medh5

One medical imaging sample — a subject, at every timepoint, with all of its ground truth — in a single self-describing HDF5 file.

Multi-modality images, segmentation in five encodings, detection boxes, keypoints, contours, meshes, classification, registration between visits, provenance and quality records, and per-object integrity digests. Format version 1.0, with a normative specification and a 117-case conformance suite any implementation can run.

import medh5

with medh5.open("case_0001.medh5") as s:
    s.identity.subject_id                              # "BRATS-GLI-01234"
    s.at("tp1").images["CT_tp1"].read(physical=True)   # HU, not raw counts
    s.annotations["organs"].dense(["liver", "spleen"]) # any encoding, one API
    s.transform_between("tp0", "tp1")                  # resolved via frames
    s.tracks("lesion")                                 # lesions joined across visits

Install

pip install medh5
pip install "medh5[torch,nifti,dicom]"

Reading and writing needs only h5py, hdf5plugin and numpy. Extras: torch, monai, nifti, dicom, dicomseg, itk, schema, interp.

Documentation

medh5.readthedocs.io — tutorials, how-to guides, the Python and CLI reference, and the normative specification.

Write your first sample · How-to guides · Python API · CLI · Specification

What the format is for

• One file per subject, not per scan — every visit in one place, so longitudinal work has a referent and splitting by file cannot leak a patient.
• Geometry is stated once and never guessed — declared grids, boxes at voxel edges, and converters that refuse rather than invent.
• Absence is not silence — a class examined and not found is recorded as such, which is a different training signal from one nobody examined.
• Every claim is checkable — per-object digests, a Merkle content_id that survives recompression, a stable diagnostic-code table, and a 117-case conformance corpus.
• Reading a patch is fast — a 64³ multi-class patch in ~4 ms, and O(1) foreground sampling once build_index() has run.

The reasoning behind each.

Write a sample

import numpy as np
import medh5
from medh5 import LabelClass, LabelSet

labels = LabelSet("demo-v1", version="1.0.0", classes=[
    LabelClass(1, "liver", "Liver", category="organ"),
    LabelClass(2, "spleen", "Spleen", category="organ"),
    LabelClass(3, "lesion", "Lesion", parents=[1], category="lesion"),
])

with medh5.create("case_0001.medh5", sample_id="case_0001",
                  subject_id="DEMO-0001") as w:
    w.label_set(labels)
    w.add_timepoint("tp0", label="baseline", days_from_baseline=0)
    w.add_grid("ct", shape=ct.shape, spacing=(2.0, 0.8, 0.8),
               origin=(-64.0, -38.4, -38.4), timepoint="tp0")
    w.add_image("CT", ct, grid="ct", modality="CT",
                value_type="quantitative", value_units="HU")
    w.add_segmentation("organs", grid="ct",
                       masks={"liver": liver, "lesion": lesion},
                       annotated_classes=["liver", "spleen", "lesion"])
    w.build_index()   # optional; foreground sampling is O(1) only with it

annotated_classes names the spleen although there is no spleen mask: that records "we looked and found none". The encoding is chosen by measuring the class overlap graph — liver and lesion overlap, so it picks one that can represent that — and the write is atomic.

Train on it

from torch.utils.data import DataLoader
from medh5.torch import PatchDataset, collate, worker_init_fn
from medh5.sampling import PatchSampler

sampler = PatchSampler((96, 96, 96), strategy="balanced",
                       foreground_classes=["liver", "lesion"])
dataset = PatchDataset(paths, sampler, images=["CT"],
                       annotations={"organs": ["liver", "lesion"]},
                       samples_per_volume=8)

loader = DataLoader(dataset, batch_size=2, num_workers=8,
                    worker_init_fn=worker_init_fn, collate_fn=collate)

worker_init_fn drops handles inherited across a fork. It is recommended rather than required: the handle cache is PID-keyed and re-checks ownership on every access, so a forked worker abandons the parent's handles on first use rather than reading through or closing them.

Command line

medh5 info case.medh5                  # grids, images, annotations, coverage
medh5 validate case.medh5 --level strict
medh5 verify case.medh5                # digests and content_id
medh5 timeline case.medh5              # visits and intervals
medh5 track case.medh5 --class lesion  # per-lesion volumes across visits

medh5 dataset index studies/ -o cohort.json
medh5 dataset split cohort.json --group-by group_id --stratify-by site_id
medh5 dataset stats cohort.json --partition train --workers 8
medh5 dataset check cohort.json --deep

medh5 convert from-dicom /studies out/     # one sample per patient, all visits
medh5 convert from-nifti case.medh5 --image CT=ct.nii.gz
medh5 convert from-rtstruct plan.dcm case.medh5 --rasterize
medh5 migrate old/*.medh5 -o new/ --group-by subject

medh5 scrub out/*.medh5 --apply --date-shift-days -117
medh5 pack cohort/*.medh5 -o shard.medh5c
medh5 recompress cohort/*.medh5 --profile training
medh5 bench                                # reproduce the performance targets
medh5 conformance publish suite/           # the suite, for another implementation

Interoperability

Every conversion returns a report distinguishing what it decided from the data and where it guessed — the encoding chosen, the class ids minted, a half-voxel convention changed, a timepoint order inferred rather than read.

COCO is deliberately unsupported: it has no world geometry, spacing or frame of reference, so importing means inventing a grid and exporting means discarding the geometry that makes a medical annotation reproducible.

Reading it without medh5

import h5py, json, hdf5plugin       # hdf5plugin only for blosc2 profiles

with h5py.File("case_0001.medh5") as f:
    doc = json.loads(f["meta"][()])
    doc["identity"]["subject_id"]
    dict(f["grids"]["ct"].attrs)     # spacing, origin, direction
    f["images"]["CT"][10:20]

medh5 recompress --profile portable writes gzip, readable by any HDF5 build.

Versioning

The format is 1.0. A minor version may add optional objects, profiles, encodings and diagnostic codes; it may not change what an existing one means (spec §16). The package follows semantic versioning from 1.0.0.

0.x files are not readable by 1.0 and are not meant to be — medh5 migrate converts them once. See Converters.

License

MIT