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# %% [markdown] # Make sure that we have the latest version of pandas-profiling. # %% !pip install -U data-profiling # %% # Standard Library Imports from pathlib import Path # Installed packages import pandas as pd # Our package from data_profiling import ProfileReport from data_profiling.utils.cache import cache_f...
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# %% import numpy as np from matplotlib.image import imread from skimage.measure import label, regionprops from skimage.color import rgb2gray, rgba2rgb points_path = 'Sample/Clandmarks.png' image_path = 'Sample/Cim.png' points_im = imread(points_path) rgb_im = rgba2rgb(points_im) im = rgb2gray(rgb_im) rgb_points = rgb...
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# %% from tqdm import tqdm # %% %load_ext autoreload %autoreload 2 # %% import logging import sys logging.basicConfig(stream=sys.stdout, level=logging.DEBUG) # %% from multicamera_acquisition.paths import DATA_DIR from multicamera_acquisition.acquisition import acquire_video # %% save_location = DATA_DIR / 'tests' ...
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# %% [markdown] # # New training set for the model. <br> The T-SNE results advocate for at least 3 Dpo labels <br> # > 1: Beta helix<br> # > 2: Beta propeller<br> # > 3: triple helix<br> # *** # ## Preparing the dataset # ### I. Old dataset # ### II. # # *** # %% import nglview as nv import os def view_pdb(file) :...
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# %% %load_ext autoreload %autoreload 2 # %% from multicamera_acquisition.paths import DATA_DIR from multicamera_acquisition.acquisition import acquire_video # %% save_location = DATA_DIR / 'tests' # %% camera_list = [ {'name': 'top', 'serial': 24535665, 'brand':'basler', 'gain': 12, 'display': False}, {'nam...
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# %% [markdown] # ## Training protocol # Iterates through synaptic network initialization parameters and executes training for each # # See 'fit_script_stage123.py' for details of training # %% import numpy as np from fit_script_stage123 import fit_script_stage123 from tools.lattices import WS_network import os nois...
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# %% [markdown] # Main notebook containing relevant analysis steps, run for each model. # # The script `notebook_per_model.py' automatically copies this notebook to an ensemble directory and executes it for newly trained ensembles using papermill. # # **Warning:** You can loose your work! Don't edit automatically cr...
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# %% [markdown] # # Detection Family Figure # %% # Imports import numpy as np import matplotlib.pyplot as plt import json plt.style.use("./style_sheet.mplstyle") col = ["xkcd:muted blue", "xkcd:coral pink"] # %% # Load data fname = "figdata/ideal_data_detection_task_family.json" data = json.load(open(fname, "r")) s...
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# %% [markdown] # # Main # %% [markdown] # ## Initialization of packages # %% import numpy as np import pandas as pd import matplotlib %matplotlib notebook import matplotlib.pyplot as plt import os import sys # %% [markdown] # ## Paths # for all Notebooks # %% paths = {'analysis': 'Analysis/', 'plot': 'Ana...
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# %% # This code should enable you to get started with using the stimuli and neural responses from the data set. # If you want more, please contact: # Ben Willmore (benjamin.willmore@dpag.ox.ac.uk), or # Michael Lohse (m.lohse@ucl.ac.uk) # %% from pcmdata import Clusters # %% # load data (dataset H) without spike ...
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# %% [markdown] # # UniFMIR: Pre-training a Foundation Model for Universal Fluorescence Microscopy Image Restoration # This demo allows you to run the models on your own images or the examples from the paper. Please refer to the paper for more details. # %% [markdown] # ## 1. Clone the repository and prepare environm...
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# %% # Core scverse libraries import scanpy as sc import anndata as ad # Data retrieval import pooch # %% adata = sc.read_h5ad("SEA-AD.h5ad") # %% sub=adata.obs[['donor_id', 'ADNC']] sub_adata=adata[adata.obs['ADNC'].isin(['Intermediate', 'Low','High','Not AD'])] print(sub_adata.obs) #from collections import C...
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# %% from pypylon import pylon # %% camera = pylon.InstantCamera(pylon.TlFactory.GetInstance().CreateFirstDevice()) camera.Open() # %% # demonstrate some feature accessdi.SetSerialNumber("2134234") new_width = camera.Width.GetValue() - camera.Width.GetInc() if new_width >= camera.Width.GetMin(): camera.Width.SetV...
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# %% from pybioportal import copy_number_segment as cns # %% df1a = cns.fetch_copy_number_segments(sample_study_ids=[ {"sample_ids": ["P-0000004-T01-IM3", "P-0000950-T01-IM3"], "study_id": "msk_met_2021"}, {"sample_ids": ["TCG...
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# %% [markdown] # # Norse # # Norse is a deep learning simulator for spiking neural networks, built on PyTorch. # # ## Import a NIR graph to Norse # %% import norse.torch as norse import torch import nir # Create a NIR Network affine_weights = torch.tensor([[1.0, 2.0], [3.0, 4.0]]) affine_bias = torch.tensor([1.0,...
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# %% [markdown] # # Yellow Taxy NYC # # ### Data Profiling in Databricks with data-profiling # %% [markdown] # Read a Delta table # %% input_table_name = "default.yellowtaxi_trips" df = spark.table(input_table_name) # %% display(df) # %% [markdown] # ## Data profiling with data-profiling # # pandas-profiling is n...
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# %% from pybioportal import patients as pts # %% df1 = pts.get_all_patients(keyword="TCGA") df1 # %% df2a = pts.fetch_patients(patient_identifiers=[ {"patient_ids": ["TCGA-3C-AAAU","TCGA-3C-AALI"], "study_id": "brca_tcga"...
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# %% import numpy as np from tensorflow.keras.models import load_model from ml4h.models.model_factory import get_custom_objects from ml4h.tensormap.ukb.demographics import age_in_days, af_dummy2, sex_dummy1 from ml4h.tensormap.ukb.survival import mgb_afib_wrt_instance2, mgb_death_wrt_instance2 # %% output_tensormaps =...
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# %% import torch import matplotlib.pyplot as plt # %% entrada = torch.rand(4,1,64,64) # %% plt.imshow(entrada[0,0]) # %% entrada.shape # %% modelo = torch.nn.Sequential( torch.nn.Conv2d(1, 64, 3, padding=1), torch.nn.Conv2d(64, 128, 3, padding=1), torch.nn.Conv2d(128, 3, 3, padding=1), ) # %% ...
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# %% import numpy as np import os import zipfile import pandas as pd import shutil # %% image_path = './Data/Images/' images = os.listdir(image_path) # %% # sav 파일 경로 지정 #file_path = './Data/231107_PSG.xlsx' file_path = './Data/231203_PSG.xlsx' # sav 파일 읽기 df = pd.read_excel(file_path) df['sex'] = df['sex'].map({'F...
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# %% import torch import norse import snntorch import snntorch.import_nirtorch import nir import importlib importlib.reload(norse) # %% nir_graph = nir.read("braille_noDelay_bias_zero.nir") net = snntorch.import_nirtorch.from_nir(nir_graph) # %% test_data_path = "data/ds_test.pt" ds_test = torch.load(test_data_path) ...
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# %% from os.path import join import xgboost as xgb import numpy as np import dask.dataframe as dd # %% DATA_PATH = '/mnt/dssmcmlfs01/merlin_cxg_2023_05_15_sf-log1p' # %% x_train = np.load(join(DATA_PATH, 'pca/x_pca_training_train_split_256.npy')) y_train = dd.read_parquet(join(DATA_PATH, 'train'), columns='cell_typ...
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# %% %load_ext autoreload %autoreload 2 # %% from multicamera_acquisition.paths import DATA_DIR from multicamera_acquisition.acquisition import acquire_video # %% import logging import sys logging.basicConfig(stream=sys.stdout, level=logging.DEBUG) # %% save_location = DATA_DIR / 'tests' # %% camera_list = [ {'...
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# %% import spyx import spyx.nn as snn import jax import jax.numpy as jnp import numpy as np import nir # %% isis = [ 6, 15, 4, 3, 0, 2, 1, 2, 0, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 13, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 5, 0, 14 ] d1 = list(np.concatenate([isi*[0]+[1] for isi in isis]))[:100] d = jnp.array([[e]...
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# %% [markdown] # # Norse # # Norse is a deep learning simulator for spiking neural networks, built on PyTorch. # # ```{include} ../../../tmp/examples/norse/supported_primitives.md # %% [markdown] # ## Import a NIR graph to Norse # %% import norse.torch as norse import torch import nir # Create a NIR Network affi...
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# %% [markdown] # # imports # %% %matplotlib inline import eelbrain as eel import numpy as np import scipy, pathlib, importlib, mne, time, os, sys from tqdm import tqdm import matplotlib.pyplot as plt import clicks, utils from pathnames import * mne.set_log_level(verbose='error') dBstrs=['66dB', '54dB', '42dB', '30dB'...
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# %% from pypylon import pylon # %% camera = pylon.InstantCamera(pylon.TlFactory.GetInstance().CreateFirstDevice()) camera.Open() # %% # set gain camera.GainAuto.SetValue("Off") # %% camera.Gain.SetValue(12) # %% # Test exposure time camera.ExposureAuto.SetValue("Off") # %% camera.ExposureTime.SetValue(2000) # %%...
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# %% # Python Script # Using emilys.optics.aberration # # by J. Barthel / Forschungszentrum Jülich GmbH, Jülich, Germany # email: ju.barthel@fz-juelich.de # # 2019 July 3 # # Part of the emilys project: https://github.com/ju-bar/emilys # published under the GNU GPL 3.0 License # # %% import numpy as np import matplotl...
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# %% from pybioportal import gene_panel_data as gpd # %% df1a = gpd.fetch_gene_panel_data(molecular_profile_ids=["brca_tcga_gistic", "acc_tcga_gistic", "brca_tcga_mutations"]) df1a # %% df1b = gpd.fetch_gene_panel_data(molecular_prof_sample_ids=[ {"molecular_profile_id": "b...
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# %% import pandas as pd import numpy as np # %% #import data = pd.read_csv('/Users/luopei/Documents/Research/Hypocretin/oxlight/SI oxlight/Zscore+F/7185_AS_VP.csv') # %% #Chop for +/-10 seconds around each new bout of NN Sniff ts = data.loc[data['Upright'] == 1]['time'].tolist() #only rows where prox_new is 1 event...
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# %% [markdown] # # Import the required packages # %% import os import json from aihwkit.experiments.runners import InferenceCloudRunner from aihwkit.cloud.client.entities import CloudJobStatus # %% [markdown] # ## Create a local runner and check the job status of the experiment # # The code is checking for the en...
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# %% [markdown] # # snnTorch # # snnTorch is a deep learning simulator for spiking neural networks, built on PyTorch. # %% [markdown] # ## Import a NIR graph to snnTorch # %% import snntorch as snn import torch import nir # Create a NIR Network affine_weights = torch.tensor([[1.0, 2.0], [3.0, 4.0]]) affine_bias = ...
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# %% [markdown] # The autoreload instruction reloads modules automatically before code execution, which is helpful for the update below. # %% %load_ext autoreload %autoreload 2 # %% [markdown] # Make sure that we have the latest version of pandas-profiling. # %% import sys !"{sys.executable}" -m pip install -U data...
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# %% from pybioportal import discrete_copy_number_alterations as dcna # %% df1 = dcna.get_discrete_copy_numbers_in_molecular_profile(molecular_profile_id="brca_tcga_gistic", sample_list_id="brca_tcga_all", ...
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# %% from pybioportal import samples as sp # %% df1 = sp.get_samples_by_keyword(keyword="TCGA") df1 # %% df2a = sp.fetch_samples(sample_identifiers=[ {"sample_ids": ["TCGA-AR-A1AR-01","TCGA-BH-A1EO-01","TCGA-BH-A1ES-01"], "study...
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# %% [markdown] # # Step 0: Data Download # %% [markdown] # We apply DeepDeWedge to a single tilt series collected from Chlamydomonas Reinhardtii. The tilt series is part of the Tomo110 dataset ([which can be downloaded here](https://download.fht.org/jug/cryoCARE/Tomo110.zip)), which was used in the tutorial for the [...
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# %% %load_ext autoreload %autoreload 2 # %% import json import os import json import wfdb import pickle import torch import tqdm import gzip import networkx import numpy as np import sak import sak.torch import sak.torch.nn import sak.torch.nn as nn import sak.torch.nn import sak.torch.train import sak.torch.data im...
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# %% import pandas as pd import matplotlib.pyplot as plt import hddm print hddm.__version__ import kabuki print kabuki.__version__ # %% data = hddm.load_csv('./hddm_input.csv') data.head(10) # %% data = hddm.utils.flip_errors(data) label_texts = ['','No stimulus','0 head / 80 tail','80 head 0 tail','80 head / 80 ta...
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# %% from pybioportal import treatments as trt # %% [markdown] # Get the Study IDs of all studies # %% from pybioportal import studies as std studies = std.get_all_studies(projection="DETAILED") std_ids = studies["studyId"].to_list() print(f"First Study IDs of {len(std_ids)}: {std_ids[0:5]}") # %% trt.fetch_status_d...
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# %% import numpy as np import pandas as pd from sergio import sergio # %% [markdown] # # Simulate Clean Data _ Steady-State Simulation # %% sim = sergio(number_genes=100, number_bins = 9, number_sc = 300, noise_params = 1, decays=0.8, sampling_state=15, noise_type='dpd') sim.build_graph(input_file_taregts ='steady-s...
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# %% [markdown] # ## This script subtracts the Buffer only noise from intersected beds # %% import os cwd = os.getcwd() main_dir = cwd print(main_dir) # %% import pybedtools from glob import glob confident_peaks_dir = main_dir + '/confident_clusters/' all_sample=sorted(glob(os.path.join(confident_peaks_dir, '*_co...
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# %% import pandas as pd # %% combo_3d = pd.read_parquet("ccs-prediction/combined_metlin_ccsbase_train_test_split_3d.parquet") # %% combo_3d.source.value_counts() # %% combo_3d.split.value_counts() # %% # train metlin combo_3d[(combo_3d.source == "metlin") & (combo_3d.split.str.contains("train"))].to_parquet("ccs-p...
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# %% import torch import torch.nn as nn import sinabs from sinabs.nir import from_nir import numpy as np import nir # %% graph = nir.read('lif_norse.nir') for nkey, node in graph.nodes.items(): print(f"{nkey:7} {node}") # %% isis = [ 6, 15, 4, 3, 0, 2, 1, 2, 0, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 13, 0, 0, ...
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# %% [markdown] # # Segmentation # %% [markdown] # ## Loading Models # %% from ultralytics import YOLO model = YOLO("yolo12n-seg.pt") # %% [markdown] # ## Training # %% results = model.train(data = "data/yolo_cropped/data.yaml", epochs = 100, imgsz = 64...
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# %% [markdown] # # Train cryo-CARE Network # # In this notebook we initialize a new model and train it. # %% from train_cryo_care import CryoCARE from csbdeep.models import Config from csbdeep.utils import plot_history import numpy as np # %% [markdown] # ## Create Model # # We use the standard `CSBDeep` config. ...
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# %% [markdown] # <a href="https://colab.research.google.com/github/hzwer/arXiv2020-RIFE/blob/main/Colab_demo.ipynb" target="_parent"><img src="https://colab.research.google.com/assets/colab-badge.svg" alt="Open In Colab"/></a> # %% !git clone https://github.com/hzwer/arXiv2020-RIFE # %% !mkdir /content/arXiv2020-RIF...
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# %% %load_ext autoreload %autoreload 2 # %% import awswrangler as wr import pandas as pd # %% [markdown] # ### Step 1: # Download the METLINCCS dataset # # Link: https://metlin.scripps.edu/landing_page.php?pgcontent=mainPage # # Click on METLIN-CCS | METLIN CCS Lipids and download the excel, export it as csv and l...
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# %% [markdown] # # Imports # %% from multisensory import ( ClassicalTask, BalancedComodulationTask, DetectionTask, MAPClassifier, ) import pickle from pathlib import Path root = Path(".") save_path = root / "ideal_data" # %% [markdown] # # Hyperparameters # %% # Tasks tasks = [ ClassicalTask(s...
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# %% import loompy import numpy as np import pandas as pd from anndata import AnnData import scanpy as sc # %% lc = loompy.connect("./raw/zeisel_2018/l5_all.loom") # %% X = lc.layers[""].sparse().T.tocsr() dict_obs = dict() for k in lc.col_attrs.keys(): if k == "Comment": continue dict_obs[k] = lc.co...
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# %% [markdown] # # Run power analysis # Steps: # 1. Define input data # - Statistical parametric map array # - Mask array # - Data type (t- or z-values) # - Analysis design (one- or two-sample) # - Sample size # - Cluster-defining threshold # - Alpha (cluster-extent threshold) # - FWHM ...
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# %% from pybioportal import molecular_data as md # %% df1a = md.fetch_molecular_data(entrez_gene_ids=["672","675"], molecular_profile_ids=["brca_tcga_mrna", "acc_tcga_rna_seq_v2_mrna"]) df1a # %% df1b = md.fetch_molecular_data(entrez_gene_ids=["672","675"], ...
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# %% # http://justinblaber.org/acquiring-stereo-images-with-spinnaker-api-hardware-trigger/ # %% import matplotlib.pyplot as plt import PySpin # %% # Set camera serial numbers camera_serials = [22181547] serial_1 = str(camera_serials[0]) # %% # Get system system = PySpin.System.GetInstance() # %% # Get camera list...
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# %% from pmlb import fetch_data, nearest_datasets import seaborn as sns import matplotlib.pyplot as plt import numpy as np import pandas as pd %matplotlib inline # %% pmlb_stats= pd.read_csv('../pmlb/all_summary_stats.tsv', sep='\t') print('potential dimensions:',[c for c in pmlb_stats.columns if c != 'dataset']) pm...
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# %% import os import json from pprint import pprint from PIL import Image import glob as glob import matplotlib.pyplot as plt from IPython.display import Video # %% [markdown] # ### This notebook walks through how to load a video stimulus and its corresponding metadata. # %% dataset_root = "/your/path/to/BOLDMoments...
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# %% import pypylon.pylon as py # %% from pypylon import pylon # %% camera_serials = [24535665, 24548223] # %% NUM_CAMERAS = 2 # %% tlf = py.TlFactory.GetInstance() # %% # create a device filter for Pylon CamEmu devices di = py.DeviceInfo() # %% di # %% devs = tlf.EnumerateDevices([di,]) # %% devs # %% devs[0]...
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# %% [markdown] # # snnTorch # # snnTorch is a deep learning simulator for spiking neural networks, built on PyTorch. # # ```{include} ../../../tmp/examples/snntorch/supported_primitives.md # %% [markdown] # ## Import a NIR graph to snnTorch # %% from snntorch.import_nir import import_from_nir import torch import ...
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# %% import torch import torch.nn as nn import snntorch as snn import numpy as np # from snntorch import export import nir import nirtorch # %% graph = nir.read('lif_norse.nir') graph.nodes # %% net = snn.import_from_nir(graph) # %% isis = [ 6, 15, 4, 3, 0, 2, 1, 2, 0, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 13, 0...
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# %% from fimpy.core import H5SplitDataset from fimpy.pipeline.twop import align_2p_volume from pathlib import Path from fimpy.loading.twop import load_2p # %% [markdown] # # Load one # %% path = Path(r"J:\_Shared\experiments\E0032_luminance\v01_flashes\IO\181024_f1") # %% load_2p(path, pattern="*im*/*mat_files*/a...
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# %% import numpy as np from matplotlib.pylab import plt import numpy as np import seaborn as sns def parse_energy_matrix(f): i,j = 0,0 energy = np.zeros((60,60)) for l in f.readlines(): if 'Energy' in l: energy[i][j] = float(l.split(' ')[-1]) j += 1 ...
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# %% [markdown] # ## Spyx # # Spyx is a JAX-based SNN/Deep learning framework that enables fully JIT compiled optimization of models. # %% import spyx import spyx.nn as snn import jax import jax.numpy as jnp import nir # %% [markdown] # ## Import a NIR graph to Spyx: # %% # Load the NIR graph from disk nir_graph ...
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# %% [markdown] # ### Example notebook for model training and inference # - Author: Xiaohui Zhang # %% %load_ext autoreload %autoreload 2 import tensorflow as tf import importlib import os, random import json import sys import numpy as np import argparse from model_attention_bilstm import model from dataloader_sleep...
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# %% [markdown] # # Spyx # # Spyx is a JAX-based SNN/Deep learning framework that enables fully JIT compiled optimization of models. # # ```{include} ../../../tmp/examples/spyx/supported_primitives.md # %% import spyx import spyx.nn as snn import jax import jax.numpy as jnp import nir # %% [markdown] # ## Import ...
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# %% # This notebook can be used to load hesin files, typecast columns type and the saving as hesin.tsv format # %% import pandas as pd import numpy as np # %% txt_file_path = "" #/home/user/hesin_oper.txt tsv_file_path = "" #/home/user/hesin_oper.tsv df=pd.read_csv("file_path", sep = "\t") df # %% df.dtypes # %% ...
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# %% import numpy as np import pandas as pd # %% # Table 2 temp_df = pd.read_excel('/n/holystore01/LABS/price_lab/Users/mjzhang/scTRS_data/single_cell_data/' 'mouse_liver_halpern_nature_2017/SuppTable3_zonation.xlsx', skiprows=2, index_col=0) # %% df_hom = pd.read_csv('/n/holystore01/LABS/pr...
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# %% import pyreadstat import numpy as np import pandas as pd import matplotlib.pyplot as plt from scipy import stats import seaborn as sns import os from Mymodule.ModelHandler import * from Mymodule.Utils import * from Mymodule.GradCam import * from Mymodule.BatchHandler import * from sklearn.metrics import roc_auc_...
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# %% from rockpool.nn.combinators import Sequential from rockpool.nn.modules import LinearTorch, LIFNeuronTorch import numpy as np import pandas as pd import torch import matplotlib.pyplot as plt # %% d0 = [0, 0, 0, 0, 0, 0, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 1, 0, 0, 0, 0, 1, 0, 0, 0, 1, 1, 0, 0, 1, 0, 1...
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# %% !pip install -q SPARQLWrapper # %% !pip install -e /dss/dsshome1/04/di93zer/git/cellnet --no-deps # %% import os from os.path import join import pandas as pd import numpy as np # %% DATA_PATH = '/mnt/dssmcmlfs01/merlin_cxg_2023_05_15_sf-log1p' # %% [markdown] # # Compute lookup matrices # %% cell_type_mappi...
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# %% input_path = "./data/GSE199460_original3000_preprocessed.h5ad" %run /geniusland/home/fangyi/jupyter/CLEAR-main/Revise.py \ --input_h5ad_path={input_path} \ --aug_prob 0.0 --obs_label_colname "" # %% count_csv_path = f"./result/CLEAR/feature_CLEAR_{name}_original{gene}_preprocessed.csv" label_csv_path=f"./result/...
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# %% import os import random import subprocess from multiprocessing.pool import ThreadPool import time import pandas as pd # Generate a list of path of filtered MSA path_proteins = "/home/conchae/ML_depolymerase/get_candidates/millard/scanned_MSA" paths = [f"{path_proteins}/{msa}" for msa in os.listdir(f"{path_protein...
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# %% [markdown] # ### formatting censor.tsv file # %% import pandas as pd import numpy as np # %% LOCAL_DATA_FOLDER = ""#this is the same path that is being referred in do_all.sh file#/mnt/disks/ana-disk/ukbiobank_project/ukbb7089_2023_07_25/ df_censor = pd.read_csv(LOCAL_DATA_FOLDER+"censor.tsv.gz",sep = "\t", comp...
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# %% [markdown] # # Make the SWORD2 prediction # *** # ### I. The prediction # ### II. Scan through the IPR results # *** # %% import os import subprocess from multiprocessing.pool import ThreadPool path_work = "/home/conchae/PhageDepo_pdb" path_pdb = f"{path_work}/phagedepo_out" path_out = f"{path_work}/sword2_ou...
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# %% !pip install celltypist # %% from os.path import join import anndata import scanpy as sc import numpy as np import pandas as pd import dask.dataframe as dd import dask.array as da from scipy.sparse import csr_matrix # %% [markdown] # # Get subset training data # %% def get_count_matrix_and_obs(ddf): x = (...
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# %% from corrts import * import numpy as np import plotly.express as px import plotly.graph_objs as go import plotly.io as pio import matplotlib.pyplot as plt pio.templates.default = "simple_white" # %% gaussian_kernel = lambda t,r: np.exp(-r*t**2/2) lags = np.arange(0,1000) rgs = np.logspace(-4,0,100)[::-1] a...
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# %% import pandas as pd import anndata from anndata import AnnData import scanpy as sc import matplotlib.pyplot as plt from os.path import join import numpy as np import glob # %% raw_dir = "raw/habib_2016/" # %% df_mat = pd.read_csv(join(raw_dir, "SCP1/expression/DATA_MATRIX_LOG_TPM.txt"), sep='\t', index_col=0) df...
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# %% # http://justinblaber.org/acquiring-stereo-images-with-spinnaker-api-hardware-trigger/ # %% import PySpin # %% # Set camera serial numbers camera_serials = [22181547,22181612] serial_1 = str(camera_serials[0]) serial_2 = str(camera_serials[1]) # %% # Get system system = PySpin.System.GetInstance() # %% # Get ...
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# %% from build_docker import * import unittest import pprint DEBUG_MODE = False this_script_path = os.path.realpath('__file__') # %% # example args for testing different scenarios EXAMPLE_BUILD_TAG = "my.example" # build from local files, and push to both Dockerhub and GCR EXAMPLE_ARGS_LOCAL = ['--targets', 'all',...
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# %% [markdown] # # Install the ml4h toolkit for machine learning on clinical data # # The following commands will install the [ml4h toolkit for machine learning on clinical data](https://github.com/broadinstitute/ml4h) on your Terra [detachable persistent disk](https://support.terra.bio/hc/en-us/articles/360047318551...
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# %% [markdown] # # Annotate relative radial distance from nuclear center # # For each read in the PGP1 dataset, find its normalized radial distance from the nuclear center. # %% import importlib import os, sys, warnings import numpy as np import pandas as pd sys.path.append(os.path.abspath(os.path.join(r"..", r".")...
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# %% import norse import numpy as np import pandas as pd import torch import matplotlib.pyplot as plt # %% d0 = [0, 0, 0, 0, 0, 0, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 1, 0, 0, 0, 0, 1, 0, 0, 0, 1, 1, 0, 0, 1, 0, 1, 0, 0, 1, 1, 0, 1, 1, 1, 1, 1, 1, 1, 1, 1, 1, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 1, 1,...
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# %% [markdown] # # Sinabs # # Sinabs is a deep learning library for spiking neural networks which is based on PyTorch and focuses on fast training as well as inference on neuromorphic hardware. # # `sinabs.to_nir` and `sinabs.from_nir` methods allow you to seemlessly navigate between `nir` and `sinabs`. Once your mo...
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# %% import numpy as np import matplotlib.pyplot as plt from emilys.image.arrayplot import arrayplot2d %matplotlib inline # %% # development imports with autoreload %load_ext autoreload %autoreload 1 # %% # development import specifics %aimport emilys.image.kernels # %% # load an image file and show it nx = 256 ny =...
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# %% # This tutorial is based on # https://mne.tools/dev/auto_tutorials/preprocessing/20_rejecting_bad_data.html import os import numpy as np import mne from jointdecorrelation import EventBasedArtifactProjector mne.set_log_level('error') # %% # download and load the MNE sample dataset sample_data_folder = mne.d...
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# %% from pybioportal import mutations as mts # %% df1 = mts.get_muts_in_mol_prof_by_sample_list_id(molecular_profile_id="brca_tcga_mutations", sample_list_id="brca_tcga_all", entrez_gene_id="672") df1 # %% df2a = mts....
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# %% [markdown] # # YData Profiling: HCC Dataset # Source of data: https://www.kaggle.com/datasets/mrsantos/hcc-dataset # # As modifiations have been introduced for the purpose of this use case, the .csv file is provided (hcc.csv). # %% [markdown] # ## Import libraries # %% import pandas as pd from data_profiling i...
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# %% import numpy as np import pandas as pd import scanpy as sc import matplotlib as mpl import matplotlib.pyplot as plt from copy import copy vir = copy(mpl.cm.viridis) vir.set_under("lightgray") sc.settings.verbosity = 3 sc.logging.print_header() sc.settings.set_figure_params(figsize = [12,10],dpi =100...
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# %% import pandas as pd import os from tqdm import tqdm from Bio import SeqIO # %% # %% seq_to_remove = SeqIO.parse(f"{path_DePP_results}/remove_benchmark.fasta", "fasta") seq_to_remove_list = [record.seq for record in seq_to_remove] # %% df_final_results = pd.read_csv(f"{path_DePP_results}/full_benchmark_dataf...
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# %% [markdown] # # Sinabs # # Sinabs is a deep learning library for spiking neural networks which is based on PyTorch and focuses on fast training as well as inference on neuromorphic hardware. # # `sinabs.to_nir` and `sinabs.from_nir` methods allow you to seemlessly navigate between `nir` and `sinabs`. Once your mo...
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# %% [markdown] # # Figure 3 # %% %load_ext autoreload %autoreload 2 from flyvis import EnsembleView # %% EnsembleView( "flow/0000", best_checkpoint_fn_kwargs={"validation_subdir": "validation", "loss_file_name": "loss"}, ) # %% [markdown] # ## a # %% task_error = ensemble.task_error() # %% embedding_and_...
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# %% [markdown] # # Test notebook Titanic # %% from pathlib import Path import numpy as np import pandas as pd from IPython.utils.capture import capture_output from ipywidgets import widgets from data_profiling import ProfileReport from data_profiling.utils.cache import cache_file # %% # Read the Titanic Dataset fi...
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# %% import numpy as np import pandas as pd # %% DIC_PATHWAY = {'Glycolysis': 'REACTOME_GLYCOLYSIS', 'Lipogenesis': 'REACTOME_TRIGLYCERIDE_BIOSYNTHESIS', 'Bile acid production':'KEGG_PRIMARY_BILE_ACID_BIOSYNTHESIS', 'Glutamine synthesis':'', 'Xenobiotic metab...
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# %% import pandas as pd import numpy as np # %% [markdown] # # Drug Targets # %% drug_targets = pd.read_csv('data/COVID/drug_target.csv') drug_targets # %% drug_targets['evidence_url'] = drug_targets['Evidence'].apply(lambda x: x[x.find('https:'):-1]) # %% drug_targets.iloc[0].evidence_url # %% drug_targets['Term...
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# %% import matplotlib.pyplot as plt import nir import numpy as np from spinnaker2 import s2_nir, brian2_sim # load NIR model nir_model = nir.read("two_lif_neurons.nir") s2_nir.add_output_to_node("lif1", nir_model, "out_lif1") # %% def run_two_neuron_model_on_s2(nir_model, duration, dt): times = np.arange(0, dur...
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# %% from lisa_user_data import genome_tools # %% import importlib # %% genome_tools = importlib.reload(genome_tools) r = [genome_tools.Region('chr1', start, end) for start, end in zip([1,10,20,30],[12,15,23,33])] r2 = [genome_tools.Region('chr1', start, end) for start, end in zip([1,10,20,30],[12,15,23,33])] r.appe...
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# %% import torch import tonic import norse import nir import numpy as np from collections import defaultdict import tqdm # %% nir_graph = nir.read("cnn_sinabs.nir") {k: type(v) for k, v in nir_graph.nodes.items()} # %% g = norse.torch.from_nir(nir_graph) # %% to_frame = tonic.transforms.ToFrame(sensor_size=tonic.da...
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# %% [markdown] # # Python tutorial for using Attentive Chrome # %% [markdown] # ## 1. Install kipoi # This can be done by using `pip`. (Ex `pip install kipoi`). Note that you need anaconda or miniconda installed. Refer to https://kipoi.org/docs/#installation for more information. # %% [markdown] # ## 2. Using Attent...
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# %% import os from os.path import join import dask.dataframe as dd import dask.array as da import numpy as np import pandas as pd from dask_ml.decomposition import IncrementalPCA # %% PATH = '/mnt/dssmcmlfs01/merlin_cxg_2023_05_15_sf-log1p' # %% def get_count_matrix(ddf): x = ( ddf['X'] .map_pa...
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# %% import pandas as pd import numpy as np # %% [markdown] # # MESH # %% important_columns_mesh = [ 'Class ID', 'Preferred Label', 'Synonyms', 'Obsolete', 'Semantic Types', 'CUI' ] # %% mesh_df = pd.read_csv( "data/MESH.csv", # relative python path to subdirectory sep=',', u...
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# %% import nir import numpy as np # %% ng1 = nir.read('braille_v2.nir') ng2 = nir.read('braille_v2a.nir') # %% sorted(ng1.edges) == sorted([('lif2', 'output'), ('input', 'fc1'), ('fc2', 'lif2'), ('lif1.lif', 'lif1.w_rec'), ('lif1.w_rec', 'lif1.lif'), ('fc1',...
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# %% import nir import numpy as np # %% ng1 = nir.read('braille_v2.nir') ng2 = nir.read('braille_v2a.nir') # %% sorted(ng1.edges) == sorted([('lif2', 'output'), ('input', 'fc1'), ('fc2', 'lif2'), ('lif1.lif', 'lif1.w_rec'), ('lif1.w_rec', 'lif1.lif'), ('fc1',...
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# %% [markdown] # # Create unit test data for comparison between matlab and Python # %% addpath('./matlab') # %% fprintf('MATLAB version\n') version clear # %% [stauts, data_path] = system('python -c "import mne; print(mne.datasets.testing.data_path(), end=str())"') # %% fname = strcat(data_path, '/MEG', '/sample',...