cgeorgiaw's picture
cgeorgiaw HF Staff
Update app.py
663b7d7 verified
import os
from typing import List
import gradio as gr
import pandas as pd
from datasets import load_dataset, Dataset
repo = 'hugging-science/m-boltz-submissions'
CONFIGS = {'antibody':'Antibody–Antigen', 'ligand':'Allosteric–Orthosteric', 'final':'final'}
# Column schemas per tab (used to create empty frames and to order columns)
COLUMNS = {
"antibody": [
"group_name",
"successful",
"high",
"medium",
"acceptable",
],
"ligand": [
"group_name",
"rmsd_top1_all",
"rmsd_top1_allosteric",
"rmsd_top1_orthosteric",
"rmsd_top5_all",
"structures_under_2a",
],
"final": [
"group_name",
"repository_url",
"commit_sha",
"challenge_type",
"description_link",
],
}
# You need a write‑enabled token available to the Space (Settings → Repository secrets)
# with name HF_TOKEN. This function raises a helpful error if it is missing.
def _hf_token() -> str:
token = os.getenv("HF_TOKEN")
if not token:
raise RuntimeError(
"Missing HF_TOKEN. Add a write-enabled token in your Space secrets."
)
return token
def _empty_df(columns: List[str]) -> pd.DataFrame:
return pd.DataFrame(columns=columns)
def load_df(config: str, columns: List[str]) -> pd.DataFrame:
"""Load the 'train' split from a Hub dataset into a pandas DataFrame.
Returns an empty DataFrame with the expected columns if the dataset doesn't exist yet.
"""
try:
ds = load_dataset(repo, config, split="train", token=_hf_token())
df = ds.to_pandas()
# Ensure all expected columns exist and in correct order
for c in columns:
if c not in df.columns:
df[c] = pd.NA
return df[columns]
except Exception:
# Fresh repo or first run: return empty with correct columns
return _empty_df(columns)
def push_df(config: str, df: pd.DataFrame) -> None:
"""Overwrite the dataset's 'train' split on the Hub with the provided DataFrame.
If the repo doesn't exist, this will create it under your account/org.
"""
# Convert to datasets.Dataset (drops pandas index)
ds = Dataset.from_pandas(df.reset_index(drop=True), preserve_index=False)
# Overwrite the dataset on the Hub. If it doesn't exist, it's created.
ds.push_to_hub(repo, config_name=config, token=_hf_token())
# --- Tab logic --------------------------------------------------------------
# Antibody–Antigen
def submit_antibody(group_name, successful, high, medium, acceptable):
config = CONFIGS["antibody"]
cols = COLUMNS["antibody"]
df = load_df(config, cols)
row = {
"group_name": group_name or "",
"successful": int(successful) if successful is not None else 0,
"high": int(high) if high is not None else 0,
"medium": int(medium) if medium is not None else 0,
"acceptable": int(acceptable) if acceptable is not None else 0,
}
# Overwrite if group_name already exists
if group_name and not df.empty:
df = df[df["group_name"] != group_name]
df = pd.concat([df, pd.DataFrame([row])], ignore_index=True)
push_df(config, df)
# Re-load to ensure what we show is exactly what's on the Hub
return load_df(config, cols)
def refresh_antibody():
return load_df(CONFIGS["antibody"], COLUMNS["antibody"])
# Allosteric–Orthosteric
def submit_ligand(group_name, rmsd_top1_all, rmsd_top1_allosteric, rmsd_top1_orthosteric, rmsd_top5_all, structures_under_2a):
config = CONFIGS["ligand"]
cols = COLUMNS["ligand"]
df = load_df(config, cols)
row = {
"group_name": group_name or "",
"rmsd_top1_all": float(rmsd_top1_all) if rmsd_top1_all is not None else None,
"rmsd_top1_allosteric": float(rmsd_top1_allosteric) if rmsd_top1_allosteric is not None else None,
"rmsd_top1_orthosteric": float(rmsd_top1_orthosteric) if rmsd_top1_orthosteric is not None else None,
"rmsd_top5_all": float(rmsd_top5_all) if rmsd_top5_all is not None else None,
"structures_under_2a": int(structures_under_2a) if structures_under_2a is not None else 0,
}
# Overwrite if group_name already exists
if group_name and not df.empty:
df = df[df["group_name"] != group_name]
df = pd.concat([df, pd.DataFrame([row])], ignore_index=True)
push_df(config, df)
return load_df(config, cols)
def refresh_ligand():
return load_df(CONFIGS["ligand"], COLUMNS["ligand"])
# Final Submission
def submit_final(group_name, repository_url, commit_sha, challenge_type, description_link):
config = CONFIGS["final"]
cols = COLUMNS["final"]
df = load_df(config, cols)
row = {
"group_name": group_name or "",
"repository_url": repository_url or "",
"commit_sha": commit_sha or "",
"challenge_type": challenge_type or "",
"description_link": description_link or "",
}
# Overwrite if group_name already exists
if group_name and not df.empty:
df = df[df["group_name"] != group_name]
df = pd.concat([df, pd.DataFrame([row])], ignore_index=True)
push_df(config, df)
return load_df(config, cols)
def refresh_final():
return load_df(CONFIGS["final"], COLUMNS["final"])
# --- UI ---------------------------------------------------------------------
with gr.Blocks(title="Binding Challenges") as app:
gr.Markdown("""# M-Boltz Hackathon\n
Welcome to the M-Boltz Hack! This is the submission portal for the two binding challenges: Antibody–Antigen Binding and Allosteric–Orthosteric Ligand Binding.\n
Please use the respective tabs to submit your results and view the leaderboard for each challenge. Once you are ready to make your final submission, please use the 'Final Submission' tab. If you have any questions or issues, don't hesistate to open a Discussion in the Community tab.\n
""")
with gr.Tab("Antibody–Antigen Binding Challenge"):
gr.Markdown("""
# Antibody-Antigen Binding Challenge
The goal of this challenge is to improve Boltz-2 accuracy for predicting the correct poses of a Fv/Fab region binding to an antigen.\n
Accuracy will be measured through the Capri-Q docking assessment classification scores and the final winner will be determined based on the number of successful top-1 predictions on our *internal* test set. However, you are encouraged to submit results on the training set during the hack to see where you stack up.\n
A prediction is deemed successful if the Capri-Q classification is either "high", "medium", or "acceptable".
If multiple entries reach the same number of successful predictions, ties are broken by looking at the number of predictions with "High" classification, then with "Medium" classification and finally with "Acceptable" classification.
If there is still a tie then, we will look at the mean RMSD across all successful predictions.
""")
aa_group = gr.Textbox(label="Group Name", placeholder="Your group name")
with gr.Row():
aa_successful = gr.Number(label="#Successful", value=0, precision=0)
aa_high = gr.Number(label="#High", value=0, precision=0)
aa_medium = gr.Number(label="#Medium", value=0, precision=0)
aa_acceptable = gr.Number(label="#Acceptable", value=0, precision=0)
with gr.Row():
aa_submit = gr.Button("Submit")
aa_refresh = gr.Button("Refresh table")
aa_df = gr.Dataframe(
value=load_df(CONFIGS["antibody"], COLUMNS["antibody"]),
label="Submissions (Antibody–Antigen)",
interactive=False,
wrap=True,
)
aa_submit.click(
submit_antibody,
inputs=[aa_group, aa_successful, aa_high, aa_medium, aa_acceptable],
outputs=aa_df,
)
aa_refresh.click(refresh_antibody, outputs=aa_df)
with gr.Tab("Allosteric–Orthosteric Ligand Binding Challenge"):
gr.Markdown("""
# Allosteric-Orthosteric Ligand Binding Challenge
The goal of this challenge is to improve Boltz-2 accuracy for predicting the binding poses of either allosteric or orthosteric ligands.\n
The winner will be determined by accuracy measured on our *internal* test set by calculating the RMSD between the top-1 prediction and the experimental pose. However, submit your intermediate results here to see where you stack up!
""")
li_group = gr.Textbox(label="Group Name", placeholder="Your group name")
with gr.Row():
li_rmsd_top1_all = gr.Number(label="RMSD top-1 (all structures)")
li_rmsd_top1_allosteric = gr.Number(label="RMSD top-1 (allosteric)")
li_rmsd_top1_orthosteric = gr.Number(label="RMSD top-1 (orthosteric)")
with gr.Row():
li_rmsd_top5_all = gr.Number(label="RMSD top-5 (all structures)")
li_structures_under_2a = gr.Number(label="#structures with RMSD < 2A", value=0, precision=0)
with gr.Row():
li_submit = gr.Button("Submit")
li_refresh = gr.Button("Refresh table")
li_df = gr.Dataframe(
value=load_df(CONFIGS["ligand"], COLUMNS["ligand"]),
label="Submissions (Ligand Binding)",
interactive=False,
wrap=True,
)
li_submit.click(
submit_ligand,
inputs=[li_group, li_rmsd_top1_all, li_rmsd_top1_allosteric, li_rmsd_top1_orthosteric, li_rmsd_top5_all, li_structures_under_2a],
outputs=li_df,
)
li_refresh.click(refresh_ligand, outputs=li_df)
'''with gr.Tab("Final Submission"):
fs_group = gr.Textbox(label="Group Name", placeholder="Your group name")
fs_repo_url = gr.Textbox(label="Repository URL")
fs_commit_sha = gr.Textbox(label="Commit SHA")
fs_challenge_type = gr.Radio(
["allosteric-orthosteric binding", "antibody-antigen binding"],
label="Challenge Type"
)
fs_description_link = gr.Textbox(label="Link to Markdown Description", placeholder="Link to a markdown page in your repo")
with gr.Row():
fs_submit = gr.Button("Submit")
fs_refresh = gr.Button("Refresh table")
fs_df = gr.Dataframe(
value=load_df(CONFIGS["final"], COLUMNS["final"]),
label="Final submissions",
interactive=False,
wrap=True,
)
fs_submit.click(
submit_final,
inputs=[fs_group, fs_repo_url, fs_commit_sha, fs_challenge_type, fs_description_link],
outputs=fs_df,
)
fs_refresh.click(refresh_final, outputs=fs_df)'''
# For local dev: `python app.py`
if __name__ == "__main__":
app.launch()