Abdelaal et al. 2019 inter-dataset brain comparison: VISp/ALM/MTG, 34-population annotation (Figure S10 Panel B)
Genuine INTER-dataset (cross-dataset, cross-species where applicable) evaluation: three brain datasets — VISp (mouse, primary visual cortex), ALM (mouse, anterior lateral motor area), MTG (human, middle temporal gyrus) — all SMART-Seq v4. VISp and ALM share GSE115746. MTG is a separate human single-nucleus dataset; combinations involving MTG include cross-species data. Some two-dataset training combinations still share the mouse study with the test dataset, so independent-study holdout must not be inferred for all nine combinations. Methods, quoted verbatim: "We used the three brain datasets, VISp, ALM, and MTG with two levels of annotations, 3 and 34 cell populations. We tested all possible train-test combinations, by either using one dataset to train and test on another (6 experiments) or using two concatenated datasets to train and test on the third (3 experiments). A total of 9 experiments[...]." This protocol scopes the deeper, 34-cell-population annotation level (Figure S10 Panel B); the separate 3-population major-lineage level (Figure S10 Panel A) is a different protocol and is not ingested here. Percentage of cells left "unlabeled" (rejected) is reported per classifier per train-test combination; this protocol ingests only the SVMrejection row (9 values), a conventional rejection-option baseline, as a bounded, coherent subset — not the other 17 classifiers shown in the same figure.
Overview
Genuine INTER-dataset (cross-dataset, cross-species where applicable) evaluation: three brain datasets — VISp (mouse, primary visual cortex), ALM (mouse, anterior lateral motor area), MTG (human, middle temporal gyrus) — all SMART-Seq v4. VISp and ALM share GSE115746. MTG is a separate human single-nucleus dataset; combinations involving MTG include cross-species data. Some two-dataset training combinations still share the mouse study with the test dataset, so independent-study holdout must not be inferred for all nine combinations. Methods, quoted verbatim: "We used the three brain datasets, VISp, ALM, and MTG with two levels of annotations, 3 and 34 cell populations. We tested all possible train-test combinations, by either using one dataset to train and test on another (6 experiments) or using two concatenated datasets to train and test on the third (3 experiments). A total of 9 experiments[...]." This protocol scopes the deeper, 34-cell-population annotation level (Figure S10 Panel B); the separate 3-population major-lineage level (Figure S10 Panel A) is a different protocol and is not ingested here. Percentage of cells left "unlabeled" (rejected) is reported per classifier per train-test combination; this protocol ingests only the SVMrejection row (9 values), a conventional rejection-option baseline, as a bounded, coherent subset — not the other 17 classifiers shown in the same figure.
Consult the linked sources for architecture or protocol details. Missing evidence is not evidence of a missing capability.
9 recorded evaluations, 9 metric rows. A comparison chart has not yet been validated for these results. The table retains the individual findings and their sources.
Results
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9 evaluations · 9 results. Different protocols are not a single leaderboard.
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Source checking is not independent reproduction. Release 2026-10-07-e11db1d1c586.
Methods and evaluation design
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Recorded evaluations
Each evaluation records what was tested and under which conditions.
- abdelaal brain svmrejection test=ALM train=MTG
- abdelaal brain svmrejection test=ALM train=VISp
- abdelaal brain svmrejection test=ALM train=VISp & MTG (concatenated)
- abdelaal brain svmrejection test=MTG train=ALM
- abdelaal brain svmrejection test=MTG train=VISp
- abdelaal brain svmrejection test=MTG train=VISp & ALM (concatenated)
- abdelaal brain svmrejection test=VISp train=ALM
- abdelaal brain svmrejection test=VISp train=ALM & MTG (concatenated)
- abdelaal brain svmrejection test=VISp train=MTG
Baseline coverage
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- Author-reported evaluations
- 9
Literature evidence is not a Rewire measurement. Executed but unpublished runs and private review status are not included.
Null control
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Regularised classifier on simple permitted features, or protocol's conventional reference
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Coverage is derived from release 2026-10-07-e11db1d1c586. Source citations describe the original records; they do not validate an unreviewed baseline proposal. No results have been generated by this audit.
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Sources and history
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Release 2026-10-07-e11db1d1c586 · Record review: source checked
2 source records and release history
- A comparison of automatic cell identification methods for single-cell RNA sequencing data · Original source · 10.1186/s13059-019-1795-z; published article XML
- A comparison of automatic cell identification methods for single-cell RNA sequencing data — Additional File 1 (Supplementary Data) · Original source · 10.1186/s13059-019-1795-z; Additional File 1 (Supplementary Data PDF)
Technical metadata and extraction receipts
Stable ID: ucc-research-protocol-abdelaal-brain-inter-34pop
- review
- method: automated_source_review; actor: Claude Sonnet cell-type-annotation-transfer evidence-research worker; reviewed at: 2026-10-07T07:44:08Z; note: Source-backed transcription of Abdelaal et al. 2019 Additional File 1 (Supplementary Data PDF), a separate byte artifact from the already-catalogued main-text XML. Originally retrieved 2026-10-06T21:17:27Z via the Springer/BMC static-content route (https://static-content.springer.com/esm/art%3A10.1186%2Fs13059-019-1795-z/MediaObjects/13059_2019_1795_MOESM1_ESM.pdf), HTTP 200, 13,495,279 bytes. Re-verified byte-identical (SHA-256 unchanged) in this pass against the cached copy in the neighboring cell-type-evidence-20261006 worktree before archiving. Figure S10 (page 15 of 18) read directly from a pdftoppm image render at 2400 dpi (not OCR, not color inference); Panel B's printed numeric cell values independently re-confirmed against the original PDF by a separate reviewer prior to this ingestion. No new model execution, independent experimental replication, or qualified human scientific review.
- source locator
- Methods, "Brain" (train-test design, main-text XML); Figure S10, Panel B caption and heatmap (Additional File 1, page 15 of 18)
- limitations
- This is a conventional rejection-option BASELINE result only: the percentage of test-set cells SVMrejection declined to label. It is NOT a known-type accuracy claim, NOT an unknown/absent-type-detection accuracy claim, and NOT a claim that SVMrejection outperforms or underperforms any other classifier — no comparison across methods is asserted by this protocol or its results.; The scored denominator (exact number of cells actually scored in each individual train-test experiment) is UNREPORTED in the retrieved main text and supplement. Table 2's raw per-dataset cell counts (VISp 12,832; ALM 8,758; MTG 14,636) are recorded on the linked dataset records as context only, not as a confirmed denominator, and must not be used to back-calculate an implied rejected-cell count.; metric_direction is recorded as "unknown" for every result under this protocol: percentage unlabeled is a coverage/rejection-rate figure, not a standalone performance metric with one universal better/worse direction; it depends on context (e.g., the correctness of the calls a classifier would otherwise have made) not captured by this figure alone.; Only the SVMrejection row (9 values: 6 single-dataset-train + 3 two-dataset-train combinations) is ingested; the other 17 classifiers shown in the same Figure S10 Panel B heatmap are not ingested in this pass.; Figure S10 Panel A (3-population major-lineage level) is a separate figure/protocol and is not ingested here.; Figure S9 Panel A (PBMC, train-test median-F1/implied-unlabeled heatmap) carries no printed digit labels in the retrieved PDF at any resolution checked (up to 4800 dpi), and separately shows a source-internal conflict between its own caption text ("median F1-score"), the page's only legend ("Unlabeled (%)"), and the figure's overall title ("Percentage of unlabeled cells"); neither is resolved, and nothing from Figure S9 Panel A is ingested.; Reference labels are the original brain-atlas studies' author-assigned cell-population annotations, not independently adjudicated ground truth.; VISp and ALM share GSE115746. MTG is a separate human single-nucleus dataset; combinations involving MTG include cross-species data. Some two-dataset training combinations still share the mouse study with the test dataset, so independent-study holdout must not be inferred for all nine combinations.; Automated source review only; independent human scientific review remains outstanding.
Related records
- dataset: VISp brain single-cell RNA-seq (scRNA-seq) dataset (Abdelaal et al. 2019, Table 2)
- dataset: ALM brain single-cell RNA-seq (scRNA-seq) dataset (Abdelaal et al. 2019, Table 2)
- dataset: MTG brain single-nucleus RNA-seq (snRNA-seq) dataset (Abdelaal et al. 2019, Table 2)
- protocol: abdelaal brain svmrejection test=ALM train=MTG
- protocol: abdelaal brain svmrejection test=ALM train=VISp
- protocol: abdelaal brain svmrejection test=ALM train=VISp & MTG (concatenated)
- protocol: abdelaal brain svmrejection test=MTG train=ALM
- protocol: abdelaal brain svmrejection test=MTG train=VISp
- protocol: abdelaal brain svmrejection test=MTG train=VISp & ALM (concatenated)
- protocol: abdelaal brain svmrejection test=VISp train=ALM
- protocol: abdelaal brain svmrejection test=VISp train=ALM & MTG (concatenated)
- protocol: abdelaal brain svmrejection test=VISp train=MTG