This project contains the tools to create the BBP Cell Atlas, using datasets from the Allen Institute for Brain Science (AIBS) and collected literature density values. The AIBS datasets files were obtained via experiments performed on P56 wild-type mouse brains. The outcome of this project is a list of volumetric files that provides cell type density estimates for each voxel of the mouse brain volume. The BBP Cell Atlas is the first model required to reconstruct BBP circuits of the mouse brain.
The tools implementation is based on the methods of Eroe et al. (2018), Rodarie et al. (2022), and Roussel et al. (2022).
The source code was originally written by Csaba Eroe, Dimitri Rodarie, Hugo Dictus, Lu Huanxiang, Wojciech Wajerowicz, Jonathan Lurie, and Yann Roussel.
The tools allow to:
- combine AIBS annotation files to reinstate missing mouse brain regions
- combine several AIBS gene marker datasets, to be used as hints for the spatial distribution of glial cells
- compute cell densities for several cell types including neurons and glial cells in the whole mouse brain
Tools can be used through a command line interface.
After installation, you can display the available command lines with the following bash command:
atlas-densities --helpgit clone https://github.com/BlueBrain/atlas-densities
cd atlas-densities
pip install -e .This project depends on the BBP python project cgal-pybind. The python project cgal-pybind needs to be installed prior to the above instructions.
Note: Depending on the size and resolution of the atlas, it can happen that some of the examples may not run with the 25um atlas from the Allen Institute due to memory requirements. For instance, 8GB of memory is often not enough for the "Combine ISH datasets for glia cells", depending on the datasets being combined.
Most the pipeline steps rely on the following AIBS reference datasets (see Rodarie et al. (2022) for more details on the different versions of these datasets):
- A Nissl volume
- An annotation volume
- A brain region hierarchy file
The AIBS Nissl reference volume is derived from high resolution image stacks of Nissl-stained coronal brain slices. These images are realigned and arranged to form a 3D brain volume. Nissl stains each cell somas. The intensity of each voxel of the Nissl volume correlates with the number of cells in this voxel. This Nissl volume has a corresponding annotation volume which maps each voxel of the Nissl volume to a brain region. The AIBS organize brain regions in a hierarchical tree, with leaves representing the finest parcellation.
These datasets are publicly available on the AIBS website.
Make data directory, and download needed annotation volumes, Nissl volume and hierarchy file:
mkdir -p data/ccfv2 data/ccfv3
# hierarchy file:
curl -o data/1.json http://api.brain-map.org/api/v2/structure_graph_download/1.json
# also available in atlas_densities/app/data/1.json
# CCFv2 annotation volumes:
curl -o data/ccfv2/annotation_25.nrrd http://download.alleninstitute.org/informatics-archive/current-release/mouse_ccf/annotation/mouse_2011/annotation_25.nrrd
curl -o data/ccfv2/annotation_fibers_25.nrrd http://download.alleninstitute.org/informatics-archive/current-release/mouse_ccf/annotation/mouse_2011/annotationFiber_25.nrrd
# CCFv3 annotation volume:
curl -o data/ccfv3/annotation_25.nrrd http://download.alleninstitute.org/informatics-archive/current-release/mouse_ccf/annotation/ccf_2017/annotation_25.nrrd
# AIBS Nissl volume:
curl -o data/ccfv2/ara_nissl_25.nrrd http://download.alleninstitute.org/informatics-archive/current-release/mouse_ccf/ara_nissl/ara_nissl_25.nrrdDepending on the chosen version for the reference volumes pairs, some additional preparation are needed.
The ccfv2 annotations are split into two volumes. One describes solely the fibers and ventricular related regions while the other contains all other brain regions. If you choose the ccfv2 version to estimate cell densities, then you should combine these two datasets:
# Here we override the ccfv2 annotation_25.nrrd file
atlas-densities combination combine-ccfv2-annotations \
--brain-annotation-ccfv2=data/ccfv2/annotation_25.nrrd \
--fiber-annotation-ccfv2=data/ccfv2/annotation_fibers_25.nrrd \
--output-path=data/ccfv2/annotation_25.nrrdThe ccfv3 annotation volume is more smooth but lacks a few brain parcellations that were present in the ccfv2 counterpart. If you choose the ccfv3 version to estimate cell densities, you can extend the ccfv3 annotation atlas with annotations of ccfv2.
# Here we override the ccfv3 annotation_25.nrrd file
atlas-densities combination combine-v2-v3-annotations \
--hierarchy-path=data/1.json \
--brain-annotation-ccfv2=data/ccfv2/annotation_25.nrrd \
--fiber-annotation-ccfv2=data/ccfv2/annotation_fibers_25.nrrd \
--brain-annotation-ccfv3=data/ccfv3/annotation_25.nrrd \
--output-path=data/ccfv3/annotation_25.nrrdIn the following examples, we will use the ccfv2 reference atlases.
The BBP Cell Atlas pipeline leverages in situ hybridization (ISH) volumetric datasets from the AIBS to estimate cell type densities in all regions of the mouse brain. These ISH datasets have to be realigned to the Nissl reference volume.
The DeepAtlas toolkit allows you to download AIBS ISH image stacks, align these images to the Nissl volume, and interpolate between them to create volumetric ISH datasets for each gene of your interest.
Glial cells express many genetic markers but none is expressed by every glial cells. We combine here in situ hybridization (ISH) volumetric datasets for glia markers and compute the glia subtypes global scaling factors, as described in Eroe et al. (2018). The list of required genes to combine for the generic glia marker can be found at combine_markers_ccfv2_config.yaml.
atlas-densities combination combine-markers \
--hierarchy-path=data/1.json \
--annotation-path=data/ccfv2/annotation_25.nrrd \
--config=atlas_densities/app/data/markers/combine_markers_ccfv2_config.yamlIn Eroe et al. (2018) (i.e., BBP Cell Atlas version 1), the excitatory neurons are distinguished from the inhibitory neurons using the Nrn1 and GAD67 (or GAD1) genetic marker.
In Rodarie et al. (2022) (i.e., BBP Cell Atlas version 2), the authors used parvalbumin (Pvalb), somatostatin (SST), vasoactive intestinal peptide (VIP) and gabaergic (GAD1) markers (see also fit_average_densities_ccfv2_config.yaml).
Compute and save the overall mouse brain cell density based on Nissl stained AIBS data.
# make output directory
mkdir -p data/ccfv2/density_volumes/
atlas-densities cell-densities cell-density \
--hierarchy-path=data/1.json \
--annotation-path=data/ccfv2/annotation_25.nrrd \
--nissl-path=data/ccfv2/ara_nissl_25.nrrd \
--output-path=data/ccfv2/density_volumes/cell_density.nrrdCompute and save the glial cell and neuron densities, based on overall cell densities from previous section and the combined ISH glia datasets (see In situ hybridization datasets section). The files glia.nrrd, oligodendrocyte.nrrd, microglia.nrrd, astrocyte.nrrd and glia_proportions.json come from the output of the ISH dataset combination step.
atlas-densities cell-densities glia-cell-densities \
--hierarchy-path=data/1.json \
--annotation-path=data/ccfv2/annotation_25.nrrd \
--cell-density-path=data/ccfv2/density_volumes/cell_density.nrrd \
--glia-density-path=data/ccfv2/relative_marker_volumes/glia.nrrd \
--astrocyte-density-path=data/ccfv2/relative_marker_volumes/astrocyte.nrrd \
--microglia-density-path=data/ccfv2/relative_marker_volumes/microglia.nrrd \
--oligodendrocyte-density-path=data/ccfv2/relative_marker_volumes/oligodendrocyte.nrrd \
--glia-proportions-path=data/ccfv2/relative_marker_volumes/glia_proportions.json \
--output-dir=data/ccfv2/density_volumesIn Rodarie et al. (2022), the authors collected density estimates from the literature for inhibitory neurons. Some estimates are in a format that can not be directly used by the pipeline (e.g., counts instead of densities). This part of the pipeline integrates the literature values into csv files, that will be used later on for the fitting.
We compile here the cell density estimates related to measurements of Kim et al. (2017) density file (mmc3.xlsx) and Rodarie et al. (2022) literature review file (gaba_papers.xlsx) into a single CSV file. Regions known to be purely excitatory or inhibitory (in terms of neuron composition) are also listed in a separate CSV file.
# make output directory
mkdir -p data/ccfv2/measurements
atlas-densities cell-densities compile-measurements \
--measurements-output-path=data/ccfv2/measurements/measurements.csv \
--homogenous-regions-output-path=data/ccfv2/measurements/homogeneous_regions.csvCompute and save average cell densities based on literature measurements and Cell Atlas data (e.g., region volumes).
WARNING: Different versions of the annotation atlas or the hierarchy file might have different sets brain regions (see Rodarie et al. (2022) for more details). The region names used by the literature measurements might therefore have no match in these datasets. Regions from the measurements that are not in the hierarchy or do not appear in the annotations will be ignored. A warning message will display these regions, allowing us to review them.
atlas-densities cell-densities measurements-to-average-densities \
--hierarchy-path=data/1.json \
--annotation-path=data/ccfv2/annotation_25.nrrd \
--cell-density-path=data/ccfv2/density_volumes/cell_density.nrrd \
--neuron-density-path=data/ccfv2/density_volumes/neuron_density.nrrd \
--measurements-path=data/ccfv2/measurements/measurements.csv \
--output-path=data/ccfv2/measurements/lit_densities.csvWe fit here transfer functions that describe the relation between mean ISH expression in regions of the mouse brain and literature regional density estimates (see Rodarie et al. (2022) for more details). This step leverages AIBS ISH marker datasets (in their expression form, see also fit_average_densities_ccfv2_config.yaml) and the previously computed literature density values. These transfer functions are used to obtain first estimates of neuron densities in regions not covered by literature.
The results of the following command includes a csv file (first_estimates.csv) storing the list of first density estimates for each neuron type and for each region of the annotation volume. The fitting.json output file contains the coefficients fitted by the algorithm together with their respective standard deviation and coefficient of determination (r_square).
# make output folder
mkdir -p data/ccfv2/first_estimates
atlas-densities cell-densities fit-average-densities \
--hierarchy-path=data/1.json \
--annotation-path=data/ccfv2/annotation_25.nrrd \
--neuron-density-path=data/ccfv2/density_volumes/neuron_density.nrrd \
--average-densities-path=data/ccfv2/measurements/lit_densities.csv \
--homogenous-regions-path=data/ccfv2/measurements/homogeneous_regions.csv \
--gene-config-path=atlas_densities/app/data/markers/fit_average_densities_ccfv2_config.yaml \
--fitted-densities-output-path=data/ccfv2/first_estimates/first_estimates.csv \
--fitting-maps-output-path=data/ccfv2/first_estimates/fitting.jsonNote: One can use the --min-data-points to require a minimum of points for the linear regression; the default is 1.
The neuron subtypes are here distinguished from each other using either the pipeline from Eroe et al. (2018) (BBP Cell Atlas version 1) or Rodarie et al. (2022) (BBP Cell Atlas version 2).
Estimate excitatory and inhibitory neuron densities from the Nrn1 and GAD1 (or GAD67) AIBS ISH markers and whole brain estimates from Kim et al. (2017) (located at mmc1.xlsx).
atlas-densities cell-densities inhibitory-and-excitatory-neuron-densities \
--hierarchy-path=data/1.json \
--annotation-path=data/ccfv2/annotation_25.nrrd \
--gad1-path=data/ccfv2/marker_volumes/gad1.nrrd \
--nrn1-path=data/ccfv2/marker_volumes/nrn1.nrrd \
--neuron-density-path=data/ccfv2/density_volumes/neuron_density.nrrd \
--inhibitory-neuron-counts-path=atlas_densities/app/data/measurements/mmc1.xlsx \
--output-dir=data/ccfv2/density_volumes/Estimate GAD67, Pvalb, SST, and VIP neuron densities from the literature and the transfer functions computed previously (first density estimates).
atlas-densities cell-densities inhibitory-neuron-densities \
--hierarchy-path=data/1.json \
--annotation-path=data/ccfv2/annotation_25.nrrd \
--neuron-density-path=data/ccfv2/density_volumes/neuron_density.nrrd \
--average-densities-path=data/ccfv2/first_estimates/first_estimates.csv \
--output-dir=data/ccfv2/density_volumes/Morphological and Electrical type densities of inhibitory neurons in the isocortex can be estimated using Roussel et al. (2022)'s pipeline. This pipeline produces a mapping from inhibitory neuron molecular types (here PV, SST, VIP and GAD67) to ME-types defined in Markram et al. (2015).
The following command creates neuron density nrrd files for the me-types listed in a probability mapping csv file (see also mtypes_probability_map_config.yaml).
atlas-densities mtype-densities create-from-probability-map \
--hierarchy-path=data/1.json \
--annotation-path=data/ccfv2/annotation_25.nrrd \
--probability-map data/probability_map01.csv \
--probability-map data/probability_map02.csv \
--synapse-class INH \
--marker gad67 data/molecular_densities/gad67.nrrd \
--marker pv data/molecular_densities/pv.nrrd \
--marker sst data/molecular_densities/sst.nrrd \
--marker vip data/molecular_densities/vip.nrrd \
--marker approx_lamp5 data/molecular_densities/approx_lamp5.nrrd \
--n-jobs 8 \
--output-dir=data/ccfv2/me-types/The molecular density of approx_lamp5 was calculated from the other molecular densities as
approx_lamp5 = gad67 - vip - sst - pv
which approximates the molecular density of lamp5.
This can be calculated via command line via:
atlas-densities combination manipulate \
--clip \
--base-nrrd data/molecular_densities/gad67.nrrd \
--subtract data/molecular_densities/vip.nrrd \
--subtract data/molecular_densities/pv.nrrd \
--subtract data/molecular_densities/sst.nrrd \
--output-path approx_lamp5.nrrdThe command outputs the density files in the output-dir and a metadata json file:
{
"SLAC": {
"bNAC": "data/ccfv2/test_regions_me-types/SLAC|bNAC_densities.nrrd",
"cAC": "data/ccfv2/test_regions_me-types/SLAC|cAC_densities.nrrd",
"cNAC": "data/ccfv2/test_regions_me-types/SLAC|cNAC_densities.nrrd"
},
"NGC-SA": {
"cNAC": "data/ccfv2/test_regions_me-types/NGC-SA|cNAC_densities.nrrd",
// ...
},
// ...
}This should run after the inhibitory/excitatory computation above. To run:
atlas-densities cell-densities excitatory-split \
--annotation-path=data/ccfv2/annotation_25.nrrd \
--hierarchy-path=data/1.json \
--neuron-density=data/ccfv2/density_volumes/neuron_density.nrrd \
--inhibitory-density=data/ccfv2/density_volumes/gad67+_density.nrrd \
--output-dir=data/ccfv2/excitatory_splitRun the following commands before submitting your code for review:
cd atlas-densities
isort -l 100 --profile black atlas_densities tests setup.py
black -l 100 atlas_densities tests setup.pyThese formatting operations will help you pass the linting check testenv:lint defined in tox.ini.
When you use this software, we kindly ask you to cite the following DOI:
The development of this software was supported by funding to the Blue Brain Project, a research center of the École polytechnique fédérale de Lausanne (EPFL), from the Swiss government’s ETH Board of the Swiss Federal Institutes of Technology.
For license and authors, see LICENSE.txt and AUTHORS.txt respectively.
Copyright (c) 2022-2024 Blue Brain Project/EPFL