A: Spatial footprints of cells. Should have dimensions (“unit_id”, “height”, “width”). --> image_masks
C: Temporal components of cells. Should have dimensions “frame” and “unit_id”. --> roi_response_denoised
b: Spatial footprint of background. Should have dimensions (“height”, “width”). --> background_image_masks
f: Temporal dynamic of background. Should have dimension “frame”. --> roi_response_neuropil
b0: Baseline fluorescence for each cell. Should have dimensions (“frame”, “unit_id”) and same shape as C --> roi_response_baseline
c0: Initial calcium decay, in theory triggered by calcium events happened before the recording starts. Should have dimensions (“frame”, “unit_id”) and same shape as C
S: Deconvolved spikes for each cell. Should have dimensions (“frame”, “unit_id”) and same shape as C --> roi_response_deconvolved
max_proj: the maximum projection --> summary_image
Add segmentation extractor for Minian output. Supported output format: Zarr (for now) Similarly to Caiman uses CNMF to perform cell identification.
Output structure (example):
image_masks
roi_response_denoised
background_image_masks
roi_response_neuropil
roi_response_baseline
roi_response_deconvolved
summary_image
TODOs