CellVGAE uses the connectivity between cells (such as k-nearest neighbour graphs) with gene expression values as node features to learn high-quality cell representations in a lower-dimensional space
Project description
CellVGAE
An unsupervised scRNA-seq analysis workflow with graph attention networks
CellVGAE uses the connectivity between cells (such as k-nearest neighbour graphs or KNN) with gene expression values as node features to learn high-quality cell representations in a lower-dimensional space, with applications in downstream analyses like (density-based) clustering, visualisation, gene set enrichment analysis and others. CellVGAE leverages both the variational graph autoencoder and graph attention networks to offer a powerful and more interpretable machine learning approach. It is implemented in PyTorch using the PyTorch Geometric library.
Requirements
Installing CellVGAE with pip will attempt to install PyTorch and PyTorch Geometric, however it is recommended that the appropriate GPU/CPU versions are installed manually beforehand. For Linux:
-
Install PyTorch GPU:
conda install pytorch torchvision torchaudio cudatoolkit=11.1 -c pytorch -c nvidia
or PyTorch CPU:
conda install pytorch torchvision torchaudio cpuonly -c pytorch
-
Install PyTorch Geometric:
conda install pyg -c pyg -c conda-forge
-
(Optional) Install Faiss CPU:
conda install -c pytorch faiss-cpu
Faiss is only required if using the option
--graph_type "KNN Faiss"
. It is a soft dependency as it is not available for some platforms (currently Apple M1). Attempting to use CellVGAE with Faiss without installing it will result in an exception.A GPU version of Faiss for CUDA 11.1 is not yet available.
-
Install CellVGAE with pip:
pip install cellvgae --pre
-
(Optional) For the attention graph visualisations of Figure 6,
igraph
is required:pip install python-igraph
If using the R preprocessing code, we recommend installing the following:
Seurat 3
, scran
, SingleCellExperiment
. scRNAseq
, BiocSingular
, igraph
, dplyr
and textshape
.
Example use
Using the example files in this repo (.h5ad file is the same as downloaded by Scanpy 1.8.1):
python -m cellvgae --input_gene_expression_path "example_data/paul15_myeloid_scanpy.h5ad" --graph_file_path "example_data/paul15_Faiss_KNN_K3_KHVG2500.txt" --graph_convolution "GAT" --num_hidden_layers 2 --hidden_dims 128 128 --num_heads 3 3 3 3 --dropout 0.4 0.4 0.4 0.4 --latent_dim 50 --epochs 50 --model_save_path "model_saved_out"
Other examples are available in examples/cellvgae_example_scripts.txt
(also consult the help section below)
Usage
Invoke the training script with python -m cellvgae
with the arguments detailed below:
usage: train [-h] [--input_gene_expression_path INPUT_GENE_EXPRESSION_PATH] [--hvg HVG] [--khvg KHVG] [--graph_type {KNN Scanpy,KNN Faiss,PKNN}] [--k K] [--graph_n_pcs GRAPH_N_PCS]
[--graph_metric {euclidean,manhattan,cosine}] [--graph_distance_cutoff_num_stds GRAPH_DISTANCE_CUTOFF_NUM_STDS] [--save_graph] [--raw_counts] [--faiss_gpu]
[--hvg_file_path HVG_FILE_PATH] [--khvg_file_path KHVG_FILE_PATH] [--graph_file_path GRAPH_FILE_PATH] [--graph_convolution {GAT,GATv2,GCN}] [--num_hidden_layers {2,3}]
[--num_heads [NUM_HEADS [NUM_HEADS ...]]] [--hidden_dims [HIDDEN_DIMS [HIDDEN_DIMS ...]]] [--dropout [DROPOUT [DROPOUT ...]]] [--latent_dim LATENT_DIM] [--loss {kl,mmd}] [--lr LR]
[--epochs EPOCHS] [--val_split VAL_SPLIT] [--test_split TEST_SPLIT] [--transpose_input] [--use_linear_decoder] [--decoder_nn_dim1 DECODER_NN_DIM1] [--name NAME] --model_save_path MODEL_SAVE_PATH [--umap] [--hdbscan]
Train CellVGAE.
optional arguments:
-h, --help show this help message and exit
--input_gene_expression_path INPUT_GENE_EXPRESSION_PATH
Input gene expression file path.
--hvg HVG Number of HVGs.
--khvg KHVG Number of KHVGs.
--graph_type {KNN Scanpy,KNN Faiss,PKNN}
Type of graph.
--k K K for KNN or Pearson (PKNN) graph.
--graph_n_pcs GRAPH_N_PCS
Use this many Principal Components for the KNN (only Scanpy).
--graph_metric {euclidean,manhattan,cosine}
--graph_distance_cutoff_num_stds GRAPH_DISTANCE_CUTOFF_NUM_STDS
Number of standard deviations to add to the mean of distances/correlation values. Can be negative.
--save_graph Save the generated graph to the output path specified by --model_save_path.
--raw_counts Enable preprocessing recipe for raw counts.
--faiss_gpu Use Faiss on the GPU (only for KNN Faiss).
--hvg_file_path HVG_FILE_PATH
HVG file if not using command line options to generate it.
--khvg_file_path KHVG_FILE_PATH
KHVG file if not using command line options to generate it. Can be the same file as --hvg_file_path if HVG = KHVG.
--graph_file_path GRAPH_FILE_PATH
Graph specified as an edge list (one edge per line, nodes separated by whitespace, not comma), if not using command line options to generate it.
--graph_convolution {GAT,GATv2,GCN}
--num_hidden_layers {2,3}
Number of hidden layers (must be 2 or 3).
--num_heads [NUM_HEADS [NUM_HEADS ...]]
Number of attention heads for each layer. Input is a list that must match the total number of layers = num_hidden_layers + 2 in length.
--hidden_dims [HIDDEN_DIMS [HIDDEN_DIMS ...]]
Output dimension for each hidden layer. Input is a list that matches --num_hidden_layers in length.
--dropout [DROPOUT [DROPOUT ...]]
Dropout for each layer. Input is a list that must match the total number of layers = num_hidden_layers + 2 in length.
--latent_dim LATENT_DIM
Latent dimension (output dimension for node embeddings).
--loss {kl,mmd} Loss function (KL or MMD).
--lr LR Learning rate for Adam.
--epochs EPOCHS Number of training epochs.
--val_split VAL_SPLIT
Validation split e.g. 0.1.
--test_split TEST_SPLIT
Test split e.g. 0.1.
--transpose_input Specify if inputs should be transposed.
--use_linear_decoder Turn on a neural network decoder, similar to traditional VAEs.
--decoder_nn_dim1 DECODER_NN_DIM1
First hidden dimenson for the neural network decoder, if specified using --use_linear_decoder.
--name NAME Name used for the written output files.
--model_save_path MODEL_SAVE_PATH
Path to save PyTorch model and output files. Will create the entire path if necessary.
--umap Compute and save the 2D UMAP embeddings of the output node features.
--hdbscan Compute and save different HDBSCAN clusterings.
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