MirrorPeptidizer / scripts /plot_ablation_dl_figures.py
dahuilangda's picture
Add MirrorPeptidizer benchmark (D/L comparison, new targets, ablation, figure data, SI)
0613483 verified
Raw History Blame Contribute Delete
10.6 kB
"""Generate publication figures for ablation and D/L comparison results."""
from pathlib import Path
import re
import matplotlib.pyplot as plt
import numpy as np
import pandas as pd
ROOT = Path(__file__).resolve().parents[2]
BENCH = ROOT / "benchmark"
FIGDIR = BENCH / "figures"
PALETTE = {
"blue_main": "#0F4D92",
"blue_secondary": "#3775BA",
"blue_light": "#7BAED4",
"orange": "#E28E2C",
"green": "#5BAA5B",
"red_strong": "#B64342",
"neutral_light": "#CFCECE",
"neutral_mid": "#767676",
"neutral_dark": "#4D4D4D",
}
MODE_LABELS = {
"chroma+proteinmpnn": "Chroma+ProteinMPNN",
"chroma+bo": "Chroma+BO",
"chroma+proteinmpnn+bo": "Chroma+ProteinMPNN+BO",
}
MODE_COLORS = {
"chroma+proteinmpnn": PALETTE["red_strong"],
"chroma+bo": PALETTE["orange"],
"chroma+proteinmpnn+bo": PALETTE["blue_main"],
}
TARGETS = ["PDL1", "MDM2", "IL23R"]
def apply_nature_style(font_size=8, axes_linewidth=0.8):
plt.rcParams["font.family"] = "sans-serif"
plt.rcParams["font.sans-serif"] = ["Arial", "DejaVu Sans", "Liberation Sans"]
plt.rcParams["svg.fonttype"] = "none"
plt.rcParams["pdf.fonttype"] = 42
plt.rcParams["axes.spines.right"] = False
plt.rcParams["axes.spines.top"] = False
plt.rcParams["axes.linewidth"] = axes_linewidth
plt.rcParams["legend.frameon"] = False
plt.rcParams["font.size"] = font_size
plt.rcParams["axes.titlesize"] = font_size + 1
plt.rcParams["axes.labelsize"] = font_size + 1
plt.rcParams["xtick.labelsize"] = font_size
plt.rcParams["ytick.labelsize"] = font_size
plt.rcParams["legend.fontsize"] = font_size
plt.rcParams["axes.grid"] = False
plt.rcParams["xtick.direction"] = "out"
plt.rcParams["ytick.direction"] = "out"
plt.rcParams["xtick.major.width"] = axes_linewidth
plt.rcParams["ytick.major.width"] = axes_linewidth
plt.rcParams["xtick.major.size"] = 3
plt.rcParams["ytick.major.size"] = 3
def add_panel_label(ax, label):
ax.text(
-0.10,
1.05,
label,
transform=ax.transAxes,
fontsize=9,
fontweight="bold",
color="black",
ha="left",
va="bottom",
)
def save_pub_fig(fig, name):
FIGDIR.mkdir(parents=True, exist_ok=True)
fig.tight_layout(pad=1.2)
fig.savefig(FIGDIR / f"{name}.svg", bbox_inches="tight")
fig.savefig(FIGDIR / f"{name}.pdf", bbox_inches="tight")
fig.savefig(FIGDIR / f"{name}.png", dpi=300, bbox_inches="tight")
plt.close(fig)
def plot_ablation():
apply_nature_style(font_size=8)
df = pd.read_csv(BENCH / "ablation" / "ablation_summary_pose_filtered.csv")
df["mode_label"] = df["ablation"].map(MODE_LABELS)
fig, axes = plt.subplots(1, 2, figsize=(6.4, 2.7))
x = np.arange(len(TARGETS))
width = 0.24
modes = ["chroma+proteinmpnn", "chroma+bo", "chroma+proteinmpnn+bo"]
offsets = [-width, 0, width]
ax = axes[0]
for mode, offset in zip(modes, offsets):
part = df[df["ablation"] == mode].set_index("target").loc[TARGETS]
ax.bar(
x + offset,
part["best_score"],
width=width,
color=MODE_COLORS[mode],
label=MODE_LABELS[mode],
)
ax.set_ylabel("Best ProteinMPNN score (lower is better)")
ax.set_xticks(x)
ax.set_xticklabels(TARGETS)
ax.set_ylim(0, 2.9)
add_panel_label(ax, "a")
ax = axes[1]
for mode, offset in zip(modes, offsets):
part = df[df["ablation"] == mode].set_index("target").loc[TARGETS]
ax.bar(
x + offset,
part["best_synthesis_penalty"],
width=width,
color=MODE_COLORS[mode],
)
ax.axhline(0.8, color=PALETTE["neutral_mid"], lw=0.8, ls="--")
ax.axhline(1.6, color=PALETTE["neutral_mid"], lw=0.8, ls=":")
ax.set_ylabel("Best synthesis penalty (lower is better)")
ax.set_xticks(x)
ax.set_xticklabels(TARGETS)
ax.set_ylim(0, 2.7)
ax.text(2.55, 0.82, "low", fontsize=7, color=PALETTE["neutral_mid"])
ax.text(2.45, 1.62, "moderate", fontsize=7, color=PALETTE["neutral_mid"])
add_panel_label(ax, "b")
handles, labels = axes[0].get_legend_handles_labels()
fig.legend(handles, labels, loc="upper center", ncol=3, bbox_to_anchor=(0.5, 1.08))
save_pub_fig(fig, "fig_ablation_bo_tradeoff")
def _parse_top_diff(diff_text):
rows = []
for item in str(diff_text).split(";"):
item = item.strip()
if not item:
continue
match = re.match(r"([A-Z]):D([0-9.]+)/L([0-9.]+)", item)
if match:
aa, d_value, l_value = match.groups()
rows.append((aa, float(d_value), float(l_value)))
return rows
def plot_dl_comparison():
apply_nature_style(font_size=8)
from sklearn.manifold import TSNE
fig, axes = plt.subplots(1, 3, figsize=(9.2, 3.0))
AAS_ORDER = list("ACDEFGHIKLMNPQRSTVWY")
TOP_N = 100
for idx, target in enumerate(TARGETS):
ax = axes[idx]
d_df = pd.read_csv(BENCH / "dl_downsampled" / f"{target}_D_peptide_filtered.csv")
l_df = pd.read_csv(BENCH / "dl_downsampled" / f"{target}_L_peptide_filtered.csv")
d_top = d_df.nsmallest(TOP_N, "score").drop_duplicates("sequence")
l_top = l_df.nsmallest(TOP_N, "score").drop_duplicates("sequence")
def _onehot_padded(sequences, max_len):
aa_to_idx = {aa: i for i, aa in enumerate(AAS_ORDER)}
vecs = []
for seq in sequences:
vec = np.zeros(max_len * len(AAS_ORDER))
for pos, aa in enumerate(str(seq)):
if aa in aa_to_idx:
vec[pos * len(AAS_ORDER) + aa_to_idx[aa]] = 1.0
vecs.append(vec)
return np.array(vecs)
all_seqs = pd.concat([d_top, l_top])["sequence"]
max_len = all_seqs.str.len().max()
d_vecs = _onehot_padded(d_top["sequence"], max_len)
l_vecs = _onehot_padded(l_top["sequence"], max_len)
X = np.vstack([d_vecs, l_vecs])
n_d = len(d_vecs)
# PCA init to reduce dimensionality before t-SNE
from sklearn.decomposition import PCA
n_pca = min(50, X.shape[1], X.shape[0] - 1)
X_pca = PCA(n_components=n_pca, random_state=42).fit_transform(X)
tsne = TSNE(n_components=2, perplexity=30, random_state=42,
learning_rate="auto", init="pca")
X_embed = tsne.fit_transform(X_pca)
ax.scatter(
X_embed[n_d:, 0], X_embed[n_d:, 1],
s=28, alpha=0.6, color=PALETTE["orange"], label="L-peptide", rasterized=True,
)
ax.scatter(
X_embed[:n_d, 0], X_embed[:n_d, 1],
s=28, alpha=0.6, color=PALETTE["blue_main"], label="D-peptide", rasterized=True,
)
ax.set_xlabel(f"{target} (top {TOP_N}) — t-SNE 1")
if idx == 0:
ax.set_ylabel("t-SNE 2")
ax.set_xticks([])
ax.set_yticks([])
panel_labels = ["a", "b", "c"]
add_panel_label(ax, panel_labels[idx])
handles = [
plt.Line2D([0], [0], marker="o", color="w", markerfacecolor=PALETTE["blue_main"],
markersize=8, label="D-peptide"),
plt.Line2D([0], [0], marker="o", color="w", markerfacecolor=PALETTE["orange"],
markersize=8, label="L-peptide"),
]
fig.legend(handles=handles, loc="upper center", ncol=2, bbox_to_anchor=(0.5, 1.04),
fontsize=8, handletextpad=0.5, columnspacing=1.5)
save_pub_fig(fig, "fig_dl_sequence_comparison")
def _load_bad_pose_keys(peptide_mode):
"""Buried (inside-target) pose keys from the geometric surface filter."""
path = BENCH / "buried_pose_inventory.csv"
if not path.exists():
return set()
df = pd.read_csv(path)
sub = df[df["peptide_mode"] == peptide_mode]
return set(zip(sub["target"], sub["length"].astype(int), sub["pose"].astype(int)))
def _load_filtered_dl_df(target, peptide_mode):
csv_path = BENCH / target / peptide_mode / "all_results.csv"
df = pd.read_csv(csv_path)
bad_keys = _load_bad_pose_keys(peptide_mode)
if bad_keys:
keys = list(zip(
[target] * len(df),
df["length"].astype(int),
df["pose"].astype(int),
))
keep = [k not in bad_keys for k in keys]
df = df.loc[keep].copy()
return df.dropna(subset=["score"])
def plot_dl_score_distribution():
apply_nature_style(font_size=8)
from scipy import stats as sp_stats
fig, axes = plt.subplots(1, 3, figsize=(9.2, 2.8))
rng = np.random.default_rng(42)
for idx, target in enumerate(TARGETS):
ax = axes[idx]
d_df = _load_filtered_dl_df(target, "D_peptide")
l_df = _load_filtered_dl_df(target, "L_peptide")
# Downsample L to match D count
n_d = len(d_df)
n_l = len(l_df)
if n_l > n_d:
l_df = l_df.sample(n=n_d, random_state=rng).copy()
d_scores = d_df["score"].values
l_scores = l_df["score"].values
bins = np.linspace(
min(d_scores.min(), l_scores.min()),
max(np.percentile(d_scores, 99), np.percentile(l_scores, 99)),
50,
)
ax.hist(
d_scores, bins=bins, density=True, alpha=0.55,
color=PALETTE["blue_main"], label="D-peptide",
)
ax.hist(
l_scores, bins=bins, density=True, alpha=0.55,
color=PALETTE["orange"], label="L-peptide",
)
ks_stat, ks_p = sp_stats.ks_2samp(d_scores, l_scores)
ax.axvline(np.median(d_scores), color=PALETTE["blue_main"], ls="--", lw=0.8)
ax.axvline(np.median(l_scores), color=PALETTE["orange"], ls="--", lw=0.8)
ax.set_xlabel(f"{target} — ProteinMPNN score (NLL)")
if idx == 0:
ax.set_ylabel("Density")
ax.text(
0.97, 0.95,
f"$n$ = {n_d}\nKS = {ks_stat:.3f}\np < {ks_p:.1e}" if ks_p < 0.001 else f"$n$ = {n_d}\nKS = {ks_stat:.3f}\np = {ks_p:.3f}",
transform=ax.transAxes, ha="right", va="top",
fontsize=7, color=PALETTE["neutral_dark"],
bbox=dict(boxstyle="round,pad=0.3", fc="white", ec=PALETTE["neutral_light"], lw=0.5),
)
if idx == 0:
ax.legend(loc="upper left", fontsize=7)
save_pub_fig(fig, "fig_dl_score_distribution")
def main():
plot_ablation()
plot_dl_comparison()
plot_dl_score_distribution()
if __name__ == "__main__":
main()