GraFT: Graph Filtered Temporal Dictionary Learning for Functional Neural Imaging

被引:8
作者
Charles, Adam S. [1 ,2 ,3 ]
Cermak, Nathan [4 ]
Affan, Rifqi O. [5 ]
Scott, Benjamin B. [5 ]
Schiller, Jackie [4 ]
Mishne, Gal [6 ,7 ]
机构
[1] Kavli Neurosci Discovery Inst, Dept Biomed Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Ctr Imaging Sci, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Math Inst Data Sci, Baltimore, MD 21287 USA
[4] Technion Israel Inst Technol, IL-31096 Haifa, Israel
[5] Boston Univ, Dept Psychol & Brain Sci, Boston, MA 02215 USA
[6] Halicioglu Data Sci Inst, La Jolla, CA 92093 USA
[7] Univ Calif San Diego, Neurosci Grad Program, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
Imaging; Calcium; Dictionaries; Machine learning; Shape; Neurons; Optical imaging; Dictionary learning; sparse coding; calcium imaging; two-photon microscopy; re-weighted l1; DIMENSIONALITY REDUCTION; FLUORESCENCE MICROSCOPY; 2-PHOTON; BRAIN; ALGORITHM; SIGNALS; FIELD;
D O I
10.1109/TIP.2022.3171414
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Optical imaging of calcium signals in the brain has enabled researchers to observe the activity of hundreds-to-thousands of individual neurons simultaneously. Current methods predominantly use morphological information, typically focusing on expected shapes of cell bodies, to better identify neurons in the field-of-view. The explicit shape constraints limit the applicability of automated cell identification to other important imaging scales with more complex morphologies, e.g., dendritic or widefield imaging. Specifically, fluorescing components may be broken up, incompletely found, or merged in ways that do not accurately describe the underlying neural activity. Here we present Graph Filtered Temporal Dictionary (GraFT), a new approach that frames the problem of isolating independent fluorescing components as a dictionary learning problem. Specifically, we focus on the time-traces-the main quantity used in scientific discovery-and learn a time trace dictionary with the spatial maps acting as the presence coefficients encoding which pixels the time-traces are active in. Furthermore, we present a novel graph filtering model which redefines connectivity between pixels in terms of their shared temporal activity, rather than spatial proximity. This model greatly eases the ability of our method to handle data with complex non-local spatial structure. We demonstrate important properties of our method, such as robustness to morphology, simultaneously detecting different neuronal types, and implicitly inferring number of neurons, on both synthetic data and real data examples. Specifically, we demonstrate applications of our method to calcium imaging both at the dendritic, somatic, and widefield scales.
引用
收藏
页码:3509 / 3524
页数:16
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