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# %% [markdown] # ### ECG Transformation Across Varying Heart Rates # %% import numpy as np import neurokit2 as nk import matplotlib.pyplot as plt from sklearn.preprocessing import FunctionTransformer from sklearn.impute import SimpleImputer import rlign # %% normalizer = rlign.Rlign(scale_method="linear", template_...
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# %% [markdown] # # Create Graph Dataset # %% import sys import os import pickle as pkl import pandas as pd import torch path = os.path.join('..', '.') if path not in sys.path: sys.path.append(os.path.abspath(path)) from src.protein_graph import pncaGraph from tqdm import tqdm # %% train_seqs = pd.read_csv('.....
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# %% from sklearn.neighbors import KNeighborsClassifier, KNeighborsRegressor from sklearn.model_selection import GridSearchCV, cross_val_score, KFold from sklearn.metrics import roc_auc_score, precision_recall_curve from sklearn.metrics import auc as calculate_auc from sklearn.metrics import mean_squared_error from sk...
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# %% import pandas as pd import numpy as np # %% # %% BASE_PATH = "/storage/Arushi/090526_EvoAge/kg_formation/data_collection/" OUT_PATH = "/storage/Arushi/090526_EvoAge/kg_formation/processed_data/stitch" # %% ## Pubchem_2_name Pubchem = pd.read_pickle(f'{BASE_PATH}databases_for_mapping/pubchem/combined_df.pkl')...
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# %% # %% Load source data and reproduce Fig 3 RT violin+slope import os import numpy as np import pandas as pd import matplotlib.pyplot as plt from matplotlib.ticker import MaxNLocator from matplotlib.patches import Patch in_xlsx = os.path.join(data_dir, "output", "SourceData_Fig3_SH_RT.xlsx") roi_order = ["lc", "sn...
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# %% [markdown] # # Visualization of Data Distribution for [THINGS-Mooney](https://github.com/wobc/things-mooney) # %% import pandas as pd import matplotlib.pyplot as plt import seaborn as sns metadata = pd.read_csv('things_mooney_metadata.csv') # %% # Set the style for the plot sns.set(style="whitegrid") # Plot th...
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# %% # =============================== # Encryption Pipeline # =============================== def encrypt_image(img_tensor, key_params): """ Applies chaotic encryption: 1) Arnold Cat Map (confusion) 2) Logistic Map + Zigzag diffusion """ img_np = img_tensor.squeeze(0).cpu().numpy() N = im...
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# %% [markdown] # # MolecularFunction → BiologicalProcess Relation Pipeline # # Builds a unified, deduplicated edge table for the **MolecularFunction–BiologicalProcess** relation. # # **Output schema:** `head | relation | tail | head_type | relation_type | tail_type | kg_source | kg_type | head_id_is | tail_id_is | h...
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# %% [markdown] # # First steps # # After installing the plugin you can open it from the napari menu under the name ```Convpaint```. # # You can use the plugin with various types of images: simple gray-scale, multi-channel, time-lapse, RGB. Note that while you can annotate stacks of slices as a single 3D image, the l...
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# %% [markdown] # # 不同类型的测量 API # %% [markdown] # ## 概述 # # TensorCircuit 允许执行与测量结果相关的两种操作。 # 这些是 (i) 条件测量,其结果可用于控制下游条件量子门,以及 (ii) 后选择,它允许用户选择与特定测量结果相对应的测量后状态。 # %% [markdown] # ## 设置 # %% import tensorcircuit as tc import numpy as np K = tc.set_backend("tensorflow") # %% [markdown] # ## 条件测量 # # # `cond_measur...
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# %% [markdown] # Reproduce Fig2 # # Here I have number of units that are close to the paper (I think because I did a mistake first in calculating constraints - using whole baseline instead of only 1500 ms?) # %% import pandas as pd import numpy as np from scipy import stats import matplotlib.pyplot as plt import se...
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# %% %load_ext autoreload %autoreload 2 import numpy as np import pandas as pd import napari from scribbles_testing.FoodSeg103_data_handler import * # %% [markdown] # ## Create scribbles # %% [markdown] # Load the ground truths as batch # %% img_nums = [n for n in range(0, 4983, 8)] #[1382] #2750 #1234 #2314 gts = ...
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# %% [markdown] # # Stats for Figure 2 # %% # imports import pandas as pd import numpy as np import sys sys.path.append('..') # needed for relative file path import with jupyter from src.cc import ccptpt from src.expparams import sim_dt from src.expparams import sim_dur from src.expparams import sim_step_num from nump...
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# %% # %% Load saved source data and reproduce Fig 4 violin+slope (Gain → Loss) import os import numpy as np import pandas as pd import matplotlib.pyplot as plt from matplotlib.ticker import MaxNLocator from matplotlib.patches import Patch in_xlsx = os.path.join(data_dir, "output", "SourceData_Fig4_SH_GainLoss.xlsx") ...
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# %% from deepscore import DeepScore from preprocessing import * import scanpy as sc import anndata as ad %load_ext rpy2.ipython %load_ext tensorboard sc.settings.set_figure_params(dpi=80, color_map='gist_earth') sc.settings.set_figure_params(figsize=('10', '10'), color_map='gist_earth') # %% #!Rscript /home/pab/pro...
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# %% #### !/usr/bin/env python # coding: utf-8 from molmap.model import RegressionEstimator, MultiClassEstimator, MultiLabelEstimator from molmap import loadmap from molmap.show import imshow_wrap import molmap from molmap import MolMap from sklearn.utils import shuffle from joblib import load, dump import numpy as n...
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# %% import pickle as pkl #import viz_sequence from scipy.stats import spearmanr, pearsonr import matplotlib.pyplot as plt from scipy.spatial.distance import jensenshannon import h5py from scipy.special import softmax import scipy import matplotlib import matplotlib.pyplot as plt import numpy as np from statsmodels.dis...
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# %% # =============================== # Environment & Reproducibility Setup # =============================== import torch import torch.nn as nn import torchvision import torchvision.transforms as transforms import matplotlib.pyplot as plt import pennylane as qml import numpy as np import random from pytorch_msssim i...
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# %% # %% Load source data and reproduce Fig 5 SH Accept vs SH Reject (violin + paired slope) import os import numpy as np import pandas as pd import matplotlib.pyplot as plt from matplotlib.ticker import MaxNLocator from matplotlib.patches import Patch in_xlsx = os.path.join(data_dir, "output", "SourceData_Fig5_SH_Ac...
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# %% import numpy as np import pandas as pd from PIL import Image from seghub import segbox from scribbles_testing import cellpose_data_handler from scribbles_testing.image_analysis_helpers import single_img_stats # %% img_folder = "/mnt/imaging.data/rschwob/cellpose_run07/" output_folder = "/mnt/imaging.data/rschwob...
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# %% [markdown] # ```{currentmodule} optimap # ``` # %% from optimap.utils import jupyter_render_animation as render # %% [markdown] # ```{tip} # Download this tutorial as a {download}`Jupyter notebook <converted/apd.ipynb>`, or as a {download}`python script <converted/apd.py>` with code cells. We highly recommend us...
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# %% [markdown] # # Tabular Examples # RNA3DB contains `Tabular`, a high-level API for interacting with Infernal's output tables for `cmscan`. # # Using the `.tbl` files we provide, we can look up Rfam family information for any RNA chain in the PDB. # %% # read an entire directory of *.tbl files, such as those provi...
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# %% [markdown] # # CellularComponent → ChemicalEntity Relation Pipeline # # Builds a unified, deduplicated edge table for the **CellularComponent–ChemicalEntity** relation. # # **Output schema:** `head | relation | tail | head_type | relation_type | tail_type | kg_source | head_id_is | tail_id_is | head_detail_name ...
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# %% import numpy as np import pandas as pd from scipy import stats import pingouin as pg # ---------------------------- # 1) Raw LH frequecny data # ---------------------------- data5D = { "ConFoff": { "Before": [18.3, 12.0, 15.0, 15.0, 17.5, 15.0], "After": [22.5, 22.5, 27.5, 20.0, 25.0, 25.0],...
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# %% [markdown] # # 量子近似优化算法 (QAOA) # %% [markdown] # ## 概述 # %% [markdown] # QAOA 是一种混合经典量子算法,它结合了量子电路与经典优化。 # 在本教程中,我们利用 QAOA 解决最大割 (MAX CUT) 组合优化问题:给定一个图 $G=(V, E)$,其中节点 $V$ 和边 $E$,找到一个子集 $S \in V$ 使得 $S$ 和 $S \backslash V$ 之间的边数最大化。 # 这个问题可以简化为寻找反铁磁伊辛模型的基态,其哈密顿量为: # # $$H_C = \frac{1}{2} \sum_{i,j\in E} C_{ij} \...
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# %% [markdown] # This notebook shows how to use JOINT to cluster data with 2 cell types and 2 features (genes) # %% import numpy as np from joint import joint from sklearn.cluster import KMeans import matplotlib.pyplot as plt from sklearn.metrics.cluster import adjusted_rand_score %matplotlib inline # %% # generate ...
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# %% # --- Instantiate and Train --- # Reset seed before each model for fair comparison set_seed(42) cnn_model = CNNAutoencoder() print("Training CNN baseline...") cnn_model, cnn_losses = train_model(cnn_model, "CNN") torch.save(cnn_model.state_dict(), "cnn_model.pt") set_seed(42) qnn_model = QNNBranch() print("\nTr...
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# %% %load_ext autoreload %autoreload 2 import numpy as np import pandas as pd from scribbles_testing.FoodSeg103_data_handler import * # %% [markdown] # Load the images as batches # %% img_nums = [0]#[n for n in range(0, 4900, 500)] #2750 #1234 #2314 imgs, gts = load_food_batch(img_nums) num_imgs = len(imgs) print(f...
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# %% import molmap import os import pandas as pd import matplotlib.pyplot as plt import seaborn as sns from molmap import feature, dataset # %% data = dataset.load_HIV() # %% aspirin = 'CC(=O)OC1=CC=CC=C1C(O)=O' #aspirin NAC = 'CC(=O)NC1=CC=CC=C1C(O)=O' #N_acetylanthranilic_acid smiles_list = [aspirin, NAC] # %% E ...
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# %% import numpy as np import pandas as pd import pickle %matplotlib inline import matplotlib import matplotlib.pyplot as plt import seaborn as sns from pathlib import Path import re import scipy.stats as stats # %% matplotlib.rcParams.update({'font.size': 10}) matplotlib.rcParams['pdf.fonttype'] = 42 matplotlib...
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# %% import numpy as np import pandas as pd import pickle %matplotlib inline import matplotlib import matplotlib.pyplot as plt import seaborn as sns from pathlib import Path import re import scipy.stats as stats # %% matplotlib.rcParams.update({'font.size': 10}) matplotlib.rcParams['pdf.fonttype'] = 42 matplotlib...
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# %% [markdown] # # Gene ↔ Mutation Relation-Wise Merge # # Merges Gene–Mutation triples from EvoAGE; # deduplicates by `(head, relation, tail)`; and saves the result. # %% [markdown] # ## 0. Configuration # %% import os import pandas as pd BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' PROC_DIR = BAS...
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# %% import pandas as pd import numpy as np # %% # %% # %% BASE_PATH = "/storage/Arushi/090526_EvoAge/kg_formation/data_collection/" OUT_PATH = "/storage/Arushi/090526_EvoAge/kg_formation/processed_data/stitch" # %% ## Pubchem_2_name Pubchem = pd.read_pickle(f'{BASE_PATH}databases_for_mapping/pubchem/combined_...
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# %% [markdown] # # SDE integrator # %% #export # Initialization from DiffOperator import DifferentialOperator # import derivativesTransferFunctions import numpy as np # import derivativesTransferFunctions # %% [markdown] # ## Reward-driven regulatory mechanism # %% #export def RegulatoryPsi(psi0, stimulusA, stimu...
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# %% %load_ext autoreload %autoreload 2 import numpy as np import napari from scribbles_testing.FoodSeg103_data_handler import * # %% [markdown] # ## Prediction # %% [markdown] # Load the images as batches # %% img_nums = [1328]#[n for n in range(0, 4500, 1000)] #2750 #1234 #2314 imgs = load_food_batch(img_nums, lo...
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# %% # This scripts creates events.tsv for the main sample of subjects # Let's consider the boop and split the imagery block into 2 blocks # %% import os from src.utils import seq2tsv from src.my_settings import settings sett = settings() # %% [markdown] # # Settings # %% feedback_task_list = ['nf','sham'] ## Loca...
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# %% [markdown] # ## Pipeline for supervised modeling # %% import os # Check if it's in the correct directory print("Current working directory:", os.getcwd()) path = os.path.abspath(os.path.join(os.getcwd(), '..', 'path.py')) %run $path # %% [markdown] # ##### Configure notebook # %% # Import data train_file = '../...
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# %% import csv # Load the csv file def load_csv(file_path): # input: csv with two columns: (id, sequence) # output: list of tuples (id, sequence) sequences = [] with open(file_path, "r") as f: reader = csv.reader(f) header = next(reader) # skip header for row in reader: ...
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# %% # %% Load saved source data and reproduce Fig 2A violin (from SourceData_Wide) import os import numpy as np import pandas as pd import matplotlib.pyplot as plt from matplotlib.ticker import MaxNLocator from matplotlib.patches import Patch in_xlsx = os.path.join(data_dir, "output", "SourceData_Fig2_stakes.xlsx") ...
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# %% from molmap import model as molmodel import molmap from molmap import dataset import matplotlib.pyplot as plt import pandas as pd from tqdm import tqdm from joblib import load, dump tqdm.pandas(ascii=True) import numpy as np import tensorflow as tf import os os.environ["CUDA_VISIBLE_DEVICES"]="3" seed = 123 np....
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# %% [markdown] # # Protein ↔ Phenotype Relation-Wise Merge # # Merges Protein–Phenotype triples from CrossBAR; # deduplicates by `(head, relation, tail)`; and saves the result. # %% [markdown] # ## 0. Configuration # %% import os import pandas as pd BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' PROC_DI...
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# %% [markdown] # # Gene ↔ Mutation Relation-Wise Merge # # Merges Gene–Mutation triples from EvoAGE; # deduplicates by `(head, relation, tail)`; and saves the result. # %% [markdown] # ## 0. Configuration # %% import os import pandas as pd BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' PROC_DIR = BAS...
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# %% [markdown] # # `Exact` explainer # # This notebooks demonstrates how to use the Exact explainer on some simple datasets. The Exact explainer is model-agnostic, so it can compute Shapley values and Owen values exactly (without approximation) for any model. However, since it completely enumerates the space of maski...
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# %% [markdown] # # Different Types of Measurement API # %% [markdown] # ## Overview # # TensorCircuit allows for two kinds of operations to be performed that are related to the outcomes of measurements. These are (i) conditional measurements, the outcomes of which can be used to control downstream conditional quant...
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# %% # =============================== # Quantum Device # =============================== dev = qml.device("default.qubit", wires=n_qubits, shots=None) @qml.qnode(dev, interface="torch", diff_method="backprop") def improved_qblock(inputs, weights): # Angle embedding qml.AngleEmbedding(inputs * np.pi, wires=...
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# %% # %% Load source data (Fig 7 Accept vs Reject) and reproduce laminar profile + superficial/deep plot import os import numpy as np import pandas as pd import matplotlib.pyplot as plt roi_tag = "dlPFC" # must match what you saved in_xlsx = os.path.join(data_dir, "output", f"SourceData_Fig7_{roi_tag}_AR_laminar.xl...
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# %% [markdown] # # Table 1. Fifteen feature vectors of DNA data calculated by repDNA # %% [markdown] # ![img](./repDNA.png) # %% from Bio.Seq import Seq from Bio import SeqIO import pandas as pd import numpy as np # %% df = pd.Series(SeqIO.to_dict(SeqIO.parse('./test.fasta', 'fasta'))) # %% s = df.iloc[0] # %% my...
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# %% #### !/usr/bin/env python # coding: utf-8 from molmap.model import RegressionEstimator, MultiClassEstimator, MultiLabelEstimator from molmap import loadmap from molmap.show import imshow_wrap import molmap from molmap import MolMap from sklearn.utils import shuffle from joblib import load, dump import numpy as n...
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# %% [markdown] # # Create Sequences for Dataset # %% import pandas as pd import numpy as np import copy import gumpy # %% [markdown] # ### Get sequences from mutations # %% reference = gumpy.Genome('../data/NC_000962.3.gbk') pnca = reference.build_gene('pncA') # %% # from fowler-lab/predict-pyrazinamide-resistance...
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# %% %load_ext autoreload %autoreload 2 from PIL import Image import napari import numpy as np import os from scribbles_creator import * from scribbles_testing.cellpose_data_handler import * # %% [markdown] # ## Define where the images are located # %% folder_path = "../cellpose_train_imgs/" # %% [markdown] # ## C...
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# %% [markdown] # # Node Feature Importance # %% import sys import os import numpy as np import pickle as pkl import matplotlib.pyplot as plt import seaborn as sns import pandas as pd import torch import torch.nn.functional as F from torch.nn import CrossEntropyLoss path = os.path.join('..', '.') if path not in sys....
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# %% from molmap import loadmap import matplotlib.pyplot as plt import matplotlib.patches as mpatches import seaborn as sns from rdkit import Chem from rdkit.Chem import Draw from rdkit.Chem.Draw import IPythonConsole #IPythonConsole.ipython_useSVG = True import numpy as np mp1 = loadmap('./descriptor.mp') mp2 = lo...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ─────────────────────────...
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# %% import pandas as pd import numpy as np # %% # %% # %% BASE_PATH = "/storage/Arushi/090526_EvoAge/kg_formation/data_collection/" OUT_PATH = "/storage/Arushi/090526_EvoAge/kg_formation/processed_data/stitch" # %% # BTO BTO = pd.read_csv(f'{BASE_PATH}databases_for_mapping/bto/Tissue.tsv', sep = '\t') BTO BTO_D...
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# %% [markdown] # # Xarray Data Structures - an fNIRS example # # This example illustrates the usage of xarray-based data structures for calculating the Beer-Lambert transformation. # %% # This cells setups the environment when executed in Google Colab. try: import google.colab !curl -s https://raw.githubuser...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ─────────────────────────...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ───────...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ...
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# %% #!/usr/bin/env python # coding: utf-8 from molmap.model import RegressionEstimator, MultiClassEstimator, MultiLabelEstimator from molmap import loadmap, dataset from molmap.show import imshow_wrap from sklearn.utils import shuffle from joblib import load, dump import numpy as np import pandas as pd import os ...
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# %% [markdown] # Makes summary df from abcTau run results. # %% import matplotlib.pyplot as plt import seaborn as sns import pickle import re from pathlib import Path import numpy as np import pandas as pd from scipy import stats from scipy.stats import gaussian_kde # add the path to the abcTau package import sys ...
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# %% import shap import tensorflow as tf from tensorflow.keras.models import load_model import chrombpnet.training.utils.losses as losses import chrombpnet.training.utils.one_hot as one_hot from tensorflow.keras.utils import get_custom_objects from tensorflow.keras.models import load_model import matplotlib.pyplot as p...
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# %% library(Seurat) library(Signac) library(glue) library(ggplot2) library(GenomicRanges) set.seed(1234) setwd("~/projects/deepscore") source("utils/multiple_scataq_analysis.R") # %% kidney.rna <- readRDS("~/projects/kidney/Nuc/kidney.rna.rds") kidney.atac <- readRDS("~/projects/kidney/Atac/kidney.atac.rds") kidney....
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ───────...
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# %% import sys import os # Add the parent directory of `notebook/` to sys.path sys.path.append(os.path.abspath("..")) import numpy as np import pandas as pd from pymatgen.symmetry.analyzer import SpacegroupAnalyzer from pymatgen.io.ase import AseAtomsAdaptor from multiprocessing import Pool, cpu_count from ase import...
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# %% [markdown] # # Description # %% [markdown] # **Classifiers**, such as Random Forest or Catboost are very powerful machine learning tools for image segmentation. The most famous example is the very popular open source software [Ilastik](https://www.ilastik.org/). There are also popular plugins to perform these tas...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # # Databases Having Gene Phenotype relation of Drosophila # %% # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC...
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# %% # %% Load source data (Fig 6) and reproduce laminar profile + superficial/deep plot import os import numpy as np import pandas as pd import matplotlib.pyplot as plt from matplotlib.ticker import MaxNLocator roi_tag = "vPFC" # <-- match what you saved ("vPFC" or "dlPFC") in_xlsx = os.path.join(data_dir, "output",...
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# %% from sklearn.neighbors import KNeighborsClassifier, KNeighborsRegressor from sklearn.model_selection import GridSearchCV, cross_val_score, KFold from sklearn.metrics import roc_auc_score, precision_recall_curve from sklearn.metrics import auc as calculate_auc from sklearn.metrics import mean_squared_error from sk...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ─────────────────────────...
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# %% import os import pandas as pd import numpy as np # %% # ── Base directories ────────────────────────────────────────────────────────── BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' PROC_DIR = BASE_DIR + 'processed_data/' DB_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' # ── Output ...
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# %% [markdown] # # NMF analysis # %% import os import itertools import joblib import numpy as np import pandas as pd pd.set_option('display.max_columns', None) import matplotlib.pyplot as plt import seaborn as sns # %% %load_ext autoreload %autoreload 2 from fruitfly_parkinson import settings as s from fruitfly_p...
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# %% [markdown] # # Demonstration of DCBC evaluation usage in volume space # This notebook shows an example of a Distance controlled boundary coefficient (DCBC) evaluation of a striatum parcellation using the Multi-domain task battery (MDTB) functional dataset (glm7). # # ## Installation and Dependencies # # Ensure ...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% # sgd/ALL_YEAST_GENE_PHENOTYPE.csv # %% [markdown] # # Databases Having Gene PHENOTYPE relation of yeast # %% # # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_c...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ───────...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ───────...
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# %% [markdown] # # This tutorial shows how to run Cytocraft on subcell-resolution ST data (MERFISH ileum dataset) # %% [markdown] # ## Preprocessing # %% [markdown] # ### Load packages # %% import os import pandas as pd import cytocraft.craft as cc gem_path = './demo/merfish_ileum/data/transcripts.gem.csv' obs_path...
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# %% # %% Load source data (Fig 7) and reproduce laminar profile + superficial/deep plot import os import numpy as np import pandas as pd import matplotlib.pyplot as plt from matplotlib.ticker import MaxNLocator roi_tag = "vPFC" # match what you saved in_xlsx = os.path.join(data_dir, "output", f"SourceData_Fig7_{roi_...
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# %% import pandas as pd import numpy as np # %% # read volumes files volumUNSAM = pd.read_csv('volumes_asegUNSAM.csv') volumRRIB= pd.read_csv('volumes_asegRRIB.csv') volumJUK = pd.read_csv('volumes_asegJUK.csv') volumADNI = pd.read_csv('volumes_asegADNI.csv') #read dataset's participants info repo_dir='/Users/parri/...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ─────────────────────────...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # # Databases Having Phenotype biologicalprocess relation of celegans # %% # Monarch/Monarch_final/Celegans/Cele_PhenotypicFeature_BiologicalProcess.csv # %% BASE_DIR = '/storage/Arushi/090526_EvoAg...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # # Databases Having Phenotype biologicalprocess relation of celegans # %% # Monarch/Monarch_final/Celegans/Cele_PhenotypicFeature_BiologicalProcess.csv # %% BASE_DIR = '/storage/Arushi/090526_EvoAg...
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# %% [markdown] # Examples of ACF calculation with epoched methods: # 1. isttc concat # 2. PearsonR trial averaged # 3. iSTTC trial averaged (works like PearsonR but with non binned data) # %% import numpy as np import pandas as pd import pickle from isttc.scripts.cfg_global import project_folder_path from isttc.spik...
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# %% [markdown] # # 梯度和变分优化 # %% [markdown] # ## 概述 # # TensorCircuit 旨在使参数化量子门的优化变得简单、快速和方便。 在本说明中,我们回顾了如何获得电路梯度和运行变分优化。 # %% [markdown] # ## 设置 # %% import numpy as np import scipy.optimize as optimize import tensorflow as tf import tensorcircuit as tc K = tc.set_backend("tensorflow") # %% [markdown] # ## PQC #...
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# %% from chembench import dataset import pandas as pd import os random_seeds = [2, 16, 32, 64, 128, 256, 512, 1024, 2048, 4096] data_save_dir = '/raid/shenwanxiang/08_Robustness/dataset_induces' if not os.path.exists(data_save_dir): os.makedirs(data_save_dir) # %% def random_split(df, random_state = 123, split...
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# %% import warnings warnings.filterwarnings('ignore') import stereo as st import random import numpy as np import scanpy as sc import matplotlib.pyplot as plt import os import torch import pandas as pd import SpatialGlue from SpatialGlue.preprocess import clr_normalize_each_cell, pca # Fix random seed from SpatialGl...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ───────...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' !mkdir Celegans_chemical_noeffect_biologic...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% # Gene → Anatomy # Monarch/Monarch_final/Celegans/Gene_Cele_Anatomy.csv # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_m...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ───────...
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# %% import pandas as pd import matplotlib.pyplot as plt import numpy as np import seaborn as sns import math # %% #Load data using pandas. Make sure that the file is within the directory or use the full path to the file. ex. ('\C:\Users\mikep\etc') data = pd.read_csv('MaleFemalePheno.csv') # %% #Get Categorical Arra...
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# %% [markdown] # # 00 settings # %% import scipy.io as scio import h5py import numpy as np import tifffile as tf from PIL import Image import hdf5storage import pandas as pd import numpy as np import math import random import copy from itertools import chain import matplotlib.pyplot as plt import matplotlib.cm as c...
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# %% import os import pandas as pd import numpy as np # %% # ── Base directories ────────────────────────────────────────────────────────── BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' PROC_DIR = BASE_DIR + 'processed_data/' DB_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' # ── Output ...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ───────...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ─────────────────────────...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # # Databases Having Gene gene relation of yeast # %% # Monarch/Monarch_final/Yeast/Gene_Yeast_MolecularFunction.csv # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BAS...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% # flybase/Flybase_Droso_Gene_Phenotype.csv # Monarch/Drosophila/Gene_Droso_Phenotype_MONARCH.csv # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data...
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# %% [markdown] # # MERA # %% [markdown] # ## Overview # # In this tutorial, we'll show you how to implement MERA (multi-scale entangled renormalization ansatz) with TensorCircuit, but not in physics perspective. # %% [markdown] # ## Background # # MERA is a kind of VQE starts from only one qubit in the $\ket{0}$ s...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ───────...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_collection/databases_for_mapping/' PROC_DIR = BASE_DIR + 'processed_data/' # ── Output path ─────────────────────────...