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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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# %% [markdown] # # 算符扩散 # %% [markdown] # ## 概述 # %% [markdown] # 在本教程中,我们将介绍作为混沌动力学和信息加扰诊断的算子扩散。我们将检查算子扩散作为电路深度 $L$ 的函数,可以将其视为离散量子系统中的时间 $t$。 此处考虑的算子扩散系数为: # $$ # C_{y}(j,t)=\frac{1}{2} \text{Tr}([O(t), \sigma^{(j)}_{y}]^{\dagger}[O(t),\sigma^{(j)}_{y}]), # $$ # 其中 $\sigma_{y}^{(j)}$ 是第 $j$ 个量子位的 Pauli-y 矩阵。 $O(0)$...
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# %% import pickle as pkl import matplotlib.pyplot as plt import os import numpy as np # %% path = "/srv/scratch/anusri/chrombpnet_paper/results/chrombpnet/ATAC/GM12878/" #universal_transfer=path+"ATAC_10.08.2021_withuniversalbias/with_universal_bias_final_model/unplug/" #invivo=path+"ATAC_10.09.2021_withinvivobias/f...
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# %% import os import subprocess import pandas as pd os.environ["CUDA_VISIBLE_DEVICES"] ="0" pythoner = "/home/sxh/anaconda3/envs/chemprop/bin/python" optimizer = "/home/sxh/Research/chemprop/hyperparameter_optimization.py" trainer = "/home/sxh/Research/chemprop/train.py" predicter = "/home/sxh/Research/chemprop/p...
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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 celegans # %% # gendr/Cele/Cele_GenDR_Gene_BioProcess.csv # Monarch/Monarch_final/Celegans/Gene_Cele_BiologicalProcess.csv # %% BASE_DIR = '/storage/A...
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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_gene # ── Output ...
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# %% from molmap import model as molmodel import molmap 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"]="0" np.random.seed(123) tf.compat.v1.set_rand...
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# %% [markdown] # # Phenotype ↔ ChemicalEntity Relation-Wise Merge # # Merges Phenotype–Chemical triples from PrimeKG; fills missing `tail_detail_name` # via PubChem IUPAC lookup; deduplicates by `(head, relation, tail)`; and saves the result. # %% [markdown] # ## 0. Configuration # %% import os import pandas as pd ...
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# %% [markdown] # # Customized Contraction # %% [markdown] # ## Overview # # If the simulated circuit has large qubit counts, we recommend users try a customized contraction setup instead of the default one, which is greedy. # %% [markdown] # ## Setup # # Please refer to the [installation documentation](https://cot...
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# %% import os, sys, logging import torch from torch import nn, tensor from functools import partial sys.path.append(os.path.join(os.getcwd(), '..')) from utils.DataLoaders_jupyter import Get_Dataset, Create_DataLoaders from utils.DataLoaders_noSplit import Get_Dataset_noSplit, Create_DataLoaders_noSplit from utils.L...
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# %% [markdown] # # ChemicalEntity ↔ Tissue Relation-Wise Merge # # Merges Chemical–Tissue triples from EvoAGE; resolves tissue names via BTO; # deduplicates by `(head, relation, tail)`; and saves the result. # %% [markdown] # ## 0. Configuration # %% import pandas as pd # ── Base directories ──────────────────────...
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# %% [markdown] # # ANATOMY ↔ GENE Relation-Wise Merge # # Merges ANATOMY–GENE triples from multiple KG sources (DRKG, PrimeKG, Hetionet, TARKG), # aligns to a common schema, deduplicates by `(head, relation, tail)`, and saves the result. # %% [markdown] # ## 0. Configuration # %% import os import pandas as pd impor...
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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 import warnings warnings.filterwa...
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# %% [markdown] # # ANATOMY ↔ GENE Relation-Wise Merge # # Merges ANATOMY–GENE triples from multiple KG sources (DRKG, PrimeKG, Hetionet, TARKG), # aligns to a common schema, deduplicates by `(head, relation, tail)`, and saves the result. # %% [markdown] # ## 0. Configuration # %% import os import pandas as pd impor...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% ! 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 ...
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# %% [markdown] # # Calculate phase dependent modulation of AP generation in response to spatially diffuse or concentrated poisson excitation and rhythmic inhibition # # The simulations had either: # 1. Rhythmic inhibition at the soma (64 Hz) or dendrites (16 Hz) # 2. Diffuse or concentrated synaptic excitation at a...
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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 biologicalprocess relation of celegans # %% # gendr/Cele/Cele_GenDR_Gene_BioProcess.csv # Monarch/Monarch_final/Celegans/Gene_Cele_BiologicalProcess.csv # %% BASE_DIR = '/s...
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# %% from molmap import model as molmodel import molmap 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"]="0" np.random.seed(123) tf.compat.v1.set_rand...
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# %% from molmap import model as molmodel import molmap 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"]="0" np.random.seed(123) tf.compat.v1.set_rand...
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# %% [markdown] # # Figure 6 — Source Data Export # # **Figure 6** examines the Hessian geometry of the GAN loss landscape and # its relationship to neural tuning curves. Panel 6C shows an example # single-unit tuning curve sampled along Hessian eigenvectors. Panel 6D # shows tuning heatmaps for preferred and non-pr...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% ! 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 ...
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# %% from molmap import model as molmodel import molmap 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"]="0" np.random.seed(123) tf.compat.v1.set_rand...
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# %% import numpy as np import pandas as pd import pickle %matplotlib inline import matplotlib.pyplot as plt import seaborn as sns from pathlib import Path import re import pickle from src import util_analysis # %% import matplotlib matplotlib.rcParams.update({'font.size': 10}) matplotlib.rcParams['pdf.fonttype'...
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# %% [markdown] # # Advanced Automatic Differentiation # %% [markdown] # ## Overview # # In this section, we review some advanced AD tricks, especially their application to circuit simulations. With these advanced AD tricks, we can evaluate some quantum quantities more efficiently. # # The advanced AD is possible in...
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# %% [markdown] # ### MACSima proteins # %% ## Call all functions %run integrate_niches_functions.ipynb # %% save_folder="/data/Combined_Analysis/Integration/FetPed_SelectedGenes_8samples/" # %% ### Maxima P7_macsima = sc.read_h5ad("./P7w_macsima.h5ad") # %% sc.pp.neighbors(P7_macsima) # %% sc.tl.leiden(P7_macsi...
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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/' DB_DIR = BASE_DIR + '...
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# %% from molmap import model as molmodel import molmap 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"]="1" np.random.seed(123) tf.compat.v1.set_rand...
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# %% [markdown] # # 电路基础 # %% [markdown] # ## 概述 # # 在这篇笔记中,我们将了解 TensorCircuit 中核心对象的基本操作-``tc.Circuit``,它支持无噪声仿真和基于蒙特卡洛轨迹的噪声仿真。更重要的是,几乎所有对 Circuit 对象的操作都是可微分的和可即时编译的,这是成功高效地进行变分量子算法模拟的关键。 # [WIP note] # %% [markdown] # ## 设置 # %% from functools import partial import inspect import sys import numpy as np import te...
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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/' DB_DIR = BASE_DIR + '...
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# %% [markdown] # # Pathway ↔ Gene Relation-Wise Merge # # Merges Pathway–Gene triples from PrimeKG; drops rows with missing `tail_detail_name`; # deduplicates by `(head, relation, tail)`; and saves the result. # %% [markdown] # ## 0. Configuration # %% import os import pandas as pd BASE_DIR = '/storage/Arushi/09...
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# %% [markdown] # # Qudit Circuit Basics # # *A gentle intro to `tensorcircuit.quditcircuit.QuditCircuit`* # %% [markdown] # # ## Overview # # This tutorial shows how to build and simulate **qudit** circuits (d‑level systems, where `d ≥ 3`) using `tensorcircuit`'s `QuditCircuit` API. # **Highlights** # - Create a `...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% # Monarch/Monarch_final/Drosophila/GENE_GENE_Droso_Droso.csv # string/dmel/string_DROSO_GENE_GENE.csv # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'd...
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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/' # ── Require...
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# %% from molmap import model as molmodel import molmap 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"]="0" np.random.seed(1) tf.compat.v1.set_random...
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# %% [markdown] # # Set Up # %% # import necessary packages import pandas as pd import numpy as np from nilearn import surface import usefulFunctions as uf import os import glob from scipy.stats import ttest_rel # %% # falg to save csvs save_csv = True # set directories base_dir = f'{os.path.dirname(os.getcwd())}/' ...
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# %% [markdown] # # Figure 2 — Source Data Export # # **Figure 2** shows an example PIT (posterior inferotemporal) neuron evolution experiment (Exp 155), # demonstrating the evolution trajectory and population PSTH dynamics across generations. # # ## Data requirements # # > **Raw neural recordings are required to ru...
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# %% # using dataframes stored in /dfs, visualize connectivity as a heatmap # %% # import packages import pandas as pd import numpy as np from matplotlib import pyplot import matplotlib.pyplot as plt import seaborn as sns import cmocean # %% # open postsynaptic connectivity table of left admn sensory neurons full_df...
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# %% [markdown] # # Set up # %% #import packages import pandas as pd from nilearn import surface import numpy as np import os import glob import usefulFunctions as uf # %% # flag to save csv save_csv = True #set paths base_dir = f'{os.path.dirname(os.getcwd())}/' roi_dir = f'{base_dir}data/labels/' psc_dir = f'{bas...
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# %% [markdown] # # Calculate phase dependent modulation of AP threshold poisson excitation and rhythmic inhibition # # The simulations had either: # 1. Rhythmic inhibition at the soma (64 Hz) or dendrites (16 Hz) # 2. Poisson excitation at the soma and dendrites # # Here we calculate voltage threshold for action p...
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# %% [markdown] # # Phenotype ↔ Phenotype Relation-Wise Merge # # Merges Phenotype–Phenotype triples from PrimeKG, GPKG, and TARKG; # deduplicates by `(head, relation, tail)`; and saves the result. # %% [markdown] # ## 0. Configuration # %% import os import pandas as pd import numpy as np BASE_DIR = '/storage/Aru...
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# %% [markdown] # This is an example of train and test pipeline for GemNet-OC model. # Same task could be performed with pre-defined config from repository root: # ```bash # python run.py --config-name gemnet-oc.yaml # python run.py --config-name gemnet-oc_test.yaml # ``` # For detailed description please refer to [R...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% # gendr/Droso/Droso_GenDR_Gene_BioProcess.csv # Monarch/Monarch_final/Drosophila/Gene_Droso_BiologicalProcess.csv # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_DIR + 'data_co...
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# %% [markdown] # # Generate tables for the empirical assessment on P1000 matched somatic +/- germline data at the patient-level # Here, we analyze results of running models on empirical data: matched somatic +/- germline data from the P1000 dataset. # # Prerequisites: # - you ran the empirical assessment experiment ...
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# %% [markdown] # # 00 settings # %% import pandas as pd import numpy as np import matplotlib.pyplot as plt import matplotlib.cm as cm import seaborn as sns from scipy.stats import pearsonr from scipy import stats from scipy import signal import pymannkendall as mk # settings duration = 10 bs_start_idx = [2306,2338,...
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# %% import pandas as pd import os # %% # ── 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 path ──────────────...
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# %% [markdown] # # 结合SKLearn实现的支持向量分类 # # [_Mark (Zixuan) Song_](https://marksong.tech) 撰写 # # 本示例结合了`sklearn`库中的`SVC`类,实现了支持向量分类。 # %% [markdown] # ## 概述 # # 本示例的目的是将量子机器学习(QML)转换器嵌入到SVC管道中并且介绍`tensorcircuit`与`scikit-learn`的一种连接方式。 # %% [markdown] # ## 设置 # # 安装 `scikit-learn` 和 `requests`. 本模型测试数据为 [德国信用]The d...
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# %% import numpy as np import pandas as pd import pickle from isttc.scripts.cfg_global import project_folder_path import matplotlib as mpl import matplotlib.pyplot as plt import seaborn as sns mpl.rcParams['pdf.fonttype'] = 42 mpl.rcParams['ps.fonttype'] = 42 plt.rcParams['svg.fonttype'] = 'none' # %% results_fold...
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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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# %% [markdown] # # Operator spreading # %% [markdown] # ## Overview # %% [markdown] # In this tutorial, we will introduce the operator spreading that serves as a diagnostic of the chaotic dynamics and information scrambling. We will examine operator spreading as a function of the circuit depth $L$ that can be regard...
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# %% [markdown] # # Circuit Basics # %% [markdown] # ## Overview # # In this note, we will learn about basic operations of the core object in TensorCircuit - ``tc.Circuit`` which supports both noiseless simulation and noisy simulation with the Monte Carlo trajectory-based method. More importantly, near all the operat...
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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 celegans # %% # fic/fic_CELE_GENE_GENE.csv # wid/wid_CELE_GENE_GENE.csv # string/celegans/string_CELE_GENE_GENE.csv # Monarch/Monarch_final/Celegans/GENE_GENE_C...
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# %% !pip install torch torchvision opencv-python tqdm # %% from google.colab import files uploaded = files.upload() # %% !unzip mini_dataset.zip # %% import os, cv2, torch from torch.utils.data import Dataset, DataLoader class MiniWMH(Dataset): def __init__(self, root="mini_dataset", size=224): self...
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# %% import matplotlib.pyplot as plt import pandas as pd import numpy as np from tqdm import tqdm from joblib import load, dump import time from molmap import dataset from molmap import loadmap from molmap import model as molmodel import molmap #use GPU, if negative value, CPUs will be used import tensorflow as tf #i...
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# %% [markdown] # # Qudit(多能级量子比特) 电路基础 # # *`tensorcircuit.quditcircuit.QuditCircuit` 的轻量入门* # %% [markdown] # # ## 概述 # # 这个教程展示了如何使用 `tensorcircuit` 的 `QuditCircuit` API 来构建和模拟 **qudit(多能级量子比特)** 电路(d 级系统,其中 `d ≥ 3`)。 # # **要点** # - 创建一个 `QuditCircuit(nqudits, dim)` with dimension `dim ∈ [3, 36]`; # - 单比特门: `X`...
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# %% import numpy as np import pandas as pd from pathlib import Path %matplotlib inline import matplotlib import matplotlib.pyplot as plt import seaborn as sns import src.util_analysis as util_analysis # %% # So that we can edit the text in illustrator matplotlib.rcParams.update({'font.size': 10}) matplotlib.rcPar...
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# %% import torch import numpy as np import cv2 import os import torch.nn.functional as F import torchvision.transforms as transforms from tqdm.auto import tqdm from google.colab import drive drive.mount('/content/drive') import sys sys.path.append('/content/drive/MyDrive/ResNetModel/src') from model import build_m...
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# %% import numpy as np from itertools import islice import pandas as pd import pickle import csv import matplotlib.pyplot as plt import seaborn as sns from isttc.scripts.cfg_global import project_folder_path from isttc.acfunc import acf_sttc, acf_pearsonr_trial_avg, acf_sttc_trial_avg, acf_sttc_trial_concat from istt...
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# %% from __future__ import print_function from __future__ import division from __future__ import unicode_literals import numpy as np import tensorflow as tf from joblib import load,dump from rdkit import Chem import pandas as pd from deepchem.models import GraphConvModel, MPNNModel import deepchem as dc from deepche...
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# %% import torch import argparse import torch.nn as nn import torch.optim as optim import time from tqdm.auto import tqdm from google.colab import drive drive.mount('/content/drive') import sys sys.path.append('/content/drive/MyDrive/ResNetModel/src') from model import build_model from findmydatasets import get_dat...
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# %% [markdown] # # Figure 5 — Source Data Export # # **Figure 5** examines the temporal dynamics of the evolution process via # time-binned PSTH analysis. Panel 5A shows the population-average PSTH at # the first (block 0) and last (block 55) evolution blocks. Panel 5C shows # how the activation trajectory changes ...
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# %% [markdown] # # mirTARbase # %% import pandas as pd # %% BASE_PATH = "/storage/Arushi/090526_EvoAge/kg_formation/data_collection/" OUT_PATH = "/storage/Arushi/090526_EvoAge/kg_formation/processed_data/mirTARbase/" # %% drerio_ncbi = pd.read_csv( f'{BASE_PATH}databases_for_mapping/ncbi/Danio_rerio.gene_info'...
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# %% [markdown] # # Support Vector Classification with SKLearn # # Authored by [_Mark (Zixuan) Song_](https://marksong.tech) # # We use the `SKLearn` library to implement `SVC` in the following tutorial. # %% [markdown] # ## Overview # # The aim of this tutorial is to implant a quantum machine learning (QML) transf...
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# %% import pandas as pd import os # %% # ── 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 path ──────────────...
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# %% [markdown] # # `bar` plot # # This notebook is designed to demonstrate (and so document) how to use the `shap.plots.bar` function. It uses an XGBoost model trained on the classic UCI adult income dataset (which is classification task to predict if people made over 50k in the 90s). # %% import xgboost import sha...
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# %% import pandas as pd import numpy as np import glob import os from tqdm import tqdm # %% !pwd # %% [markdown] # %% # Monarch/Monarch_final/Zebrafish/GENE_GENE_Zebrafish_Zebrafish.csv # string/drer/string_Zebra_GENE_GENE.csv # %% BASE_DIR = '/storage/Arushi/090526_EvoAge/kg_formation/' MAPPING_DIR = BASE_D...
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# %% import os import re 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/' #...
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# %% [markdown] # # Experiment 7 figure generation and statistics # %% import pickle as pkl import pandas as pd import numpy as np from pathlib import Path %matplotlib inline import matplotlib import matplotlib.pyplot as plt from matplotlib.lines import Line2D # So that we can edit the text in illustrator matplotlib....
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# %% [markdown] # This is an example of train and test pipeline for PaiNN model from schnetpack library. # Same task could be performed with pre-defined config from repository root: # ```bash # python run.py --config-name painn.yaml # ``` # For detailed description please refer to [README](../nablaDFT/README.md). # ...
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# %% [markdown] # # AMPD - Automatic Multiscale Peak Detection # # This notebook provides an end-to-end pipeline for processing and analyzing fNIRS data collected during a finger-tapping task. The primary goal is to identify peaks in the time series data using an **Optimized AMPD** algorithm. # # The **AMPD** algorit...
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# %% # using dataframes stored in /dfs, compute cosine similarity between each left ADMN sensory neuron # %% # import packages import pandas as pd import numpy as np from matplotlib import pyplot,patches import matplotlib.pyplot as plt import seaborn as sns import cmocean from sklearn.metrics.pairwise import cosine_...
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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 sys.path.append('/Users/midani/OneDrive/proj/leap/manuscript') import os import numpy as np import pandas as pd from typing import Tuple from functools import reduce import repo_code.lib_aux as lib_aux subsetDf = lib_aux.subsetDf remove_zero_cols = lib_aux.remove_zero_cols remove_zero_rows = lib_aux...
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# %% [markdown] # # 00 settings # %% import pandas as pd import h5py import hdf5storage import numpy as np import matplotlib.pyplot as plt import matplotlib.cm as cm import seaborn as sns from scipy.stats import pearsonr from scipy import stats from scipy import signal import pymannkendall as mk # settings duration =...
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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("..")) # model import torch import torch.nn as nn import torch.nn.functional as F import torch_geometric as tg import torch_scatter import e3nn from e3nn import o3 from typing import Dict, Union # crystal ...
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# %% [markdown] # todo here some parametric runs: # %% import pandas as pd import numpy as np import csv import random import matplotlib.pyplot as plt import seaborn as sns from isttc.scripts.cfg_global import project_folder_path from isttc.acfunc import acf_pearsonr_trial_avg, acf_sttc_trial_avg # %% [markdown] # #...
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# %% from molmap import model as molmodel import molmap 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"]="1" # %% def get_attentiveFP_idx(df): ...
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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 numpy as np import pandas as pd import pickle %matplotlib inline import matplotlib.pyplot as plt import seaborn as sns from pathlib import Path import re from tqdm.auto import tqdm from pathlib import Path %matplotlib inline import matplotlib.pyplot as plt from matplotlib.lines import Line2D import matpl...
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# %% from molmap import model as molmodel import molmap 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"]="0" def get_attentiveFP_idx(df, file = './sp...
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# %% from molmap import model as molmodel import molmap 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"]="0" def get_attentiveFP_idx(df, file = './sp...
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# %% [markdown] # # Display 3D neuron with crystals # %% [markdown] # Load img # %% import nrrd lab_n, _ = nrrd.read(r"D:\Zuohan\neuron\neuron.nrrd") lab_c, _ = nrrd.read(r"D:\Zuohan\neuron\crystal.nrrd") import yaml from CrystalTracer3D.io import CrystalReader with open('config.yml', 'r') as ymlfile: cfg = yaml...
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# %% [markdown] # Loading dataset from Allen repository: # # * we use stimulus set "Functional Connectivity", spontaneous 30 minute block (animals are shown gray screen), 26 mice (4 genotypes) # * data is loaded from warehouse once (60Gb) and then used locally # * spikes from spontaneous session are loaded and stored ...
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# %% [markdown] # # Extended Figure 4 — Source Data Export # # **Extended Figure 4** provides additional temporal detail for the attribution # and trajectory analyses in Figure 5. Panel 4B shows time-binned # differential attribution scores for five bin sizes (5, 10, 20, 25, 50 ms). # Panel 4C replicates the time-bin...
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# %% import numpy as np import pandas as pd import pickle %matplotlib inline import matplotlib.pyplot as plt import seaborn as sns from pathlib import Path import re from tqdm.auto import tqdm from pathlib import Path %matplotlib inline import matplotlib.pyplot as plt from matplotlib.lines import Line2D import matpl...
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# %% from molmap import model as molmodel import molmap 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"]="0" np.random.seed(123) tf.compat.v1.set_rand...
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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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# %% from molmap import model as molmodel import molmap 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"]="1" np.random.seed(123) tf.compat.v1.set_rand...
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# %% [markdown] # # Analyse user response data # %% import pandas as pd import matplotlib.pyplot as pl import numpy as np import json import shap # %% responses = [] with open("trial_data2_3_3_2019.csv") as f: lines = f.readlines() for line in lines: parts = line.replace('""', "'").replace('"', "").sp...
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# %% from molmap import model as molmodel import molmap 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"]="0" np.random.seed(123) tf.compat.v1.set_rand...
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# %% [markdown] # # MolecularFunction → ChemicalEntity Relation Pipeline # # Builds a unified, deduplicated edge table for the strictly **MolecularFunction–ChemicalEntity** relation (no swapping, only native MolecularFunction → ChemicalEntity). # # **Output schema:** `head | relation | tail | head_type | relation_typ...
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# %% [markdown] # Plot info about Allen dataset subset that we use. # # We use 8 areas: 6 visual cortical areas (V1, LM, AL, RL, AM, PM) and 2 thalamic (LGN, LP). # # below mapping from Rudelt at el (found in github code): # structures = ["VISp", "VISl", "VISrl", "VISal", "VISpm", "VISam", "LGd", "LP"] # stru...
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# %% # OS interface for interacting with the file system import os # Core data manipulation and visualisation libraries import numpy as np # Numerical computing (arrays, math functions) from scipy.linalg import logm, sqrtm # Matrix operations for Riemannian geometry # ✅ Confirmati...
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# %% [markdown] # # Biomarker search # Predictors of neurofeedback success? # %% import os import pandas as pd import src.my_settings as settings sett = settings.settings() # %% # Read participants.tsv df_p = pd.read_csv(os.path.join(sett["git_path"], "data", "participants.tsv"), sep="\t") # remove sub-07 and sub-1...
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# %% import sys sys.path.append('/Users/midani/OneDrive/proj/leap/manuscript') import os import numpy as np import pandas as pd from typing import Tuple from functools import reduce import repo_code.lib_aux as lib_aux subsetDf = lib_aux.subsetDf remove_zero_cols = lib_aux.remove_zero_cols remove_zero_rows = lib_aux...
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# %% # %% # %% import os import pandas as pd # ── Change only these two lines to relocate all I/O ────────────────────────── BASE_PATH = "/storage/Arushi/090526_EvoAge/kg_formation/data_collection/" # all raw input files live here OUT_PATH = "/storage/Arushi/090526_EvoAge/kg_formation/processed_data/" # all ...
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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/' # ── Requir...
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# %% [markdown] # # Experiment 7 figure generation and statistics # %% import pickle as pkl import pandas as pd import numpy as np from pathlib import Path %matplotlib inline import matplotlib import matplotlib.pyplot as plt from matplotlib.lines import Line2D # So that we can edit the text in illustrator matplotlib....
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# %% import numpy as np import pandas as pd import pickle %matplotlib inline import matplotlib.pyplot as plt import seaborn as sns from pathlib import Path import re # get utils for thresholds from src import util_analysis from src import util_process_prolific as util_process import importlib from tqdm.auto import ...
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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 numpy as np from statsmodels.distributions.empirical_distribution import ECDF #uncorrected mode...