app.py

import gradio as gr
import joblib
from huggingface_hub import hf_hub_download
import pandas as pd
import numpy as np
from collections import Counter

# --- Download model from HF Hub ---
repo_id = "Ym420/Peptide-Function"  # replace with your HF repo
model_filename = "xgb_multilabel_model_full.pkl"

model_path = hf_hub_download(repo_id=repo_id, filename=model_filename)
model_package = joblib.load(model_path)
model = model_package['model']
feature_columns = model_package['feature_columns']

# --- Metadata ---
aa_list = model_package['aa_list']
dipeptides = model_package['dipeptides']
hydrophobicity_scale = model_package['hydrophobicity_scale']
eisenberg_scale = model_package['eisenberg_scale']
aa_mass = model_package['aa_mass']
aa_charge = model_package['aa_charge']
aa_boman = model_package['aa_boman']
aa_flexibility = model_package['aa_flexibility']
aa_polarizability = model_package['aa_polarizability']
aa_aliphatic = model_package['aa_aliphatic']
aa_deltaG = model_package['aa_deltaG']

# --- Target cells ---
TARGET_CELLS = ["Gram+", "Fungus", "Mammalian Cell", "Cancer", "Gram-"]

# --- Feature extraction ---
def extract_features_app(seq: str) -> pd.DataFrame:
    seq = seq.upper()
    
    # --- 1. Dipeptide composition ---
    count = Counter([seq[i:i+2] for i in range(len(seq)-1)])
    total = max(len(seq)-1, 1)
    dipep_features = [count.get(dp, 0) / total for dp in dipeptides]

    # --- 2. Physicochemical features ---
    def g(aa, table): return table.get(aa, 0)
    def h(dp, table): return (g(dp[0], table) + g(dp[1], table)) / 2.0

    dipeptides_seq = [seq[i:i+2] for i in range(len(seq)-1)]
    
    if len(seq) < 2:
        physchem_features = [0]*12
    else:
        mw = np.mean([h(dp, aa_mass) for dp in dipeptides_seq])
        charge = np.mean([h(dp, aa_charge) for dp in dipeptides_seq])
        hydro = np.mean([h(dp, hydrophobicity_scale) for dp in dipeptides_seq])
        aromatic = np.mean([(dp[0] in 'FWY') + (dp[1] in 'FWY') for dp in dipeptides_seq]) / 2.0
        pI = np.mean([h(dp, {aa: 7 + (int(aa in 'KRH') - int(aa in 'DE')) for aa in aa_list}) for dp in dipeptides_seq])
        instability = np.mean([((dp[0] in 'DEKR') + (dp[1] in 'DEKR')) / 2.0 for dp in dipeptides_seq])
        hydro_moment = np.sqrt(np.mean([(h(dp, eisenberg_scale))**2 for dp in dipeptides_seq]))
        aliphatic = np.mean([h(dp, aa_aliphatic) for dp in dipeptides_seq])
        boman = np.mean([h(dp, aa_boman) for dp in dipeptides_seq])
        flexibility = np.mean([h(dp, aa_flexibility) for dp in dipeptides_seq])
        polarizability = np.mean([h(dp, aa_polarizability) for dp in dipeptides_seq])
        deltag = np.mean([h(dp, aa_deltaG) for dp in dipeptides_seq])

        physchem_features = [mw, charge, hydro, aromatic, pI, instability,
                             hydro_moment, aliphatic, boman, flexibility, polarizability, deltag]
    
    features = dipep_features + physchem_features
    
    df = pd.DataFrame([features], columns=feature_columns)
    df = df.astype('float32')  # ensure same type as training
    return df

# --- Prediction function ---
def predict_peptide(sequence: str):
    seq = "".join(sequence.split()).upper()
    if not seq:
        return []

    X = extract_features_app(seq)
    
    probs_list = model.predict_proba(X)  # list of arrays per target
    # --- probs_list: list of arrays from each estimator ---
    #probs_list = [est.predict_proba(X) for est in model]  # model is a list

    table = []
    for i, target in enumerate(TARGET_CELLS):
        prob = float(probs_list[i][0][1])
        table.append([target, round(prob, 4)])
    return table


# --- Gradio Interface ---
custom_css = """
footer, .footer {display:none !important;}
"""

with gr.Blocks(css=custom_css, theme="default") as demo:
    gr.Markdown("## Peptide Antimicrobial Predictor\nEnter a peptide sequence to predict efficacy/toxicity.")
    
    seq_input = gr.Textbox(label="Enter Peptide Sequence")
    
    with gr.Row():
        predict_btn = gr.Button("Predict", variant="primary")
        clear_btn = gr.Button("Clear")
    
    table_output = gr.Dataframe(
        headers=["Target Cell", "Probability of Efficacy/Toxicity"],
        datatype=["str","number"],
        interactive=False
    )
    
    predict_btn.click(fn=predict_peptide, inputs=seq_input, outputs=table_output)
    clear_btn.click(fn=lambda: ("", []), outputs=[seq_input, table_output])
    
    # API endpoint for iOS app
    gr.api(predict_peptide, api_name="predict_peptide")

#if __name__ == "__main__": 
#    demo.launch()

if __name__ == "__main__": 
    demo.launch(show_error=True)