rewirebio.iobenchmarks
Dataset

Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)

Long-read input in Lin et al. 2026.

Research readiness

These checks assess whether the evidence supports a reproducible investigation. A source-checked score alone does not meet these requirements.

Release 2026-10-10-7b8f80935f90 · Evidence verified: Not verified

Evidence incomplete

Replay metrics

Exact outcomes, predictions, identifiers and evaluator are connected.

Missing or unresolved evidence

  • No verified artifact manifest is linked to this exact record.
  • artifact hashes: verification is missing
  • join integrity: verification is missing
  • score semantics: verification is missing
  • metric replay: verification is missing

Verified: Not verified

Evidence incomplete

Investigate discrepancies

Replay evidence includes annotations and an assessment of dependence. Unknown independence permits descriptive analysis only.

Missing or unresolved evidence

  • No verified artifact manifest is linked to this exact record.
  • artifact hashes: verification is missing
  • join integrity: verification is missing
  • score semantics: verification is missing
  • metric replay: verification is missing
  • annotations: verification is missing
  • dependence: verification is missing

Verified: Not verified

Evidence incomplete

Run locally

A pinned recipe describes the inputs, environment and resource requirements.

Missing or unresolved evidence

  • No verified artifact manifest is linked to this exact record.
  • artifact hashes: verification is missing
  • join integrity: verification is missing
  • score semantics: verification is missing
  • recipe pinned: verification is missing
  • resource estimate: verification is missing

Verified: Not verified

Evidence incomplete

Validate independently

Separate data and exposure records support an independent test.

Missing or unresolved evidence

  • No verified artifact manifest is linked to this exact record.
  • artifact hashes: verification is missing
  • join integrity: verification is missing
  • score semantics: verification is missing
  • independent validation: verification is missing
  • overlap checked: verification is missing

Verified: Not verified

Readiness describes the evidence in this release. Availability on your computer is checked separately when an investigation runs. Existing data exposure can prevent independent validation even when files are available.

Artifacts and reproduction

No verified artifact manifest is connected to this record yet. The gaps above identify what is needed before analysis can begin.

Read reviewed discrepancy investigations

Evaluation results

8 evaluations · 32 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: FUSILLI on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.86 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

FUSILLI on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'FUSILLI', column 'F1'
Configuration: FUSILLI on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.92 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

FUSILLI on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'FUSILLI', column 'Precision'
Configuration: FUSILLI on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.81 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

FUSILLI on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'FUSILLI', column 'Sensitivity (recall)'
Configuration: FUSILLI on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.92 specificity
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

FUSILLI on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'FUSILLI', column 'Specificity'
Configuration: FUSILLI on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, low-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 6)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.42 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

FUSILLI on paediatric B-ALL nanopore WTS, low-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-low-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 6, row 'FUSILLI', column 'F1'
Configuration: FUSILLI on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, low-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 6)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.92 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

FUSILLI on paediatric B-ALL nanopore WTS, low-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-low-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 6, row 'FUSILLI', column 'Precision'
Configuration: FUSILLI on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, low-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 6)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.27 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

FUSILLI on paediatric B-ALL nanopore WTS, low-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-low-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 6, row 'FUSILLI', column 'Sensitivity (recall)'
Configuration: FUSILLI on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, low-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 6)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.95 specificity
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

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

FUSILLI on paediatric B-ALL nanopore WTS, low-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-low-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 6, row 'FUSILLI', column 'Specificity'
Configuration: FusionSeeker on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.76 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

FusionSeeker on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'FusionSeeker', column 'F1'
Configuration: FusionSeeker on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.94 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

FusionSeeker on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'FusionSeeker', column 'Precision'
Configuration: FusionSeeker on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.63 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

FusionSeeker on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'FusionSeeker', column 'Sensitivity (recall)'
Configuration: FusionSeeker on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.96 specificity
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FusionSeeker on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'FusionSeeker', column 'Specificity'
Configuration: FusionSeeker on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, low-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 6)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.16 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

FusionSeeker on paediatric B-ALL nanopore WTS, low-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-low-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 6, row 'FusionSeeker', column 'F1'
Configuration: FusionSeeker on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, low-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 6)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
1 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

FusionSeeker on paediatric B-ALL nanopore WTS, low-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-low-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 6, row 'FusionSeeker', column 'Precision'
Configuration: FusionSeeker on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, low-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 6)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.09 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

FusionSeeker on paediatric B-ALL nanopore WTS, low-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-low-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 6, row 'FusionSeeker', column 'Sensitivity (recall)'
Configuration: FusionSeeker on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, low-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 6)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
1 specificity
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FusionSeeker on paediatric B-ALL nanopore WTS, low-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-low-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 6, row 'FusionSeeker', column 'Specificity'
Configuration: JAFFAL on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.78 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

JAFFAL on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'JAFFAL', column 'F1'
Configuration: JAFFAL on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.79 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

JAFFAL on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'JAFFAL', column 'Precision'
Configuration: JAFFAL on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.76 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

JAFFAL on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'JAFFAL', column 'Sensitivity (recall)'
Configuration: JAFFAL on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.81 specificity
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

JAFFAL on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'JAFFAL', column 'Specificity'
Configuration: JAFFAL on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, low-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 6)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.36 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

JAFFAL on paediatric B-ALL nanopore WTS, low-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-low-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 6, row 'JAFFAL', column 'F1'
Configuration: JAFFAL on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, low-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 6)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.9 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

JAFFAL on paediatric B-ALL nanopore WTS, low-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-low-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 6, row 'JAFFAL', column 'Precision'
Configuration: JAFFAL on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, low-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 6)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.23 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

JAFFAL on paediatric B-ALL nanopore WTS, low-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-low-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 6, row 'JAFFAL', column 'Sensitivity (recall)'
Configuration: JAFFAL on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, low-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 6)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.95 specificity
fraction · higher

Uncertainty: Not reported by the source

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

JAFFAL on paediatric B-ALL nanopore WTS, low-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-low-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 6, row 'JAFFAL', column 'Specificity'
Configuration: LongGF on nanopore cDNA reads (Lin et al. 2026)Protocol: Paediatric B-ALL nanopore WTS, high-depth cohort, dominant-fusion classification (Lin et al. 2026 Table 3)
Dataset: Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
0.81 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

LongGF on paediatric B-ALL nanopore WTS, high-depth (Lin et al. 2026)

rna-fusion-20261009-protocol-lin2026-high-depth

Aggregation: Not reported

Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia · Table 3, row 'LongGF', column 'F1'

Source checking is not independent reproduction. Release 2026-10-10-7b8f80935f90.

Dataset and evaluation context

A dataset supplies biological observations. The evaluation protocol defines how those observations are split, used and scored.

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.

6 evidence rows matching the loaded filters

Claims, original sources and review scope · Release 2026-10-10-7b8f80935f90
Property and statementOriginal source and locationReview and provenance
attributes.assay
ONT PCR-cDNA barcoding, R9.4.1 flow cells, Guppy high-accuracy base calling
Context-only references
Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia

Original source ↗

Materials and Methods 'Samples', 'Library Preparation', 'Fusion Performance Evaluations'; Tables 1-2

Version: Journal of Molecular Diagnostics 28(5):406, published 2026-02-10; PMC13197905 full-text XML
Retrieved: 2026-10-09T20:38:17Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.assay

Source artifact SHA-256: 8cc3b4bca5e2fe9b068a1e891366854d974f3df3102425959e600b9ea19f87b6

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

attributes.population
High-depth cohort: 51 samples (27 with a known B-ALL fusion), mean 11.2 M reads; low-depth cohort: 119 sequencing runs of 68 samples (79 runs with a known fusion per Methods 'Fusion Performance Evaluations'; Results give 81 samples with known genomic subtypes), mean 1.4 M reads. The high-depth samples are a subset of the low-depth samples.
Context-only references
Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia

Original source ↗

Materials and Methods 'Samples', 'Library Preparation', 'Fusion Performance Evaluations'; Tables 1-2

Version: Journal of Molecular Diagnostics 28(5):406, published 2026-02-10; PMC13197905 full-text XML
Retrieved: 2026-10-09T20:38:17Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.population

Source artifact SHA-256: 8cc3b4bca5e2fe9b068a1e891366854d974f3df3102425959e600b9ea19f87b6

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

attributes.source_locator
Materials and Methods 'Samples', 'Library Preparation', 'Fusion Performance Evaluations'; Tables 1-2
Context-only references
Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia

Original source ↗

Materials and Methods 'Samples', 'Library Preparation', 'Fusion Performance Evaluations'; Tables 1-2

Version: Journal of Molecular Diagnostics 28(5):406, published 2026-02-10; PMC13197905 full-text XML
Retrieved: 2026-10-09T20:38:17Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.source_locator

Source artifact SHA-256: 8cc3b4bca5e2fe9b068a1e891366854d974f3df3102425959e600b9ea19f87b6

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

attributes.split
Two cohorts; the high-depth cohort is a subset of the low-depth samples
Context-only references
Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia

Original source ↗

Materials and Methods 'Samples', 'Library Preparation', 'Fusion Performance Evaluations'; Tables 1-2

Version: Journal of Molecular Diagnostics 28(5):406, published 2026-02-10; PMC13197905 full-text XML
Retrieved: 2026-10-09T20:38:17Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.split

Source artifact SHA-256: 8cc3b4bca5e2fe9b068a1e891366854d974f3df3102425959e600b9ea19f87b6

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

description
Long-read input in Lin et al. 2026.
Context-only references
Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia

Original source ↗

Materials and Methods 'Samples', 'Library Preparation', 'Fusion Performance Evaluations'; Tables 1-2

Version: Journal of Molecular Diagnostics 28(5):406, published 2026-02-10; PMC13197905 full-text XML
Retrieved: 2026-10-09T20:38:17Z

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Field: description

Source artifact SHA-256: 8cc3b4bca5e2fe9b068a1e891366854d974f3df3102425959e600b9ea19f87b6

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Inspected artifact

name
Paediatric B-ALL nanopore PCR-cDNA whole-transcriptome sequencing (UNC, St Jude, ECOG-ACRIN)
Context-only references
Long-Read Whole-Transcriptome Sequencing and Selective Gene Panel Profiling Enable Sensitive Detection of Fusion Oncogenes in Pediatric B-Cell Acute Lymphoblastic Leukemia

Original source ↗

Materials and Methods 'Samples', 'Library Preparation', 'Fusion Performance Evaluations'; Tables 1-2

Version: Journal of Molecular Diagnostics 28(5):406, published 2026-02-10; PMC13197905 full-text XML
Retrieved: 2026-10-09T20:38:17Z

not individually reviewed

No individual claim review recorded

Audit details

Field: name

Source artifact SHA-256: 8cc3b4bca5e2fe9b068a1e891366854d974f3df3102425959e600b9ea19f87b6

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Sources and history

Release 2026-10-10-7b8f80935f90 · Record review: source checked

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Technical metadata and extraction receipts

Stable ID: rna-fusion-20261009-data-lin2026-ball-nanopore

areas
rna-transcriptomes
contexts
clinical_research
population
High-depth cohort: 51 samples (27 with a known B-ALL fusion), mean 11.2 M reads; low-depth cohort: 119 sequencing runs of 68 samples (79 runs with a known fusion per Methods 'Fusion Performance Evaluations'; Results give 81 samples with known genomic subtypes), mean 1.4 M reads. The high-depth samples are a subset of the low-depth samples.
assay
ONT PCR-cDNA barcoding, R9.4.1 flow cells, Guppy high-accuracy base calling
split
Two cohorts; the high-depth cohort is a subset of the low-depth samples
source locator
Materials and Methods 'Samples', 'Library Preparation', 'Fusion Performance Evaluations'; Tables 1-2
missing metadata
version: reason: unreported
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