Christina Theodoris
Fix isp perturb_group dims, reformat cell states dict to keyed, add attn mask
c2679c4 | """ | |
| Geneformer embedding extractor. | |
| Usage: | |
| from geneformer import EmbExtractor | |
| embex = EmbExtractor(model_type="CellClassifier", | |
| num_classes=3, | |
| emb_mode="cell", | |
| cell_emb_style="mean_pool", | |
| filter_data={"cell_type":["cardiomyocyte"]}, | |
| max_ncells=1000, | |
| max_ncells_to_plot=1000, | |
| emb_layer=-1, | |
| emb_label=["disease","cell_type"], | |
| labels_to_plot=["disease","cell_type"], | |
| forward_batch_size=100, | |
| nproc=16) | |
| embs = embex.extract_embs("path/to/model", | |
| "path/to/input_data", | |
| "path/to/output_directory", | |
| "output_prefix") | |
| embex.plot_embs(embs=embs, | |
| plot_style="heatmap", | |
| output_directory="path/to/output_directory", | |
| output_prefix="output_prefix") | |
| """ | |
| # imports | |
| import logging | |
| import anndata | |
| import matplotlib.pyplot as plt | |
| import numpy as np | |
| import pandas as pd | |
| import pickle | |
| import scanpy as sc | |
| import seaborn as sns | |
| import torch | |
| from collections import Counter | |
| from pathlib import Path | |
| from tqdm.notebook import trange | |
| from transformers import BertForMaskedLM, BertForTokenClassification, BertForSequenceClassification | |
| from .tokenizer import TOKEN_DICTIONARY_FILE | |
| from .in_silico_perturber import downsample_and_sort, \ | |
| gen_attention_mask, \ | |
| get_model_input_size, \ | |
| load_and_filter, \ | |
| load_model, \ | |
| mean_nonpadding_embs, \ | |
| pad_tensor_list, \ | |
| quant_layers | |
| logger = logging.getLogger(__name__) | |
| # average embedding position of goal cell states | |
| def get_embs(model, | |
| filtered_input_data, | |
| emb_mode, | |
| layer_to_quant, | |
| pad_token_id, | |
| forward_batch_size): | |
| model_input_size = get_model_input_size(model) | |
| total_batch_length = len(filtered_input_data) | |
| if ((total_batch_length-1)/forward_batch_size).is_integer(): | |
| forward_batch_size = forward_batch_size-1 | |
| embs_list = [] | |
| for i in trange(0, total_batch_length, forward_batch_size): | |
| max_range = min(i+forward_batch_size, total_batch_length) | |
| minibatch = filtered_input_data.select([i for i in range(i, max_range)]) | |
| max_len = max(minibatch["length"]) | |
| original_lens = torch.tensor(minibatch["length"]).to("cuda") | |
| minibatch.set_format(type="torch") | |
| input_data_minibatch = minibatch["input_ids"] | |
| input_data_minibatch = pad_tensor_list(input_data_minibatch, | |
| max_len, | |
| pad_token_id, | |
| model_input_size) | |
| with torch.no_grad(): | |
| outputs = model( | |
| input_ids = input_data_minibatch.to("cuda"), | |
| attention_mask = gen_attention_mask(minibatch) | |
| ) | |
| embs_i = outputs.hidden_states[layer_to_quant] | |
| if emb_mode == "cell": | |
| mean_embs = mean_nonpadding_embs(embs_i, original_lens) | |
| embs_list += [mean_embs] | |
| del outputs | |
| del minibatch | |
| del input_data_minibatch | |
| del embs_i | |
| del mean_embs | |
| torch.cuda.empty_cache() | |
| embs_stack = torch.cat(embs_list) | |
| return embs_stack | |
| def label_embs(embs, downsampled_data, emb_labels): | |
| embs_df = pd.DataFrame(embs.cpu()) | |
| if emb_labels is not None: | |
| for label in emb_labels: | |
| emb_label = downsampled_data[label] | |
| embs_df[label] = emb_label | |
| return embs_df | |
| def plot_umap(embs_df, emb_dims, label, output_file, kwargs_dict): | |
| only_embs_df = embs_df.iloc[:,:emb_dims] | |
| only_embs_df.index = pd.RangeIndex(0, only_embs_df.shape[0], name=None).astype(str) | |
| only_embs_df.columns = pd.RangeIndex(0, only_embs_df.shape[1], name=None).astype(str) | |
| vars_dict = {"embs": only_embs_df.columns} | |
| obs_dict = {"cell_id": list(only_embs_df.index), | |
| f"{label}": list(embs_df[label])} | |
| adata = anndata.AnnData(X=only_embs_df, obs=obs_dict, var=vars_dict) | |
| sc.tl.pca(adata, svd_solver='arpack') | |
| sc.pp.neighbors(adata) | |
| sc.tl.umap(adata) | |
| sns.set(rc={'figure.figsize':(10,10)}, font_scale=2.3) | |
| sns.set_style("white") | |
| default_kwargs_dict = {"palette":"Set2", "size":200} | |
| if kwargs_dict is not None: | |
| default_kwargs_dict.update(kwargs_dict) | |
| sc.pl.umap(adata, color=label, save=output_file, **default_kwargs_dict) | |
| def gen_heatmap_class_colors(labels, df): | |
| pal = sns.cubehelix_palette(len(Counter(labels).keys()), light=0.9, dark=0.1, hue=1, reverse=True, start=1, rot=-2) | |
| lut = dict(zip(map(str, Counter(labels).keys()), pal)) | |
| colors = pd.Series(labels, index=df.index).map(lut) | |
| return colors | |
| def gen_heatmap_class_dict(classes, label_colors_series): | |
| class_color_dict_df = pd.DataFrame({"classes": classes, "color": label_colors_series}) | |
| class_color_dict_df = class_color_dict_df.drop_duplicates(subset=["classes"]) | |
| return dict(zip(class_color_dict_df["classes"],class_color_dict_df["color"])) | |
| def make_colorbar(embs_df, label): | |
| labels = list(embs_df[label]) | |
| cell_type_colors = gen_heatmap_class_colors(labels, embs_df) | |
| label_colors = pd.DataFrame(cell_type_colors, columns=[label]) | |
| for i,row in label_colors.iterrows(): | |
| colors=row[0] | |
| if len(colors)!=3 or any(np.isnan(colors)): | |
| print(i,colors) | |
| label_colors.isna().sum() | |
| # create dictionary for colors and classes | |
| label_color_dict = gen_heatmap_class_dict(labels, label_colors[label]) | |
| return label_colors, label_color_dict | |
| def plot_heatmap(embs_df, emb_dims, label, output_file, kwargs_dict): | |
| sns.set_style("white") | |
| sns.set(font_scale=2) | |
| plt.figure(figsize=(15, 15), dpi=150) | |
| label_colors, label_color_dict = make_colorbar(embs_df, label) | |
| default_kwargs_dict = {"row_cluster": True, | |
| "col_cluster": True, | |
| "row_colors": label_colors, | |
| "standard_scale": 1, | |
| "linewidths": 0, | |
| "xticklabels": False, | |
| "yticklabels": False, | |
| "figsize": (15,15), | |
| "center": 0, | |
| "cmap": "magma"} | |
| if kwargs_dict is not None: | |
| default_kwargs_dict.update(kwargs_dict) | |
| g = sns.clustermap(embs_df.iloc[:,0:emb_dims].apply(pd.to_numeric), **default_kwargs_dict) | |
| plt.setp(g.ax_row_colors.get_xmajorticklabels(), rotation=45, ha="right") | |
| for label_color in list(label_color_dict.keys()): | |
| g.ax_col_dendrogram.bar(0, 0, color=label_color_dict[label_color], label=label_color, linewidth=0) | |
| l1 = g.ax_col_dendrogram.legend(title=f"{label}", | |
| loc="lower center", | |
| ncol=4, | |
| bbox_to_anchor=(0.5, 1), | |
| facecolor="white") | |
| plt.savefig(output_file, bbox_inches='tight') | |
| class EmbExtractor: | |
| valid_option_dict = { | |
| "model_type": {"Pretrained","GeneClassifier","CellClassifier"}, | |
| "num_classes": {int}, | |
| "emb_mode": {"cell","gene"}, | |
| "cell_emb_style": {"mean_pool"}, | |
| "filter_data": {None, dict}, | |
| "max_ncells": {None, int}, | |
| "emb_layer": {-1, 0}, | |
| "emb_label": {None, list}, | |
| "labels_to_plot": {None, list}, | |
| "forward_batch_size": {int}, | |
| "nproc": {int}, | |
| } | |
| def __init__( | |
| self, | |
| model_type="Pretrained", | |
| num_classes=0, | |
| emb_mode="cell", | |
| cell_emb_style="mean_pool", | |
| filter_data=None, | |
| max_ncells=1000, | |
| emb_layer=-1, | |
| emb_label=None, | |
| labels_to_plot=None, | |
| forward_batch_size=100, | |
| nproc=4, | |
| token_dictionary_file=TOKEN_DICTIONARY_FILE, | |
| ): | |
| """ | |
| Initialize embedding extractor. | |
| Parameters | |
| ---------- | |
| model_type : {"Pretrained","GeneClassifier","CellClassifier"} | |
| Whether model is the pretrained Geneformer or a fine-tuned gene or cell classifier. | |
| num_classes : int | |
| If model is a gene or cell classifier, specify number of classes it was trained to classify. | |
| For the pretrained Geneformer model, number of classes is 0 as it is not a classifier. | |
| emb_mode : {"cell","gene"} | |
| Whether to output cell or gene embeddings. | |
| cell_emb_style : "mean_pool" | |
| Method for summarizing cell embeddings. | |
| Currently only option is mean pooling of gene embeddings for given cell. | |
| filter_data : None, dict | |
| Default is to extract embeddings from all input data. | |
| Otherwise, dictionary specifying .dataset column name and list of values to filter by. | |
| max_ncells : None, int | |
| Maximum number of cells to extract embeddings from. | |
| Default is 1000 cells randomly sampled from input data. | |
| If None, will extract embeddings from all cells. | |
| emb_layer : {-1, 0} | |
| Embedding layer to extract. | |
| The last layer is most specifically weighted to optimize the given learning objective. | |
| Generally, it is best to extract the 2nd to last layer to get a more general representation. | |
| -1: 2nd to last layer | |
| 0: last layer | |
| emb_label : None, list | |
| List of column name(s) in .dataset to add as labels to embedding output. | |
| labels_to_plot : None, list | |
| Cell labels to plot. | |
| Shown as color bar in heatmap. | |
| Shown as cell color in umap. | |
| Plotting umap requires labels to plot. | |
| forward_batch_size : int | |
| Batch size for forward pass. | |
| nproc : int | |
| Number of CPU processes to use. | |
| token_dictionary_file : Path | |
| Path to pickle file containing token dictionary (Ensembl ID:token). | |
| """ | |
| self.model_type = model_type | |
| self.num_classes = num_classes | |
| self.emb_mode = emb_mode | |
| self.cell_emb_style = cell_emb_style | |
| self.filter_data = filter_data | |
| self.max_ncells = max_ncells | |
| self.emb_layer = emb_layer | |
| self.emb_label = emb_label | |
| self.labels_to_plot = labels_to_plot | |
| self.forward_batch_size = forward_batch_size | |
| self.nproc = nproc | |
| self.validate_options() | |
| # load token dictionary (Ensembl IDs:token) | |
| with open(token_dictionary_file, "rb") as f: | |
| self.gene_token_dict = pickle.load(f) | |
| self.pad_token_id = self.gene_token_dict.get("<pad>") | |
| def validate_options(self): | |
| # first disallow options under development | |
| if self.emb_mode == "gene": | |
| logger.error( | |
| "Extraction and plotting of gene-level embeddings currently under development. " \ | |
| "Current valid option for 'emb_mode': 'cell'" | |
| ) | |
| raise | |
| # confirm arguments are within valid options and compatible with each other | |
| for attr_name,valid_options in self.valid_option_dict.items(): | |
| attr_value = self.__dict__[attr_name] | |
| if type(attr_value) not in {list, dict}: | |
| if attr_value in valid_options: | |
| continue | |
| valid_type = False | |
| for option in valid_options: | |
| if (option in [int,list,dict]) and isinstance(attr_value, option): | |
| valid_type = True | |
| break | |
| if valid_type: | |
| continue | |
| logger.error( | |
| f"Invalid option for {attr_name}. " \ | |
| f"Valid options for {attr_name}: {valid_options}" | |
| ) | |
| raise | |
| if self.filter_data is not None: | |
| for key,value in self.filter_data.items(): | |
| if type(value) != list: | |
| self.filter_data[key] = [value] | |
| logger.warning( | |
| "Values in filter_data dict must be lists. " \ | |
| f"Changing {key} value to list ([{value}]).") | |
| def extract_embs(self, | |
| model_directory, | |
| input_data_file, | |
| output_directory, | |
| output_prefix): | |
| """ | |
| Extract embeddings from input data and save as results in output_directory. | |
| Parameters | |
| ---------- | |
| model_directory : Path | |
| Path to directory containing model | |
| input_data_file : Path | |
| Path to directory containing .dataset inputs | |
| output_directory : Path | |
| Path to directory where embedding data will be saved as csv | |
| output_prefix : str | |
| Prefix for output file | |
| """ | |
| filtered_input_data = load_and_filter(self.filter_data, self.nproc, input_data_file) | |
| downsampled_data = downsample_and_sort(filtered_input_data, self.max_ncells) | |
| model = load_model(self.model_type, self.num_classes, model_directory) | |
| layer_to_quant = quant_layers(model)+self.emb_layer | |
| embs = get_embs(model, | |
| downsampled_data, | |
| self.emb_mode, | |
| layer_to_quant, | |
| self.pad_token_id, | |
| self.forward_batch_size) | |
| embs_df = label_embs(embs, downsampled_data, self.emb_label) | |
| # save embeddings to output_path | |
| output_path = (Path(output_directory) / output_prefix).with_suffix(".csv") | |
| embs_df.to_csv(output_path) | |
| return embs_df | |
| def plot_embs(self, | |
| embs, | |
| plot_style, | |
| output_directory, | |
| output_prefix, | |
| max_ncells_to_plot=1000, | |
| kwargs_dict=None): | |
| """ | |
| Plot embeddings, coloring by provided labels. | |
| Parameters | |
| ---------- | |
| embs : pandas.core.frame.DataFrame | |
| Pandas dataframe containing embeddings output from extract_embs | |
| plot_style : str | |
| Style of plot: "heatmap" or "umap" | |
| output_directory : Path | |
| Path to directory where plots will be saved as pdf | |
| output_prefix : str | |
| Prefix for output file | |
| max_ncells_to_plot : None, int | |
| Maximum number of cells to plot. | |
| Default is 1000 cells randomly sampled from embeddings. | |
| If None, will plot embeddings from all cells. | |
| kwargs_dict : dict | |
| Dictionary of kwargs to pass to plotting function. | |
| """ | |
| if plot_style not in ["heatmap","umap"]: | |
| logger.error( | |
| "Invalid option for 'plot_style'. " \ | |
| "Valid options: {'heatmap','umap'}" | |
| ) | |
| raise | |
| if (plot_style == "umap") and (self.labels_to_plot is None): | |
| logger.error( | |
| "Plotting UMAP requires 'labels_to_plot'. " | |
| ) | |
| raise | |
| if max_ncells_to_plot > self.max_ncells: | |
| max_ncells_to_plot = self.max_ncells | |
| logger.warning( | |
| "max_ncells_to_plot must be <= max_ncells. " \ | |
| f"Changing max_ncells_to_plot to {self.max_ncells}.") | |
| if (max_ncells_to_plot is not None) \ | |
| and (max_ncells_to_plot < self.max_ncells): | |
| embs = embs.sample(max_ncells_to_plot, axis=0) | |
| if self.emb_label is None: | |
| label_len = 0 | |
| else: | |
| label_len = len(self.emb_label) | |
| emb_dims = embs.shape[1] - label_len | |
| if self.emb_label is None: | |
| emb_labels = None | |
| else: | |
| emb_labels = embs.columns[emb_dims:] | |
| if plot_style == "umap": | |
| for label in self.labels_to_plot: | |
| if label not in emb_labels: | |
| logger.warning( | |
| f"Label {label} from labels_to_plot " \ | |
| f"not present in provided embeddings dataframe.") | |
| continue | |
| output_prefix_label = "_" + output_prefix + f"_umap_{label}" | |
| output_file = (Path(output_directory) / output_prefix_label).with_suffix(".pdf") | |
| plot_umap(embs, emb_dims, label, output_prefix_label, kwargs_dict) | |
| if plot_style == "heatmap": | |
| for label in self.labels_to_plot: | |
| if label not in emb_labels: | |
| logger.warning( | |
| f"Label {label} from labels_to_plot " \ | |
| f"not present in provided embeddings dataframe.") | |
| continue | |
| output_prefix_label = output_prefix + f"_heatmap_{label}" | |
| output_file = (Path(output_directory) / output_prefix_label).with_suffix(".pdf") | |
| plot_heatmap(embs, emb_dims, label, output_file, kwargs_dict) | |