metadata.yaml

about:
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  name: rostrolateral visual area
  schemaKey: Anatomy
- identifier: http://purl.obolibrary.org/obo/UBERON_0035894
  name: anterolateral visual area
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- identifier: http://purl.obolibrary.org/obo/UBERON_0002436
  name: primary visual cortex
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acknowledgement: Supported by Intelligence Advanced Research Projects Activity (IARPA)
  via Department of Interior/ Interior Business Center (DoI/IBC) contract numbers
  D16PC00003, D16PC00004, and D16PC0005. NIH/NINDS U19 NS104648, NIH/NEI R01 EY027036,
  NIH/NIMH U01 MH114824, NIH/NIMH U01 MH117072 NIH/NINDS R01 NS104926, NIH/NIMH RF1
  MH117815, NIH/NIMH RF1 MH123400, Mathers Foundation, NSF CAREER grant IOS-1552868,
  NSF NeuroNex grant 1707400, National Institute of Mental Health and National Institute
  of Neurological Disorders And Stroke under Award Number U19MH114830.
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  species:
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  variableMeasured:
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  Yu, Szi-chieh (2023) MICrONS Two Photon Functional Imaging (Version 0.230307.2132)
  [Data set]. DANDI archive. https://doi.org/10.48324/dandi.000402/0.230307.2132"
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dateCreated: '2023-01-04T10:47:01.770484+00:00'
datePublished: '2023-03-07T21:32:06.168531+00:00'
description: "The light microscopic images were acquired from a cubic millimeter volume
  that spanned portions of primary visual cortex and three higher visual cortical
  areas. The volume was imaged in vivo by two-photon random access mesoscope (2P-RAM)
  from postnatal days P75 to P81 in a male mouse expressing a genetically encoded
  calcium indicator in excitatory cells, while the mouse viewed natural movies and
  parametric stimuli. The calcium imaging data includes the single-cell responses
  of an estimated 75,000 pyramidal cells imaged over a volume of approximately 1200
  x 1100 x 500 \u03BCm3 (anteroposterior x mediolateral x radial depth). The center
  of the volume was placed at the junction of primary visual cortex (VISp) and three
  higher visual areas, lateromedial area (VISlm), rostrolateral area (VISrl) and anterolateral
  area (VISal). During imaging, the animal was head-restrained, and the stimulus was
  presented to the left visual field. Treadmill rotation (single axis) and video of
  the animal's left eye were captured throughout the scan, yielding the locomotion
  velocity, eye movements, and pupil diameter data included here.\n\nThe functional
  data were co-registered with electron microscopy (EM) data. The structural identifiers
  of the matched cells are added as plane segmentation columns extracted from the
  CAVE database. To access the latest revision see the notebook that is linked to
  this dandiset. The structural ids might not be present for all plane segmentations."
doi: 10.48324/dandi.000402/0.230307.2132
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name: MICrONS Two Photon Functional Imaging
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