Metadata-Version: 2.1
Name: LFPykernels
Version: 0.1.1
Summary: Causal spike-signal impulse response functions for finite-sized neuronal network models
Home-page: https://github.com/LFPy/LFPykernels
Author: LFPy-team
Author-email: lfpy@users.noreply.github.com
Classifier: Programming Language :: Python :: 3
Classifier: Programming Language :: Python :: 3.7
Classifier: Programming Language :: Python :: 3.8
Classifier: Programming Language :: Python :: 3.9
Classifier: Programming Language :: Python :: 3.10
Classifier: License :: OSI Approved :: GNU General Public License (GPL)
Classifier: Operating System :: OS Independent
Classifier: Topic :: Scientific/Engineering
Classifier: Topic :: Scientific/Engineering :: Physics
Classifier: Topic :: Utilities
Classifier: Intended Audience :: Developers
Classifier: Intended Audience :: Science/Research
Classifier: Development Status :: 4 - Beta
Provides: lfpykernels
Requires-Python: >=3.7
Description-Content-Type: text/markdown
Provides-Extra: tests
Provides-Extra: docs
License-File: LICENSE

# LFPykernels

The ``LFPykernels`` package incorporates forward-model based calculations of causal spike-signal
impulse response functions for finite-sized neuronal network models.

## Build Status

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## Citation

These codes correspond to results shown in the peer-reviewed manuscript:

Hagen E, Magnusson SH, Ness TV, Halnes G, Babu PN, et al. (2022)
Brain signal predictions from multi-scale networks using a linearized framework.
PLOS Computational Biology 18(8): e1010353. <https://doi.org/10.1371/journal.pcbi.1010353>

Bibtex format:

    @article{10.1371/journal.pcbi.1010353,
        doi = {10.1371/journal.pcbi.1010353},
        author = {Hagen, Espen AND Magnusson, Steinn H. AND Ness, Torbjørn V. AND Halnes, Geir AND Babu, Pooja N. AND Linssen, Charl AND Morrison, Abigail AND Einevoll, Gaute T.},
        journal = {PLOS Computational Biology},
        publisher = {Public Library of Science},
        title = {Brain signal predictions from multi-scale networks using a linearized framework},
        year = {2022},
        month = {08},
        volume = {18},
        url = {https://doi.org/10.1371/journal.pcbi.1010353},
        pages = {1-51},
        number = {8},
    }

If you use this software, please cite it as (change `<version>/<git-SHA>/<git-tag>` accordingly):

    Hagen, Espen. (2021). LFPykernels (<version>/<git-SHA>/<git-tag>). Zenodo. https://doi.org/10.5281/zenodo.5720619

BibTex format:

    @software{hagen_espen_2021_5720619,
      author       = {Hagen, Espen},
      title        = {LFPykernels},
      month        = nov,
      year         = 2021,
      note         = {If you use this software, please cite it as below.},
      publisher    = {Zenodo},
      version      = {<version>/<git-SHA>/<git-tag>},
      doi          = {10.5281/zenodo.5720619},
      url          = {https://doi.org/10.5281/zenodo.5720619}
    }

If you use or refer to this work, please cite it as above.
Adaptations or modifications of this work should comply with the provided `LICENSE` file provided with this repository.  

## Features

The ``LFPykernels`` package incorporates forward-model based calculations of causal spike-signal
impulse response functions for finite-sized neuronal network models.
The signals considered are low-frequency extracellular potentials ("local field potential" - LFP)
or current dipole moments (and by extension EEG and MEG like signals) that are
thought to mainly stem from synaptic currents and associated return currents.
The basic idea is that the effect of any spike event in each presynaptic
population on each signal type can be captured by single linearised multicompartment neuron
models representative of each population and simultaneously accounting for known distributions of
cells and synapses in space, distributions of delays, synaptic currents and associated return currents.

The present methodology is described in detail by [Hagen E et al., 2022](https://doi.org/10.1371/journal.pcbi.1010353).
The intended use for filter kernels predicted using ``LFPykernels`` is forward-model based signal predictions
from neuronal network simulation frameworks using simplified neuron representations like leaky integrate-and-fire
point neurons or rate-based neurons, but can also be used with biophysically detailed network models.

Let `$\nu_X(t)$` describe presynaptic population spike rates in units of spikes/dt
and `$H_{YX}(\mathbf{R}, \tau)$` predicted spike-signal kernels for the connections between presynaptic populations `$X$` and
postsynaptic populations `$Y$` the full signal may then be computed via the sum over linear convolutions:

``` math
V(\mathbf{R}, t) = \sum_X \sum_Y (\nu_X \ast H_{YX})(\mathbf{R}, t)
```

A more elaborate example combining kernel predictions with a spiking point-neuron network simulation is provided in the example notebook
<https://github.com/LFPy/LFPykernels/blob/main/examples/LIF_net_forward_model_predictions.ipynb>

For questions, please raise an issue at <https://github.com/LFPy/LFPykernels/issues>.

## Usage

Example prediction of kernel function `$H(\mathbf{R},\tau)$` mapping spike events of a
presynaptic inhibitory population `$X==\mathrm{I}$` to extracellular potential contributions by a
postsynaptic excitatory population `$Y==\mathrm{E}$` (see <https://github.com/LFPy/LFPykernels/blob/main/examples/README_example.ipynb>):

    import matplotlib.pyplot as plt
    import scipy.stats as st
    import numpy as np
    from lfpykernels import GaussCylinderPotential, KernelApprox
    import neuron

    # recompile mod files if needed
    mech_loaded = neuron.load_mechanisms('mod')
    if not mech_loaded:
        os.system('cd mod && nrnivmodl && cd -')
        mech_loaded = neuron.load_mechanisms('mod')
    print(f'mechanisms loaded: {mech_loaded}')

    # misc parameters
    dt = 2**-4  # time resolution (ms)
    t_X = 500  # time of synaptic activations (ms)
    tau = 50  # duration of impulse response function after onset (ms)
    Vrest = -65  # assumed average postsynaptic potential (mV)

    X=['E', 'I']   # presynaptic population names
    N_X = np.array([8192, 1024])  # presynpatic population sizes
    Y = 'E' # postsynaptic population
    N_Y = 8192  # postsynaptic population size
    C_YX = np.array([0.05, 0.05])  # pairwise connection probability between populations X and Y
    nu_X = {'E': 2.5, 'I': 5.0}  # assumed spike rates of each population (spikes/s)
    g_eff = True  # account for changes in passive leak due to persistent synaptic activations

    def set_passive(cell, Vrest):
        """Insert passive leak channel across all sections

        Parameters
        ----------
        cell: object
            LFPy.NetworkCell like object
        Vrest: float
            Steady state potential
        """
        for sec in cell.template.all:
            sec.insert('pas')
            sec.g_pas = 0.0003  # (S/cm2)
            sec.e_pas = Vrest  # (mV)

    # parameters for LFPy.NetworkCell representative of postsynaptic population
    cellParameters={
        'templatefile': 'BallAndSticksTemplate.hoc',
        'templatename': 'BallAndSticksTemplate',
        'custom_fun': [set_passive],
        'custom_fun_args': [{'Vrest': Vrest}],
        'templateargs': None,
        'delete_sections': False,
        'morphology': 'BallAndSticks_E.hoc'}

    populationParameters={
            'radius': 150.0,  # population radius (µm)
            'loc': 0.0,  # average depth of cell bodies (µm)
            'scale': 75.0}  # standard deviation (µm)

    # Predictor for extracellular potentials across depth assuming planar disk source
    # elements convolved with Gaussian along z-axis.
    # See https://lfpykernels.readthedocs.io/en/latest/#class-gausscylinderpotential for details
    probe = GaussCylinderPotential(
        cell=None,
        z=np.linspace(1000., -200., 13),  # depth of contacts (µm)
        sigma=0.3,  # tissue conductivity (S/m)
        R=populationParameters['radius'],  #
        sigma_z=populationParameters['scale'],
        )

    # Create KernelApprox object. See https://lfpykernels.readthedocs.io/en/latest/#class-kernelapprox for details
    kernel = KernelApprox(
        X=X,
        Y=Y,
        N_X=N_X,
        N_Y=N_Y,
        C_YX=C_YX,
        cellParameters=cellParameters,
        populationParameters=populationParameters,
        # function and parameters used to estimate average multapse count:
        multapseFunction=st.truncnorm,
        multapseParameters=[
            {'a': (1 - 2.) / .6, 'b': (10 - 2.) / .6, 'loc': 2.0, 'scale': 0.6},
            {'a': (1 - 5.) / 1.1, 'b': (10 - 5.) / 1.1, 'loc': 5.0, 'scale': 1.1}],
        # function and parameters for delay distribution from connections between a
        # population in X onto population Y:
        delayFunction=st.truncnorm,
        delayParameters=[{'a': -2.2, 'b': np.inf, 'loc': 1.3, 'scale': 0.5},
                         {'a': -1.5, 'b': np.inf, 'loc': 1.2, 'scale': 0.6}],
        # parameters for synapses from connections by populations X onto Y
        synapseParameters=[
            {'weight': 0.00012, 'syntype': 'Exp2Syn', 'tau1': 0.2, 'tau2': 1.8, 'e': 0.0},
            {'weight': 0.002, 'syntype': 'Exp2Syn', 'tau1': 0.1, 'tau2': 9.0, 'e': -80.0}],
        # parameters for spatial synaptic connectivity by populations X onto Y
        synapsePositionArguments=[
            {'section': ['apic', 'dend'],
             'fun': [st.norm],
             'funargs': [{'loc': 50.0, 'scale': 100.0}],
             'funweights': [1.0]},
            {'section': ['soma', 'apic', 'dend'],
             'fun': [st.norm],
             'funargs': [{'loc': -100.0, 'scale': 100.0}],
             'funweights': [1.0]}],
        # parameters for extrinsic synaptic input
        extSynapseParameters={'syntype': 'Exp2Syn', 'weight': 0.0002, 'tau1': 0.2, 'tau2': 1.8, 'e': 0.0},
        nu_ext=40.,  # external activation rate (spikes/s)
        n_ext=450,  # number of extrinsic synapses  
        nu_X=nu_X,
    )

    # make kernel predictions for connection from populations X='I' onto Y='E'
    H = kernel.get_kernel(
        probes=[probe],
        Vrest=Vrest, dt=dt, X='I', t_X=t_X, tau=tau,
        g_eff=g_eff)

## Physical units

Notes on physical units used in `LFPykernels`:

- There are no explicit checks for physical units

- Transmembrane currents are assumed to be in units of (nA)

- Spatial information is assumed to be in units of (µm)

- Voltages are assumed to be in units of (mV)

- Extracellular conductivities are assumed to be in units of (S/m)

- current dipole moments are assumed to be in units of (nA µm)

- Magnetic fields are assumed to be in units of (nA/µm)

- Simulation times are assumed to be in units of (ms) with step size ∆t

- Spike rates are assumed to be in units of (# spikes / ∆t)

## Documentation

The online Documentation of `LFPykernels` can be found here:
<https://lfpykernels.readthedocs.io/en/latest>

## Dependencies

`LFPykernels` is implemented in Python and is written (and continuously tested) for `Python >= 3.7` (older versions may or may not work).
The main `LFPykernels` module depends on ``LFPy`` (<https://github.com/LFPy/LFPy>, <https://LFPy.readthedocs.io>).

Running all unit tests and example files may in addition require `py.test`, `matplotlib`,
`LFPy`.

## Installation

### From development sources (<https://github.com/LFPy/LFPykernels>)

Install the current development version on <https://GitHub.com> using `git` (<https://git-scm.com>):

    git clone https://github.com/LFPy/LFPykernels.git
    cd LFPykernels
    python setup.py install  # --user optional

or using `pip`:

    pip install .  # --user optional

For active development, link the repository location

    pip install -e .  # --user optional

### Installation of stable releases on PyPI.org (<https://www.pypi.org>)

Installing stable releases from the Python Package Index (<https://www.pypi.org/project/lfpykernels>):

    pip install lfpykernels  # --user optional

To upgrade the installation using pip:

    pip install --upgrade --no-deps lfpykernels

## Docker

We provide a Docker (<https://www.docker.com>) container recipe file with LFPykernels etc.
To get started, install Docker and issue either:

    # build Dockerfile from GitHub
    docker build -t lfpykernels https://raw.githubusercontent.com/LFPy/LFPykernels/main/Dockerfile
    docker run -it -p 5000:5000 lfpykernels

or

    # build local Dockerfile (obtained by cloning repo, checkout branch etc.)
    docker build -t lfpykernels - < Dockerfile
    docker run -it -p 5000:5000 lfpykernels

If the docker file should fail for some reason it is possible to store the build log and avoid build caches by issuing

    docker build --no-cache --progress=plain -t lfpykernels - < Dockerfile 2>&1 | tee lfpykernels.log

For successful builds, the ``--mount`` option can be used to mount a folder on the host to a target folder as:

    docker run --mount type=bind,source="$(pwd)",target=/opt/data -it -p 5000:5000 lfpykernels

which mounts the present working dirctory (``$(pwd)``) to the ``/opt/data`` directory of the container.
Try mounting the ``LFPykernels`` source directory for example (by setting ``source="<path-to-LFPykernels>"``).
Various example files can then be found in the folder ``/opt/data/examples/``
when the container is running.

Jupyter notebook servers running from within the
container can be accessed after invoking them by issuing:

    cd /opt/data/examples/
    jupyter-notebook --ip 0.0.0.0 --port=5000 --no-browser --allow-root

and opening the resulting URL in a browser on the host computer, similar to:
<http://127.0.0.1:5000/?token=dcf8f859f859740fc858c568bdd5b015e0cf15bfc2c5b0c1>

## Acknowledgements

This work was supported by the European Union Horizon 2020 Research and
Innovation Programme under Grant Agreement No. 785907 and No. 945539 Human Brain Project (HBP) SGA2 and SGA3.
We also acknowledge the use of Fenix Infrastructure resources,
which are partially funded from the European Union’s Horizon 2020 Research and Innovation Programme
through the ICEI Project under the Grant Agreement No. 800858; The Helmholtz Alliance through the Initiative and
Networking Fund of the Helmholtz Association and the Helmholtz Portfolio theme Supercomputing
and Modeling for the Human Brain; and The Excellence Strategy of the Federal Government and
the La¨nder [G:(DE-82)EXS-PF-JARA-SDS005, G: (DE-82)EXS-SF-neuroIC002].
