Data Io Loading

OmicVerse Data I/O

OmicVerse provides its own data readers under ov.io. These replace scanpy's IO functions with better format handling, spatial geometry support, and Rust backend options. When working in an OmicVerse project, always use ov.io.* for data loading — never fall back to sc.read_* or scanpy.read_*.

Why this matters

OmicVerse's readers are not thin wrappers — they are independent implementations that handle edge cases scanpy misses:

• 10x H5/MTX: Proper v2/v3 format detection, flexible prefix/compression options
• Visium: Auto-resolves tissue positions (parquet > csv > legacy csv), loads images + scale factors
• Visium HD: Cell segmentation with GeoJSON→WKT polygon conversion (not available in scanpy at all)
• Nanostring SMI: Auto-detects column names across CosMx format variants (not in scanpy)

Migration table: scanpy → OmicVerse

Access paths

ov.read(path)                          # Top-level universal reader (lazy attr)
ov.io.read_h5ad(filename)              # h5ad
ov.io.read_10x_h5(filename)            # 10x Genomics H5
ov.io.read_10x_mtx(path)              # 10x Matrix Market directory
ov.io.spatial.read_visium(path)        # Visium (standard Space Ranger)
ov.io.read_visium_hd(path)            # Visium HD (auto-detect bin vs seg)
ov.io.read_visium_hd_bin(path)        # Visium HD bin-level
ov.io.read_visium_hd_seg(path)        # Visium HD cell segmentation
ov.io.read_nanostring(path, ...)      # Nanostring SMI / CosMx
ov.io.read_csv(**kwargs)              # CSV/TSV wrapper
ov.io.save(obj, path)                 # Pickle serialization
ov.io.load(path)                      # Pickle deserialization

Note: read_visium (standard) is under ov.io.spatial, not directly under ov.io. All other readers are at ov.io level.

Universal reader: ov.read(path, backend='python')

Auto-detects format by file extension and returns the appropriate object:

import omicverse as ov

# h5ad → AnnData
adata = ov.read('pbmc3k.h5ad')

# CSV → DataFrame
df = ov.read('counts.csv')

# Gzipped TSV → DataFrame
df = ov.read('metadata.tsv.gz')

# Rust backend for large h5ad files (requires snapatac2)
adata = ov.read('large_dataset.h5ad', backend='rust')
# Remember: call adata.close() when done with Rust backend

Single-cell readers

ov.io.read_h5ad(filename, **kwargs)

Direct h5ad reader. All kwargs forwarded to anndata.read_h5ad().

adata = ov.io.read_h5ad('sample.h5ad')
adata = ov.io.read_h5ad('large.h5ad', backed='r')  # Backed mode for large files

ov.io.read_10x_h5(filename, *, genome=None, gex_only=True)

Read 10x Genomics HDF5 count matrices. Handles both legacy (v2) and v3+ formats automatically.

adata = ov.io.read_10x_h5('filtered_feature_bc_matrix.h5')

# Multi-genome file: filter by genome
adata = ov.io.read_10x_h5('raw_feature_bc_matrix.h5', genome='GRCh38')

# Keep all feature types (Gene Expression + Antibody Capture + CRISPR Guide)
adata = ov.io.read_10x_h5('filtered_feature_bc_matrix.h5', gex_only=False)

ov.io.read_10x_mtx(path, *, var_names='gene_symbols', make_unique=True, gex_only=True, prefix=None, compressed=True)

Read 10x Matrix Market directory (contains matrix.mtx, features.tsv/genes.tsv, barcodes.tsv).

adata = ov.io.read_10x_mtx('filtered_feature_bc_matrix/')

# Use Ensembl gene IDs instead of symbols
adata = ov.io.read_10x_mtx('filtered_feature_bc_matrix/', var_names='gene_ids')

# STARsolo output (uncompressed files)
adata = ov.io.read_10x_mtx('Solo.out/Gene/filtered/', compressed=False)

Spatial readers

ov.io.spatial.read_visium(path, *, count_file='filtered_feature_bc_matrix.h5', library_id=None, load_images=True, ...)

Read standard 10x Visium Space Ranger output. Loads count matrix, tissue positions, images, and scale factors.

adata = ov.io.spatial.read_visium('spaceranger_output/outs/')

# Use raw counts
adata = ov.io.spatial.read_visium('outs/', count_file='raw_feature_bc_matrix.h5')

# Skip image loading (faster, less memory)
adata = ov.io.spatial.read_visium('outs/', load_images=False)

Output structure:

• adata.obsm['spatial'] — spot pixel coordinates
• adata.uns['spatial'][library_id]['images'] — hires/lowres images
• adata.uns['spatial'][library_id]['scalefactors'] — scale factors
• adata.obs['in_tissue'], array_row, array_col — tissue position metadata

ov.io.read_visium_hd(path, ...) / read_visium_hd_bin / read_visium_hd_seg

Read Visium HD data. The unified read_visium_hd auto-detects bin vs segmentation format.

# Auto-detect
adata = ov.io.read_visium_hd('spaceranger_hd_output/outs/')

# Explicit bin-level (specify bin size)
adata = ov.io.read_visium_hd_bin('outs/binned_outputs/square_016um/', binsize=16)

# Cell segmentation (includes GeoJSON polygon geometry)
adata = ov.io.read_visium_hd_seg('outs/segmented_outputs/')
# adata.obs['geometry'] contains WKT polygon strings

ov.io.read_nanostring(path, counts_file, meta_file, fov_file=None)

Read Nanostring Spatial Molecular Imager (CosMx) data.

adata = ov.io.read_nanostring(
    path='cosmx_output/',
    counts_file='exprMat_file.csv',
    meta_file='metadata_file.csv',
    fov_file='fov_positions_file.csv',  # optional
)
# adata.obsm['spatial'] — cell center coordinates
# adata.obs['geometry'] — cell polygon WKT strings

Serialization

# Save any Python object (uses cloudpickle with pickle fallback)
ov.io.save(my_model, 'model.pkl')

# Load it back
my_model = ov.io.load('model.pkl')

Defensive validation

from pathlib import Path

# Before reading: verify file exists
path = Path('data.h5ad')
assert path.exists(), f"File not found: {path}"

# Before read_10x_mtx: verify directory structure
mtx_dir = Path('filtered_feature_bc_matrix/')
assert (mtx_dir / 'matrix.mtx.gz').exists() or (mtx_dir / 'matrix.mtx').exists(), \
    f"No matrix.mtx found in {mtx_dir}"

# Before read_visium: verify Space Ranger output
outs_dir = Path('outs/')
assert (outs_dir / 'filtered_feature_bc_matrix.h5').exists(), \
    f"No count matrix in {outs_dir}. Is this a Space Ranger output directory?"
assert (outs_dir / 'spatial').is_dir(), \
    f"No spatial/ directory in {outs_dir}"

Troubleshooting

• FileNotFoundError from read_10x_h5: Verify the .h5 file path is correct. Cell Ranger output is typically at outs/filtered_feature_bc_matrix.h5.
• ValueError: The type is not supported from ov.read(): The file extension is not recognized. Use format-specific readers (read_10x_h5, read_10x_mtx) for non-standard extensions.
• ImportError: snapatac2 from ov.read(..., backend='rust'): Install with pip install snapatac2. The Rust backend is optional.
• Duplicate gene names warning: read_10x_mtx with var_names='gene_symbols' auto-deduplicates by default (make_unique=True). If you need original names, set make_unique=False.
• read_visium missing tissue positions: The reader auto-detects .parquet, .csv, and legacy .csv formats. If using a custom directory layout, verify the spatial/ subdirectory contains a tissue positions file.
• Visium HD segmentation missing polygons: Requires geopandas and shapely. Install with pip install geopandas shapely.
• Large h5ad OOM: Use backed mode ov.io.read_h5ad('large.h5ad', backed='r') or Rust backend ov.read('large.h5ad', backend='rust').

Quick copy-paste commands

See reference.md for complete code blocks organized by format.