)) in enumerate(zip(axes, panels)):
r = json.load(open(path))
rep = r["per_class_report"]
# collect (class, f1, support)
rows = [(c, rep[c]["f1-score"], int(rep[c]["support"]))
for c in rep.keys()
if c not in ("accuracy", "macro avg", "weighted avg")]
# sort descending by F1 (best first at top)
rows.sort(key=lambda t: t[1], reverse=True)
classes = [t[0] for t in rows]
f1s = [t[1] for t in rows]
supports = [t[2] for t in rows]
colors = [color_for(c) for c in classes]
y = np.arange(len(classes))
bars = ax.barh(y, f1s, color=colors, edgecolor="white", linewidth=0.6)
# per-bar n annotations (outside)
for b, s in zip(bars, supports):
ax.text(b.get_width() + 0.012, b.get_y() + b.get_height() / 2,
f"n={s:,}", va="center", fontsize=ANNOT_FS, color="#333")
# scale
ax.set_xlim(0, 1.22)
ax.set_xticks([0.0, 0.25, 0.5, 0.75, 1.0])
ax.set_xticklabels(["0.0", "0.25", "0.50", "0.75", "1.00"],
fontsize=TICK_FS)
ax.set_xlabel("held-out F1", fontsize=LABEL_FS)
# y-axis: shrink font slightly if many classes
y_fs = TICK_FS + 1 if len(classes) <= 13 else TICK_FS
ax.set_yticks(y)
ax.set_yticklabels(classes, fontsize=y_fs)
# panel title with n_cells; small acc/AUROC subtitle below
n_cells = int(r["n_cells"])
acc = r["mean_acc"]; auc = r["mean_auc"]
ax.set_title(f"{title} (n_cells={n_cells:,})", fontsize=TITLE_FS, pad=32)
ax.text(0.5, 1.01,
f"acc = {acc:.3f} · macro AUROC = {auc:.3f}",
transform=ax.transAxes, ha="center", va="bottom",
fontsize=ANNOT_FS, color="#555555")
# F1=0.9 marker
ax.axvline(0.9, color="#888888", linestyle="--", linewidth=1.1,
alpha=0.4, zorder=0)
ax.grid(axis="x", alpha=0.25, linestyle=":", zorder=0)
ax.invert_yaxis()
_panel_letter(ax, "abc"[i], x=-0.32, y=1.02, fontsize=PANEL_FS)
plt.savefig(FIG / "fig1_perclass_f1.pdf", bbox_inches="tight")
plt.close()
print(f"[fig1] wrote {FIG}/fig1_perclass_f1.pdf")
def fig3_dahlin_heatmap():
"""dahlin within-class module-score heatmap (Kit_W41 minus WT)."""
p = Path(f"{ROOT_STR}/discovery/hematopoiesis/marker/57_pathway_analysis.csv")
if not p.exists(): print(f"[fig3] {p} not found"); return
df = pd.read_csv(p)
pivot = df.pivot(index="module_name", columns="class", values="delta")
pivot_p = df.pivot(index="module_name", columns="class", values="mannu_p_adj_bonferroni")
row_order = ["Kit_signaling", "Kit_ligand", "MYC_targets", "Integrated_stress",
"Apoptosis_pro", "Apoptosis_anti", "Cell_cycle",
"Erythropoiesis_early", "Erythropoiesis_late",
"OXPHOS_ETC", "Glycolysis",
"Redox_glutathione", "LT_HSC_quiescence"]
row_order = [r for r in row_order if r in pivot.index]
col_order = ["LT-HSC", "MPP", "erythroid", "myeloid", "megakaryocyte",
"lymphoid", "basophil-mast", "monocyte", "macrophage"]
col_order = [c for c in col_order if c in pivot.columns]
P = pivot.loc[row_order, col_order]
Pp = pivot_p.loc[row_order, col_order]
fig, ax = plt.subplots(figsize=(11, 8), constrained_layout=True)
vmax = np.nanmax(np.abs(P.values))
im = ax.imshow(P.values, cmap="RdBu_r", vmin=-vmax, vmax=vmax, aspect="auto")
# cell annotations
for i in range(P.shape[0]):
for j in range(P.shape[1]):
v = P.values[i, j]; pv = Pp.values[i, j]
if np.isnan(v): continue
star = "**" if pv < 1e-3 else "*" if pv < 0.05 else ""
if abs(v) > 0.1:
label = f"{v:+.2f}"
if star: label = f"{label} {star}"
color = "white" if abs(v) >= vmax * 0.6 else "black"
ax.text(j, i, label, ha="center", va="center",
fontsize=ANNOT_FS, color=color)
elif star:
ax.text(j, i, star, ha="center", va="center",
fontsize=ANNOT_FS, color="black")
# col labels (rotated 45)
ax.set_xticks(range(len(col_order)))
ax.set_xticklabels(col_order, rotation=45, ha="right", fontsize=TICK_FS)
# row labels (module names)
ax.set_yticks(range(len(row_order)))
ax.set_yticklabels(row_order, fontsize=TICK_FS)
# color the x tick labels (class names) using canonical palette
for tl, cls in zip(ax.get_xticklabels(), col_order):
tl.set_color(color_for(cls))
tl.set_fontweight("bold")
cbar = plt.colorbar(im, ax=ax, shrink=0.85, pad=0.02)
cbar.set_label("Δ module score (Kit_W41 − WT)", fontsize=CBAR_LABEL_FS)
cbar.ax.tick_params(labelsize=TICK_FS)
ax.set_title("Dahlin: Kit-W41 vs WT within-class pathway module contrast",
fontsize=TITLE_FS, pad=14)
fig.text(0.5, -0.01,
"* p<0.05 ** p<10$^{-3}$ (Mann–Whitney, Bonferroni)",
ha="center", fontsize=ANNOT_FS, color="#555555")
plt.savefig(FIG / "fig3_dahlin_heatmap.pdf", bbox_inches="tight")
plt.close()
print(f"[fig3] wrote {FIG}/fig3_dahlin_heatmap.pdf")
def fig4_sharon_stage_stack():
"""stacked-bar class fractions across veres stages 3-6, class-colored via palette."""
import re
p = Path(f"{ROOT_STR}/discovery/pancreas/marker/veres_predictions.csv")
if not p.exists(): print(f"[fig4] {p} not found"); return
pred = pd.read_csv(p)
stg_re = re.compile(r"_S(\d)c_")
stages = pred["cell_id"].astype(str).apply(
lambda s: int(stg_re.search(s).group(1)) if stg_re.search(s) else np.nan)
pred = pred.assign(stage=stages).dropna(subset=["stage"])
pred["stage"] = pred["stage"].astype(int)
n_staged = len(pred); n_pre = len(stages); n_drop = n_pre - n_staged
print(f"[fig4] staged cells: {n_staged:,} (dropped {n_drop:,} primary-islet cells)")
ct = (pred.groupby(["stage", "pred_label"]).size()
.unstack("pred_label", fill_value=0))
frac = ct.div(ct.sum(axis=1), axis=0)
priority = ["pancreatic-progenitor", "proliferating",
"endocrine-progenitor", "endocrine-progenitor-primed",
"Fev-EP", "beta_progenitor", "beta",
"alpha_progenitor", "alpha", "delta", "gamma", "epsilon",
"acinar", "ductal", "exocrine",
"mesenchyme", "endothelial", "immune"]
present = list(frac.columns)
ordered = [c for c in priority if c in present] + \
[c for c in sorted(present, key=lambda x: -frac[x].sum())
if c not in priority]
frac = frac[ordered]
fig, ax = plt.subplots(figsize=(12, 7), constrained_layout=True)
bottom = np.zeros(frac.shape[0])
x = np.arange(frac.shape[0])
for cls in ordered:
vals = frac[cls].values
ax.bar(x, vals, bottom=bottom, label=cls,
color=color_for(cls), edgecolor="white", linewidth=0.6)
bottom += vals
for xi, s in zip(x, frac.index):
n_stage = int(ct.loc[s].sum())
ax.text(xi, 1.03, f"n = {n_stage:,}", ha="center", va="bottom",
fontsize=ANNOT_FS, color="#222222")
ax.set_xticks(x)
ax.set_xticklabels([f"Stage {int(s)}" for s in frac.index], fontsize=TICK_FS)
ax.set_xlabel("Veres protocol stage", fontsize=LABEL_FS)
ax.set_ylabel("Predicted class fraction", fontsize=LABEL_FS)
ax.set_title("Veres 2019 pancreatic differentiation", fontsize=TITLE_FS,
pad=12)
# legend reversed so it reads top-of-stack first (matches the visual)
handles, labels = ax.get_legend_handles_labels()
ax.legend(handles[::-1], labels[::-1],
bbox_to_anchor=(1.02, 1), loc="upper left", fontsize=LEGEND_FS,
frameon=False, title="Predicted class",
title_fontsize=LEGEND_TITLE_FS,
handlelength=1.6, borderaxespad=0.4)
ax.set_ylim(0, 1.12)
ax.set_yticks([0.0, 0.25, 0.5, 0.75, 1.0])
ax.tick_params(axis="y", labelsize=TICK_FS)
plt.savefig(FIG / "fig4_veres_stage_stack.pdf", bbox_inches="tight")
plt.close()
print(f"[fig4] wrote {FIG}/fig4_veres_stage_stack.pdf "
f"({len(ordered)} classes over stages {list(frac.index)})")
if __name__ == "__main__":
fig1_perclass_f1()
fig3_dahlin_heatmap()
fig4_sharon_stage_stack()
print(f"\nAll figures in {FIG}/")
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