spacr 0.0.35__py3-none-any.whl → 0.0.61__py3-none-any.whl

spacr/foldseek.py

@@ -1,26 +1,12 @@
-import os, shutil, subprocess, tarfile, glob, requests, time, random
-import pandas as pd
-from scipy.stats import fisher_exact
-from statsmodels.stats.multitest import multipletests
-from concurrent.futures import ProcessPoolExecutor, as_completed
-import seaborn as sns
-import matplotlib.pyplot as plt
+import os, shutil, subprocess, tarfile, requests
 import numpy as np
-
-import requests, time, random
-from concurrent.futures import ProcessPoolExecutor, as_completed
-
 import pandas as pd
 from scipy.stats import fisher_exact
 from statsmodels.stats.multitest import multipletests
 from concurrent.futures import ProcessPoolExecutor, as_completed
-import pandas as pd
-from sklearn.metrics import precision_score, recall_score, f1_score, accuracy_score
-
 import seaborn as sns
 import matplotlib.pyplot as plt
-import numpy as np
-from matplotlib.ticker import FixedLocator
+from sklearn.metrics import precision_score, recall_score, f1_score, accuracy_score
 
 def run_command(command):
     print(f"Executing: {command}")

spacr/graph_learning.py

@@ -1,276 +1,320 @@
 import os
-import torch
-import torch.nn as nn
-import torch.nn.functional as F
-from collections import defaultdict
-from torch.utils.data import Dataset, DataLoader
+os.environ['DGLBACKEND'] = 'pytorch'
+import torch, dgl
 import pandas as pd
-import numpy as np
-import torch.optim as optim
-
-def generate_graphs(sequencing, scores, cell_min, gene_min_read):
-    # Load and preprocess sequencing (gene) data
-    gene_df = pd.read_csv(sequencing)
-    gene_df = gene_df.rename(columns={'prc': 'well_id', 'grna': 'gene_id', 'count': 'read_count'})
-    # Filter out genes with read counts less than gene_min_read
-    gene_df = gene_df[gene_df['read_count'] >= gene_min_read]
-    total_reads_per_well = gene_df.groupby('well_id')['read_count'].sum().reset_index(name='total_reads')
-    gene_df = gene_df.merge(total_reads_per_well, on='well_id')
-    gene_df['well_read_fraction'] = gene_df['read_count'] / gene_df['total_reads']
-
-    # Load and preprocess cell score data
-    cell_df = pd.read_csv(scores)
-    cell_df = cell_df[['prcfo', 'prc', 'pred']].rename(columns={'prcfo': 'cell_id', 'prc': 'well_id', 'pred': 'score'})
-
-    # Create a global mapping of gene IDs to indices
-    unique_genes = gene_df['gene_id'].unique()
-    gene_id_to_index = {gene_id: index for index, gene_id in enumerate(unique_genes)}
-
-    graphs = []
-    for well_id in pd.unique(gene_df['well_id']):
-        well_genes = gene_df[gene_df['well_id'] == well_id]
-        well_cells = cell_df[cell_df['well_id'] == well_id]
-
-        # Skip wells with no cells or genes or with fewer cells than threshold
-        if well_cells.empty or well_genes.empty or len(well_cells) < cell_min:
-            continue
-
-        # Initialize gene features tensor with zeros for all unique genes
-        gene_features = torch.zeros((len(gene_id_to_index), 1), dtype=torch.float)
-
-        # Update gene features tensor with well_read_fraction for genes present in this well
-        for _, row in well_genes.iterrows():
-            gene_index = gene_id_to_index[row['gene_id']]
-            gene_features[gene_index] = torch.tensor([[row['well_read_fraction']]])
-
-        # Prepare cell features (scores)
-        cell_features = torch.tensor(well_cells['score'].values, dtype=torch.float).view(-1, 1)
-
-        num_genes = len(gene_id_to_index)
-        num_cells = cell_features.size(0)
-        num_nodes = num_genes + num_cells
-
-        # Create adjacency matrix connecting each cell to all genes in the well
-        adj = torch.zeros((num_nodes, num_nodes), dtype=torch.float)
-        for _, row in well_genes.iterrows():
-            gene_index = gene_id_to_index[row['gene_id']]
-            adj[num_genes:, gene_index] = 1
-
-        graph = {
-            'adjacency_matrix': adj,
-            'gene_features': gene_features,
-            'cell_features': cell_features,
-            'num_cells': num_cells,
-            'num_genes': num_genes
-        }
-        graphs.append(graph)
-
-    print(f'Generated dataset with {len(graphs)} graphs')
-    return graphs, gene_id_to_index
-
-def print_graphs_info(graphs, gene_id_to_index):
-    # Invert the gene_id_to_index mapping for easy lookup
-    index_to_gene_id = {v: k for k, v in gene_id_to_index.items()}
-
-    for i, graph in enumerate(graphs, start=1):
-        print(f"Graph {i}:")
-        num_genes = graph['num_genes']
-        num_cells = graph['num_cells']
-        gene_features = graph['gene_features']
-        cell_features = graph['cell_features']
-
-        print(f"  Number of Genes: {num_genes}")
-        print(f"  Number of Cells: {num_cells}")
-
-        # Identify genes present in the graph based on non-zero feature values
-        present_genes = [index_to_gene_id[idx] for idx, feature in enumerate(gene_features) if feature.item() > 0]
-        print("  Genes present in this Graph:", present_genes)
-
-        # Display gene features for genes present in the graph
-        print("  Gene Features:")
-        for gene_id in present_genes:
-            idx = gene_id_to_index[gene_id]
-            print(f"    {gene_id}: {gene_features[idx].item()}")
-
-        # Display a sample of cell features, for brevity
-        print("  Cell Features (sample):")
-        for idx, feature in enumerate(cell_features[:min(5, len(cell_features))]):
-            print(f"    Cell {idx+1}: {feature.item()}")
-
-        print("-" * 40)
-
-class Attention(nn.Module):
-    def __init__(self, feature_dim, attn_dim, dropout_rate=0.1):
-        super(Attention, self).__init__()
-        self.query = nn.Linear(feature_dim, attn_dim)
-        self.key = nn.Linear(feature_dim, attn_dim)
-        self.value = nn.Linear(feature_dim, feature_dim)
-        self.scale = 1.0 / (attn_dim ** 0.5)
-        self.dropout = nn.Dropout(dropout_rate)
-
-    def forward(self, gene_features, cell_features):
-        # Queries come from the cell features
-        q = self.query(cell_features)
-        # Keys and values come from the gene features
-        k = self.key(gene_features)
-        v = self.value(gene_features)
-        
-        # Compute attention weights
-        attn_weights = torch.matmul(q, k.transpose(-2, -1)) * self.scale
-        attn_weights = F.softmax(attn_weights, dim=-1)
-        # Apply dropout to attention weights
-        attn_weights = self.dropout(attn_weights)  
-
-        # Apply attention weights to the values
-        attn_output = torch.matmul(attn_weights, v)
-        
-        return attn_output, attn_weights
-
-class GraphTransformer(nn.Module):
-    def __init__(self, gene_feature_size, cell_feature_size, hidden_dim, output_dim, attn_dim, dropout_rate=0.1):
-        super(GraphTransformer, self).__init__()
-        self.gene_transform = nn.Linear(gene_feature_size, hidden_dim)
-        self.cell_transform = nn.Linear(cell_feature_size, hidden_dim)
-        self.dropout = nn.Dropout(dropout_rate)
-
-        # Attention layer to let each cell attend to all genes
-        self.attention = Attention(hidden_dim, attn_dim)
-
-        # This layer is used to transform the combined features after attention
-        self.combine_transform = nn.Linear(2 * hidden_dim, hidden_dim)
-
-        # Output layer for predicting cell scores, ensuring it matches the number of cells
-        self.cell_output = nn.Linear(hidden_dim, output_dim)
+import torch.nn as nn
+from torchvision import datasets, transforms
+from sklearn.preprocessing import StandardScaler
+from PIL import Image
+import dgl.nn.pytorch as dglnn
+from sklearn.datasets import make_classification
+from .utils import SelectChannels
+
+# approach outline
+#
+#    1. Data Preparation:
+#        Test Mode: Load MNIST data and generate synthetic gRNA data.
+#        Real Data: Load image paths and sequencing data as fractions.
+#
+#    2. Graph Construction:
+#        Each well is represented as a graph.
+#        Each graph has cell nodes (with image features) and gRNA nodes (with gRNA fraction features).
+#        Each cell node is connected to each gRNA node within the same well.
+#
+#    3. Model Training:
+#        Use an encoder-decoder architecture with the Graph Transformer model.
+#        The encoder processes the cell and gRNA nodes.
+#        The decoder outputs the phenotype score for each cell node.
+#        The model is trained on all wells (including positive and negative controls).
+#        The model learns to score the gRNA in column 1 (negative control) as 0 and the gRNA in column 2 (positive control) as 1 based on the cell features.
+#
+#    4. Model Application:
+#        Apply the trained model to all wells to get classification probabilities.
+#
+#    5. Evaluation:
+#        Evaluate the model's performance using the control wells.
+#
+#    6. Association Analysis:
+#        Analyze the association between gRNAs and the classification scores.
+#
+# The model learns the associations between cell features and phenotype scores based on the controls and then generalizes this learning to the screening wells.
+
+# Load MNIST data for testing
+def load_mnist_data():
+    transform = transforms.Compose([
+        transforms.Resize((28, 28)),
+        transforms.ToTensor(),
+        transforms.Normalize((0.1307,), (0.3081,))
+    ])
+    mnist_train = datasets.MNIST(root='./data', train=True, download=True, transform=transform)
+    mnist_test = datasets.MNIST(root='./data', train=False, download=True, transform=transform)
+    return mnist_train, mnist_test
+
+# Generate synthetic gRNA data
+def generate_synthetic_grna_data(n_samples, n_features):
+    X, y = make_classification(n_samples=n_samples, n_features=n_features, n_informative=5, n_redundant=0, n_classes=2, random_state=42)
+    synthetic_data = pd.DataFrame(X, columns=[f'feature_{i}' for i in range(n_features)])
+    synthetic_data['label'] = y
+    return synthetic_data
+
+# Preprocess image
+def preprocess_image(image_path, image_size=224, channels=[1,2,3], normalize=True):
+
+    if normalize:
+        preprocess = transforms.Compose([
+            transforms.ToTensor(),
+            transforms.CenterCrop(size=(image_size, image_size)),
+            SelectChannels(channels),
+            transforms.Normalize(mean=(0.5, 0.5, 0.5), std=(0.5, 0.5, 0.5))])
+    else:
+        preprocess = transforms.Compose([
+            transforms.ToTensor(),
+            transforms.CenterCrop(size=(image_size, image_size)),
+            SelectChannels(channels)])
+    
+    image = Image.open(image_path).convert('RGB')
+    return preprocess(image)
+
+def extract_metadata_from_path(path):
+    """
+    Extract metadata from the image path.
+    The path format is expected to be plate_well_field_objectnumber.png
+
+    Parameters:
+    path (str): The path to the image file.
+
+    Returns:
+    dict: A dictionary with the extracted metadata.
+    """
+    filename = os.path.basename(path)
+    name, ext = os.path.splitext(filename)
+
+    # Ensure the file has the correct extension
+    if ext.lower() != '.png':
+        raise ValueError("Expected a .png file")
+
+    # Split the name by underscores
+    parts = name.split('_')
+    if len(parts) != 4:
+        raise ValueError("Expected filename format: plate_well_field_objectnumber.png")
+
+    plate, well, field, object_number = parts
+
+    return {'plate': plate, 'well': well,'field': field, 'object_number': object_number}
+
+# Load images
+def load_images(image_paths, image_size=224, channels=[1,2,3], normalize=True):
+    images = []
+    metadata_list = []
+    for path in image_paths:
+        image = preprocess_image(path, image_size, channels, normalize)
+        images.append(image)
+        metadata = extract_metadata_from_path(path)  # Extract metadata from image path or database
+        metadata_list.append(metadata)
+    return torch.stack(images), metadata_list
+
+# Normalize sequencing data
+def normalize_sequencing_data(sequencing_data):
+    scaler = StandardScaler()
+    sequencing_data.iloc[:, 2:] = scaler.fit_transform(sequencing_data.iloc[:, 2:])
+    return sequencing_data
+
+# Construct graph for each well
+def construct_well_graph(images, image_metadata, grna_data):
+    cell_nodes = len(images)
+    grna_nodes = grna_data.shape[0]
+    
+    graph = dgl.DGLGraph()
+    graph.add_nodes(cell_nodes + grna_nodes)
 
-    def forward(self, adjacency_matrix, gene_features, cell_features):
-        # Apply initial transformation to gene and cell features
-        transformed_gene_features = F.relu(self.gene_transform(gene_features))
-        transformed_cell_features = F.relu(self.cell_transform(cell_features))
+    cell_features = torch.stack(images)
+    grna_features = torch.tensor(grna_data).float()
 
-        # Incorporate attention mechanism
-        attn_output, attn_weights = self.attention(transformed_gene_features, transformed_cell_features)
+    features = torch.cat([cell_features, grna_features], dim=0)
+    graph.ndata['features'] = features
 
-        # Combine the transformed cell features with the attention output features
-        combined_cell_features = torch.cat((transformed_cell_features, attn_output), dim=1)
-        
-        # Apply dropout here as well
-        combined_cell_features = self.dropout(combined_cell_features)  
+    for i in range(cell_nodes):
+        for j in range(cell_nodes, cell_nodes + grna_nodes):
+            graph.add_edge(i, j)
+            graph.add_edge(j, i)
+    
+    return graph
 
-        combined_cell_features = F.relu(self.combine_transform(combined_cell_features))
+def create_graphs_for_wells(images, metadata_list, sequencing_data):
+    graphs = []
+    labels = []
 
-        # Combine gene and cell features for message passing
-        combined_features = torch.cat((transformed_gene_features, combined_cell_features), dim=0)
+    for well in sequencing_data['well'].unique():
+        well_images = [img for img, meta in zip(images, metadata_list) if meta['well'] == well]
+        well_metadata = [meta for meta in metadata_list if meta['well'] == well]
+        well_grna_data = sequencing_data[sequencing_data['well'] == well].iloc[:, 2:].values
 
-        # Apply message passing via adjacency matrix multiplication
-        message_passed_features = torch.matmul(adjacency_matrix, combined_features)
+        graph = construct_well_graph(well_images, well_metadata, well_grna_data)
+        graphs.append(graph)
 
-        # Predict cell scores from the post-message passed cell features
-        cell_scores = self.cell_output(message_passed_features[-cell_features.size(0):])
+        if well_metadata[0]['column'] == 1:  # Negative control
+            labels.append(0)
+        elif well_metadata[0]['column'] == 2:  # Positive control
+            labels.append(1)
+        else:
+            labels.append(-1)  # Screen wells, will be used for evaluation
+
+    return graphs, labels
+
+# Define Encoder-Decoder Transformer Model
+class Encoder(nn.Module):
+    def __init__(self, in_feats, hidden_feats):
+        super(Encoder, self).__init__()
+        self.conv1 = dglnn.GraphConv(in_feats, hidden_feats)
+        self.conv2 = dglnn.GraphConv(hidden_feats, hidden_feats)
+
+    def forward(self, g, features):
+        x = self.conv1(g, features)
+        x = torch.relu(x)
+        x = self.conv2(g, x)
+        x = torch.relu(x)
+        return x
+
+class Decoder(nn.Module):
+    def __init__(self, hidden_feats, out_feats):
+        super(Decoder, self).__init__()
+        self.linear = nn.Linear(hidden_feats, out_feats)
+
+    def forward(self, x):
+        return self.linear(x)
 
-        return cell_scores, attn_weights
-    
-def train_graph_transformer(graphs, lr=0.01, dropout_rate=0.1, weight_decay=0.00001, epochs=100, save_fldr='', acc_threshold = 0.1):
-    device = torch.device('cuda' if torch.cuda.is_available() else 'cpu')
-    model = GraphTransformer(gene_feature_size=1, cell_feature_size=1, hidden_dim=256, output_dim=1, attn_dim=128, dropout_rate=dropout_rate).to(device)
+class GraphTransformer(nn.Module):
+    def __init__(self, in_feats, hidden_feats, out_feats):
+        super(GraphTransformer, self).__init__()
+        self.encoder = Encoder(in_feats, hidden_feats)
+        self.decoder = Decoder(hidden_feats, out_feats)
 
-    criterion = nn.MSELoss()
-    #optimizer = torch.optim.Adam(model.parameters(), lr=lr)
-    optimizer = optim.AdamW(model.parameters(), lr=lr, weight_decay=weight_decay)
+    def forward(self, g, features):
+        x = self.encoder(g, features)
+        with g.local_scope():
+            g.ndata['h'] = x
+            hg = dgl.mean_nodes(g, 'h')
+        return self.decoder(hg)
 
-    training_log = []
-    
-    accumulate_grad_batches=1
-    threshold=acc_threshold
-    
+def train(graphs, labels, model, loss_fn, optimizer, epochs=100):
     for epoch in range(epochs):
         model.train()
         total_loss = 0
-        total_correct = 0
-        total_samples = 0
-        optimizer.zero_grad()
-        batch_count = 0  # Initialize batch_count
+        correct = 0
+        total = 0
         
-        for graph in graphs:
-            adjacency_matrix = graph['adjacency_matrix'].to(device)
-            gene_features = graph['gene_features'].to(device)
-            cell_features = graph['cell_features'].to(device)
-            num_cells = graph['num_cells']
-            predictions, attn_weights = model(adjacency_matrix, gene_features, cell_features)
-            predictions = predictions.squeeze()
-            true_scores = cell_features[:num_cells, 0]
-            loss = criterion(predictions, true_scores) / accumulate_grad_batches
+        for graph, label in zip(graphs, labels):
+            if label == -1:
+                continue  # Skip screen wells for training
+            
+            features = graph.ndata['features']
+            logits = model(graph, features)
+            loss = loss_fn(logits, torch.tensor([label]))
+
+            optimizer.zero_grad()
             loss.backward()
-
-            # Calculate "accuracy"
-            with torch.no_grad():
-                correct_predictions = (torch.abs(predictions - true_scores) / true_scores <= threshold).sum().item()
-                total_correct += correct_predictions
-                total_samples += num_cells
-
-            batch_count += 1  # Increment batch_count
-            if batch_count % accumulate_grad_batches == 0 or batch_count == len(graphs):
-                optimizer.step()
-                optimizer.zero_grad()
-
-            total_loss += loss.item() * accumulate_grad_batches
+            optimizer.step()
+            
+            total_loss += loss.item()
+            _, predicted = torch.max(logits, 1)
+            correct += (predicted == label).sum().item()
+            total += 1
         
-        accuracy = total_correct / total_samples
-        training_log.append({"Epoch": epoch+1, "Average Loss": total_loss / len(graphs), "Accuracy": accuracy})
-        print(f"Epoch {epoch+1}, Loss: {total_loss / len(graphs)}, Accuracy: {accuracy}", end="\r", flush=True)
-    
-    # Save the training log and model as before
-    os.makedirs(save_fldr, exist_ok=True)
-    log_path = os.path.join(save_fldr, 'training_log.csv')
-    training_log_df = pd.DataFrame(training_log)
-    training_log_df.to_csv(log_path, index=False)
-    print(f"Training log saved to {log_path}")
-    
-    model_path = os.path.join(save_fldr, 'model.pth')
-    torch.save(model.state_dict(), model_path)
-    print(f"Model saved to {model_path}")
+        accuracy = correct / total if total > 0 else 0
+        print(f'Epoch {epoch}, Loss: {total_loss / total:.4f}, Accuracy: {accuracy * 100:.2f}%')
 
-    return model
-        
-def annotate_cells_with_genes(graphs, model, gene_id_to_index):
-    device = torch.device('cuda' if torch.cuda.is_available() else 'cpu')
-    model.to(device)
+def apply_model(graphs, model):
     model.eval()
-    annotated_data = []
+    results = []
 
     with torch.no_grad():
         for graph in graphs:
-            adjacency_matrix = graph['adjacency_matrix'].to(device)
-            gene_features = graph['gene_features'].to(device)
-            cell_features = graph['cell_features'].to(device)
-
-            predictions, attn_weights = model(adjacency_matrix, gene_features, cell_features)
-            predictions = np.atleast_1d(predictions.squeeze().cpu().numpy())
-            attn_weights = np.atleast_2d(attn_weights.squeeze().cpu().numpy())
-
-            # This approach assumes all genes in gene_id_to_index are used in the model.
-            # Create a list of gene IDs present in this specific graph.
-            present_gene_ids = [key for key, value in gene_id_to_index.items() if value < gene_features.size(0)]
-
-            for cell_idx in range(cell_features.size(0)):
-                true_score = cell_features[cell_idx, 0].item()
-                predicted_score = predictions[cell_idx]
-                
-                # Find the index of the most probable gene. 
-                most_probable_gene_idx = attn_weights[cell_idx].argmax()
-
-                if len(present_gene_ids) > most_probable_gene_idx:  # Ensure index is within the range
-                    most_probable_gene_id = present_gene_ids[most_probable_gene_idx]
-                    most_probable_gene_score = attn_weights[cell_idx, most_probable_gene_idx] if attn_weights.ndim > 1 else attn_weights[most_probable_gene_idx]
-
-                    annotated_data.append({
-                        "Cell ID": cell_idx,
-                        "Most Probable Gene": most_probable_gene_id,
-                        "Cell Score": true_score,
-                        "Predicted Cell Score": predicted_score,
-                        "Probability Score for Highest Gene": most_probable_gene_score
-                    })
-                else:
-                    # Handle the case where the index is out of bounds - this should not happen but is here for robustness
-                    print("Error: Gene index out of bounds. This might indicate a mismatch in the model's output.")
-
-    return pd.DataFrame(annotated_data)
+            features = graph.ndata['features']
+            logits = model(graph, features)
+            probabilities = torch.softmax(logits, dim=1)
+            results.append(probabilities[:, 1].item())
+    
+    return results
+
+def analyze_associations(probabilities, sequencing_data):
+    # Analyze associations between gRNAs and classification scores
+    sequencing_data['positive_prob'] = probabilities
+    return sequencing_data.groupby('gRNA').positive_prob.mean().sort_values(ascending=False)
+
+def train_graph_transformer(src, lr=0.01, epochs=100, hidden_feats=128, n_classes=2, row_limit=None, image_size=224, channels=[1,2,3], normalize=True, test_mode=False):
+    if test_mode:
+        # Load MNIST data
+        mnist_train, mnist_test = load_mnist_data()
+        
+        # Generate synthetic gRNA data
+        synthetic_grna_data = generate_synthetic_grna_data(len(mnist_train), 10)  # 10 synthetic features
+        sequencing_data = synthetic_grna_data
+        
+        # Load MNIST images and metadata
+        images = [] 
+        metadata_list = []
+        for idx, (img, label) in enumerate(mnist_train):
+            images.append(img)
+            metadata_list.append({'index': idx, 'plate': 'plate1', 'well': idx, 'column': label})
+        images = torch.stack(images)
+
+        # Normalize synthetic sequencing data
+        sequencing_data = normalize_sequencing_data(sequencing_data)
+    
+    else:
+        from .io import _read_and_join_tables
+        from .utils import get_db_paths, get_sequencing_paths, correct_paths
+
+        db_paths = get_db_paths(src)
+        seq_paths = get_sequencing_paths(src)
+
+        if isinstance(src, str):
+            src = [src]
+
+        sequencing_data = pd.DataFrame()
+        for seq in seq_paths:
+            sequencing_df = pd.read_csv(seq)
+            sequencing_data = pd.concat([sequencing_data, sequencing_df], axis=0)
+
+        all_df = pd.DataFrame()
+        for db_path in db_paths:
+            df = _read_and_join_tables(db_path, table_names=['png_list'])
+            all_df = pd.concat([all_df, df], axis=0)
+
+        tables = ['png_list']
+        all_df = pd.DataFrame()
+        image_paths = []
+        for i, db_path in enumerate(db_paths):
+            df = _read_and_join_tables(db_path, table_names=tables)
+            df, image_paths_tmp = correct_paths(df, src[i])
+            all_df = pd.concat([all_df, df], axis=0)
+            image_paths.extend(image_paths_tmp)
+
+        if row_limit is not None:
+            all_df = all_df.sample(n=row_limit, random_state=42)
+
+        images, metadata_list = load_images(image_paths, image_size, channels, normalize)
+        sequencing_data = normalize_sequencing_data(sequencing_data)
+
+    # Step 1: Create graphs for each well
+    graphs, labels = create_graphs_for_wells(images, metadata_list, sequencing_data)
+
+    # Step 2: Train Graph Transformer Model
+    in_feats = graphs[0].ndata['features'].shape[1]
+    model = GraphTransformer(in_feats, hidden_feats, n_classes)
+    loss_fn = nn.CrossEntropyLoss()
+    optimizer = torch.optim.Adam(model.parameters(), lr=lr)
+
+    # Train the model
+    train(graphs, labels, model, loss_fn, optimizer, epochs)
+
+    # Step 3: Apply the model to all wells (including screen wells)
+    screen_graphs = [graph for graph, label in zip(graphs, labels) if label == -1]
+    probabilities = apply_model(screen_graphs, model)
+
+    # Step 4: Analyze associations between gRNAs and classification scores
+    associations = analyze_associations(probabilities, sequencing_data)
+    print("Top associated gRNAs with positive control phenotype:")
+    print(associations.head())
+
+    return model, associations