IDEAS home Printed from https://ideas.repec.org/a/plo/pcbi00/1011904.html
   My bibliography  Save this article

Connectivity Matrix Seriation via Relaxation

Author

Listed:
  • Alexander Borst

Abstract

Volume electron microscopy together with computer-based image analysis are yielding neural circuit diagrams of ever larger regions of the brain. These datasets are usually represented in a cell-to-cell connectivity matrix and contain important information about prevalent circuit motifs allowing to directly test various theories on the computation in that brain structure. Of particular interest are the detection of cell assemblies and the quantification of feedback, which can profoundly change circuit properties. While the ordering of cells along the rows and columns doesn’t change the connectivity, it can make special connectivity patterns recognizable. For example, ordering the cells along the flow of information, feedback and feedforward connections are segregated above and below the main matrix diagonal, respectively. Different algorithms are used to renumber matrices such as to minimize a given cost function, but either their performance becomes unsatisfying at a given size of the circuit or the CPU time needed to compute them scales in an unfavorable way with increasing number of neurons. Based on previous ideas, I describe an algorithm which is effective in matrix reordering with respect to both its performance as well as to its scaling in computing time. Rather than trying to reorder the matrix in discrete steps, the algorithm transiently relaxes the integer program by assigning a real-valued parameter to each cell describing its location on a continuous axis (‘smooth-index’) and finds the parameter set that minimizes the cost. I find that the smooth-index algorithm outperforms all algorithms I compared it to, including those based on topological sorting.Author summary: Connectomic data provide researchers with neural circuit diagrams of ever larger regions of the brain. These datasets are usually represented in a cell-to-cell connectivity matrix and contain important information about prevalent circuit motifs. Such motifs, however, only become visible if the connectivity matrix is reordered appropriately. For example, ordering the cells along the flow of information, feedback and feedforward connections are segregated above and below the main matrix diagonal, respectively. While most previous approaches rely on topological sorting, my method relaxes the discrete vertex indices to real numbers (‘smooth-index’) along independent parameter axes and defines a differentiable cost function, thus, allowing gradient-based algorithms to find a minimum. The parameter set at this minimum is then re-discretized to reorder the connectivity matrix accordingly. I find my method to scale favorably with the circuit size and to outperform all algorithms I compared it to.

Suggested Citation

  • Alexander Borst, 2024. "Connectivity Matrix Seriation via Relaxation," PLOS Computational Biology, Public Library of Science, vol. 20(2), pages 1-18, February.
  • Handle: RePEc:plo:pcbi00:1011904
    DOI: 10.1371/journal.pcbi.1011904
    as

    Download full text from publisher

    File URL: https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1011904
    Download Restriction: no

    File URL: https://journals.plos.org/ploscompbiol/article/file?id=10.1371/journal.pcbi.1011904&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pcbi.1011904?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Kevin L. Briggman & Moritz Helmstaedter & Winfried Denk, 2011. "Wiring specificity in the direction-selectivity circuit of the retina," Nature, Nature, vol. 471(7337), pages 183-188, March.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Jason S Prentice & Olivier Marre & Mark L Ioffe & Adrianna R Loback & Gašper Tkačik & Michael J Berry II, 2016. "Error-Robust Modes of the Retinal Population Code," PLOS Computational Biology, Public Library of Science, vol. 12(11), pages 1-32, November.
    2. Brad Busse & Stephen Smith, 2013. "Automated Analysis of a Diverse Synapse Population," PLOS Computational Biology, Public Library of Science, vol. 9(3), pages 1-14, March.
    3. Elishai Ezra-Tsur & Oren Amsalem & Lea Ankri & Pritish Patil & Idan Segev & Michal Rivlin-Etzion, 2021. "Realistic retinal modeling unravels the differential role of excitation and inhibition to starburst amacrine cells in direction selectivity," PLOS Computational Biology, Public Library of Science, vol. 17(12), pages 1-31, December.
    4. repec:plo:pone00:0094292 is not listed on IDEAS
    5. Anna Kreshuk & Ullrich Koethe & Elizabeth Pax & Davi D Bock & Fred A Hamprecht, 2014. "Automated Detection of Synapses in Serial Section Transmission Electron Microscopy Image Stacks," PLOS ONE, Public Library of Science, vol. 9(2), pages 1-11, February.
    6. Sichen Tao & Yuki Todo & Zheng Tang & Bin Li & Zhiming Zhang & Riku Inoue, 2022. "A Novel Artificial Visual System for Motion Direction Detection in Grayscale Images," Mathematics, MDPI, vol. 10(16), pages 1-32, August.
    7. Umberto Esposito & Michele Giugliano & Mark van Rossum & Eleni Vasilaki, 2014. "Measuring Symmetry, Asymmetry and Randomness in Neural Network Connectivity," PLOS ONE, Public Library of Science, vol. 9(7), pages 1-16, July.
    8. Stefano Recanatesi & Gabriel Koch Ocker & Michael A Buice & Eric Shea-Brown, 2019. "Dimensionality in recurrent spiking networks: Global trends in activity and local origins in connectivity," PLOS Computational Biology, Public Library of Science, vol. 15(7), pages 1-29, July.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pcbi00:1011904. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: ploscompbiol (email available below). General contact details of provider: https://journals.plos.org/ploscompbiol/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.