Liam Paninski - US grants
Affiliations: | Columbia University, New York, NY |
Area:
Computation & TheoryWebsite:
http://www.stat.columbia.edu/~liam/We are testing a new system for linking grants to scientists.
The funding information displayed below comes from the NIH Research Portfolio Online Reporting Tools and the NSF Award Database.The grant data on this page is limited to grants awarded in the United States and is thus partial. It can nonetheless be used to understand how funding patterns influence mentorship networks and vice-versa, which has deep implications on how research is done.
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High-probability grants
According to our matching algorithm, Liam Paninski is the likely recipient of the following grants.Years | Recipients | Code | Title / Keywords | Matching score |
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2007 — 2015 | Paninski, Liam | N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Career: Using Advanced Statistical Techniques to Decipher the Neural Code @ Columbia University Project Summary The central problem in systems neuroscience is to understand the neural code, at both large and small physiological scales. Progress has been limited by a lack of sufficiently rich experimental data, a shortage of quantitative techniques to characterize and analyze the data, and an insufficient number of interdisciplinary researchers skilled in both systems neurophysiology and advanced statistical methods. Recent developments open new possibilities for collaborative efforts to tackle these basic problems. First, advances in multi-electrode recordings make it possible to study the simultaneous activity of large ensembles of neurons in a wide variety of experimental settings. Similarly, recent improvements in high-resolution voltage- and calcium-sensitive imaging technology now provide data capable of constraining highly-detailed biophysical models of information processing in single cells. A major bottleneck now is in analyzing and quantitatively understanding this data. Specific methodological advances in four fields are proposed: 1) encoding and decoding information in population spike trains; 2) single spike-train analysis and optimal stimulus design; 3) highly-detailed biophysical models and optimal processing of dendritic imaging data; and 4) information-theoretic analyses of sparse neural data. In each case, the investigator and his research group will develop novel mathematical models and tools for fitting these models directly to the observed data. Computer code implementing these novel techniques will be made publicly available to enhance the infrastructure for research and education. This work will have impact on the burgeoning field of neural prosthetics, which will require substantial improvements in our ability to design signaling interfaces between artificial and real neural tissue. Understanding encoding and decoding in populations of neurons and developing models that allow us to predict the effects of experimental perturbations to their behavior is key to this endeavor. This research on neural coding will also likely lead to mathematical results and statistical techniques which are of independent general interest and utility, with fundamental impacts on information theory, image processing, and optimal filtering and prediction of point processes (which in turn impact hundreds of other disciplines). In addition, the investigator is developing an advanced training course for graduate students and postdocs in statistical neuroscience (the first course of this kind in the world), as well as an introductory undergraduate course. Lecture notes will be made publicly available online and will shape a textbook in progress in advanced neural data analysis. Training opportunities will be pursued at Columbia University (strengthening already close ties with the Department of Statistics and Center for Theoretical Neuroscience) and with collaborators in the U.S. and internationally. |
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2009 — 2013 | Yuste, Rafael (co-PI) [⬀] Paninski, Liam |
N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Optical Reconstruction of Cortical Connectivity @ Columbia University One of the greatest challenges in computational neuroscience is to reconstruct the connectivity of large, complex neuronal networks. The ability to decipher circuit connectivity would have a fundamental impact on our understanding of the dynamical properties and the functional organization of the nervous system. Knowledge of prevalent connectivity patterns will also shed light on the developmental constraints and learning rules under which the network might be operating. |
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2014 — 2018 | Paninski, Liam | N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
@ Columbia University Vision begins in the retina, where light is converted into electrical signals, processed to extract and compress visual information, and transmitted through the optic nerve to the brain. Despite decades of research, a full understanding of these transformations remains incomplete. In particular, most studies have documented specific properties of the responses of single retinal cells in isolation, using specialized artificial visual stimuli. The research performed under this grant aims to develop a full, unified computational model of retinal processing, including spatial and temporal filtering, nonlinear transformations, and adaptation to local luminance and contrast, in complete populations of neurons. The model will be tested by comparing its predictions to data from large-scale multi-electrode recordings of primate retinal ganglion cells (RGCs), verifying that it can mimic known retinal responses, and critically, testing its ability to explain responses to natural visual images, including the effects of fixational and saccadic eye movements. The resulting model will provide a compact encapsulation of the "neural code" of the retina, which will serve as a substrate for understanding all subsequent visual processing in the brain. In addition, the model will provide an essential component in the development of high-acuity retinal prostheses for people blinded by diseases of photoreceptor degeneration. Finally, the model will offer a useful tool for the development and testing of new display technologies. |
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2015 — 2019 | Paninski, Liam Carloni, Luca (co-PI) [⬀] Shepard, Kenneth [⬀] |
N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
@ Columbia University Understanding how the brain works is arguably one of the most significant scientific challenges of our time and the focus of the BRAIN initiative. It is widely believed that neural circuit function is emergent, the result of complex interactions between constituents with individual neurons forming synaptic connections with thousands of other neurons. Mapping of these complex circuits has been virtually impossible because of the reliance on electrophysiological recordings which sample these networks extremely sparsely. These tools for extracellular spike recordings are only able to simultaneously record from several tens to a few hundred neurons. Raw signals from these recording electrodes are first filtered to remove out-of-band signals. Putative spike events are then detected and extracted. Finally, these snippets of time-series event are sorted, typically on the basis of waveform shapes, into clusters. Even at the very modest bandwidths for these systems, computing systems struggle to save the data and process the resulting data sets. Scalability of these measurement techniques by many orders of magnitude in recording density and channels will be essential to future progress in understanding neuron circuits. |
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2016 — 2018 | Paninski, Liam M Peterka, Darcy S [⬀] |
R21Activity Code Description: To encourage the development of new research activities in categorical program areas. (Support generally is restricted in level of support and in time.) |
Optimal Calcium Imaging With Shaped Excitation @ Columbia University Health Sciences Optimal calcium imaging with shaped excitation Understanding information flow in the brain is dependent on simultaneously recording the activity of large neuronal populations. It seems impossible to interrogate neurons serially, and still image large populations of neurons with high temporal resolution and high signal to noise. This is linked to the inverse relationship between volume scanned, and the signal collected per voxel, at fixed spatial and temporal resolution. However, this is not a hard limit. The goal of most functional imaging is to recover and assign activity signals from neurons; here we demonstrate that nearly all past approaches have dramatically oversampled spatially to create human-interpretable images. This is not necessary ? once the spatial footprints of the observed neurons are known, constrained non-negative matrix factorization methods can extract highly accurate temporal activity signals from very low spatial resolution movies. Reducing the number of samples required in imaging allows us to significantly speed up acquisition. In this proposal we introduce a new fast computational imaging method, leveraging modern computational demixing methods with simple optical hardware to increase imaging speeds by an order of magnitude. We proposed to use modern spatial light modulator systems to provide a flexible and powerful tool for optically implementing our proposed spatial downsampling approach, while taking better advantage of laser power and avoiding standard problems with diffraction- limited imaging caused by limited dwell times on the sample. The resulting combined hardware- software solution will be inexpensive, easy to implement and maintain, and widely applicable in the hundreds of labs currently using multi-photon imaging methods. Thus, the proposed approach will enable a critical leap towards achieving the goals of the BRAIN initiative. |
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2017 — 2019 | Paninski, Liam Cunningham, John (co-PI) [⬀] Miller, Kenneth (co-PI) [⬀] Abbott, Laurence Fusi, Stefano (co-PI) [⬀] |
N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Neuronex Theory Team: Columbia University Theoretical Neuroscience Center @ Columbia University Understanding how a healthy brain interprets sensory signals and guides actions, and why an unhealthy brain fails to perform these functions properly, is a profound and ambitious goal of 21st century science. Integrating knowledge of neural circuit function into a coherent picture of perception, cognition and action requires extraordinary cooperation and coordination between three research areas: experimentation, data analysis and modeling. The National Science Foundation Theory Team at Columbia University will unite exceptional resources in statistical data analysis and theoretical modeling with an extensive network of experimental collaborators to address the enormous challenges facing neuroscience. Never has the need been greater for theoretical insights and sophisticated data analysis. The field of neuroscience is facing a torrent of complex data from a system that is, itself, extraordinarily complex. Future progress requires developing the ability to extract knowledge and understanding from these data through analyses and modeling that capture the essence of what they mean. The goal of the NeuroNex Theory Team at Columbia is to establish, through the quality of its research, the excellence of its trainees, and the impact of its visitor, dissemination, and outreach programs, a new cooperative paradigm that will move neuroscience to unprecedented levels of discovery and understanding. |
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2018 — 2021 | Paninski, Liam M | U19Activity Code Description: To support a research program of multiple projects directed toward a specific major objective, basic theme or program goal, requiring a broadly based, multidisciplinary and often long-term approach. A cooperative agreement research program generally involves the organized efforts of large groups, members of which are conducting research projects designed to elucidate the various aspects of a specific objective. Substantial Federal programmatic staff involvement is intended to assist investigators during performance of the research activities, as defined in the terms and conditions of award. The investigators have primary authorities and responsibilities to define research objectives and approaches, and to plan, conduct, analyze, and publish results, interpretations and conclusions of their studies. Each research project is usually under the leadership of an established investigator in an area representing his/her special interest and competencies. Each project supported through this mechanism should contribute to or be directly related to the common theme of the total research effort. The award can provide support for certain basic shared resources, including clinical components, which facilitate the total research effort. These scientifically meritorious projects should demonstrate an essential element of unity and interdependence. |
@ Columbia University Health Sciences SUMMARY The major theme of this proposal is a tightly closed loop of experiment, theory, and data analysis. Sophisticated, scalable data science methods are a critical component of this loop. The Data Science Core serves two primary purposes. First, we will apply and refine sophisticated data analysis algorithms directly related to the project?s scientific goals. This project will generate massive streams of data from multiple recording and simulation modalities: whole-cell electrophysiology and anatomy, large-scale calcium imaging, spatiotemporally-complex optogenetic perturbations, RNA sequencing images, in addition to massive simulations of networks of spiking neurons. A correspondingly major effort is needed to manage this data, to distill it into new scientific knowledge, and to design new experiments, theoretical analyses, and simulations to close the theory-experiment-analysis loop. This will entail the application and iterative refinement of algorithms for preprocessing the data (e.g., taking calcium imaging video and extracting demixed and denoised neural activity from each cell visible in the field of view); aligning, registering, and performing statistical inferences on data across multiple modalities (e.g, calcium imaging, optogenetic stimulation, and seqFISH); functionally characterizing the stimulus preferences and correlation structure of the activity in the observed cells; and developing closed-loop optimal experimental design methods to obtain richer, more informative data. Second, this Core will build a collaborative infrastructure allowing the multiple laboratories in this project to act as one: sharing data and analysis tools, and closely integrating theorists and experimentalists. This infrastructure will: be completely open source; build on current efforts to standardize neuroscience data; be modular and extensible to allow for rapid iterative improvement of each stage of the algorithmic pipeline; enforce automatic archiving and recording of algorithmic metadata describing versioning and parameter choices for easy searchability and reproducibility; and allow for straightforward benchmarking. As we develop these practices and tools for data and analysis pipeline sharing, we will make them immediately available to the community. Thus we will provide a model platform for vastly improving reproducibility, keeping analysis pipelines up to date as improved methods are developed, and most importantly saving researchers from re- developing and re-implementing analysis software and data storage/sharing solutions. We aim to make it easy for groups of labs anywhere in the world to unite and crack large-scale neural circuits. This will transform the way neuroscience is done. |
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2019 — 2022 | Hobert, Oliver (co-PI) [⬀] Paninski, Liam Blumberg, Andrew Rabadan, Raul [⬀] |
N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
@ Columbia University The development of the nervous system, specifically the dynamics of neuronal development and wiring to build brain architecture and their constructive role in emergent brain activity, constitutes a central unexplained phenomenon in living systems. The study of developing brains requires a comprehensive and systematic characterization of the brain of an organism at different ages and a suitable mathematical framework, able to capture the structure of the growing nervous system and the emerging networks therein. We propose to address this fundamental challenge by developing such a mathematical framework capable of characterizing underlying network changes in living brains and their consequences for functional neural activity and resulting behavior. This mathematical framework will be applied to analyze the complete nervous system, at single-cell precision, of the model organism C. elegans. To address these important challenges, we have assembled an interdisciplinary team with expertise in topology, computational biology, statistics, theoretical physics, neuroscience and biology of the model organism. Our group will develop new mathematical, statistical, and computational tools to characterize the structure of developing brain networks. This analysis will reveal shared-organizational, emergent principles of nervous-system development and function. Based on the widespread representation of biological data as complex networks and the universality of the mathematical, statistical, and computational methods we will develop, we expect wide applicability beyond the original system. |
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