Version history

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

  1. Live e8ce2f808ea7
    5/17/2026, 4:35:28 PM
    Content snapshot
    {
      "scope": "mouse, GE (E13.5 MGE / E14.5 CGE+LGE) → P10 cortex scRNA-seq",
      "claim_text": "Postmitotic ganglionic-eminence cells diverge into transcriptionally distinct precursor states corresponding to non-overlapping cardinal interneuron classes (Pvalb, Sst, Vip, Id2, Th, Nos1, Igfbp6), with Vip and Id2 cardinal markers (Vip/Synpr/Igf1, Reln/Mpped1/Id2) becoming statistically detectable by E18.5.",
      "raw_fields": {
        "n": null,
        "doi": "10.1038/nature25999",
        "claim": "Postmitotic ganglionic-eminence cells diverge into transcriptionally distinct precursor states corresponding to non-overlapping cardinal interneuron classes (Pvalb, Sst, Vip, Id2, Th, Nos1, Igfbp6), with Vip and Id2 cardinal markers (Vip/Synpr/Igf1, Reln/Mpped1/Id2) becoming statistically detectable by E18.5.",
        "title": null,
        "cite_key": "Mayer2018",
        "evidence": "Single-cell RNA-seq across mouse developmental timecourse, integrated MGE (E13.5)+CGE/LGE (E14.5) progenitors with postnatal P10 reference; cardinal-type segregation of Sst-Martinotti vs non-Martinotti, Vip bipolar vs multipolar visible by P10.",
        "effect_size": "7 cardinal classes; Vip-cardinal markers detectable by E18.5; clear bipolar vs multipolar Vip segregation by P10",
        "figure_data": [
          {
            "type": "developmental_marker_emergence",
            "unit": "embryonic day",
            "value": 18.5,
            "metric": "earliest E-stage with statistically conserved Vip cardinal markers",
            "source": "Mayer Fig.4 / Ext.Data Fig.7-9",
            "context": "Vip markers Vip/Synpr/Igf1; Id2 markers Reln/Mpped1/Id2"
          }
        ],
        "text_access": "fulltext",
        "study_system": "mouse, GE (E13.5 MGE / E14.5 CGE+LGE) → P10 cortex scRNA-seq",
        "_source_cluster": "cluster_02_development_lineage",
        "replication_status": "primary",
        "_source_cluster_index": 81,
        "claim_source_sentence": "These could be allocated into non-overlapping cardinal types of cortical interneurons (Pvalb, Sst, Vip, Id2, Th, Nos1, Igfbp6). A minority of E13.5 cells also mapped to Vip and Id2 subsets, but conserved transcriptomic markers did not pass statistical significance until E18.5 (E18.5 markers of Vip neurons: Vip , Synpr , Igf1 ; E18.5 markers of Id2 neurons: Reln , Mpped1, Id2 ).",
        "replication_evidence_dois": [
          "10.1038/nature25980"
        ],
        "effect_size_source_sentence": "Based on this alignment, P10 cells exhibited strong evidence of transcriptomic separation beyond cardinal types, ( Fig. 4B ), including clear segregation between Sst Martinotti versus non-Martinotti (X94), Vip bipolar versus multipolar, and Id2 neurogliaform versus non-neurogliaform interneuron subtypes ( Fig. 4E ; Extended Data Fig. 7 – 9 )."
      },
      "section_id": "section_03",
      "source_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewVIP/blob/95e761177f7d2ec565983d3307c14ec238f9677c/evidence/section_03_evidence_package.json",
      "effect_size": "7 cardinal classes; Vip-cardinal markers detectable by E18.5; clear bipolar vs multipolar Vip segregation by P10",
      "review_repo": "ComputationalReviewVIP",
      "section_ref": "wiki_page:computationalreviewvip-03-development",
      "source_kind": "review_finding",
      "source_path": "evidence/section_03_evidence_package.json",
      "source_refs": [
        "paper:paper-c3e9fd7af6d3"
      ],
      "source_span": "These could be allocated into non-overlapping cardinal types of cortical interneurons (Pvalb, Sst, Vip, Id2, Th, Nos1, Igfbp6). A minority of E13.5 cells also mapped to Vip and Id2 subsets, but conserved transcriptomic markers did not pass statistical significance until E18.5 (E18.5 markers of Vip neurons: Vip , Synpr , Igf1 ; E18.5 markers of Id2 neurons: Reln , Mpped1, Id2 ).",
      "study_system": "mouse, GE (E13.5 MGE / E14.5 CGE+LGE) → P10 cortex scRNA-seq",
      "evidence_refs": [
        {
          "ref": "paper:paper-c3e9fd7af6d3"
        }
      ],
      "section_title": "Developmental Origins and Postnatal Maturation",
      "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": "95e761177f7d2ec565983d3307c14ec238f9677c",
        "source_repository_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewVIP"
      },
      "evidence_summary": "Single-cell RNA-seq across mouse developmental timecourse, integrated MGE (E13.5)+CGE/LGE (E14.5) progenitors with postnatal P10 reference; cardinal-type segregation of Sst-Martinotti vs non-Martinotti, Vip bipolar vs multipolar visible by P10.",
      "review_bundle_ref": "analysis_bundle:ab-2ce40c33e827",
      "replication_status": "primary",
      "review_package_ref": "analysis_bundle:ab-2ce40c33e827",
      "source_artifact_ref": "wiki_page:computationalreviewvip-03-development",
      "origin_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewVIP/blob/95e761177f7d2ec565983d3307c14ec238f9677c/evidence/section_03_evidence_package.json",
      "commit_sha": "95e761177f7d2ec565983d3307c14ec238f9677c",
      "created_by": "persona-jerome-lecoq-gbo-neuroscience",
      "repository_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewVIP"
    }