Curriculum vitae

Postdoctoral Fellow, Zhang Lab, Harvard University · sahil.moza@gmail.com · sahilmoza@fas.harvard.edu · ORCID · Google Scholar · GitHub

Research program

  • Brain-wide mechanisms of learning and behavioral flexibility in C. elegans.
  • Computational frameworks linking connectome structure to neural dynamics and behavior.
  • Research software for multimodal neural data integration, simulation and optimization.

Ongoing research

  • Whole-brain learning dynamics in C. elegansCo-leading a multi-institutional project on context-gated reorganization of neural activity; manuscript under revision
    2023–present
  • CeDNeConnectome-driven framework for integrating multimodal data with simulation and optimization workflows; preprint posted
    2024–present

Positions

  • Postdoctoral FellowDepartment of Organismic and Evolutionary Biology, Harvard University, CambridgeMentor Yun Zhang
    Sep 2022–present
  • Postdoctoral ResearcherBoston Children's Hospital and Harvard Medical School, Boston
    Jul 2021–Sep 2022
  • Scientist, EBRAINS, Human Brain ProjectKTH Royal Institute of Technology, Stockholm
    Oct 2020–Jul 2021

Education

  • PhD, Neuroscience and Systems BiologyNational Centre for Biological Sciences, TIFR, BangaloreAdvisor Upinder S. Bhalla · Thesis, Robust memory and precise balance, computation with biological network motifs
    2020
  • ME, Computational and Systems BiologyJawaharlal Nehru University, New Delhi
    2012
  • BE, BiotechnologyPanjab University, Chandigarh
    2010

Publications

  1. bioRxiv

    Aversive learning induces context-gated global reorganization of neural dynamics in Caenorhabditis elegans

    J. Liang*, S. Moon*, S. Moza*, H.J. Lee*, P.E. Eleftheriadis, J. Chen, M. Ge, M. Chen, H. Lu, Y. Zhang

    bioRxiv (2025) · Under revision

    Abstract

    Learning generates experience-dependent changes to the brain. However, how neurons of diverse functions and connectivity reorganize and modulate their activities to generate coherent changes while preserving essential functions is not well understood. Here, we address this question using an aversive olfactory learning paradigm whereby Caenorhabditis elegans learns to reduce its olfactory preference for pathogenic bacteria. Using functional imaging during olfactory stimulation in naive and trained animals, we show that, at brain-wide scale, cell type-by-cell type, learning induces context-gated reconfiguration of the organization of neural activity throughout the brain to alter neural responses only during bacteria-discrimination task, while leaving intact bacteria-sensing functions. We found that the context-gated encoding of learning is globally distributed across layers of the nervous system, composed of neurons carrying information of context or learning experience. In particular, aversive training modulates multiple functional connections within the nervous system, including those between sensory neurons and interneurons, as well as those among interneurons, in a context-gated manner. At the systems level, training modulates correlated activity of neural populations; we found that low-dimensional temporal patterns of population activity correlate well with locomotory gaits that express olfactory preferences. Upon training, the rotation and contraction of the low-dimensional neural manifolds shifts the brain into predisposed states for the context-gated display of learned behavior. Because animals encounter unpredictable environments in life, efficient learning about relevant cues while maintaining other functions is essential for survival. Our findings uncover network-level mechanisms that help explain how the brain reorganizes its activity patterns to both encode new experience and preserve essential functions.

    BibTeX
    @article{liang2025aversive,
      title = {Aversive learning induces context-gated global reorganization of neural dynamics in Caenorhabditis elegans},
      author = {Liang, Jingting and Moon, Sihoon and Moza, Sahil and Lee, Hyun Jee and Eleftheriadis, Panagiotis E. and Chen, Juan and Ge, Minghai and Chen, Maoting and Lu, Hang and Zhang, Yun},
      journal = {bioRxiv},
      year = {2025},
      month = nov,
      doi = {10.1101/2025.10.31.685731},
      note = {Under revision}
    }
  2. bioRxiv

    CeDNe: a multi-scale computational framework for modeling structure-function relationships in the C. elegans nervous system

    S. Moza, Y. Zhang

    bioRxiv (2025)

    Abstract

    Understanding how neural circuits generate behavior requires integrating structural and functional data across scales. C. elegans with its complete connectome, genetically identifiable neurons, single-cell transcriptome, neuropeptide-receptor distribution, and an amenability to simultaneous measurement of brain-wide neural activity and behavior presents a unique opportunity for such a multiscale circuit analysis. However, the absence of a unifying framework to connect these diverse datasets limits our ability to connect network structure and attributes with function. Here we introduce CeDNe (C. elegans Dynamical Network), an open-source computational framework that integrates anatomical, molecular, and imaging datasets into a unified graph-based representation that enables multimodal data analysis by cross-referencing different omics layers in a single computational environment. Specifically, CeDNe provides modular tools for visualizing and analyzing network connectivity, motif distribution, and circuit paths. Further, it incorporates a computational framework that simulates neural dynamics and optimizes network models to bridge structural connectivity with neural activity. Thus, CeDNe establishes a scalable foundation for data-driven modeling of the nervous system. This open-source tool not only facilitates computational connectomics and multimodal analyses in C. elegans but also serves as a generalizable framework for investigating structure-function relationships in neural networks of other organisms.

    BibTeX
    @article{moza2025cedne,
      title = {CeDNe: a multi-scale computational framework for modeling structure-function relationships in the C. elegans nervous system},
      author = {Moza, Sahil and Zhang, Yun},
      journal = {bioRxiv},
      year = {2025},
      month = nov,
      doi = {10.1101/2025.11.03.683805}
    }
  3. bioRxiv

    Network modularity reveals context and state-dependent reorganization of time-varying functional connectivity in single-cell resolved neural activity recordings

    S. Moon, J. Liang, H.J. Lee, A. Maalouf, Z. Yu, S. Moza, Y. Zhang, H. Lu

    bioRxiv (2025)

    Abstract

    An important goal of neuroscience is to understand how biological neural networks organize activity at multiple scales to enable complex information processing and behavioral output. To address this challenge, large-scale neural activity datasets with increased resolution and wider coverage have become more prevalent across many model systems. However, bridging the gap in scale between changes in pairwise functional connectivity between neurons and changes in brain-wide organization of activity remains a key challenge. In this work, we demonstrate application of modularity-based community detection and network modularity to single-cell resolved recordings, for the first time, as a method to summarize complex changes in time-varying functional connectivity, facilitating comparisons across multiple time windows, recordings, and conditions. We apply these methods to both single-cell resolved multi-cell and whole-brain activity recordings. In the multi-cell recordings, we find that food odor changes functional connectivity between existing network modules in a C. elegans locomotory interneuron network, rather than reorganizing them. In spontaneous whole-brain activity, we identify several key hub neurons and combinations that significantly destabilize module assignments when silenced. Together, these results demonstrate community detection and modularity as a method for detecting context and network state-dependent changes in functional connectivity at the intermediate scale of network modules in single-cell resolved neural activity. Results from these analyses facilitate future investigation of mechanisms that mediate organization of neural activity at intermediate scales.

    BibTeX
    @article{moon2025modularity,
      title = {Network modularity reveals context and state-dependent reorganization of time-varying functional connectivity in single-cell resolved neural activity recordings},
      author = {Moon, Sihoon and Liang, Jingting and Lee, Hyun Jee and Maalouf, Ava and Yu, Zikai and Moza, Sahil and Zhang, Yun and Lu, Hang},
      journal = {bioRxiv},
      year = {2025},
      month = nov,
      doi = {10.1101/2025.11.02.686048}
    }
  4. Bioinformatics

    SWITCHES: Searchable Web Interface for Topologies of CHEmical Switches

    G.V. HarshaRani, S. Moza, N. Ramakrishnan, U.S. Bhalla

    Bioinformatics (2021)

    BibTeX
    @article{harsharani2021switches,
      title = {SWITCHES: Searchable Web Interface for Topologies of CHEmical Switches},
      author = {HarshaRani, G. V. and Moza, Sahil and Ramakrishnan, Naren and Bhalla, Upinder S.},
      journal = {Bioinformatics},
      year = {2021},
      month = jan,
      doi = {10.1093/bioinformatics/btab006}
    }
  5. Book chapter

    Patterned optogenetic stimulation using a DMD projector

    A. Bhatia, S. Moza, U.S. Bhalla

    In Channelrhodopsin: Methods and Protocols, Humana, New York (2020)

    BibTeX
    @incollection{bhatia2020patterned,
      title = {Patterned optogenetic stimulation using a DMD projector},
      author = {Bhatia, Aanchal and Moza, Sahil and Bhalla, Upinder S.},
      booktitle = {Channelrhodopsin: Methods and Protocols},
      publisher = {Humana, New York},
      pages = {173--188},
      year = {2020},
      month = sep,
      doi = {10.1007/978-1-0716-0830-2_11}
    }
  6. PhD thesis

    Robust memory and precise balance: computation with biological network motifs

    S. Moza

    PhD thesis, National Centre for Biological Sciences, Tata Institute of Fundamental Research (2020)

    BibTeX
    @phdthesis{moza2020thesis,
      title = {Robust memory and precise balance: computation with biological network motifs},
      author = {Moza, Sahil},
      school = {National Centre for Biological Sciences, Tata Institute of Fundamental Research},
      year = {2020},
      month = jul
    }
  7. eLife

    Precise excitation-inhibition balance controls gain and timing in the hippocampus

    A. Bhatia*, S. Moza*, U.S. Bhalla

    eLife 8, e43415 (2019)

    Faculty Opinions "Exceptional" recommendation

    BibTeX
    @article{bhatia2019precise,
      title = {Precise excitation-inhibition balance controls gain and timing in the hippocampus},
      author = {Bhatia, Aanchal and Moza, Sahil and Bhalla, Upinder S.},
      journal = {eLife},
      volume = {8},
      pages = {e43415},
      year = {2019},
      month = apr,
      doi = {10.7554/eLife.43415}
    }

* equal contribution

Research software

  • CeDNeGraph-based framework for multimodal connectome modeling, simulation and optimization
    2025
  • NeuroRD-SBMLBiophysical model translation and standardization
    2022
  • LHSMDULatin Hypercube Sampling with Multi-Dimensional Uniformity, parameter sampling library
    2020

Talks, conferences and workshops

  • Kempner Institute 2026 ConferenceHarvard University, Cambridge
    Sep 2026
  • Neuroscience 2025, Society for NeuroscienceSan Diego
    Nov 2025
  • Analysis and Modeling of ConnectomesJanelia Research Campus
    Jun 2025
  • CeNeuro 2024Madison, Wisconsin
    Jun 2024
  • Neuronal CircuitsCold Spring Harbor Laboratory
    Mar 2024
  • Harvard Museum of Comparative Zoology seminar seriesCambridge
    May 2023
  • NeuroMatch Conferenceonline
    Mar 2020
  • No Garlands NeuroscienceIISER Pune
    Jan 2020
  • Transylvanian Experimental Neuroscience Summer SchoolRomania
    Jun 2019
  • Molecules and MemoryNCBS, Bengaluru
    Mar 2019
  • Quantitative Approaches to Behaviour and Neural SystemsLisbon
    Oct 2018
  • Spikes lecture series, Centre for NeuroscienceIISc Bengaluru
    Jan 2018
  • Neuroscience 2017, Society for NeuroscienceWashington, DC
    Nov 2017
  • No Garlands NeuroscienceIISER Pune
    Oct 2017
  • BSSE SymposiumIISc Bengaluru
    Jan 2017
  • Molecular Mechanisms at the SynapseJanelia Research Campus
    May 2016

Teaching and mentoring

  • Scienspur: Introduction to Computational Neuroscience I and IIFree online life-science courses for undergraduates worldwideInstructor
    Winter 2023
  • Computational Approaches to Memory and Plasticity (CAMP)National Centre for Biological Sciences, BangaloreTeaching assistant and organizer, five summer schools
    Summers 2014–2018
  • Boston Bangalore Biosciences Beginnings (B4) Neuroscience SchoolHarvard University and NCBSTeaching assistant and organization
    Winter 2016
  • Master's thesis student, Zhang LabWhole-brain imaging and behaviour; co-author on the whole-brain learning preprintNow a PhD student at a Max Planck institute
    2023–2025

Professional service

  • ReviewereNeuro (2023–), Journal of Computational Neuroscience (2025–), Journal of Biosciences (2022–)
  • Co-reviewerNeuron, Nature Neuroscience, eLife and Cell, with senior collaborators

Fellowships

  • Senior Research Fellowship, BiologyCouncil of Scientific and Industrial Research (CSIR)
    2014–2017
  • Junior Research Fellowship, Biology, All India Rank 36Council of Scientific and Industrial Research (CSIR)
    2012–2014
  • DBT Bioinformatics National Certification, All India Rank 33Department of Biotechnology, Government of India
    2011
  • Master's FellowshipJawaharlal Nehru University
    2010–2012

Travel awards

  • IBRO-PERC, The Brain Prize and FENS stipend
    May 2019
  • Wellcome Trust Travel Award
    Sep 2018
  • Infosys Travel Award, Infosys Foundation
    Dec 2017
  • Department of Biotechnology Travel Award, Government of India
    Nov 2017

Skills

Modeling

Large-scale simulation, dynamical systems, information theory, control-based system identification, chemical reaction network modeling, stochastic simulation (Langevin, Gillespie), optimization.

Analysis

High-dimensional volumetric (4D) neural data, neural population geometry and manifold analysis, neural time-series modeling, connectome topology, tensor decomposition (SVD, CP, Tucker), graph-based learning, unsupervised learning and clustering.

Tools

Python, PyTorch, JAX, scikit-learn, Optuna, NetworkX, NumPy, pandas, MOOSE, COPASI, Brian. UNIX, multiprocessing, SLURM and SGE clusters.

Experimental

C. elegans and Drosophila melanogaster: genetics, optogenetics, calcium imaging, behavior.