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Update cellfinder CLI name to brainmapper
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willGraham01 committed Jan 2, 2024
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32 changes: 16 additions & 16 deletions README.md
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Expand Up @@ -24,15 +24,15 @@ You can also find the documentation for the backend BrainGlobe tools these workf

At present, the package offers the following workflows to users:

- [cellfinder](#cellfinder): a command-line tool for whole-brain detection, registration, and analysis.
- [brainmapper](#brainmapper-command-line-interface-cli): A command-line tool for whole-brain detection, registration, and analysis.

Additionally, this repository provides functionalities to support code developers. See [Developers documentation](#developers-documentation) for further details.
Additionally, this repository provides functionalities to support code developers. See the [developer documentation](#developer-documentation) for further details.

## User documentation

### Installation

### Installation of the cellfinder CLI tool
At the moment, users can install the cellfinder CLI tool as a standalone tool, by running `pip install` in your desired environment:
At the moment, users can install all available workflows by running `pip install` in your desired environment:

```bash
pip install brainglobe-workflows
Expand All @@ -41,43 +41,45 @@ pip install brainglobe-workflows
`brainglobe-workflows` is built using BrainGlobe tools, and it will automatically fetch the tools that it needs and install them into your environment.
Once BrainGlobe version 1 is available, this package will fetch all BrainGlobe tools and handle their install into your environment, to prevent potential conflicts from partial-installs.

See the sections below for more information about the workflows and command-line tools provided.

### Cellfinder Command Line Interface (CLI)
#### `brainmapper` Command Line Interface (CLI)

Whole-brain cell detection, registration and analysis.

If you want to just use the cell detection part of `cellfinder`, please see the standalone [cellfinder](https://github.com/brainglobe/cellfinder-core) package, or the [cellfinder plugin](https://github.com/brainglobe/cellfinder-napari) for [napari](https://napari.org/).

If you want to just use the cell detection part of `brainmapper`, please see the standalone [cellfinder](https://github.com/brainglobe/cellfinder) package and its [`napari`](https://napari.org/) plugin.
`cellfinder` is a collection of tools developed by [Adam Tyson](https://github.com/adamltyson), [Charly Rousseau](https://github.com/crousseau) and [Christian Niedworok](https://github.com/cniedwor) in the [Margrie Lab](https://www.sainsburywellcome.org/web/groups/margrie-lab), generously supported by the [Sainsbury Wellcome Centre](https://www.sainsburywellcome.org/web/).

`cellfinder` is designed for the analysis of whole-brain imaging data such as [serial-section imaging](https://sainsburywellcomecentre.github.io/OpenSerialSection/) and lightsheet imaging in cleared tissue.
`brainmapper` is a workflow designed for the analysis of whole-brain imaging data such as [serial-section imaging](https://sainsburywellcomecentre.github.io/OpenSerialSection/) and lightsheet imaging in cleared tissue.
The aim is to provide a single solution for:

- Cell detection (initial cell candidate detection and refinement using deep learning) (using the [cellfinder](https://github.com/brainglobe/cellfinder-core) backend package),
- Cell detection (initial cell candidate detection and refinement using deep learning) (using the [cellfinder](https://github.com/brainglobe/cellfinder) backend package),
- Atlas registration (using [brainreg](https://github.com/brainglobe/brainreg)),
- Analysis of cell positions in a common space.

Basic usage:

```bash
cellfinder -s signal_images -b background_images -o output_dir --metadata metadata
brainmapper -s signal_images -b background_images -o output_dir --metadata metadata
```

Full documentation can be found [here](https://brainglobe.info/documentation/cellfinder/index.html).

NOTE: The `brainmapper` workflow previously used the name "cellfinder", but this has been discontinued following the release of the [unified `cellfinder`](https://github.com/brainglobe/cellfinder) backend package to avoid conflation of terms.
See our [blog post](https://brainglobe.info/blog/version1/cellfinder-core-and-plugin-merge.html) from the release for more information.

## Developer documentation

This repository also includes workflow scripts that are benchmarked to support code development.
These benchmarks are run regularly to ensure performance is stable, as the tools are developed and extended.
* Developers can install these benchmarks locally via `pip install .[dev]`. By executing `asv run`, the benchmarks will run with default parameters on a small dataset that is downloaded from [GIN](https://gin.g-node.org/G-Node/info/wiki). See [the asv docs](https://asv.readthedocs.io/en/v0.6.1/using.html#running-benchmarks) for further details on how to run benchmarks.
* Developers can also run these benchmarks on data they have stored locally, by specifying the relevant paths in an input (JSON) file.
* We also maintain an internal runner that benchmarks the workflows over a large, exemplar dataset, of the scale we expect users to be handling. The result of these benchmarks are made publicly available.

- Developers can install these benchmarks locally via `pip install .[dev]`. By executing `asv run`, the benchmarks will run with default parameters on a small dataset that is downloaded from [GIN](https://gin.g-node.org/G-Node/info/wiki). See [the asv docs](https://asv.readthedocs.io/en/v0.6.1/using.html#running-benchmarks) for further details on how to run benchmarks.
- Developers can also run these benchmarks on data they have stored locally, by specifying the relevant paths in an input (JSON) file.
- We also maintain an internal runner that benchmarks the workflows over a large, exemplar dataset, of the scale we expect users to be handling. The result of these benchmarks are made publicly available.

Contributions to BrainGlobe are more than welcome.
Please see the [developer guide](https://brainglobe.info/developers/index.html).


## Citing `brainglobe-workflows`

**If you use any tools in the [brainglobe suite](https://brainglobe.info/documentation/index.html), please [let us know](mailto:[email protected]?subject=cellfinder), and we'd be happy to promote your paper/talk etc.**
Expand All @@ -87,5 +89,3 @@ If you find [`cellfinder`](#cellfinder) useful, and use it in your research, ple
[https://doi.org/10.1371/journal.pcbi.1009074](https://doi.org/10.1371/journal.pcbi.1009074)
>
If you use any of the image registration functions in `cellfinder`, please also cite [`brainreg`](https://github.com/brainglobe/brainreg#citing-brainreg).

---
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Expand Up @@ -18,7 +18,7 @@
from brainglobe_utils.general.system import ensure_directory_exists
from brainglobe_utils.pandas.misc import safe_pandas_concat, sanitise_df

from brainglobe_workflows.cellfinder_brainreg.export.export import (
from brainglobe_workflows.brainmapper.export.export import (
export_points,
)

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@@ -1,7 +1,7 @@
from brainglobe_workflows.cellfinder_brainreg.export.abc4d import (
from brainglobe_workflows.brainmapper.export.abc4d import (
export_points as abc4d_export,
)
from brainglobe_workflows.cellfinder_brainreg.export.brainrender import (
from brainglobe_workflows.brainmapper.export.brainrender import (
export_points as brainrender_export,
)

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Expand Up @@ -22,10 +22,10 @@
from tifffile import tifffile
from tqdm import tqdm

from brainglobe_workflows.cellfinder_brainreg.tools import (
from brainglobe_workflows.brainmapper.tools import (
image_processing as img_tools,
)
from brainglobe_workflows.cellfinder_brainreg.tools import system
from brainglobe_workflows.brainmapper.tools import system


class StackSizeError(Exception):
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@@ -1,6 +1,6 @@
import logging

from brainglobe_workflows.cellfinder_brainreg.figures import heatmap
from brainglobe_workflows.brainmapper.figures import heatmap


def run(args, atlas, downsampled_shape):
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Expand Up @@ -44,7 +44,7 @@ def main():
suppress_tf_logging(tf_suppress_log_messages)
from brainreg.core.main import main as register

from brainglobe_workflows.cellfinder_brainreg.tools import prep
from brainglobe_workflows.brainmapper.tools import prep

start_time = datetime.now()
args, arg_groups, what_to_run, atlas = prep.prep_cellfinder_general()
Expand Down Expand Up @@ -105,9 +105,9 @@ def run_all(args, what_to_run, atlas):
from cellfinder.core.tools import prep
from cellfinder.core.tools.IO import read_with_dask

from brainglobe_workflows.cellfinder_brainreg.analyse import analyse
from brainglobe_workflows.cellfinder_brainreg.figures import figures
from brainglobe_workflows.cellfinder_brainreg.tools.prep import (
from brainglobe_workflows.brainmapper.analyse import analyse
from brainglobe_workflows.brainmapper.figures import figures
from brainglobe_workflows.brainmapper.tools.prep import (
prep_candidate_detection,
prep_channel_specific_general,
)
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Expand Up @@ -18,9 +18,9 @@
from fancylog import fancylog

import brainglobe_workflows as program_for_log
import brainglobe_workflows.cellfinder_brainreg.tools.parser as parser
from brainglobe_workflows.cellfinder_brainreg.tools import system, tools
from brainglobe_workflows.cellfinder_brainreg.tools.parser import (
import brainglobe_workflows.brainmapper.tools.parser as parser
from brainglobe_workflows.brainmapper.tools import system, tools
from brainglobe_workflows.brainmapper.tools.parser import (
cellfinder_parser,
)

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2 changes: 1 addition & 1 deletion pyproject.toml
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Expand Up @@ -74,7 +74,7 @@ napari = ["napari[pyqt5]", "brainglobe-napari-io", "cellfinder[napari]>=1.0.0"]

[project.scripts]
cellfinder-workflow = "brainglobe_workflows.cellfinder_core.cellfinder:main_app_wrapper"
cellfinder = "brainglobe_workflows.cellfinder_brainreg.main:main"
brainmapper = "brainglobe_workflows.brainmapper.main:main"

[build-system]
requires = ["setuptools>=45", "wheel", "setuptools_scm[toml]>=6.2"]
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Expand Up @@ -6,7 +6,7 @@
import brainglobe_utils.IO.cells as cell_io
import pytest

from brainglobe_workflows.cellfinder_brainreg.main import (
from brainglobe_workflows.brainmapper.main import (
main as cellfinder_run,
)

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2 changes: 1 addition & 1 deletion tests/cellfinder_brainreg/test_integration/test_extract.py
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Expand Up @@ -12,7 +12,7 @@
from brainglobe_utils.IO.cells import get_cells
from tifffile import tifffile

from brainglobe_workflows.cellfinder_brainreg.extract import (
from brainglobe_workflows.brainmapper.extract import (
extract_cubes as extract_cubes,
)

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Expand Up @@ -7,7 +7,7 @@
import pytest
from imio.load import load_any

from brainglobe_workflows.cellfinder_brainreg.main import (
from brainglobe_workflows.brainmapper.main import (
main as cellfinder_run,
)

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2 changes: 1 addition & 1 deletion tests/cellfinder_brainreg/test_unit/test_analyse.py
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Expand Up @@ -4,7 +4,7 @@

import pytest

from brainglobe_workflows.cellfinder_brainreg.analyse.analyse import (
from brainglobe_workflows.brainmapper.analyse.analyse import (
Point,
get_region_totals,
)
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Expand Up @@ -2,7 +2,7 @@

import numpy as np

from brainglobe_workflows.cellfinder_brainreg.tools import (
from brainglobe_workflows.brainmapper.tools import (
image_processing as img_tools,
)

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Expand Up @@ -3,7 +3,7 @@
import pytest
from brainglobe_utils.general.exceptions import CommandLineInputError

from brainglobe_workflows.cellfinder_brainreg.tools import prep
from brainglobe_workflows.brainmapper.tools import prep

# import shutil

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Expand Up @@ -6,7 +6,7 @@
from brainglobe_utils.general.exceptions import CommandLineInputError
from brainglobe_utils.general.system import ensure_directory_exists

import brainglobe_workflows.cellfinder_brainreg.tools.system as system
import brainglobe_workflows.brainmapper.tools.system as system

data_dir = Path(__file__).parents[4] / Path("tests", "data")
background_im_dir = os.path.join(data_dir, "background")
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Expand Up @@ -3,7 +3,7 @@
import numpy as np
import pytest

import brainglobe_workflows.cellfinder_brainreg.tools.tools as tools
import brainglobe_workflows.brainmapper.tools.tools as tools

a = [1, "a", 10, 30]
b = [30, 10, "c", "d"]
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