DeepType
Deep Learning Approach to Identifying Breast Cancer Subtypes Using High-Dimensional Genomic Data
Code Organization
This software contains these codes:
Requirements
Implement and Activate Tensorflow Environment under Conda
Implement: conda create -n tensorflow_env tensorflow
Activation: conda activate tensorflow_env
Use the software
1. Data format: filename.mat file
2. Variables:
Data: D*N numerical matrix. Each row is a gene, and each column is a sample. The genes should be ranked in the descending order by variances across samples.
targets: N*1 numerical vector. The ith element denotes the class that the ith sample belongs to.
3. Set parameters in flags.py:
NUM_GENES_1: the number of input genes.
NUM_CLUSTERS: the number of clusters K.
NUM_HIDDEN: the number of hidden layers.
NUM_NODES: numerical vector, the numbers of nodes in the hidden layers.
NUM_CLASSES: the number of unique classes of samples.
NUM_TRAIN_SIZE: the number of samples in the training set.
NUM_VALIDATION_SIZE: the number of samples in the validation set.
NUM_TEST_SIZE: the number of samples in the test set.
NUM_SAMPLE_SIZE: the number of samples in the whole dataset.
NUM_BATCH_SIZE: batch size.
NUM_LEARNING_RATE: learning rate.
NUM_SUPERVISED_BATCHES: the number of training steps in the supervised initialization.
NUM_TRAIN_BATCHES: the number of training steps in each epoch.
LAMBDA: sparsity penalty coefficient.
ALPHA: K-means loss coefficient.
DATA_DIR: Directory to put the training data.
RESULT_DIR: Directory to put the results.
4. Run the program
python DeepType.py
5. Data available
Due to the file size limit of Github, the breast cancer dataset is available at https://drive.google.com/file/d/1ao1zu3DS8GkYF-tHxpQ-1ev2psxXL-fx/view?usp=sharing