""" Geneformer in silico perturber stats generator. Usage: from geneformer import InSilicoPerturberStats ispstats = InSilicoPerturberStats(mode="goal_state_shift", combos=0, anchor_gene=None, cell_states_to_model={"disease":(["dcm"],["ctrl"],["hcm"])}) ispstats.get_stats("path/to/input_data", None, "path/to/output_directory", "output_prefix") """ import os import logging import numpy as np import pandas as pd import pickle import statsmodels.stats.multitest as smt from pathlib import Path from scipy.stats import ranksums from tqdm.notebook import trange from .tokenizer import TOKEN_DICTIONARY_FILE GENE_NAME_ID_DICTIONARY_FILE = Path(__file__).parent / "gene_name_id_dict.pkl" logger = logging.getLogger(__name__) # invert dictionary keys/values def invert_dict(dictionary): return {v: k for k, v in dictionary.items()} # read raw dictionary files def read_dictionaries(dir, cell_or_gene_emb): dict_list = [] for file in os.listdir(dir): # process only _raw.pickle files if file.endswith("_raw.pickle"): with open(f"{dir}/{file}", "rb") as fp: cos_sims_dict = pickle.load(fp) if cell_or_gene_emb == "cell": cell_emb_dict = {k: v for k, v in cos_sims_dict.items() if v and "cell_emb" in k} dict_list += [cell_emb_dict] return dict_list # get complete gene list def get_gene_list(dict_list): gene_set = set() for dict_i in dict_list: gene_set.update([k[0] for k, v in dict_i.items() if v]) gene_list = list(gene_set) gene_list.sort() return gene_list def n_detections(token, dict_list): cos_sim_megalist = [] for dict_i in dict_list: cos_sim_megalist += dict_i.get((token, "cell_emb"),[]) return len(cos_sim_megalist) def get_fdr(pvalues): return list(smt.multipletests(pvalues, alpha=0.05, method="fdr_bh")[1]) def isp_stats(cos_sims_df, dict_list, cell_states_to_model): random_tuples = [] for i in trange(cos_sims_df.shape[0]): token = cos_sims_df["Gene"][i] for dict_i in dict_list: random_tuples += dict_i.get((token, "cell_emb"),[]) goal_end_random_megalist = [goal_end for goal_end,alt_end,start_state in random_tuples] alt_end_random_megalist = [alt_end for goal_end,alt_end,start_state in random_tuples] start_state_random_megalist = [start_state for goal_end,alt_end,start_state in random_tuples] # downsample to improve speed of ranksums if len(goal_end_random_megalist) > 100_000: random.seed(42) goal_end_random_megalist = random.sample(goal_end_random_megalist, k=100_000) if len(alt_end_random_megalist) > 100_000: random.seed(42) alt_end_random_megalist = random.sample(alt_end_random_megalist, k=100_000) if len(start_state_random_megalist) > 100_000: random.seed(42) start_state_random_megalist = random.sample(start_state_random_megalist, k=100_000) names=["Gene", "Gene_name", "Ensembl_ID", "Shift_from_goal_end", "Shift_from_alt_end", "Goal_end_vs_random_pval", "Alt_end_vs_random_pval"] cos_sims_full_df = pd.DataFrame(columns=names) for i in trange(cos_sims_df.shape[0]): token = cos_sims_df["Gene"][i] name = cos_sims_df["Gene_name"][i] ensembl_id = cos_sims_df["Ensembl_ID"][i] token_tuples = [] for dict_i in dict_list: token_tuples += dict_i.get((token, "cell_emb"),[]) goal_end_cos_sim_megalist = [goal_end for goal_end,alt_end,start_state in token_tuples] alt_end_cos_sim_megalist = [alt_end for goal_end,alt_end,start_state in token_tuples] mean_goal_end = np.mean(goal_end_cos_sim_megalist) mean_alt_end = np.mean(alt_end_cos_sim_megalist) pval_goal_end = ranksums(goal_end_random_megalist,goal_end_cos_sim_megalist).pvalue pval_alt_end = ranksums(alt_end_random_megalist,alt_end_cos_sim_megalist).pvalue data_i = [token, name, ensembl_id, mean_goal_end, mean_alt_end, pval_goal_end, pval_alt_end] cos_sims_df_i = pd.DataFrame(dict(zip(names,data_i)),index=[i]) cos_sims_full_df = pd.concat([cos_sims_full_df,cos_sims_df_i]) cos_sims_full_df["Goal_end_FDR"] = get_fdr(list(cos_sims_full_df["Goal_end_vs_random_pval"])) cos_sims_full_df["Alt_end_FDR"] = get_fdr(list(cos_sims_full_df["Alt_end_vs_random_pval"])) return cos_sims_full_df class InSilicoPerturberStats: valid_option_dict = { "mode": {"goal_state_shift","vs_null","vs_random"}, "combos": {0,1,2}, "anchor_gene": {None, str}, "cell_states_to_model": {None, dict}, } def __init__( self, mode="vs_random", combos=0, anchor_gene=None, cell_states_to_model=None, token_dictionary_file=TOKEN_DICTIONARY_FILE, gene_name_id_dictionary_file=GENE_NAME_ID_DICTIONARY_FILE, ): """ Initialize in silico perturber stats generator. Parameters ---------- mode : {"goal_state_shift","vs_null","vs_random"} Type of stats. "goal_state_shift": perturbation vs. random for desired cell state shift "vs_null": perturbation vs. null from provided null distribution dataset "vs_random": perturbation vs. random gene perturbations in that cell (no goal direction) combos : {0,1,2} Whether to perturb genes individually (0), in pairs (1), or in triplets (2). anchor_gene : None, str ENSEMBL ID of gene to use as anchor in combination perturbations. For example, if combos=1 and anchor_gene="ENSG00000148400": anchor gene will be perturbed in combination with each other gene. cell_states_to_model: None, dict Cell states to model if testing perturbations that achieve goal state change. Single-item dictionary with key being cell attribute (e.g. "disease"). Value is tuple of three lists indicating start state, goal end state, and alternate possible end states. token_dictionary_file : Path Path to pickle file containing token dictionary (Ensembl ID:token). gene_name_id_dictionary_file : Path Path to pickle file containing gene name to ID dictionary (gene name:Ensembl ID). """ self.mode = mode self.combos = combos self.anchor_gene = anchor_gene self.cell_states_to_model = cell_states_to_model self.validate_options() # load token dictionary (Ensembl IDs:token) with open(token_dictionary_file, "rb") as f: self.gene_token_dict = pickle.load(f) # load gene name dictionary (gene name:Ensembl ID) with open(gene_name_id_dictionary_file, "rb") as f: self.gene_name_id_dict = pickle.load(f) if anchor_gene is None: self.anchor_token = None else: self.anchor_token = self.gene_token_dict[self.anchor_gene] def validate_options(self): 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.cell_states_to_model is not None: if (len(self.cell_states_to_model.items()) == 1): for key,value in self.cell_states_to_model.items(): if (len(value) == 3) and isinstance(value, tuple): if isinstance(value[0],list) and isinstance(value[1],list) and isinstance(value[2],list): if len(value[0]) == 1 and len(value[1]) == 1: all_values = value[0]+value[1]+value[2] if len(all_values) == len(set(all_values)): continue else: logger.error( "Cell states to model must be a single-item dictionary with " \ "key being cell attribute (e.g. 'disease') and value being " \ "tuple of three lists indicating start state, goal end state, and alternate possible end states. " \ "Values should all be unique. " \ "For example: {'disease':(['start_state'],['ctrl'],['alt_end'])}") raise if self.anchor_gene is not None: self.anchor_gene = None logger.warning( "anchor_gene set to None. " \ "Currently, anchor gene not available " \ "when modeling multiple cell states.") def get_stats(self, input_data_directory, null_dist_data_directory, output_directory, output_prefix): """ Get stats for in silico perturbation data and save as results in output_directory. Parameters ---------- input_data_directory : Path Path to directory containing cos_sim dictionary inputs null_dist_data_directory : Path Path to directory containing null distribution cos_sim dictionary inputs output_directory : Path Path to directory where perturbation data will be saved as .csv output_prefix : str Prefix for output .dataset """ self.gene_token_id_dict = invert_dict(self.gene_token_dict) self.gene_id_name_dict = invert_dict(self.gene_name_id_dict) if self.mode == "goal_state_shift": dict_list = read_dictionaries(input_data_directory,"cell") else: logger.error( "Currently, only mode available is stats for goal_state_shift.") raise # obtain total gene list gene_list = get_gene_list(dict_list) # initiate results dataframe cos_sims_df_initial = pd.DataFrame({"Gene": gene_list, "Gene_name": [self.token_to_gene_name(item) \ for item in gene_list], \ "Ensembl_ID": [self.gene_token_id_dict[genes[1]] \ if isinstance(genes,tuple) else \ self.gene_token_id_dict[genes] \ for genes in gene_list]}, \ index=[i for i in range(len(gene_list))]) # # add ENSEMBL ID for genes # cos_sims_df_initial["Ensembl_ID"] = [self.gene_token_id_dict[genes[1]] if isinstance(genes,tuple) else self.gene_token_id_dict[genes] for genes in list(cos_sims_df_initial["Gene"])] cos_sims_df = isp_stats(cos_sims_df_initial, dict_list, self.cell_states_to_model) # quantify number of detections of each gene cos_sims_df["N_Detections"] = [n_detections(i, dict_list) for i in cos_sims_df["Gene"]] # sort by shift to desired state cos_sims_df = cos_sims_df.sort_values(by=["Shift_from_goal_end", "Goal_end_FDR"]) # save perturbation stats to output_path output_path = (Path(output_directory) / output_prefix).with_suffix(".csv") cos_sims_df.to_csv(output_path) def token_to_gene_name(self, item): if isinstance(item,int): return self.gene_id_name_dict.get(self.gene_token_id_dict.get(item, np.nan), np.nan) if isinstance(item,tuple): return tuple([self.gene_id_name_dict.get(self.gene_token_id_dict.get(i, np.nan), np.nan) for i in item])