Details

scope
Fluorescence imaging (calcium and voltage) across awake behaving mammals, primarily mouse cortex
section_id
section_15
source_url
https://github.com/AllenNeuralDynamics/ComputationalReviewRecurrence/blob/79ce062d54a924ce05953ec90aa9d26044d2b48f/evidence/section_15_evidence_package.json
review_repo
ComputationalReviewRecurrence
section_ref
wiki_page:computationalreviewrecurrence-15-methods-limits
source_kind
review_finding
source_path
evidence/section_15_evidence_package.json
study_system
Fluorescence imaging (calcium and voltage) across awake behaving mammals, primarily mouse cortex
evidence_summary
Comprehensive review framing the methodological landscape of mouse-cortex imaging and its limits.
review_bundle_ref
analysis_bundle:ab-d9c479db9be9
replication_status
single-study
review_package_ref
analysis_bundle:ab-d9c479db9be9
source_artifact_ref
wiki_page:computationalreviewrecurrence-15-methods-limits
origin_url
https://github.com/AllenNeuralDynamics/ComputationalReviewRecurrence/blob/79ce062d54a924ce05953ec90aa9d26044d2b48f/evidence/section_15_evidence_package.json
commit_sha
79ce062d54a924ce05953ec90aa9d26044d2b48f
created_by
persona-jerome-lecoq-gbo-neuroscience
repository_url
https://github.com/AllenNeuralDynamics/ComputationalReviewRecurrence
Raw fields (7)
claim_text
Recent fluorescence imaging advances allow observation of the dynamics of thousands of individual neurons across multiple brain areas for extended durations in awake behaving mammals, with calcium imaging providing area-interaction tracking at cellular resolution and high-speed voltage imaging revealing spiking patterns of targeted cell types.
raw_fields
{
  "n": 0,
  "doi": "10.1016/j.cell.2021.12.007",
  "claim": "Recent fluorescence imaging advances allow observation of the dynamics of thousands of individual neurons across multiple brain areas for extended durations in awake behaving mammals, with calcium imaging providing area-interaction tracking at cellular resolution and high-speed voltage imaging revealing spiking patterns of targeted cell types.",
  "cite_key": "Kim2022",
  "evidence": "Comprehensive review framing the methodological landscape of mouse-cortex imaging and its limits.",
  "effect_size": null,
  "text_access": "abstract_only",
  "study_system": "Fluorescence imaging (calcium and voltage) across awake behaving mammals, primarily mouse cortex",
  "argument_role": "supporting",
  "replication_status": "single-study",
  "claim_source_sentence": "Recent progress in fluorescence imaging allows neuroscientists to observe the dynamics of thousands of individual neurons, identified genetically or by their connectivity, across multiple brain areas and for extended durations in awake behaving mammals.",
  "source_provenance_status": "non_substring_match",
  "replication_evidence_dois": [],
  "effect_size_source_sentence": null
}
source_refs
[
  "paper:paper-89a449ba5293"
]
source_span
Recent progress in fluorescence imaging allows neuroscientists to observe the dynamics of thousands of individual neurons, identified genetically or by their connectivity, across multiple brain areas and for extended durations in awake behaving mammals.
evidence_refs
[
  {
    "ref": "paper:paper-89a449ba5293"
  }
]
section_title
15. Methodological limits and emerging tools — what current mouse-cortex tools cannot yet measure about E→E recurrence (subthreshold network activity, fast plasticity in vivo, millimetre-scale dynamic connectomes), and what is on the near horizon
source_policy
{
  "mode": "public_source_pointer_with_short_context",
  "notes": [
    "Local review repositories are read-only inputs.",
    "SciDEX stores paper metadata, structured evidence, file pointers, and short citation contexts; it does not copy full review prose."
  ],
  "source_commit_sha": "79ce062d54a924ce05953ec90aa9d26044d2b48f",
  "source_repository_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewRecurrence"
}

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