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Libella

Memory-Optimized Spatial Transcriptomics GNN Pipeline

Libella is an end-to-end Graph Neural Network (GNN) framework designed to discover spatial ecotypes and map topological interfaces across spatial transcriptomics cohorts. By using contiguous spatial batching with $k$-hop preservation, it achieves $O(N)$ compute scalability and $O(1)$ peak memory footprint relative to dataset size. Natively supports NVIDIA CUDA and Apple Silicon (MPS).


Quick Start

Execution is fully CLI-driven via a single .csv manifest file pointing to your .h5ad datasets.

# Standard discovery run
libella manifest.csv --out-dir ./results --mode DISCOVERY

# Fast development test (restricts epochs & cell counts)
libella manifest.csv --out-dir ./results_dev --mode DEV

Installation

Requires Python $\ge$ 3.9.

pip install libella

Data Preparation

Input .h5ad files must feature Human HGNC gene symbols (e.g., CD8A) in adata.var_names.

  • Mouse / Rat Data: Automatically converted to uppercase (e.g., Sox2 $\rightarrow$ SOX2) for cross-species compatibility.
  • Ensembl IDs: Must be converted to HGNC symbols before execution.
import mygene
import scanpy as sc

# Load data
adata = sc.read_h5ad("my_data.h5ad")

# Query Ensembl to HGNC mapping
mg = mygene.MyGeneInfo()
results = mg.querymany(
    adata.var_names, 
    scopes="ensembl.gene", 
    fields="symbol", 
    species="human"
)

# Remap gene symbols
symbol_map = {res["query"]: res.get("symbol", res["query"]) for res in results}
adata.var_names = [symbol_map.get(g, g) for g in adata.var_names]

adata.write_h5ad("my_data_mapped.h5ad")

Manifest Schema

The manifest.csv defines the pipeline execution graph. It requires filepath, discovery, and projection fields.

filepath,dataset_id,patient_id,discovery,projection
/path/to/sample1.h5ad,Dataset_A,Patient_1,True,True
/path/to/sample2.h5ad,Dataset_A,Patient_2,False,True
Flag Value Description
discovery True Computes consensus genes, biological priors, and trains the core GNN.
projection True Projects the trained GNN model onto the sample to extract spatial topology.

Note: Samples marked with discovery=False and projection=True are evaluated as hold-out validation cohorts.


Configuration & Hyperparameters

All pipeline parameters can be overridden at runtime via CLI arguments.

libella manifest.csv \
  --out-dir ./results \
  --epochs 100 \
  --batch-size 15000 \
  --lr-base 0.0005

Core Parameters

Parameter Default Description
--epochs 30 Number of GNN training iterations
--batch-size 10000 Spatial chunk size for memory bounding
--top-n-genes 2000 Number of spatial consensus genes to extract
--k-neighbors 11 Physical graph neighbors constructed per node
--k-hops 2 GNN message-passing neighborhood depth
--dict-temp 0.3 Softmax temperature for spatial dictionary learning
--entropy-pruning True Toggles batch-effect artifact pruning

Run libella -h to inspect the full list of CLI flags.


Output Directory Structure

Executing the pipeline populates --out-dir with the following structure:

results/
├── graphs/
│   └── *.pt                                  # Serialized PyTorch Geometric spatial graphs
├── individual_samples/
│   └── *.csv                                 # Sample-specific topological metrics
└── out/
    ├── final_gnn_model.pt                    # Trained GNN weights checkpoint
    ├── Global_Smoothed_Macro_Domains.parquet # Cell-level spatial domain assignments
    └── Global_Meta_Topology_Continuous_Matrix.csv # Cohort-wide topological matrix

Release files for libella 0.1.7.1

For a detailed explanation of source distributions (sdists) and built distributions (wheels), please see the package formats documentation.

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