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# MultiMolecule
# Copyright (C) 2024-Present  MultiMolecule

# This file is part of MultiMolecule.

# MultiMolecule is free software: you can redistribute it and/or modify
# it under the terms of the GNU Affero General Public License as published by
# the Free Software Foundation, either version 3 of the License, or
# any later version.

# MultiMolecule is distributed in the hope that it will be useful,
# but WITHOUT ANY WARRANTY; without even the implied warranty of
# MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE.  See the
# GNU Affero General Public License for more details.

# You should have received a copy of the GNU Affero General Public License
# along with this program.  If not, see <http://www.gnu.org/licenses/>.

# For additional terms and clarifications, please refer to our License FAQ at:
# <https://multimolecule.danling.org/about/license-faq>.

from __future__ import annotations

import json
import math
import tempfile
import time
from collections.abc import Mapping
from datetime import datetime, timezone
from functools import lru_cache
from pathlib import Path
from typing import Any
from urllib.parse import parse_qs, urlparse

import gradio as gr
import matplotlib
import numpy as np
import pandas as pd
import torch
from Bio import SeqIO
from transformers import pipeline

matplotlib.use("Agg")
import matplotlib.pyplot as plt  # noqa: E402
import multimolecule  # noqa: E402, F401 - registers MultiMolecule models and pipelines with Transformers

MODEL_OPTIONS = {
    "MMSplice": "multimolecule/mmsplice",
    "MTSplice": "multimolecule/mtsplice",
    "HAL": "multimolecule/hal",
    "MaxEntScan score5": "multimolecule/maxentscan-score5",
    "MaxEntScan score3": "multimolecule/maxentscan-score3",
    "Pangolin": "multimolecule/pangolin",
    "SpTransformer": "multimolecule/sptransformer",
}
MODEL_LABELS = {model_id: label for label, model_id in MODEL_OPTIONS.items()}
FASTA_SUFFIXES = {".fa", ".fasta", ".fna"}
VALID_DNA = set("ACGTNRYSWKMBDHVX")
META_COLUMNS = {"scope", "position", "nucleotide", "sequence", "label", "type"}

DEFAULT_REFERENCE = "ACGT" * 25 + "CCCCCCCCCCCCCCCCCCCC" + "TGCA" * 25
DEFAULT_ALTERNATIVE = "ACGT" * 25 + "CCCCCCCCCCCTCCCCCCCC" + "TGCA" * 25


def _device() -> int:
    return 0 if torch.cuda.is_available() else -1


@lru_cache(maxsize=len(MODEL_OPTIONS))
def load_predictor(model_id: str):
    return pipeline("splice-variant-effect", model=model_id, device=_device())


def clean_sequence(sequence: str, label: str) -> str:
    sequence = "".join(str(sequence or "").split()).upper().replace("U", "T")
    if not sequence:
        raise gr.Error(f"{label} sequence is empty.")

    invalid = sorted(set(sequence) - VALID_DNA)
    if invalid:
        raise gr.Error(f"{label} sequence contains unsupported DNA symbols: {', '.join(invalid)}.")
    return sequence


def validate_pair(reference: str, alternative: str) -> tuple[str, str]:
    reference = clean_sequence(reference, "Reference")
    alternative = clean_sequence(alternative, "Alternative")
    if len(reference) != len(alternative):
        raise gr.Error(
            "Reference and alternative sequences must have the same length. "
            "This app does not perform genome-coordinate lookup or sequence reconstruction."
        )
    return reference, alternative


def load_fasta_pair(input_file: Any):
    if input_file is None:
        return gr.update(), gr.update()

    path = Path(getattr(input_file, "name", input_file))
    if path.suffix.lower() not in FASTA_SUFFIXES:
        raise gr.Error("Upload a FASTA file with two records: reference first, alternative second.")

    records = list(SeqIO.parse(path, "fasta"))
    if len(records) != 2:
        raise gr.Error(f"Expected exactly two FASTA records, found {len(records)}.")

    reference, alternative = validate_pair(str(records[0].seq), str(records[1].seq))
    return reference, alternative


def _json_safe(value: Any) -> Any:
    if isinstance(value, torch.Tensor):
        return _json_safe(value.detach().cpu().tolist())
    if isinstance(value, np.ndarray):
        return _json_safe(value.tolist())
    if isinstance(value, np.generic):
        return value.item()
    if isinstance(value, Mapping):
        return {str(key): _json_safe(item) for key, item in value.items()}
    if isinstance(value, (list, tuple)):
        return [_json_safe(item) for item in value]
    return value


def _is_scalar(value: Any) -> bool:
    if isinstance(value, (str, bytes)) or value is None:
        return False
    try:
        float(value)
    except (TypeError, ValueError):
        return False
    return True


def _number(value: Any) -> float | Any:
    if not _is_scalar(value):
        return value
    number = float(value)
    if math.isfinite(number):
        return number
    return value


def _position_key(key: Any) -> bool:
    try:
        int(str(key))
    except ValueError:
        return False
    return True


def _vector_row(values: list[Any], channels: list[str], scalar_column: str, scope: str = "sequence") -> dict[str, Any]:
    row: dict[str, Any] = {"scope": scope}
    if channels and len(values) == len(channels):
        row.update({channel: _number(value) for channel, value in zip(channels, values)})
    elif len(values) == 1:
        row[scalar_column] = _number(values[0])
    else:
        row.update({f"{scalar_column}_{index}": _number(value) for index, value in enumerate(values)})
    return row


def _flatten_mapping(
    mapping: Mapping[str, Any],
    channels: list[str],
    scalar_column: str,
    prefix: str | None = None,
) -> dict[str, Any]:
    row: dict[str, Any] = {}
    for key, value in mapping.items():
        key = str(key)
        column = f"{prefix}_{key}" if prefix else key
        value = _json_safe(value)
        if _is_scalar(value) or value is None or isinstance(value, str):
            row[column] = _number(value)
        elif isinstance(value, Mapping):
            row.update(_flatten_mapping(value, channels, scalar_column, prefix=column))
        elif isinstance(value, list) and all(_is_scalar(item) for item in value):
            if key in META_COLUMNS:
                row[column] = value
            elif channels and len(value) == len(channels):
                row.update({channel: _number(item) for channel, item in zip(channels, value)})
            else:
                row.update({f"{column}_{index}": _number(item) for index, item in enumerate(value)})
        else:
            row[column] = value
    return row


def normalize_score_rows(score_value: Any, channels: list[str], scalar_column: str) -> list[dict[str, Any]]:
    score_value = _json_safe(score_value)
    if score_value is None:
        return []

    if _is_scalar(score_value):
        return [{"scope": "sequence", scalar_column: _number(score_value)}]

    if isinstance(score_value, Mapping):
        if score_value and not all(_position_key(key) for key in score_value):
            series_lengths = {
                len(value)
                for value in score_value.values()
                if isinstance(value, list) and all(_is_scalar(item) for item in value)
            }
            if len(series_lengths) == 1:
                length = series_lengths.pop()
                if length > 1 and all(isinstance(value, list) for value in score_value.values()):
                    return [
                        {
                            "position": position,
                            **{str(key): _number(value[position]) for key, value in score_value.items()},
                        }
                        for position in range(length)
                    ]
        if score_value and all(_position_key(key) for key in score_value):
            rows = []
            for key, value in score_value.items():
                row = {"position": int(str(key))}
                if isinstance(value, Mapping):
                    row.update(_flatten_mapping(value, channels, scalar_column))
                elif isinstance(value, list):
                    row.update(_vector_row(value, channels, scalar_column, scope="position"))
                    row.pop("scope", None)
                else:
                    row[scalar_column] = _number(value)
                rows.append(row)
            return rows
        return [_flatten_mapping(score_value, channels, scalar_column)]

    if isinstance(score_value, list):
        if not score_value:
            return []
        if all(_is_scalar(item) for item in score_value):
            return [_vector_row(score_value, channels, scalar_column)]
        rows = []
        for index, item in enumerate(score_value):
            item = _json_safe(item)
            if isinstance(item, Mapping):
                rows.append(_flatten_mapping(item, channels, scalar_column))
            elif isinstance(item, list):
                row = {"position": index}
                row.update(_vector_row(item, channels, scalar_column, scope="position"))
                row.pop("scope", None)
                rows.append(row)
            elif _is_scalar(item):
                rows.append({"position": index, scalar_column: _number(item)})
        return rows

    return [{"scope": "sequence", scalar_column: score_value}]


def result_table(result: Mapping[str, Any], score_key: str, scores_key: str, scalar_column: str) -> pd.DataFrame:
    channels = [str(channel) for channel in result.get("channels", [])]
    score_value = result.get(scores_key, result.get(score_key))
    rows = normalize_score_rows(score_value, channels, scalar_column)
    if not rows:
        return pd.DataFrame()

    table = pd.DataFrame(rows)
    ordered = [column for column in ("scope", "position", "nucleotide", "sequence", "label", "type") if column in table]
    remaining = [column for column in table.columns if column not in ordered]
    return table[ordered + remaining]


def dataframe_records(table: pd.DataFrame) -> list[dict[str, Any]]:
    if table.empty:
        return []
    return json.loads(table.to_json(orient="records"))


def difference_summary(reference: str, alternative: str) -> dict[str, Any]:
    differences = [
        {
            "position": index,
            "reference": ref_base,
            "alternative": alt_base,
        }
        for index, (ref_base, alt_base) in enumerate(zip(reference, alternative))
        if ref_base != alt_base
    ]
    return {
        "count": len(differences),
        "positions": differences[:25],
        "positions_truncated": len(differences) > 25,
    }


def make_delta_plot(delta_table: pd.DataFrame, model_label: str):
    fig, ax = plt.subplots(figsize=(7, 2.8))
    values: list[tuple[str, float]] = []

    if not delta_table.empty:
        numeric_columns = [
            column
            for column in delta_table.columns
            if column not in META_COLUMNS and pd.api.types.is_numeric_dtype(delta_table[column])
        ]
        for _, row in delta_table.iterrows():
            position = row.get("position")
            for column in numeric_columns:
                value = row.get(column)
                if pd.notna(value):
                    suffix = f"@{int(position)}" if position is not None and pd.notna(position) else ""
                    values.append((f"{column}{suffix}", float(value)))

    values = sorted(values, key=lambda item: abs(item[1]), reverse=True)[:20]
    values.reverse()
    if not values:
        ax.text(0.5, 0.5, "No numeric delta scores", ha="center", va="center")
        ax.set_axis_off()
        fig.tight_layout()
        return fig

    labels, scores = zip(*values)
    colors = ["#2563eb" if score >= 0 else "#dc2626" for score in scores]
    ax.barh(labels, scores, color=colors)
    ax.axvline(0, color="#111827", linewidth=0.8)
    ax.set_title(f"{model_label} top delta scores")
    ax.set_xlabel("alternative - reference")
    ax.tick_params(axis="y", labelsize=8)
    fig.tight_layout()
    return fig


def write_result_files(
    metadata: dict[str, Any],
    result: Mapping[str, Any],
    delta_table: pd.DataFrame,
    reference_table: pd.DataFrame,
    alternative_table: pd.DataFrame,
) -> tuple[str, str]:
    csv_tables = []
    for score_set, table in (
        ("delta", delta_table),
        ("reference", reference_table),
        ("alternative", alternative_table),
    ):
        if not table.empty:
            csv_table = table.copy()
            csv_table.insert(0, "score_set", score_set)
            csv_tables.append(csv_table)
    csv_payload = pd.concat(csv_tables, ignore_index=True, sort=False) if csv_tables else pd.DataFrame()

    csv_file = tempfile.NamedTemporaryFile("w", suffix=".csv", delete=False, newline="")
    csv_path = csv_file.name
    csv_file.close()
    csv_payload.to_csv(csv_path, index=False)

    json_payload = {
        "metadata": metadata,
        "result": _json_safe(result),
        "tables": {
            "delta": dataframe_records(delta_table),
            "reference": dataframe_records(reference_table),
            "alternative": dataframe_records(alternative_table),
        },
    }
    json_file = tempfile.NamedTemporaryFile("w", suffix=".json", delete=False)
    json_path = json_file.name
    json_file.close()
    with open(json_path, "w") as handle:
        json.dump(json_payload, handle, indent=2)

    return csv_path, json_path


def unpack_prediction_result(result: Any) -> Mapping[str, Any]:
    result = _json_safe(result)
    if isinstance(result, list):
        if len(result) != 1:
            raise gr.Error(f"Expected one prediction result, got {len(result)}.")
        result = result[0]
    if not isinstance(result, Mapping):
        raise gr.Error(f"Expected a prediction dictionary, got {type(result).__name__}.")
    return result


def predict(model_label: str, reference: str, alternative: str):
    started = time.perf_counter()
    model_id = MODEL_OPTIONS[model_label]
    reference, alternative = validate_pair(reference, alternative)

    try:
        predictor = load_predictor(model_id)
        result = unpack_prediction_result(predictor(reference, alternative=alternative))
    except gr.Error:
        raise
    except Exception as exc:
        raise gr.Error(f"Prediction failed for {model_label}: {exc}") from exc

    delta_table = result_table(result, "delta_score", "delta_scores", "delta_score")
    reference_table = result_table(result, "reference_score", "reference_scores", "reference_score")
    alternative_table = result_table(result, "alternative_score", "alternative_scores", "alternative_score")
    metadata = {
        "task": "splice-variant-effect",
        "model": model_id,
        "model_label": model_label,
        "device": "cuda" if torch.cuda.is_available() else "cpu",
        "reference_length": len(reference),
        "alternative_length": len(alternative),
        "differences": difference_summary(reference, alternative),
        "channels": result.get("channels", []),
        "output_fields": sorted(result.keys()),
        "runtime_seconds": round(time.perf_counter() - started, 3),
        "timestamp_utc": datetime.now(timezone.utc).isoformat(),
    }
    csv_path, json_path = write_result_files(metadata, result, delta_table, reference_table, alternative_table)
    delta_plot = make_delta_plot(delta_table, model_label)
    return delta_table, reference_table, alternative_table, metadata, delta_plot, csv_path, json_path


def initial_model(request: gr.Request):
    if request is None:
        return "MMSplice"

    query_params = getattr(request, "query_params", None)
    model_id = None
    if query_params is not None:
        model_id = query_params.get("model")
    if not model_id and getattr(request, "url", None):
        parsed = parse_qs(urlparse(str(request.url)).query)
        model_values = parsed.get("model")
        model_id = model_values[0] if model_values else None

    return MODEL_LABELS.get(model_id, "MMSplice")


with gr.Blocks(title="Splice Variant Effect") as demo:
    gr.Markdown(
        "# Splice Variant Effect\n"
        "Score paired reference and alternative DNA windows with MultiMolecule splice variant-effect models."
    )

    model = gr.Dropdown(
        choices=list(MODEL_OPTIONS.keys()),
        value="MMSplice",
        label="Checkpoint",
    )

    with gr.Row():
        reference = gr.Textbox(
            label="Reference DNA sequence",
            value=DEFAULT_REFERENCE,
            lines=5,
        )
        alternative = gr.Textbox(
            label="Alternative DNA sequence",
            value=DEFAULT_ALTERNATIVE,
            lines=5,
        )

    input_file = gr.File(
        label="Upload paired FASTA (reference record first, alternative record second)",
        file_types=[".fa", ".fasta", ".fna"],
    )
    run = gr.Button("Run variant effect", variant="primary")

    with gr.Row():
        delta_scores = gr.Dataframe(label="Delta scores")
        run_metadata = gr.JSON(label="Run metadata")

    with gr.Row():
        reference_scores = gr.Dataframe(label="Reference scores")
        alternative_scores = gr.Dataframe(label="Alternative scores")

    delta_plot = gr.Plot(label="Top delta scores")

    with gr.Row():
        csv_download = gr.File(label="Download CSV")
        json_download = gr.File(label="Download JSON")

    run.click(
        predict,
        inputs=[model, reference, alternative],
        outputs=[
            delta_scores,
            reference_scores,
            alternative_scores,
            run_metadata,
            delta_plot,
            csv_download,
            json_download,
        ],
    )
    input_file.change(load_fasta_pair, inputs=input_file, outputs=[reference, alternative])
    demo.load(initial_model, outputs=model)


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