scPTR / analyses /run_mirna_analysis.py
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#!/usr/bin/env python
"""miRNA-target analysis: test whether miRNA-targeted genes have higher gamma.
Uses TargetScan 8.0 predictions to identify miRNA-target relationships,
then tests whether predicted targets have systematically higher degradation
rates (gamma) than non-targets using Mann-Whitney U tests.
This addresses Aim 4 of the research plan: post-transcriptional regulatory networks.
"""
from __future__ import annotations
import json
import sys
from pathlib import Path
import matplotlib
matplotlib.use("Agg")
import matplotlib.pyplot as plt
import numpy as np
import pandas as pd
from scipy import stats
sys.path.insert(0, str(Path(__file__).parent))
from _common import set_figure_style
import scptr
OUTPUT_DIR = Path(__file__).parent.parent / "output" / "mirna_analysis"
def save_fig(fig, name, subdir="figures"):
out_dir = OUTPUT_DIR / subdir
out_dir.mkdir(parents=True, exist_ok=True)
path = out_dir / f"{name}.png"
fig.savefig(path, dpi=150, bbox_inches="tight")
plt.close(fig)
print(f" Saved: {path}")
def run_mirna_analysis(adata, dataset_name, mirna_targets):
"""Run miRNA-gamma correlation analysis on a dataset."""
print(f"\n{'='*60}")
print(f"miRNA ANALYSIS: {dataset_name}")
print(f"{'='*60}")
# Run scPTR pipeline
import copy
adata = copy.deepcopy(adata)
scptr.pp.filter_genes(adata)
scptr.pp.normalize_layers(adata)
scptr.pp.neighbors(adata, n_neighbors=30)
scptr.pp.smooth_layers(adata)
scptr.tl.estimate_beta(adata)
scptr.tl.estimate_gamma(adata)
# Run miRNA-gamma correlation
print(f" Running miRNA-gamma correlation...")
result_df = scptr.tl.mirna_gamma_correlation(
adata, mirna_targets, n_top_targets=200, min_cells_expressing=50
)
if len(result_df) == 0:
print(f" No miRNA families with sufficient targets found.")
return None
# Summary statistics
n_tested = len(result_df)
n_sig = (result_df["fdr"] < 0.05).sum()
n_sig_10 = (result_df["fdr"] < 0.10).sum()
n_enriched = (result_df["fold_enrichment"] > 1.0).sum()
print(f"\n Results:")
print(f" miRNA families tested: {n_tested}")
print(f" Significant (FDR < 0.05): {n_sig} ({100*n_sig/n_tested:.1f}%)")
print(f" Significant (FDR < 0.10): {n_sig_10} ({100*n_sig_10/n_tested:.1f}%)")
print(f" Enriched (fold > 1.0): {n_enriched} ({100*n_enriched/n_tested:.1f}%)")
print(f" Median fold enrichment: {result_df['fold_enrichment'].median():.3f}")
# Top significant miRNAs
top_sig = result_df[result_df["fdr"] < 0.10].head(20)
if len(top_sig) > 0:
print(f"\n Top significant miRNAs (FDR < 0.10):")
for _, row in top_sig.iterrows():
print(f" {row['representative_mirna']:>25s} "
f"n_targets={row['n_targets_in_data']:3d} "
f"fold={row['fold_enrichment']:.2f} "
f"p={row['mannwhitney_p']:.2e} "
f"FDR={row['fdr']:.3f}")
# Top miRNAs by effect size regardless of significance
top_effect = result_df.nlargest(10, "fold_enrichment")
print(f"\n Top miRNAs by fold enrichment:")
for _, row in top_effect.iterrows():
print(f" {row['representative_mirna']:>25s} "
f"fold={row['fold_enrichment']:.2f} "
f"FDR={row['fdr']:.3f}")
# Aggregate test: all miRNA targets vs non-targets
gamma = np.median(adata.layers["gamma"], axis=0)
gene_names_upper = [g.upper() for g in adata.var_names]
all_target_genes = set()
for _, row in mirna_targets.iterrows():
all_target_genes.add(str(row["gene_symbol"]).upper())
informative = (adata.layers["gamma"] > 0).mean(axis=0) >= 0.1
target_gamma = []
nontarget_gamma = []
for i, g in enumerate(gene_names_upper):
if not informative[i]:
continue
if g in all_target_genes:
target_gamma.append(gamma[i])
else:
nontarget_gamma.append(gamma[i])
if len(target_gamma) >= 10 and len(nontarget_gamma) >= 10:
u, p = stats.mannwhitneyu(target_gamma, nontarget_gamma, alternative="greater")
print(f"\n Aggregate test (all targets vs non-targets):")
print(f" Target genes in data: {len(target_gamma)}")
print(f" Non-target genes: {len(nontarget_gamma)}")
print(f" Target median gamma: {np.median(target_gamma):.6f}")
print(f" Non-target median gamma: {np.median(nontarget_gamma):.6f}")
print(f" Fold: {np.median(target_gamma) / (np.median(nontarget_gamma) + 1e-8):.3f}")
print(f" Mann-Whitney p: {p:.2e}")
# Save results
res_dir = OUTPUT_DIR / "results"
res_dir.mkdir(parents=True, exist_ok=True)
result_df.to_csv(res_dir / f"mirna_gamma_{dataset_name}.csv", index=False)
# Figures
fig, axes = plt.subplots(1, 3, figsize=(16, 5))
# Panel 1: Volcano plot (fold enrichment vs -log10 p)
neg_log_p = -np.log10(result_df["mannwhitney_p"].clip(lower=1e-50))
sig_mask = result_df["fdr"] < 0.05
axes[0].scatter(result_df["fold_enrichment"][~sig_mask], neg_log_p[~sig_mask],
s=10, alpha=0.3, color="gray", label="NS")
axes[0].scatter(result_df["fold_enrichment"][sig_mask], neg_log_p[sig_mask],
s=20, alpha=0.7, color="red", label=f"FDR<0.05 (n={sig_mask.sum()})")
axes[0].axhline(y=-np.log10(0.05), color="blue", linestyle="--", alpha=0.5)
axes[0].axvline(x=1.0, color="black", linestyle="--", alpha=0.3)
axes[0].set_xlabel("Fold enrichment (target/non-target gamma)")
axes[0].set_ylabel("-log10(p)")
axes[0].set_title(f"miRNA Target Enrichment ({dataset_name})")
axes[0].legend()
# Panel 2: Distribution of fold enrichments
axes[1].hist(result_df["fold_enrichment"], bins=30, color="steelblue",
edgecolor="black", linewidth=0.5)
axes[1].axvline(x=1.0, color="red", linestyle="--", label="No enrichment")
axes[1].axvline(x=result_df["fold_enrichment"].median(), color="green",
linestyle="--", label=f"Median={result_df['fold_enrichment'].median():.2f}")
axes[1].set_xlabel("Fold enrichment")
axes[1].set_ylabel("Count")
axes[1].set_title("Distribution of Fold Enrichments")
axes[1].legend()
# Panel 3: Aggregate target vs non-target boxplot
if len(target_gamma) >= 10:
box_data = [target_gamma, nontarget_gamma]
bp = axes[2].boxplot(box_data, labels=["miRNA\ntargets", "Non-\ntargets"],
patch_artist=True)
bp["boxes"][0].set_facecolor("coral")
bp["boxes"][1].set_facecolor("lightblue")
axes[2].set_ylabel("Median gamma per gene")
axes[2].set_title(f"Aggregate: targets vs non-targets\np={p:.2e}")
axes[2].set_yscale("symlog", linthresh=0.001)
fig.suptitle(f"miRNA-Gamma Analysis: {dataset_name}", fontsize=13, y=1.02)
fig.tight_layout()
save_fig(fig, f"mirna_analysis_{dataset_name}")
return {
"n_families_tested": n_tested,
"n_significant_005": int(n_sig),
"n_significant_010": int(n_sig_10),
"n_enriched": int(n_enriched),
"median_fold_enrichment": float(result_df["fold_enrichment"].median()),
"aggregate_p": float(p) if len(target_gamma) >= 10 else None,
}
def main():
set_figure_style()
OUTPUT_DIR.mkdir(parents=True, exist_ok=True)
# Load TargetScan predictions
print("=" * 60)
print("LOADING TARGETSCAN PREDICTIONS")
print("=" * 60)
cache_dir = Path(__file__).parent.parent / ".cache" / "targetscan"
try:
mirna_targets = scptr.tl.load_targetscan_predictions(
species_id=9606, # Human
min_context_score=-0.2,
cache_dir=cache_dir,
)
print(f" Loaded {len(mirna_targets)} human miRNA-target predictions")
print(f" miRNA families: {mirna_targets['mirna_family'].nunique()}")
print(f" Target genes: {mirna_targets['gene_symbol'].nunique()}")
except FileNotFoundError as e:
print(f" ERROR: {e}")
print(" Please download TargetScan data first.")
sys.exit(1)
# Also load mouse predictions for mouse datasets
try:
mirna_targets_mouse = scptr.tl.load_targetscan_predictions(
species_id=10090, # Mouse
min_context_score=-0.2,
cache_dir=cache_dir,
)
print(f" Loaded {len(mirna_targets_mouse)} mouse miRNA-target predictions")
print(f" miRNA families: {mirna_targets_mouse['mirna_family'].nunique()}")
print(f" Target genes: {mirna_targets_mouse['gene_symbol'].nunique()}")
except Exception as e:
print(f" Mouse predictions not available: {e}")
mirna_targets_mouse = mirna_targets # Fallback: use human
# Load datasets
print("\n" + "=" * 60)
print("LOADING DATASETS")
print("=" * 60)
adata_pan = scptr.datasets.pancreas()
adata_dg = scptr.datasets.dentate_gyrus()
# Try to load sci-fate
try:
adata_sci = scptr.datasets.sci_fate()
except Exception:
adata_sci = None
# Run analysis on each dataset
all_results = {}
# Pancreas (mouse) - use mouse predictions
all_results["pancreas"] = run_mirna_analysis(
adata_pan, "pancreas", mirna_targets_mouse
)
# Dentate Gyrus (mouse) - use mouse predictions
all_results["dentate_gyrus"] = run_mirna_analysis(
adata_dg, "dentate_gyrus", mirna_targets_mouse
)
# sci-fate (human A549) - use human predictions
if adata_sci is not None:
all_results["sci_fate"] = run_mirna_analysis(
adata_sci, "sci_fate", mirna_targets
)
# Save summary
res_dir = OUTPUT_DIR / "results"
res_dir.mkdir(parents=True, exist_ok=True)
with open(res_dir / "mirna_summary.json", "w") as f:
json.dump(all_results, f, indent=2)
# Summary table
print(f"\n{'='*60}")
print("miRNA ANALYSIS SUMMARY")
print(f"{'='*60}")
print(f"{'Dataset':>15s} {'Tested':>7s} {'Sig(5%)':>7s} {'Sig(10%)':>8s} "
f"{'Enriched':>8s} {'Med.Fold':>8s} {'Agg.p':>10s}")
for name, res in all_results.items():
if res is None:
continue
print(f"{name:>15s} {res['n_families_tested']:>7d} "
f"{res['n_significant_005']:>7d} {res['n_significant_010']:>8d} "
f"{res['n_enriched']:>8d} {res['median_fold_enrichment']:>8.3f} "
f"{res['aggregate_p']:>10.2e}" if res['aggregate_p'] else "")
print(f"\nResults saved to: {OUTPUT_DIR.resolve()}")
if __name__ == "__main__":
main()