Version history

12 versions on record. Newest first; the live version sits at the top with a live indicator.

  1. Live
    4/27/2026, 2:59:17 PM
    Content snapshot
    {
      "question": "What cell types are most vulnerable in Alzheimers Disease based on SEA-AD transcriptomic data from the Allen Brain Cell Atlas? Identify mechanisms of cell-type-specific vulnerability in neurons, microglia, astrocytes, and oligodendrocytes. Focus on gene expression patterns, pathway dysregulation, and therapeutic implications.",
      "domain": "neurodegeneration",
      "status": "completed",
      "triggered_by": "autonomous",
      "gap_id": "gap-seaad-v4-20260402065846",
      "world_model_rank": 0.738471,
      "kg_impact_score": 346.5,
      "completed_at": "2026-04-03T16:33:37.274852-07:00",
      "report_url": "/analyses/sda-2026-04-03-gap-seaad-v4-20260402065846.html",
      "reproducibility_class": "observational"
    }
  2. v11
    4/3/2026, 4:33:37 PM
    Content snapshot
    {
      "question": "What cell types are most vulnerable in Alzheimers Disease based on SEA-AD transcriptomic data from the Allen Brain Cell Atlas? Identify mechanisms of cell-type-specific vulnerability in neurons, microglia, astrocytes, and oligodendrocytes. Focus on gene expression patterns, pathway dysregulation, and therapeutic implications.",
      "domain": "neurodegeneration",
      "status": "completed",
      "triggered_by": "autonomous",
      "gap_id": "gap-seaad-v4-20260402065846",
      "completed_at": "2026-04-03T16:33:37.274852-07:00",
      "report_url": "/analyses/sda-2026-04-03-gap-seaad-v4-20260402065846.html"
    }
  3. v10
    4/3/2026, 4:33:37 PM
    Content snapshot
    {
      "question": "What cell types are most vulnerable in Alzheimers Disease based on SEA-AD transcriptomic data from the Allen Brain Cell Atlas? Identify mechanisms of cell-type-specific vulnerability in neurons, microglia, astrocytes, and oligodendrocytes. Focus on gene expression patterns, pathway dysregulation, and therapeutic implications.",
      "domain": "neurodegeneration",
      "status": "completed",
      "triggered_by": "autonomous",
      "gap_id": "gap-seaad-v4-20260402065846",
      "completed_at": "2026-04-03T16:33:37.274852-07:00",
      "report_url": "/analyses/sda-2026-04-03-gap-seaad-v4-20260402065846.html"
    }
  4. v9
    4/3/2026, 4:33:37 PM
    Content snapshot
    {
      "question": "What cell types are most vulnerable in Alzheimers Disease based on SEA-AD transcriptomic data from the Allen Brain Cell Atlas? Identify mechanisms of cell-type-specific vulnerability in neurons, microglia, astrocytes, and oligodendrocytes. Focus on gene expression patterns, pathway dysregulation, and therapeutic implications.",
      "domain": "neurodegeneration",
      "status": "completed",
      "triggered_by": "autonomous",
      "gap_id": "gap-seaad-v4-20260402065846",
      "completed_at": "2026-04-03T16:33:37.274852-07:00",
      "report_url": "/analyses/sda-2026-04-03-gap-seaad-v4-20260402065846.html"
    }
  5. v8
    4/3/2026, 4:33:37 PM
    Content snapshot
    {
      "question": "What cell types are most vulnerable in Alzheimers Disease based on SEA-AD transcriptomic data from the Allen Brain Cell Atlas? Identify mechanisms of cell-type-specific vulnerability in neurons, microglia, astrocytes, and oligodendrocytes. Focus on gene expression patterns, pathway dysregulation, and therapeutic implications.",
      "domain": "neurodegeneration",
      "status": "completed",
      "triggered_by": "autonomous",
      "gap_id": "gap-seaad-v4-20260402065846",
      "completed_at": "2026-04-03T16:33:37.274852-07:00",
      "report_url": "/analyses/sda-2026-04-03-gap-seaad-v4-20260402065846.html"
    }
  6. v7
    4/3/2026, 4:33:37 PM
    Content snapshot
    {
      "question": "What cell types are most vulnerable in Alzheimers Disease based on SEA-AD transcriptomic data from the Allen Brain Cell Atlas? Identify mechanisms of cell-type-specific vulnerability in neurons, microglia, astrocytes, and oligodendrocytes. Focus on gene expression patterns, pathway dysregulation, and therapeutic implications.",
      "domain": "neurodegeneration",
      "status": "completed",
      "triggered_by": "autonomous",
      "gap_id": "gap-seaad-v4-20260402065846",
      "completed_at": "2026-04-03T16:33:37.274852-07:00",
      "report_url": "/analyses/sda-2026-04-03-gap-seaad-v4-20260402065846.html"
    }
  7. v6
    4/3/2026, 4:33:37 PM
    Content snapshot
    {
      "question": "What cell types are most vulnerable in Alzheimers Disease based on SEA-AD transcriptomic data from the Allen Brain Cell Atlas? Identify mechanisms of cell-type-specific vulnerability in neurons, microglia, astrocytes, and oligodendrocytes. Focus on gene expression patterns, pathway dysregulation, and therapeutic implications.",
      "domain": "neurodegeneration",
      "status": "completed",
      "triggered_by": "autonomous",
      "gap_id": "gap-seaad-v4-20260402065846",
      "completed_at": "2026-04-03T16:33:37.274852-07:00",
      "report_url": "/analyses/sda-2026-04-03-gap-seaad-v4-20260402065846.html"
    }
  8. v5
    4/3/2026, 4:33:37 PM
    Content snapshot
    {
      "question": "What cell types are most vulnerable in Alzheimers Disease based on SEA-AD transcriptomic data from the Allen Brain Cell Atlas? Identify mechanisms of cell-type-specific vulnerability in neurons, microglia, astrocytes, and oligodendrocytes. Focus on gene expression patterns, pathway dysregulation, and therapeutic implications.",
      "domain": "neurodegeneration",
      "status": "completed",
      "triggered_by": "autonomous",
      "gap_id": "gap-seaad-v4-20260402065846",
      "completed_at": "2026-04-03T16:33:37.274852-07:00",
      "report_url": "/analyses/sda-2026-04-03-gap-seaad-v4-20260402065846.html"
    }
  9. v4
    4/3/2026, 4:33:37 PM
    Content snapshot
    {
      "question": "What cell types are most vulnerable in Alzheimers Disease based on SEA-AD transcriptomic data from the Allen Brain Cell Atlas? Identify mechanisms of cell-type-specific vulnerability in neurons, microglia, astrocytes, and oligodendrocytes. Focus on gene expression patterns, pathway dysregulation, and therapeutic implications.",
      "domain": "neurodegeneration",
      "status": "completed",
      "triggered_by": "autonomous",
      "gap_id": "gap-seaad-v4-20260402065846",
      "completed_at": "2026-04-03T16:33:37.274852-07:00",
      "report_url": "/analyses/sda-2026-04-03-gap-seaad-v4-20260402065846.html"
    }
  10. v3
    4/3/2026, 4:33:37 PM
    Content snapshot
    {
      "question": "What cell types are most vulnerable in Alzheimers Disease based on SEA-AD transcriptomic data from the Allen Brain Cell Atlas? Identify mechanisms of cell-type-specific vulnerability in neurons, microglia, astrocytes, and oligodendrocytes. Focus on gene expression patterns, pathway dysregulation, and therapeutic implications.",
      "domain": "neurodegeneration",
      "status": "completed",
      "triggered_by": "autonomous",
      "gap_id": "gap-seaad-v4-20260402065846",
      "completed_at": "2026-04-03T16:33:37.274852-07:00",
      "report_url": "/analyses/sda-2026-04-03-gap-seaad-v4-20260402065846.html"
    }
  11. v2
    4/3/2026, 4:33:37 PM
    Content snapshot
    {
      "question": "What cell types are most vulnerable in Alzheimers Disease based on SEA-AD transcriptomic data from the Allen Brain Cell Atlas? Identify mechanisms of cell-type-specific vulnerability in neurons, microglia, astrocytes, and oligodendrocytes. Focus on gene expression patterns, pathway dysregulation, and therapeutic implications.",
      "domain": "neurodegeneration",
      "status": "completed",
      "triggered_by": "autonomous",
      "gap_id": "gap-seaad-v4-20260402065846",
      "completed_at": "2026-04-03T16:33:37.274852-07:00",
      "report_url": "/analyses/sda-2026-04-03-gap-seaad-v4-20260402065846.html"
    }
  12. v1
    4/3/2026, 4:33:37 PM
    Content snapshot
    {
      "question": "What cell types are most vulnerable in Alzheimers Disease based on SEA-AD transcriptomic data from the Allen Brain Cell Atlas? Identify mechanisms of cell-type-specific vulnerability in neurons, microglia, astrocytes, and oligodendrocytes. Focus on gene expression patterns, pathway dysregulation, and therapeutic implications.",
      "domain": "neurodegeneration",
      "status": "completed",
      "triggered_by": "autonomous",
      "gap_id": "gap-seaad-v4-20260402065846",
      "completed_at": "2026-04-03T16:33:37.274852-07:00",
      "report_url": "/analyses/sda-2026-04-03-gap-seaad-v4-20260402065846.html"
    }