rewirebio.iobenchmarks
Protocol

All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)

Per-algorithm TP, FP, FN, TPR, PPV and F1 for all fusions on conventional RNA-seq.

12 evaluations · 72 results

Overview

Per-algorithm TP, FP, FN, TPR, PPV and F1 for all fusions on conventional RNA-seq.

Consult the linked sources for architecture or protocol details. Missing evidence is not evidence of a missing capability.

12 recorded evaluations, 72 metric rows. A comparison chart has not yet been validated for these results. The table retains the individual findings and their sources.

View coverage and remaining gaps across all benchmarks

Results

Results are available, but no reviewed comparison panel is linked in this release.

All evaluations

12 evaluations · 72 results. Different protocols are not a single leaderboard.

Filter evaluations

Applied filters: All linked evaluations

Exact evaluated configurations and original reported results
Tested configurationProtocol and datasetFindingEvidence and details
Configuration: Arriba v2.1.0 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0.14 f1-score
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Arriba on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'Arriba', column 'F1' (PDF page text)
Configuration: Arriba v2.1.0 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
677 false-negative-count
count · lower

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Arriba on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'Arriba', column 'False negative' (PDF page text)
Configuration: Arriba v2.1.0 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
9,567 false-positive-count
count · lower

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Arriba on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'Arriba', column 'False positive' (PDF page text)
Configuration: Arriba v2.1.0 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0.08 precision
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Arriba on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'Arriba', column 'Positive predictive value' (PDF page text)
Configuration: Arriba v2.1.0 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0.56 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Arriba on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'Arriba', column 'True positive rate' (PDF page text)
Configuration: Arriba v2.1.0 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
857 true-positive-count
count · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

Arriba on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'Arriba', column 'True positive' (PDF page text)
Configuration: EricScript v0.5.5 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0.01 f1-score
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

EricScript on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'EricScript', column 'F1' (PDF page text)
Configuration: EricScript v0.5.5 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
665 false-negative-count
count · lower

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

EricScript on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'EricScript', column 'False negative' (PDF page text)
Configuration: EricScript v0.5.5 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
160,271 false-positive-count
count · lower

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

EricScript on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'EricScript', column 'False positive' (PDF page text)
Configuration: EricScript v0.5.5 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0 precision
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

EricScript on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'EricScript', column 'Positive predictive value' (PDF page text)
Configuration: EricScript v0.5.5 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0.54 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

EricScript on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'EricScript', column 'True positive rate' (PDF page text)
Configuration: EricScript v0.5.5 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
785 true-positive-count
count · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

EricScript on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'EricScript', column 'True positive' (PDF page text)
Configuration: FusionCatcher v1.33 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0.08 f1-score
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FusionCatcher on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'FusionCatcher', column 'F1' (PDF page text)
Configuration: FusionCatcher v1.33 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
295 false-negative-count
count · lower

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FusionCatcher on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'FusionCatcher', column 'False negative' (PDF page text)
Configuration: FusionCatcher v1.33 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
22,445 false-positive-count
count · lower

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FusionCatcher on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'FusionCatcher', column 'False positive' (PDF page text)
Configuration: FusionCatcher v1.33 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0.04 precision
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FusionCatcher on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'FusionCatcher', column 'Positive predictive value' (PDF page text)
Configuration: FusionCatcher v1.33 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0.77 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FusionCatcher on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'FusionCatcher', column 'True positive rate' (PDF page text)
Configuration: FusionCatcher v1.33 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
971 true-positive-count
count · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FusionCatcher on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'FusionCatcher', column 'True positive' (PDF page text)
Configuration: Genomon v2.6.3 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0.31 f1-score
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

Genomon on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'Genomon', column 'F1' (PDF page text)
Configuration: Genomon v2.6.3 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
1,044 false-negative-count
count · lower

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

Genomon on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'Genomon', column 'False negative' (PDF page text)
Configuration: Genomon v2.6.3 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
1,932 false-positive-count
count · lower

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

Genomon on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'Genomon', column 'False positive' (PDF page text)
Configuration: Genomon v2.6.3 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0.26 precision
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

Genomon on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'Genomon', column 'Positive predictive value' (PDF page text)
Configuration: Genomon v2.6.3 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0.4 recall
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

Genomon on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'Genomon', column 'True positive rate' (PDF page text)
Configuration: Genomon v2.6.3 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
683 true-positive-count
count · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

Genomon on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'Genomon', column 'True positive' (PDF page text)
Configuration: InFusion v0.8 (Tamura et al. 2026)Protocol: All fusions, conventional RNA-seq of haematologic cell lines, consensus truth (Tamura et al. 2026 Supplementary Table 3)
Dataset: CCLE haematologic malignancy cell lines, conventional RNA-seq (170 cell lines)
0.19 f1-score
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

InFusion on all fusions, conventional RNA-seq (Tamura et al. 2026)

rna-fusion-20261009-protocol-tamura2026-all-conventional

Aggregation: Not reported

Comparison of gene fusion detection algorithms reveals frequently overlooked driver fusions in hematologic malignancies; Tamura et al. 2026, Supplementary Information (Supplementary Tables 1-12) · Supplementary Table 3, 'Conventional RNA-seq of cell lines', row 'InFusion', column 'F1' (PDF page text)

Source checking is not independent reproduction. Release 2026-10-09-ba02f2f4a36e.

Methods and evaluation design

Procedure, tasks and evaluated configurations

Recorded evaluations

Each evaluation records what was tested and under which conditions.

Baseline coverage

Reference methods help show what a model adds beyond simple controls. We track a null control and a conventional method for each protocol.

0 of 2 active baseline roles have published Rewire measurements in this release. Measurements on a selected protocol do not establish coverage of an entire suite.

No execution recipe linked to this protocol. Recipe availability does not establish a completed evaluation.

Author-reported evaluations
1
External evaluations
11

Literature evidence is not a Rewire measurement. Executed but unpublished runs and private review status are not included.

Null control

Proposed control: requires review

Select a task-valid null control after reviewing inputs and metric

Protocol-specific applicability, permitted inputs, access, split, evaluator and execution requirements need review before implementation or execution.

This is a suggested selection rule, not a validated method or a measured score.

Conventional reference

Proposed control: requires review

Select an upstream conventional reference after reviewing the full protocol

Protocol-specific applicability, permitted inputs, access, split, evaluator and execution requirements need review before implementation or execution.

This is a suggested selection rule, not a validated method or a measured score.

Protocol coverage CSV (gzip) · Model evaluation matrix (gzip) · Source table (gzip) · Release and checksums (gzip)

Coverage is derived from release 2026-10-09-ba02f2f4a36e. Source citations describe the original records; they do not validate an unreviewed baseline proposal. No results have been generated by this audit.

Run instructions

No runnable recipe has been reviewed for this protocol. Dataset access, model requirements, licences and compute requirements must be checked against its sources before execution.

Strengths, limitations and unresolved questions

Evidence

Source checking verifies the cited claim or transcription. It does not establish independent reproduction.

Evidence table

Inspect claims, sources and review details

Trace each statement to its source and review. A context-only reference supports the record generally; it does not verify an individual field. Source checking does not reproduce an experiment.

One row per statement and cited source. Multiple citations are not independent evaluations. Shared locators are labelled explicitly.

0 evidence rows matching the loaded filters

Claims, original sources and review scope · Release 2026-10-09-ba02f2f4a36e
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Sources and history

Release 2026-10-09-ba02f2f4a36e · Record review: source checked

2 source records and release historyDownload this release (gzip)
Technical metadata and extraction receipts

Stable ID: rna-fusion-20261009-protocol-tamura2026-all-conventional

areas
rna-transcriptomes
contexts
clinical_research
protocol
Truth: fusion-cell line pairs detected by at least four algorithms other than the one evaluated (TrinityFusion modes count as one vote); false positives: fusions detected by that algorithm alone; TPR, PPV and F1 by standard formulas. Default or recommended parameters, GRCh38.
version
Supplementary Table 3, 'Conventional RNA-seq of cell lines'
metric
recall
limitations
Haematologic cancer cell lines only (170 for conventional, 26 for targeted RNA-seq); no solid tumours, FFPE tissue or clinical specimens. Per-caller results on 165 clinical samples are only in a figure.; Truth is consensus: fusion-cell line pairs detected by at least four algorithms other than the one scored (TrinityFusion modes count as one vote), without orthogonal validation except for driver pairs, so it favours callers that agree with the majority.; False positives are fusions detected by that algorithm alone; fusions called by two or three algorithms count as neither TP nor FP. PPV is therefore not precision against a validated truth, and single-caller calls may include real fusions.; Truth-set size differs by algorithm (printed per row and stored as the evaluation denominator).; Genomon rows are author_reported: a co-author is first author of the Genomon fusion paper; the other 11 algorithms were developed elsewhere.; Default or recommended parameters only; the authors show that parameter changes recover some missed driver fusions (Results).
source locator
Supplementary Table 3, sub-table 'Conventional RNA-seq of cell lines'; Methods 'Comparison of detection algorithms'
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