ulmshare/README.md

---
pretty_name: "OpenH-RF — ULMShare (in vivo mouse transcranial ULM)"
license: cc-by-4.0
task_categories:
  - image-to-image
tags:
  - ultrasound
  - iq
  - openh-rf
  - ulm
  - super-resolution
  - microbubbles
  - in-vivo
  - mouse
  - brain
language:
  - en
size_categories:
  - 10K<n<100K
---

# ULMShare — in vivo mouse transcranial ULM

## Dataset Description

Pre-beamformed, plane-wave **IQ channel data** from transcranial ultrasound
localization microscopy (ULM) of the mouse brain, converted from the public
[ULMShare](https://arxiv.org/abs/2606.07851) release into the zea format. Each
acquisition is a contrast-enhanced (microbubble) plane-wave sequence over the
intact skull of an anesthetized mouse; compounding the transmits gives a
Power-Doppler movie of the cerebral microvasculature, and localizing and
tracking individual microbubbles across frames gives a super-resolved density
map of the vessels.

This is **in vivo animal data**, not phantom or simulated. It is a conversion of the upstream release, which holds 99 acquisitions from 61 mice
(approximately 30 TB of original-source raw data, distinct from the stored HF release below) recorded between March 2022 and March 2025 at the Provost
Ultrasound Lab (Polytechnique Montréal) and partner sites.

## Dataset Contributor(s)

**Original dataset (ULMShare).** Brice Rauby, Nin Ghigo, Gerardo
Ramos-Palacios, Alexis Leconte, Stephen A. Lee, Alice Wu, Paul Xing, Oleksandra
Gulenko, Louis Caron, Antoine Malescot, Eric Martineau, Jonathan Porée, Maxime
Gasse, Ravi L. Rungta, Abbas F. Sadikot, and Jean Provost — Provost Ultrasound
Lab, Polytechnique Montréal.

**zea conversion and reconstruction (this submission).** Oisín Nolan
<o.i.nolan@tue.nl>, Eindhoven University of Technology.

## Dataset Creation Date

08/21/2026 (zea conversion). The underlying acquisitions were recorded between
March 2022 and March 2025.

## License / Terms of Use

CC BY 4.0. See [LICENSE](./LICENSE).

## Intended Usage

Ultrasound localization microscopy: microbubble detection and localization,
frame-to-frame tracking, super-resolved vascular density and velocity mapping,
and clutter filtering / tissue suppression.

## Dataset Characterization

- **Data Collection Method:** in vivo animal (mouse), contrast-enhanced.
- **Labeling Method:** none. A reference ULM density map rendered by the
  original authors is stored alongside the acquisitions as a
  `density_map` custom element — a visualization, not a ground-truth label.
- **Acquisition system:** Verasonics Vantage 256. See files for further acquisition details.

## Dataset Format

zea (HDF5), current release `zea_version` 0.1.4.

Each acquisition is **one HDF5 file with a single track**.

```
/
├── probe/                       name, type, probe_geometry, probe_center_frequency
├── metadata/
│   ├── credit                   DOI of the ULMShare publication
│   ├── subject/                 id, type, sex, genetic_strain, weight
│   └── text_report              procedure notes (where recorded)
├── custom/                      acquisition context (see table below)
└── tracks/track_0/
    ├── data/raw_data            (n_frames, n_tx, n_ax, n_el, 2) int16
    ├── scan/                    sampling_frequency, center_frequency,
    │                            demodulation_frequency, sound_speed,
    │                            initial_times, t0_delays, polar_angles,
    │                            azimuth_angles, focus_distances,
    │                            transmit_origins, tx_apodizations,
    │                            tgc_gain_curve
    └── transmit_only            False
```

**Large acquisitions split for upload:** The HuggingFace file-size limit is 500 GB. Four
acquisitions are near or above it, so each one is split into two parts. These are
`mouse_58/acquisition_1` (616 GB) and `mouse_59/acquisition_1` to `acquisition_3` (499 GB each).
The split is at frame 240,000, into `_part1of2.hdf5` and `_part2of2.hdf5`. Both parts hold the
same metadata: probe geometry, subject information, and clinical fields. To rebuild an
acquisition, join `raw_data` from the two parts along axis 0.

### Per-sample feature table

| Feature | Shape | Dtype | Units | Description |
|---|---|---|---|---|
| `data/raw_data` | `(n_frames, n_tx, n_ax, n_el, 2)` | `int16` | ADC counts | Baseband IQ channel data, `[I, Q]` (`I + jQ`) |
| `probe/probe_geometry` | `(n_el, 3)` | `float32` | m | Element positions `(x, y, z)` |
| `probe/probe_center_frequency` | `()` | `float32` | Hz | Probe center frequency |
| `scan/sampling_frequency` | `()` | `float32` | Hz | IQ sampling rate (`fc` for BS100BW, `fc/2` for BS50BW) |
| `scan/center_frequency`, `scan/demodulation_frequency` | `()` | `float32` | Hz | Transmit carrier / demodulation frequency |
| `scan/sound_speed` | `()` | `float32` | m/s | 1540 |
| `scan/polar_angles` | `(n_tx,)` | `float32` | rad | Plane-wave steering angles, ping-pong order |
| `scan/azimuth_angles` | `(n_tx,)` | `float32` | rad | Zero (2D imaging) |
| `scan/focus_distances` | `(n_tx,)` | `float32` | m | `inf` (unfocused plane waves) |
| `scan/t0_delays` | `(n_tx, n_el)` | `float32` | s | Transmit delays, min 0 |
| `scan/initial_times` | `(n_tx,)` | `float32` | s | Zero (MUST adds no per-transmit offset) |
| `scan/tx_apodizations` | `(n_tx, n_el)` | `float32` | – | Ones (full aperture; see Known Issues) |
| `scan/transmit_origins` | `(n_tx, 3)` | `float32` | m | Zero |
| `scan/tgc_gain_curve` | `(n_ax,)` | `float32` | – | 8 source control points interpolated per sample |
| `metadata/subject/weight` | `()` | `float32` | kg | Mouse body weight |
| `custom/density_map` | `(H, W, 3)` or `(H, W)` | `uint8` | – | Reference ULM density map PNG |

### Custom elements

Acquisition context with no zea spec field, stored as strings exactly as
recorded upstream: `anesthesia`, `injection_type`, `mb_dilution`,
`volume_mb_injected`, `frame_rate_hz`, `npulse`, `voltage`, `mouse_weight`,
`mouse_age_days`, `mouse_animal_protocol_id`, `flush`, and (where non-blank)
`procedure_type`, `slice_position`, `temperature`, `syringe_gauge`.

## Dataset Quantification

**Current OpenH-RF release:** 103 HDF5 files; 20.74 TB (20,735,658,275,478 bytes) stored; root `zea_version` **0.1.4**. Sizes include all HDF5 contents and use decimal units (MB = 10^6 bytes, GB = 10^9 bytes, TB = 10^12 bytes), not decoded-array memory or original-source download sizes.

- **Acquisitions:** 99, from 61 mice — one zea HDF5 file per acquisition.
- **Stored HDF5 size:** 20.74 TB (20,735,658,275,478 bytes).
- **Split:** none.

## Subject Metadata

Aggregate only; the subjects are mice, so no PHI applies. Subject attributes
are counted per mouse (n = 61); probe and imaging plane per acquisition
(n = 99).

- **Subjects:** 61 mice, 99 acquisitions.
- **Sex:** 36 female, 22 male, 3 unrecorded.
- **Strain:** C57BL/6J (48), C57BL/6N (13).
- **Age:** 22–216 days (recorded for 56 of 61).
- **Weight:** 11.3–31.0 g (recorded for 55 of 61).
- **Anatomy:** whole-brain transcranial, through the intact skull. An imaging
  plane is named for 23 of 99 acquisitions: striatum, hippocampus, midbrain,
  pons, cerebellum.
- **Pathology:** none — all animals are healthy.
- **Probe model:** L22-14v (77), GEL818iD (15), L22-14vX (7).
- **Sites:** McGill University (43 mice), ICM / Paris Brain Institute (12),
  Université de Montréal (6).

## Data Validation

- Standard B-mode and B-mode with tissue suppression `zea` pipelines available in `pipeline_bmode.yaml` and `pipeline_tissue_suppression.yaml`, respectively.

## Known Issues

- N/A

## Ethical Considerations

- **Data tier:** in vivo animal (mouse). No human subjects, no protected health
  information, and no participant-consent or IRB requirement applies.
- **Animal use approval:** acquisitions were performed under an institutional
  animal use protocol. `custom/mouse_animal_protocol_id` records the identifier
  per acquisition. Recording sites are McGill University, the ICM (Institut de cardiologie de Montréal), and Université de Montréal. The approval statements themselves
  belong to the original ULMShare authors and should be reproduced from their
  publication when this conversion is published, rather than inferred from the
  protocol identifiers alone.
- **Animal welfare (ARRIVE 2.0):** the essential-10 reporting items that this
  dataset can carry are recorded per acquisition and summarized under Subject
  Metadata — species and strain, sex, age, weight, health status (all healthy;
  no disease model), anesthetic protocol, contrast-agent route and dose, and
  recording site. Items that belong to the original study design rather than
  the released data — sample-size rationale, randomization, blinding, and
  outcome definitions — are not reproduced here and should be taken from the
  ULMShare publication.
- **De-identification:** not applicable to animal subjects. Subject IDs are
  coded (`mouse_18`), and no date of birth is carried into the zea files —
  only age in days.
- **Procedures:** no terminal procedure is represented; imaging is transcranial
  through the intact skull.

## Citation

CC BY 4.0 requires attribution to the original authors. Cite the **dataset**:

Rauby, B., Ghigo, N., Ramos-Palacios, G., Leconte, A., Lee, S., Wu, A.,
Xing, P., Gulenko, O., Caron, L., Malescot, A., Martineau, É., Porée, J.,
Gasse, M., Rungta, R., Sadikot, A., Provost, J. (2026). *ULMShare: A
Large-Scale In Vivo Ultrasound Localization Microscopy Dataset for
Microvascular Imaging.* Federated Research Data Repository.
[doi:10.20383/103.01550](https://doi.org/10.20383/103.01550)

and, where the methods are relevant, the accompanying preprint:
[arXiv:2606.07851](https://doi.org/10.48550/arXiv.2606.07851).

Note that `metadata/credit` inside the converted files carries the source
`acquisition.json`'s `doi_citations` where those are recorded, and otherwise
falls back to the preprint DOI above; the FRDR dataset DOI is the canonical
citation target for the data itself.