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# %% [markdown] # ## Example of InfoGraph # %% [markdown] # ### Graph level representation learning # %% from dig.sslgraph.utils import Encoder from dig.sslgraph.dataset import get_dataset from dig.sslgraph.evaluation import GraphUnsupervised from dig.sslgraph.method import InfoGraph # %% [markdown] # #### Loading d...
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# %% [markdown] # ## Load necessary imports for downloading LDA50 database and converting to NiMARE dataset file # %% import os from pprint import pprint from nimare.extract import download_abstracts, fetch_neuroquery, fetch_neurosynth from nimare.io import convert_neurosynth_to_dataset # %% [markdown] # ## Download...
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# %% import os os.chdir('../') # %% from DeepPurpose import DTI as models from DeepPurpose import utils, dataset # %% [markdown] # There are two ways to load the pretrained model, the first way is to load from local model directory. # # A model directory should consist of two files: # # config.pkl that describes...
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# %% class Matter(object): pass lump = Matter() # %% from transitions import Machine, State # %% states = ['solid','liquid','gas','plasma'] transitions = [ { 'trigger': 'melt', 'source': 'solid', 'dest': 'liquid' }, { 'trigger': 'evaporate', 'source': 'liquid', 'dest': 'gas' }, { 'trigger': 'sublima...
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# %% import scanpy as sc import matplotlib.pyplot as plt import pickle # %% with open('DLPFC.pkl', 'rb') as fp: adata = pickle.load(fp) # %% fig, ax = plt.subplots(2, 9, figsize=(18,4)) for key, i in zip(mapping_names.keys(), ax[0].flatten()): adata = data[key] sc.pl.umap(adata, color="batch", ax=i,...
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# %% import torch from monai.transforms import Resize from models import InversionTimeLSTM, FeatureExtractor from utils import load_parameters import json device = torch.device("cuda" if torch.cuda.is_available() else "cpu") device # %% def load_model(p): with open(f'{p}/config.json', 'r') as f: config = ...
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# %% import os os.chdir('../') # %% import DeepPurpose.oneliner as oneliner from DeepPurpose import dataset # %% target, target_name = dataset.load_SARS_CoV_Protease_3CL() train_drug, train_target, train_y = dataset.load_AID1706_SARS_CoV_3CL('./data', seed = 1234) X_repurpose, drug_names, drug_CID = dataset.load_anti...
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# %% import pandas as pd # %% xtb_cols = ['GFN2_TOTAL_ENERGY', 'GFN2_ATOMIC_ENERGY', 'GFN2_FORMATION_ENERGY', 'GFN2_HOMO_ENERGY', 'GFN2_LUMO_ENERGY', 'GFN2_ROT_CONSTANT_A', 'GFN2_ROT_CONSTANT_B', 'GFN2_ROT_CONSTANT_C', 'GFN2_DIPOLE_X', 'GFN2_DIPOLE_Y', 'GFN2_DIPOLE_Z', 'GFN2_DIPOLE_TOT'] dft_co...
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# %% import os os.chdir('../') import DeepPurpose.DTI as models from DeepPurpose.utils import * from DeepPurpose.dataset import * # %% X_drug, X_target, y = load_process_KIBA('./data/', binary=False) drug_encoding = 'CNN' target_encoding = 'CNN' train, val, test = data_process(X_drug, X_target, y, ...
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# %% import os os.chdir('../') import DeepPurpose.DTI as models from DeepPurpose.utils import * from DeepPurpose.dataset import * # %% X_drug, X_target, y = load_process_DAVIS('./data/', binary=True) drug_encoding = 'CNN' target_encoding = 'CNN' train, val, test = data_process(X_drug, X_target, y, ...
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# %% [markdown] # ## Example of MVGRL # %% [markdown] # ### Graph level representation learning # %% from dig.sslgraph.utils import Encoder from dig.sslgraph.evaluation import GraphUnsupervised from dig.sslgraph.dataset import get_dataset from dig.sslgraph.method import MVGRL # %% [markdown] # #### Loading dataset ...
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# %% import os os.chdir('../') # %% import DeepPurpose.oneliner as oneliner from DeepPurpose import dataset # %% target, target_name = dataset.load_SARS_CoV_Protease_3CL() train_drug, train_target, train_y = dataset.load_AID1706_SARS_CoV_3CL('./data', seed = 1234) X_repurpose, drug_names, drug_CID = dataset.load_anti...
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# %% import sys sys.path.append('../../../../') # %% %load_ext autoreload %autoreload 2 import torch from jtvae import JTVAE import jtnn import fast_jtnn path_adj = "./" # %% from rdkit import Chem from rdkit import RDLogger RDLogger.DisableLog('rdApp.*') # %% from dig.ggraph.dataset import ZINC800 from dig.ggrap...
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# %% import os os.chdir('../') from DeepPurpose import utils from DeepPurpose import DTI as models import gradio model_binding = models.model_pretrained(model = 'MPNN_CNN_BindingDB') model_kiba = models.model_pretrained(model = 'MPNN_CNN_KIBA') model_davis = models.model_pretrained(model = 'MPNN_CNN_DAVIS') def DTI_...
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# %% import os os.chdir('../') import DeepPurpose.DTI as models from DeepPurpose.utils import * from DeepPurpose.dataset import * # %% X_drug, X_target, y = process_BindingDB('../data/BindingDB_All.tsv', y = 'Kd', binary = False, ...
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# %% import os os.chdir('../') import DeepPurpose.DTI as models from DeepPurpose.utils import * from DeepPurpose.dataset import * # %% X_drug, X_target, y = load_process_DAVIS('./data/', binary=False) drug_encoding = 'CNN' target_encoding = 'CNN' train, val, test = data_process(X_drug, X_target, y, ...
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# %% import numpy as np import jPCA import matplotlib.pyplot as plt from jPCA.util import load_churchland_data, plot_projections # %% # Load publicly available data from Mark Churchland's group path = "/Users/Bantin/Documents/Stanford/Linderman-Shenoy/jPCA_ForDistribution/exampleData.mat" datas, times = load_churchlan...
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# %% import numpy as np import pandas as pd # %% # -*- coding: utf-8 -*- import gibbslda import pandas as pd # load dataset f = 'E:/word_embeding_TM/GLDAW_model/test_rus_docs.csv' df = pd.read_csv(f, delimiter=';',decimal='.', encoding='ANSI') texts = [[text for text in doc.split()] for doc in df['original data']] ...
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# %% import sys sys.path.append('../') import pandas as pd import seaborn as sns; sns.set(style='darkgrid', context='notebook') from figures.plotting import plot_eigenspectrum, annotate_corr from matplotlib import pyplot as plt eigmetric = 'effective dimensionality' eigspec = pd.read_csv(f'../results/counter-example|...
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# %% %matplotlib inline %load_ext autoreload %autoreload 2 # %% from configuration import * from figure_estimation import * # %% plt.rcParams.update({ 'font.size': 12, 'xtick.labelsize': 12, 'ytick.labelsize': 12, }) # %% figure_folder = base_folder / 'figures' / 'estimation' figure_folder.mkdir(exist_o...
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# %% [markdown] # ## Example of GraphCL with grid search # %% from dig.sslgraph.utils import Encoder from dig.sslgraph.dataset import get_dataset from dig.sslgraph.evaluation import GraphSemisupervised from sslgraph.method import GraphCL # %% [markdown] # ### 1. Semi-supervised learning on DD # # #### Load dataset #...
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# %% import os, glob import numpy as np import matplotlib. pyplot as plt import pandas as pd import seaborn as sns from skimage.io import imread, imsave from tqdm.notebook import tqdm from scipy.fftpack import dct import pickle from skimage.morphology import remove_small_holes, binary_dilation, disk, binary_erosion fro...
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# %% [markdown] # ## Sheet to process the Archer (2018) proteomics and RNA data # Generally used for Figure 4 and SHHa/SHHb split # %% import os import pandas as pd # %% [markdown] # ### Load and process proteomics data per Archer 2018 # %% base_folder = '../data/' # %% ## Load proteomics Data bpdf = pd.read_excel(...
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# %% [markdown] # ## Example of GRACE # %% [markdown] # ### Node-level representation learning on CORA # %% from dig.sslgraph.utils import Encoder from dig.sslgraph.evaluation import NodeUnsupervised from dig.sslgraph.dataset import get_node_dataset from dig.sslgraph.method import GRACE # %% [markdown] # #### Loadin...
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# %% import os os.chdir('../') # %% import DeepPurpose.DTI as models from DeepPurpose.utils import * from DeepPurpose.dataset import * # %% from time import time t1 = time() X_drug, X_target, y = load_process_KIBA('./data/', binary=False) drug_encoding = 'MPNN' target_encoding = 'AAC' train, val, test = data_proces...
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# %% import os os.chdir('../') # %% import DeepPurpose.DTI as models from DeepPurpose.utils import * from DeepPurpose.dataset import * # %% from time import time t1 = time() X_drug, X_target, y = load_process_KIBA('./data/', binary=False) drug_encoding = 'MPNN' target_encoding = 'CNN' train, val, test = data_proces...
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# %% library(DESeq2) library(tidyverse) library(ggplot2) # %% counts = read_csv('../03_build_meta_and_counts/counts.csv') %>% column_to_rownames('gene') counts %>% head # %% meta = read_csv('../04_cleanup/meta_qc.csv') %>% filter(!is.na(name)) %>% column_to_rownames("name") %>% mutate(name = rownames(.)) meta %>% hea...
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# %% import chromadb from chromadb.utils import embedding_functions sentence_transformer_ef = embedding_functions.SentenceTransformerEmbeddingFunction(model_name="all-MiniLM-L6-v2") client = chromadb.Client() # client.heartbeat() # client.reset() collection = client.get_or_create_collection("test-where-list", embed...
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# %% import os os.chdir('../') # %% import DeepPurpose.DTI as models from DeepPurpose.utils import * from DeepPurpose.dataset import * # %% from time import time t1 = time() X_drug, X_target, y = load_process_DAVIS('./data/', binary=False) drug_encoding = 'MPNN' target_encoding = 'AAC' train, val, test = data_proce...
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# %% import os os.chdir('../') # %% import DeepPurpose.DTI as models from DeepPurpose.utils import * from DeepPurpose.dataset import * # %% from time import time t1 = time() X_drug, X_target, y = load_process_DAVIS('./data/', binary=False) drug_encoding = 'MPNN' target_encoding = 'CNN' train, val, test = data_proce...
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# %% import os os.chdir('../') # %% import DeepPurpose.DTI as models from DeepPurpose.utils import * from DeepPurpose.dataset import * # %% from time import time t1 = time() X_drug, X_target, y = load_process_DAVIS('./data/', binary=False) drug_encoding = 'CNN' target_encoding = 'Transformer' train, val, test = dat...
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# %% import os os.chdir('../') # %% import DeepPurpose.DTI as models from DeepPurpose.utils import * from DeepPurpose.dataset import * # %% from time import time t1 = time() X_drug, X_target, y = load_process_KIBA('./data/', binary=False) drug_encoding = 'CNN' target_encoding = 'Transformer' train, val, test = data...
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# %% [markdown] # # trying to check that the res model is working sitewise # %% [markdown] # # 1 checking that the data loaded is working site-wise # %% import gvp import gvp.atom3d from atom3d.datasets import LMDBDataset from functools import partial import torch_geometric # %% # inspecting the first element in da...
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# %% def forced_choice_permutation_accuracy(data1, data2, model, n_permutations=10000, metric='correlation'): '''Compute one-tailed p-values for forced choice accuracy using permutation test Args: data1: (Brain_Data) Brain_Data instance of Condition1(must be same subject order across conditions) ...
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# %% import sys import os import glob import random from itertools import combinations import numpy as np import scipy import matplotlib as mpl import matplotlib.pyplot as plt from matplotlib import ticker import seaborn as sns import prettypyplot as pplt import pyemma import mdtraj as md import MDAnalysis as mda #...
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# %% import os import time import numpy as np import pandas as pd from matplotlib import pyplot as plt from tqdm.auto import tqdm from foldingdiff import sampling, plotting # %% def time_to_sample_length(length: int, num_samples: int, **kwargs) -> float: """Returns the time to sample a given number of samples f...
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# %% import os os.chdir('../') import DeepPurpose.DTI as models from DeepPurpose.utils import * from DeepPurpose.dataset import * # %% X_drug, X_target, y = load_AID1706_SARS_CoV_3CL('./kh278/DeepPurpose/data', oversample_num = 30) drug_encoding = 'CNN' target_encoding = 'CNN' train, val, test = data_process(X_drug,...
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# %% import sys sys.path.append('./../..') import dynaphos import matplotlib.pyplot as plt import numpy as np import os import pandas as pd from dynaphos import utils import seaborn as sns import matplotlib as mpl results = pd.read_csv('results/performance_best_GPU.csv',) # Load colorstyles plt.style.use('../_figure...
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# %% [markdown] # # Compare Embedding Models # # This notebook walks through how to compare various embedding models with your custom benchmark results. # %% [markdown] # ## 1. Setup # %% [markdown] # ### 1.1 Install & Import # # Install the necessary packages. # %% %pip install -r requirements.txt # %% %load_ext...
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# %% import sys sys.path.append('../../../../') # %% %load_ext autoreload %autoreload 2 import torch from jtvae import JTVAE from fast_jtnn.datautils import MolTreeFolder, PairTreeFolder, MolTreeDataset path_adj = "./" # %% from rdkit import Chem from rdkit import RDLogger RDLogger.DisableLog('rdApp.*') # %% from ...
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# %% import sys sys.path.append('./../..') import dynaphos import matplotlib.pyplot as plt import numpy as np import os import pandas as pd from dynaphos import utils import seaborn as sns import matplotlib as mpl results = pd.read_csv('results/performance_best_GPU.csv',) # Load colorstyles plt.style.use('../_figure...
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# %% ## if you are using the pip version, please comment out the below two lines import os os.chdir('../') from DeepPurpose import CompoundPred as models from DeepPurpose.utils import * from tdc import BenchmarkGroup group = BenchmarkGroup(name = 'ADMET_Group', path = 'data/') import warnings warnings.filterwarnings(...
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# %% import os os.chdir('../') import DeepPurpose.DTI as models from DeepPurpose.utils import * from DeepPurpose.dataset import * # %% X_drug, X_target, y = load_AID1706_SARS_CoV_3CL('./kh278/DeepPurpose/data', oversample_num = 30) drug_encoding = 'MPNN' target_encoding = 'CNN' train, val, test = data_process(X_drug...
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# %% %matplotlib inline %load_ext autoreload %autoreload 2 from visualize import PyramidVisualizer, get_dataset, simple_visualizer from metroem.aligner import Aligner from collections import defaultdict import random import cloudvolume as cv import numpy as np # %% cv_path = 'gs://h01-release/data/20210601/c3' # %% ...
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# %% import numpy as np # %% import tensorflow as tf # %% saved_model_dir = "../../data/osfstorage/deep-learning-qc/saved-models/report-model" model = tf.keras.models.load_model(saved_model_dir) # %% def rename(model, layer, new_name): def _get_node_suffix(name): for old_name in old_nodes: if...
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# %% import numpy as np import dynfc as dyn import scipy as sc import scipy.io import matplotlib.pyplot as plt # %% mat_dbg = sc.io.loadmat('../data/dbg.mat', squeeze_me = True) # %% signal = mat_dbg['RSsig_t'].transpose() # %% flp = 0.03 fhi = 0.07 delt = 0.392 k = 2 base = 2 nBits = 8 # %% timeserie = np.zero...
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# %% [markdown] # ## Example of GraphEBM: Compositional Generation # %% import os import torch from torch_geometric.loader import DenseDataLoader from rdkit import RDLogger from dig.ggraph.dataset import ZINC250k from dig.ggraph.method import GraphEBM # %% device = torch.device('cuda:1') # %% [markdown] # #### Prep...
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# %% import os, glob import numpy as np import matplotlib. pyplot as plt import pandas as pd import seaborn as sns from skimage.io import imread, imsave from tqdm.notebook import tqdm from scipy.fftpack import dct import pickle from skimage.morphology import remove_small_holes, binary_dilation, disk, binary_erosion fro...
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# %% import pickle # %% with open("/media/Data/zhangchao/zhangchao/BatchEffectEvaluationPipeline/analysis/OB/OB_res.pkl", "rb") as f: data = pickle.load(f) # %% names = ["Raw", "Harmony", "Combat", "BBKNN", "Scanorama", "MNN", "PRECAST", "spatiA...
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# %% CODE_REPO_PATH='/YOUR_PATH/Converting_allo_goal_to_ego_steering/analysis/' import warnings warnings.filterwarnings('ignore') from importlib import reload import sys import os import neuprint from neuprint import Client sys.path.insert(0, CODE_REPO_PATH) import em %config InlineBackend.figure_format = 'retina...
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# %% import os import pickle import pandas as pd import numpy as np # %% # run # указываем каталог, в котором лежат матрицы phi results0 = 'E:/word_embeding_TM/Renyi_entropy/phi_matrix/' results1 = 'E:/word_embeding_TM/Renyi_entropy/' # %% #for i in os.listdir(results0): # print('file name: ', i) # df = pd.re...
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# %% import numpy as np import os, sys sys.path.append(os.getcwd()+"/..") from rnn_scripts.utils import * from rnn_scripts.train import * cls= green_blue_colours() import matplotlib.pyplot as plt %matplotlib inline # %% # Load training data from three models fig_dir=os.getcwd()+"/../figures/" model_dir = os.getcwd(...
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# %% [markdown] # # Local Peristence Demo # This notebook demonstrates how to configure Chroma to persist to disk, then load it back in. # %% import chromadb # %% # Create a new Chroma client with persistence enabled. persist_directory = "db" client = chromadb.PersistentClient(path=persist_directory) # Create a n...
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# %% [markdown] # ## Start with the necessary imports # %% import os import nipype import nibabel as nib import numpy as np from nilearn.plotting import plot_roi from nilearn import plotting from nimare.dataset import Dataset from nimare.decode import discrete from nimare.utils import get_resource_path # %% [markdo...
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# %% library(tidyverse) library(DESeq2) # %% preprocessed_list = qs::qread('../04_cleanup/preprocessed_list.qs') # %% deg_results_tibble = tibble() for (name in c("0010_HY", "0010_HPF", "0010_SC", "0010_IC", "0010_PFC", "0037_HY", "0037_HPF", "0037_SC", "0037_IC", "0037_ZI")){ seq_run = str_split(name, '_') %>%...
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# %% import numpy as np import pandas as pd from glob import glob # %% with open('../scripts/preprocessing-stimulus/splits.txt') as f: splits = f.readlines() # %% def convert_to_seconds(hhmmss): h, m, s = hhmmss.split(':') s = float(h) * 3600 + float(m) * 60 + float(s) return s # %% splits = [s.strip...
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# %% import pandas as pd import numpy as np import matplotlib.pyplot as plt import sys # %% loc = sys.argv[1] loc = "IZH.csv" df = pd.read_csv(loc, index_col=0) # %% list(df.script_name.unique()) # %% sizes = df["size"].unique() sizes.sort() groups = df.groupby(["size"]) all_df = [] all_index = [] for size in s...
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# %% import importlib import os import sys import matplotlib as mpl import matplotlib.pyplot as plt import mdtraj as md import numpy as np import prettypyplot as pplt import scipy import seaborn as sns from matplotlib import ticker import extq # %% pplt.load_cmaps() plt.style.use("custom") # custom style sheet plt....
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# %% library(tidyverse) library(gprofiler2) # %% dir.create('wgcna_output/renamed_tables', recursive = TRUE, showWarnings = FALSE) # %% kme = read_csv('wgcna_output/tables/dmb_ds4_mcs20_pF_kME_cellModEmbed.csv.gz') kme %>% head # %% modules = colnames(kme) %>% `[`(-(1:3)) %>% enframe %>% rename(index = name, old_nam...
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# %% import sys sys.path.append('../') import pandas as pd import seaborn as sns; sns.set(style='darkgrid', context='poster') from figures.plotting import plot_eigenspectrum from matplotlib import pyplot as plt pooling = True dataset = 'imagenet' grayscale = False data = pd.read_csv(f'../results/eigspectra|dataset:{da...
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# %% library(tidyverse) library(broom) # %% # load the mouse brain ESMU. Part of this repo and at https://github.com/perslab/CELLECT/wiki/Precomputed-CELLEX-datasets esmu = read_csv('esmu/mousebrain.mu.csv.gz') esmu %>% head # %% # load the kmes file kmes = read_csv('wgcna_output/renamed_tables/wgcna_output_ds4_mcs20...
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# %% [markdown] # Step 1: Define our imports (assumes `Binary.py` lives in the same directory as this notebook) # %% import Binary from glob import glob import os import numpy as np import matplotlib.pyplot as plt # %% [markdown] # Step 2: Point to data directory and load. This directory contains data from one cont...
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# %% CODE_REPO_PATH='/YOUR_PATH/Converting_allo_goal_to_ego_steering/analysis/' import warnings warnings.filterwarnings('ignore') from importlib import reload import sys sys.path.insert(0, CODE_REPO_PATH) import model as model %config InlineBackend.figure_format = 'retina' # %% FIGURE_PATH='/YOUR_PATH/Converting_all...
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# %% [markdown] # ## Example of GCA # %% [markdown] # ### Node-level representation learning on Amazon Photos # %% from dig.sslgraph.utils import Encoder from dig.sslgraph.evaluation import NodeUnsupervised from dig.sslgraph.dataset import get_node_dataset from dig.sslgraph.method import pGRACE from dig.sslgraph.util...
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# %% !pip install --no-use-pep517 "napari[all]" !sudo apt-get install --reinstall libxcb-xinerama0 !python3 -m pip install pyvirtualdisplay !sudo apt-get install xvfb !sudo apt-get install python3-pyqt5 # %% import random import torch import numpy as np import cloudvolume as cv import torch from visualize import Pyr...
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# %% import live2p from live2p.analysis import process_data, clean_data, min_subtract, baseline_subtract from pathlib import Path import matplotlib.pyplot as plt import numpy as np import json import scipy.stats as stats import sklearn # %% import h5py # %% %load_ext autoreload %autoreload 2 # %% base = 'D:/Frankenr...
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# %% import numpy as np import matplotlib.pyplot as plt from scipy.signal import convolve # %% with open('recordedWaveforms.bin','rb') as file: data = np.fromfile(file,dtype='int16').astype('float32') LED = data[0::4] x_feedback = data[1::4] x_control = data[2::4] photodiode = data[3::4] # %% # Define a functio...
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# %% # check if used pathways match # MelBrainSys_PhDProject_TKraft/DataSets/Annotations/geneset_with_cancerGenes_merged.txt & Co # compared to annotation/pathway-definitions.ods # %% library(xlsx) # %% basePath = "/data/bcu_projects/MelBrainSys_PostdocProject_Gruetzmann/publications/2022-my-MelBrainSys-paper/scripts...
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# %% import pandas as pd import numpy as np import matplotlib.pyplot as plt import sys # %% loc = sys.argv[1] loc = "LIF.csv" df = pd.read_csv(loc, index_col=0) # %% list(df.script_name.unique()) # %% sizes = df["size"].unique() sizes.sort() groups = df.groupby(["size"]) all_df = [] all_index = [] for size in s...
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# %% import sys sys.path.append('../') import pandas as pd import seaborn as sns; sns.set(style='darkgrid', context='notebook') from matplotlib import pyplot as plt from figures.plotting import annotate_corr_grid, annotate_corr benchmark = 'dicarlo.MajajHong2015.IT.public-pls' eigmetric = 'effective dimensionality' po...
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# %% ## loading package import numpy as np import pandas as pd import matplotlib.pyplot as plt from matplotlib import pylab import seaborn as sns from sklearn.metrics.pairwise import cosine_similarity from statannot import add_stat_annotation import matplotlib as mpl from scipy import stats, cluster import glob impo...
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# %% import os import sys from pprint import pprint import numpy as np import pandas as pd import matplotlib.pyplot as plt project_root = ".." sys.path.append(project_root) from sleeprnn.common import viz DATASETS_PATH = os.path.join(project_root, 'resources', 'datasets', 'nsrr') viz.notebook_full_width() # %% [ma...
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# %% import pandas as pd from glob import glob import numpy as np # %% subjects = [s.split('/')[-1] for s in sorted(glob('../data/sub-*'))] # %% def load_confounds(subject): confounds = sorted(glob(f"../outputs/fmriprep/{subject}/func/*.tsv")) dfs = [pd.read_csv(c, sep='\t') for c in confounds] return dfs...
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# %% # import libraries import serial import pandas as pd from pandas import DataFrame import numpy as np import matplotlib.pyplot as plt from matplotlib.animation import FuncAnimation import threading import os # configure Matplotlib backend import matplotlib matplotlib.use('TkAgg') # functions # reads in the press...
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# %% import eelbrain as eel import numpy as np import cochlea, tqdm, pathlib, time from pathnames import * # %% [markdown] # # load stimulus recorded on EEG Erg1 sensor channel # %% datadict = eel.load.unpickle(preprocessed_path / f'part_001_in_speech_Cz_reref_ergs.pkl') ergs = [e.sub(time=(1, 245)) for e in datadict...
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# %% import os os.chdir('../') from DeepPurpose import dataset import numpy as np import pandas as pd # %% SMILES, Target_seq, y = dataset.load_process_DAVIS() # %% X_drug, X_target, y = dataset.process_BindingDB('../data/BindingDB_All.tsv', y = 'Kd', ...
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# %% [markdown] # # Tutorial 4: Integration of heterogeneous-structure datasets # %% [markdown] # In this tutorial, we utilized three mouse hippocampal slices from Slide-seq to assess the performance of spatiAlign in integrating heterogeneous-structure datasets with distinct biological characteristics. # %% [markdown...
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# %% [markdown] # ## Taurine Barplots for Figure 6 # Used for Figure 6 # # Author: Max Gold # %% import matplotlib import matplotlib.pyplot as plt import pandas as pd import seaborn as sns # %% # Say, "the default sans-serif font is COMIC SANS" matplotlib.rcParams['font.sans-serif'] = "Helvetica" # Then, "ALWAYS use...
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# %% import os, sys from pathlib import Path import json import numpy as np from scipy import stats from matplotlib import pyplot as plt import seaborn as sns PLOT_DIR = Path(os.path.join(os.path.dirname(os.getcwd()), "plots")) assert PLOT_DIR.is_dir() PLOT_DIR # %% BASELINE_SCTM_SCORES_JSON = "/home/wukevin/project...
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# %% [markdown] # # K-Means clustering on a Riemannian Manifold # # Lead authors: Thomas Gerald and Hadi Zaatiti. # # In this notebook, we demonstrate how run a K-mean clustering algorithm on a Riemannian Manifold. Generate data on a sphere from a Von Mises Fisher distribution and apply a rotation sampled randomly fr...
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# %% import nibabel as nib import scipy.linalg as la import pandas as pd from glob import glob import matplotlib.pyplot as plt %matplotlib inline import numpy as np # %% import seaborn as sns # %% import nilearn.plotting # %% !ls ../outputs/datapaper/tsnr/ # %% subjects = [path.split('/')[-1] for path in glob('../o...
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# %% library(xlsx) # %% basePath = "/data/bcu_projects/MelBrainSys_PostdocProject_Gruetzmann/publications/2022-my-MelBrainSys-paper/scripts-etc-for-publication/" setwd(basePath) # %% immunePWs = read.xlsx(file = "annotation/pathway-definitions.xls", header = T, sheetName = "ImmunePathways") colnames(immunePWs) = gsub...
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# %% import os, glob from tqdm import tqdm import numpy as np from skimage.io import imread, imsave import matplotlib.pyplot as plt from matplotlib import rc plt.rcParams.update({'font.size': 20}) # plt.style.use('dark_background') rc('pdf', fonttype=42) import funcs import imp imp.reload(funcs) # %% folder = os.pat...
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# %% [markdown] # # Tutorial 3: Integrating DLPFC dataset # %% [markdown] # In this tutorial, we illustrate the application of spatiAlign for integrating a series of 10x Genomics Visium datasets from the human dorsolateral prefrontal cortex (DLPFC). # %% [markdown] # - ### Import packages # %% import scanpy as sc f...
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# %% [markdown] # # scoring antitoxin mutations with evMutation # # ### Inputs: # - the experimentally measured antitoxin variant effects # - evCouplings model # # ### Outputs: # - score file # %% import evcouplings from evcouplings.couplings import CouplingsModel import pandas as pd plt.style.use('../../src/paper_...
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# %% import sys sys.path.append('../') import pandas as pd import seaborn as sns; sns.set(style='darkgrid', context='poster') from matplotlib import pyplot as plt from matplotlib.gridspec import GridSpec benchmark = 'dicarlo.MajajHong2015.IT.public-pls' pooling = False data = pd.read_csv(f'../results/encoding|benchma...
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# %% [markdown] # ## Example of GraphEBM: Random Generation # %% import os import torch from torch_geometric.loader import DenseDataLoader from rdkit import RDLogger from dig.ggraph.dataset import QM9, ZINC250k from dig.ggraph.method import GraphEBM from dig.ggraph.evaluation import RandGenEvaluator # %% device = to...
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# %% import sys sys.path.append('../') import pandas as pd import seaborn as sns; sns.set(style='darkgrid', context='notebook') from matplotlib import pyplot as plt from figures.plotting import annotate_corr_grid benchmark = 'bonner.Object2Vec.pls.roi=LOC' intrinsic_metric = 'intra-ID' pooling_enc = False dataset_intr...
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# %% import sys sys.path.append('../') import pandas as pd import seaborn as sns; sns.set(style='darkgrid', context='poster') from matplotlib import pyplot as plt from matplotlib.gridspec import GridSpec eigmetric = 'effective dimensionality' pooling = True dataset = 'imagenet' grayscale = False data = pd.read_csv(f'....
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# %% # Bunch of imports # System path should be changed to where the git repo is. import sys sys.path.append('..') import tensorflow as tf import src.models as models import lattice_filter_op_loader custom_module = lattice_filter_op_loader.module # %% # Set GPU and batch size # Can set a different batch size, or skip...
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# %% import pandas as pd import numpy as np # %% slideseq_df = pd.DataFrame( data=np.array([0.6230, 0.3583, 0.5567, 0.7615, 0.6074, 0.5778, 0.4514, 0.4348, 0.5064]).reshape(1, -1), columns=["spatiAlign", "PRECAST", "GraphST", "SCALEX", "Harmony", "Combat", "BBKNN", "Scanorama", "MNN"], ) # %% slideseq_df # ...
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# %% [markdown] # ## Tutorial 2: Integrating datasets measured by different platforms. # In this tutorial, we demonstrate how to apply Spatialign to integrate datasets that were measured by different platforms. As an example, we used three mouse olfactory bulb datasets. One slice was profiled by 10x Genomics Vi...
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# %% # Bunch of imports # System path should be changed to where the git repo is. import sys import tensorflow as tf import models as models import lattice_filter_op_loader import os custom_module = lattice_filter_op_loader.module # %% # Set GPU and batch size # Can set a different batch size, or skip if CPU strategy...
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# %% [markdown] # It seems that redirecting error message works only in jupyter notebook (in another process) # # http://rdkit.blogspot.com/2016/03/capturing-error-information.html # %% from io import StringIO import sys from rdkit import Chem import os.path as osp from tqdm import tqdm import pickle # %% with open(...
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# %% [markdown] # # Tutorial 5: Integration of time-series mouse embryonic brain # %% [markdown] # In this tutorial, we utilized a series of mouse brain datasets extracted from multiple developing mouse embryos, measured by Stereo-seq, to demonstrate the benefits of spatiAlign for downstream gene-level analysis. # %...
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# %% %matplotlib inline %load_ext autoreload %autoreload 2 # %% from configuration import * import pandas as pd from spikeinterface.sortingcomponents.benchmark.benchmark_motion_interpolation import BenchmarkMotionInterpolationMearec from figure_interpolation import (figure_sorting_accuracies, ...
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# %% # computes network flow/impact matrix of each gene on each other gene for each sample # outputs in TrainNetwork-*/NetworkPropagation/NetworkFlow/ # %% library(parallel) # %% basePath = "/data/bcu_projects/MelBrainSys_PostdocProject_Gruetzmann/publications/2022-my-MelBrainSys-paper/scripts-etc-for-publication/" m...
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# %% import numpy as np import matplotlib.pyplot as plt import seaborn as sns # %% class UnnormedMVNormalPDF: def __init__(self, eigvecs): if not isinstance(eigvecs, np.ndarray): eigvecs = np.array(eigvecs) self.eigvecs = eigvecs self.cov = eigvecs.T @ eigvecs self.cov_...
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# %% import numpy as np from torch.utils.data import DataLoader import os, sys sys.path.append(os.getcwd()+"/..") from rnn_scripts.model import * from rnn_scripts.train import * from rnn_scripts.utils import * from tasks.seqDS import * import matplotlib.pyplot as plt %matplotlib inline # %% # Load models fig_dir=os.ge...
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# %% import os import pandas as pd # supress warnings about having no GPU os.environ['TF_CPP_MIN_LOG_LEVEL'] = '3' from Humatch.align import get_padded_seq from Humatch.model import load_cnn from Humatch.classify import predict_from_list_of_seq_strs, get_class_and_score_of_max_predictions_only from Humatch.plot import...