geniml
DevelopmentMachine learning toolkit for genomic interval (BED) data; use it when you need to tokenize BED collections and train embeddings for regions/cells/labels, build consensus peak universes, or run similarity search and downstream ML on chromatin accessibility datasets.
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When to Use
- You have many BED files and need numeric features for clustering, similarity search, or downstream supervised learning (e.g., ChIP-seq/ATAC-seq region sets).
- You want unsupervised embeddings of genomic regions to compare region sets across experiments (Region2Vec).
- You need joint embeddings of regions and metadata labels (e.g., tissue/cell type/condition) to enable cross-modal queries like Region → Label or Label → Region (BEDspace).
- You are analyzing single-cell ATAC-seq and want cell embeddings for clustering/annotation and integration with Scanpy workflows (scEmbed).
- You need a consensus peak set (“universe”) built from multiple BED files to standardize tokenization and region definitions across datasets (Universe construction).
Key Features
- Region2Vec: Word2vec-style unsupervised embeddings for genomic regions from tokenized BED data.
- BEDspace: StarSpace-based joint embedding space for region sets and metadata labels; supports similarity search and cross-modal retrieval.
- scEmbed: Single-cell ATAC-seq embedding workflow (tokenize cells → train → encode cells) compatible with Scanpy.
- Universe (Consensus Peaks) Builder: Generates reference peak sets using multiple statistical approaches (CC, CCF, ML, HMM).
- Utilities:
- Tokenization: Universe-based tokenization (hard/soft tokenization patterns).
- Evaluation: Embedding quality metrics (e.g., silhouette, Davies–Bouldin).
- BEDshift: Region randomization/null-model generation while preserving genomic context.
- BBClient / caching: Faster repeated access to BED resources.
- Text2BedNN: Neural search backend for genomic queries.
Additional details are commonly documented in:
references/region2vec.md,references/bedspace.md,references/scembed.md,references/consensus_peaks.md,references/utilities.md.
Dependencies
- Python: 3.9+ (recommended)
- geniml: latest from PyPI (or GitHub main)
- Optional ML extras:
geniml[ml](typically pulls PyTorch and related ML dependencies) - Scanpy stack (for scEmbed workflows):
scanpy(plusanndata,numpy,scipy) - StarSpace (for BEDspace training): external binary from https://github.com/facebookresearch/StarSpace
- Universe coverage generation:
uniwig(used to generate coverage tracks in universe workflows)
Example Usage
1) Install
# Base install
uv pip install geniml
# With ML extras (e.g., PyTorch and related dependencies)
uv pip install "geniml[ml]"
# Development version
uv pip install git+https://github.com/databio/geniml.git
2) End-to-end: Build a universe → tokenize BEDs → train Region2Vec → evaluate
# (A) Build coverage tracks (example pattern)
cat bed_files/*.bed > combined.bed
uniwig -m 25 combined.bed chrom.sizes coverage/
# (B) Build a universe (coverage cutoff method)
geniml universe build cc \
--coverage-folder coverage/ \
--output-file universe.bed \
--cutoff 5 \
--merge 100 \
--filter-size 50
# (C) Tokenize BED files, train Region2Vec, and evaluate embeddings
from geniml.tokenization import hard_tokenization
from geniml.region2vec import region2vec
from geniml.evaluation import evaluate_embeddings
# 1) Tokenize BED files against the universe
hard_tokenization(
src_folder="bed_files/",
dst_folder="tokens/",
universe_file="universe.bed",
p_value_threshold=1e-9,
)
# 2) Train Region2Vec
region2vec(
token_folder="tokens/",
save_dir="model/",
num_shufflings=1000,
embedding_dim=100,
)
# 3) Evaluate (requires labels/metadata aligned to embeddings)
metrics = evaluate_embeddings(
embeddings_file="model/embeddings.npy",
labels_file="metadata.csv",
)
print(metrics)
3) Single-cell ATAC-seq: tokenize cells → train scEmbed → cluster with Scanpy
import scanpy as sc
from geniml.scembed import ScEmbed
from geniml.io import tokenize_cells
# 1) Load AnnData
adata = sc.read_h5ad("scatac_data.h5ad")
# 2) Tokenize cells using a universe
tokenize_cells(
adata="scatac_data.h5ad",
universe_file="universe.bed",
output="tokens.parquet",
)
# 3) Train scEmbed
model = ScEmbed(embedding_dim=100)
model.train(dataset="tokens.parquet", epochs=100)
# 4) Encode cells and attach embeddings to AnnData
embeddings = model.encode(adata)
adata.obsm["scembed_X"] = embeddings
# 5) Standard Scanpy neighborhood graph + clustering + UMAP
sc.pp.neighbors(adata, use_rep="scembed_X")
sc.tl.leiden(adata)
sc.tl.umap(adata)
Implementation Details
Tokenization (Universe-based)
- Goal: Convert genomic intervals into discrete “tokens” defined by a reference universe (consensus peak set).
- Hard tokenization: Assigns intervals to universe bins/peaks deterministically (commonly used for Region2Vec/scEmbed pipelines).
- Key parameter:
p_value_thresholdcontrols stringency of mapping/overlap significance (lower is stricter; overly strict thresholds can reduce coverage).
Region2Vec (Region Embeddings)
- Core idea: Treat each BED file (or region set) like a “document” and each universe peak like a “word”; learn embeddings using a word2vec-style objective.
- Important knobs:
embedding_dim: dimensionality of learned vectors (e.g., 50–300).num_shufflings: increases training signal by shuffling/co-occurrence augmentation; higher values increase runtime.
BEDspace (Joint Region + Label Embeddings)
- Core idea: Learn a shared vector space for region sets and metadata labels using StarSpace, enabling:
- Region → Label retrieval (predict likely labels for a query region set)
- Label → Region retrieval (find region sets associated with a label)
- Operational requirement: StarSpace must be installed and its path provided/configured for training.
scEmbed (Single-cell Embeddings)
- Core idea: Apply Region2Vec-like training on tokenized single-cell accessibility profiles to produce cell embeddings.
- Best practice: Pre-tokenize cells (e.g., to Parquet) to reduce repeated preprocessing and speed up training.
- Downstream: Use embeddings as
adata.obsm[...]and run standard Scanpy steps (neighbors, Leiden, UMAP).
Universe Construction (Consensus Peaks)
- Purpose: Create a stable reference peak set for tokenization and cross-dataset comparability.
- Methods:
- CC (Coverage Cutoff): threshold-based peak calling from coverage.
- CCF (Coverage Cutoff Flexible): cutoff with flexible boundaries/confidence intervals.
- ML (Maximum Likelihood): probabilistic modeling of peak positions.
- HMM (Hidden Markov Model): state-based segmentation; typically most computationally intensive.
- Typical parameters:
--cutoff: minimum coverage to call peaks (CC/CCF).--merge: merge distance for nearby peaks.--filter-size: minimum peak length to keep.