In vivo calcium imaging enables simultaneous recording of large neuronal ensembles engaged in complex operations. Many experiments require monitoring and identification of cell populations across multiple sessions. Population cell tracking across multiple sessions is complicated by non-rigid transformations induced by cell movement and imaging field shifts. We introduce SCOUT (Single-Cell spatiOtemporal longitUdinal Tracking), a fast, robust cell-tracking method utilizing multiple cell-cell similarity metrics, probabilistic inference, and an adaptive clustering methodology, to perform cell identification across multiple sessions. By comparing SCOUT with earlier cell-tracking algorithms on simulated, 1-photon, and 2-photon recordings, w...
Abstract — Automated visual-tracking of cell populations in vitro using phase contrast time-lapse mi...
Recent improvements in high performance fluorescent sensors and scientific CMOS cameras enable optic...
<div><p>We discuss methods for fast spatiotemporal smoothing of calcium signals in dendritic trees, ...
In vivo calcium imaging enables simultaneous recording of large neuronal ensembles engaged in c...
Identifying and tracking cell location in long-term longitudinal studies is critical for identifying...
Summary: Ca2+ imaging techniques permit time-lapse recordings of neuronal activity from large popula...
SummaryRecent advances in fluorescence imaging permit studies of Ca2+ dynamics in large numbers of c...
To understand how networks of neurons process information, it is essential to monitor their activity...
Accurate tracking of the same neurons across multiple days is crucial for studying changes in neuron...
Understanding the mechanisms that control critical biological events of neural cell populations, suc...
Cell tracking is a key task in the high-throughput quantitative study of important biological proces...
We present an algorithm for detecting the location of cells from two-photon calcium imaging data. In...
Understanding the mechanisms that control critical biological events of neural cell populations, suc...
We have developed methods for segmentation and track-ing of cells in time-lapse phase-contrast micro...
In vivo two-photon calcium imaging is a powerful approach in neuroscience. However, processing two-p...
Abstract — Automated visual-tracking of cell populations in vitro using phase contrast time-lapse mi...
Recent improvements in high performance fluorescent sensors and scientific CMOS cameras enable optic...
<div><p>We discuss methods for fast spatiotemporal smoothing of calcium signals in dendritic trees, ...
In vivo calcium imaging enables simultaneous recording of large neuronal ensembles engaged in c...
Identifying and tracking cell location in long-term longitudinal studies is critical for identifying...
Summary: Ca2+ imaging techniques permit time-lapse recordings of neuronal activity from large popula...
SummaryRecent advances in fluorescence imaging permit studies of Ca2+ dynamics in large numbers of c...
To understand how networks of neurons process information, it is essential to monitor their activity...
Accurate tracking of the same neurons across multiple days is crucial for studying changes in neuron...
Understanding the mechanisms that control critical biological events of neural cell populations, suc...
Cell tracking is a key task in the high-throughput quantitative study of important biological proces...
We present an algorithm for detecting the location of cells from two-photon calcium imaging data. In...
Understanding the mechanisms that control critical biological events of neural cell populations, suc...
We have developed methods for segmentation and track-ing of cells in time-lapse phase-contrast micro...
In vivo two-photon calcium imaging is a powerful approach in neuroscience. However, processing two-p...
Abstract — Automated visual-tracking of cell populations in vitro using phase contrast time-lapse mi...
Recent improvements in high performance fluorescent sensors and scientific CMOS cameras enable optic...
<div><p>We discuss methods for fast spatiotemporal smoothing of calcium signals in dendritic trees, ...