BayesianTracker (btrack
) is a Python library for multi object tracking,
used to reconstruct trajectories in crowded fields. Here, we use a
probabilistic network of information to perform the trajectory linking. This
method uses spatial information as well as appearance information for track linking.
The tracking algorithm assembles reliable sections of track that do not contain splitting events (tracklets). Each new tracklet initiates a probabilistic model, and utilises this to predict future states (and error in states) of each of the objects in the field of view. We assign new observations to the growing tracklets (linking) by evaluating the posterior probability of each potential linkage from a Bayesian belief matrix for all possible linkages.
The tracklets are then assembled into tracks by using multiple hypothesis testing and integer programming to identify a globally optimal solution. The likelihood of each hypothesis is calculated for some or all of the tracklets based on heuristics. The global solution identifies a sequence of high-likelihood hypotheses that accounts for all observations.
We developed btrack
for cell tracking in time-lapse microscopy data.
Automated cell tracking and lineage tree reconstruction. Visualization is provided by our plugin to Napari, arboretum.
Video of tracking, showing automatic lineage determination
Read about the science:
http://lowe.cs.ucl.ac.uk/cellx.html
You can also --> ⭐ 😉
BayesianTracker has been tested with Python 3.7+ on OS X, Linux and Win10. The tracker and hypothesis engine are mostly written in C++ with a Python wrapper.
$ pip install btrack
If you would rather install the latest development version, and/or compile directly from source, you can clone and install from this repo:
$ git clone https://github.com/quantumjot/BayesianTracker.git
$ conda env create -f ./BayesianTracker/environment.yml
$ conda activate btrack
$ cd BayesianTracker
$ pip install -e .
Addtionally, the build.sh
script will download Eigen source, run the makefile
and pip install.
If you do not want to install a local copy, you can run the tracker in a Colab notebook. Please note that these examples are work in progress and may change:
You can run btrack with a GUI and visualize the output using our plugin (called arboretum
) for the open source image viewer Napari
.
Status | Notebook | Link |
---|---|---|
In progress | Visualizing btrack output using arboretum | GitHub |
BayesianTracker can be used simply as follows:
import btrack
from btrack.dataio import import_CSV
# NOTE(arl): This should be from your image segmentation code
objects = import_CSV('/path/to/your/objects.csv')
# initialise a tracker session using a context manager
with btrack.BayesianTracker() as tracker:
# configure the tracker using a config file
tracker.configure_from_file('/path/to/your/models/cell_config.json')
# append the objects to be tracked
tracker.append(objects)
# set the volume (Z axis volume is set very large for 2D data)
tracker.volume=((0,1200),(0,1600),(-1e5,1e5))
# track them (in interactive mode)
tracker.track_interactive(step_size=100)
# generate hypotheses and run the global optimizer
tracker.optimize()
# get the tracks as a python list
tracks = tracker.tracks
Tracks themselves are python objects with properties:
# get the first track
track_zero = tracks[0]
# print the length of the track
print(len(track_zero))
# print all of the xyzt positions in the track
print(track_zero.x)
print(track_zero.y)
print(track_zero.z)
print(track_zero.t)
# print the fate of the track
print(track_zero.fate)
# print the track ID, root node, parent node, children and generational depth
print(track_zero.ID)
print(track_zero.root)
print(track_zero.parent)
print(track_zero.children)
print(track_zero.generation)
There are many additional options, including the ability to define object models.
Observations can be provided in several basic formats:
- a simple CSV or JSON file
- HDF5 for larger/more complex datasets, or
- using your own code from numpy arrays or pandas data arrays.
For example, CSV data of the format:
t x y z
0 300 300 0
1 301 299 1
2 302 288 2
...
can be imported:
from btrack.dataio import import_CSV
objects = import_CSV('/path/to/your/objects.csv')
More detail the colab notebooks above.
Tracks can also be exported in CSV and/or the LBEP format:
from btrack.dataio import export_CSV
from btrack.dataio import export_LBEP
# export tracks in CSV format
export_CSV('/path/to/your/tracks.csv', tracks)
# export the LBEP table of lineage information
export_LBEP('/path/to/your/lbep_tracks.txt', tracks)
btrack supports three different methods:
EXACT
- (DEFAULT) exact calculation of Bayesian belief matrix, but can be slow on large datasetsAPPROXIMATE
- approximate calculation, faster, for use with large datasets. This has an additionalmax_search_radius
parameter, which sets the local spatial search radius (isotropic, pixels) of the algorithm.CUDA
- GPU implementation of the EXACT method (in progress)
For most cell datasets (<1000 cells per time point) we recommend EXACT
. If you have larger datasets, we recommend APPROXIMATE
.
If the tracking does not complete, and is stuck on the optimization step, this means that your configuration is poorly suited to your data. Try turning off optimization, followed by modifying the parameters of the config file.
import btrack
from btrack.constants import BayesianUpdates
with btrack.BayesianTracker() as tracker:
# configure the tracker and change the update method
tracker.configure_from_file('/path/to/your/models/cell_config.json')
tracker.update_method = BayesianUpdates.APPROXIMATE
tracker.max_search_radius = 100
...
More details of how this type of tracking approach can be applied to tracking cells in time-lapse microscopy data can be found in the following publications:
Automated deep lineage tree analysis using a Bayesian single cell tracking approach
Ulicna K, Vallardi G, Charras G and Lowe AR.
bioRxiv (2020)
https://www.biorxiv.org/content/early/2020/09/10/2020.09.10.276980
Local cellular neighbourhood controls proliferation in cell competition
Bove A, Gradeci D, Fujita Y, Banerjee S, Charras G and Lowe AR.
Mol. Biol. Cell (2017)
https://doi.org/10.1091/mbc.E17-06-0368
@article {Ulicna2020.09.10.276980,
author = {Ulicna, Kristina and Vallardi, Giulia and Charras, Guillaume and Lowe, Alan R.},
title = {Automated deep lineage tree analysis using a Bayesian single cell tracking approach},
elocation-id = {2020.09.10.276980},
year = {2020},
doi = {10.1101/2020.09.10.276980},
publisher = {Cold Spring Harbor Laboratory},
URL = {https://www.biorxiv.org/content/early/2020/09/10/2020.09.10.276980},
eprint = {https://www.biorxiv.org/content/early/2020/09/10/2020.09.10.276980.full.pdf},
journal = {bioRxiv}
}
@article{Bove07112017,
author = {Bove, Anna and Gradeci, Daniel and Fujita, Yasuyuki and Banerjee,
Shiladitya and Charras, Guillaume and Lowe, Alan R.},
title = {Local cellular neighborhood controls proliferation in cell competition},
volume = {28},
number = {23},
pages = {3215-3228},
year = {2017},
doi = {10.1091/mbc.E17-06-0368},
URL = {http://www.molbiolcell.org/content/28/23/3215.abstract},
eprint = {http://www.molbiolcell.org/content/28/23/3215.full.pdf+html},
journal = {Molecular Biology of the Cell}
}