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89dec6b | 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 | #!/usr/bin/env python3
"""Combined figure: (a) Motif Preservation (A1 + A2 stacked) and (b) JS heatmap, in one row."""
import os
import numpy as np
import pandas as pd
import matplotlib.pyplot as plt
import matplotlib as mpl
import seaborn as sns
from matplotlib.colors import LinearSegmentedColormap
from matplotlib.gridspec import GridSpec, GridSpecFromSubplotSpec
# ββ Data ββ
df_summary = pd.read_csv(
"/data/n5huang/dna_token/tokenizer_evaluation/motif_eval_outputs_new/summary_by_tokenizer.csv"
)
df_js = pd.read_csv(
"/data/n5huang/dna_token/enrichment_analysis/js_vs_random_matrix.csv",
index_col=0,
)
# ββ Method config (shared) ββ
METHODS = ["DNAbert2", "Grover", "cCRE_region_BPE", "motif_region_BPE", "DNAMotifTokenizer"]
DISPLAY_NAMES = {
"DNAbert2": "DNABERT-2",
"Grover": "Grover",
"cCRE_region_BPE": "cCRE-Region BPE",
"motif_region_BPE": "Motif-Region BPE",
"DNAMotifTokenizer": "DNAMotif",
}
METHOD_COLORS = {
"DNAbert2": "#6C5CE7", # purple (from C)
"Grover": "#E74C3C", # red (from T)
"cCRE_region_BPE": "#52BE80", # green (from A)
"motif_region_BPE": "#F4D03F", # yellow (Token Characterization)
"DNAMotifTokenizer": "#E67E22", # orange (Fine-tuning Ability)
}
HEATMAP_REGIONS = ["promoter", "enhancer", "exon"]
JS_INDEX_DISPLAY = [DISPLAY_NAMES.get(n, n) for n in df_js.index]
# ββ Plot style ββ
mpl.rcParams.update({
"font.family": "sans-serif",
"font.size": 58,
"axes.labelsize": 64,
"axes.titlesize": 66,
"axes.titleweight": "bold",
"xtick.labelsize": 58,
"ytick.labelsize": 58,
})
def get_value(method, source_df, col_name):
row = source_df[source_df["Tokenizer"] == method]
if len(row) == 0:
return float("nan")
return row[col_name].values[0]
def draw_bar_panel(ax, title, ylabel, col_name, higher_better, title_pad=30, ylabel_y=0.5):
vals = [get_value(m, df_summary, col_name) for m in METHODS]
colors = [METHOD_COLORS[m] for m in METHODS]
x_labels = [DISPLAY_NAMES[m] for m in METHODS]
x = np.arange(len(METHODS)) * 0.3
bars = ax.bar(x, vals, color=colors, edgecolor="white", linewidth=0.5, alpha=0.85, width=0.2)
for i, v in enumerate(vals):
if np.isnan(v):
continue
y_off = max(vals) * 0.02
fmt = f"{v:.2f}" if abs(v) >= 1 else f"{v:.4f}"
ax.text(x[i], v + y_off, fmt, ha="center", va="bottom", fontsize=62, fontweight="bold")
ax.set_xticks(x)
ax.set_xticklabels(x_labels, rotation=15, ha="right")
ax.set_xlim(x[0] - 0.2, x[-1] + 0.2)
ax.set_ylabel(ylabel)
# Pin ylabel position in axes coords so A1 and A2 line up regardless of tick-label widths.
ax.yaxis.set_label_coords(-0.08, ylabel_y)
ax.set_title(title, pad=title_pad)
ax.tick_params(axis="x", pad=10)
ax.tick_params(axis="y", pad=15)
ax.spines["top"].set_visible(False)
ax.spines["right"].set_visible(False)
ax.grid(axis="y", alpha=0.3, linewidth=0.8)
valid = [v for v in vals if not np.isnan(v)]
if valid:
best = (np.nanargmax if higher_better else np.nanargmin)(vals)
bars[best].set_edgecolor("black")
bars[best].set_linewidth(2)
# ββ Figure layout: 1 row, 2 top-level columns ββ
fig = plt.figure(figsize=(50, 26))
gs = GridSpec(1, 2, figure=fig, width_ratios=[1, 0.9], wspace=0.30)
# Left column (panel a): 2 stacked subplots
gs_a = GridSpecFromSubplotSpec(2, 1, subplot_spec=gs[0, 0], hspace=0.8)
ax_a1 = fig.add_subplot(gs_a[0, 0])
ax_a2 = fig.add_subplot(gs_a[1, 0])
# Right column (panel b): heatmap
ax_b = fig.add_subplot(gs[0, 1])
# ββ Draw panel a (A1 + A2) ββ
draw_bar_panel(ax_a1, "Perfect Match Rate", "Perfect match rate (%)",
"Perfect_Match_Rate", higher_better=True, title_pad=80, ylabel_y=0.35)
draw_bar_panel(ax_a2, "Motif Fragmentation", "Avg tokens per motif",
"Avg_Tokens_Per_Motif", higher_better=False, title_pad=80)
# ββ Draw panel b (heatmap) ββ
df_disp = df_js.copy()
df_disp.index = JS_INDEX_DISPLAY
cmap = LinearSegmentedColormap.from_list("evo_heat", ["white", "#AED6F1", "#5DADE2", "#2E86C1"])
sns.heatmap(
df_disp,
ax=ax_b,
annot=True,
fmt=".4f",
annot_kws={"size": 62, "fontweight": "bold"}, # matches bar-value annotation size
cmap=cmap,
vmin=0.0,
vmax=float(df_disp.values.max()) or 0.001,
linewidths=0.5,
cbar_kws={"label": "Jensen-Shannon distance"},
)
ax_b.set_title("Region vs random-genome separation",
fontsize=66, fontweight="bold", pad=80)
ax_b.set_xlabel("Genomic region", fontsize=64, labelpad=15)
ax_b.set_ylabel("")
ax_b.tick_params(axis="x", labelsize=58)
ax_b.tick_params(axis="y", labelsize=58, rotation=0)
cbar = ax_b.collections[0].colorbar
cbar.ax.tick_params(labelsize=58)
cbar.set_label("Jensen-Shannon distance", size=64)
fig.subplots_adjust(left=0.06, right=0.98, top=0.88, bottom=0.10)
# ββ Panel labels (a), (b) on same line as titles ββ
# Use axes-relative y so they line up with titles (which sit just above each axes top).
ax_a1.text(-0.08, 1.234, "(a)", transform=ax_a1.transAxes,
fontsize=66, fontweight="bold", va="center", ha="center")
ax_b.text(-0.30, 1.083, "(b)", transform=ax_b.transAxes,
fontsize=66, fontweight="bold", va="center", ha="center")
out_dir = "/data/n5huang/dna_token/paper_figures"
os.makedirs(out_dir, exist_ok=True)
out = os.path.join(out_dir, "combined_panel_a_b.pdf")
fig.savefig(out, dpi=300)
fig.savefig(out.replace(".pdf", ".png"), dpi=80)
print(f"Saved: {out}")
print(f"Saved: {out.replace('.pdf', '.png')}")
plt.close(fig)
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