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SegmentNT human genome annotation lncRNA auPRC: lncRNA: per-nucleotide annotation (auPRC)

lncRNA: per-nucleotide annotation (auPRC). Scored with Area under precision-recall curve on Human genome lncRNA test chromosomes 20 and 21. Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

21 evaluations · 21 metric rows

Overview

lncRNA: per-nucleotide annotation (auPRC). Scored with Area under precision-recall curve on Human genome lncRNA test chromosomes 20 and 21. Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

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Results

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SegmentNT human genome annotation lncRNA auPRC: lncRNA: per-nucleotide annotation (auPRC)

auprc (dimensionless) · Higher values are better.

Every method SegmentNT human genome annotation reports on lncRNA: per-nucleotide annotation (auPRC), scored with Area under precision-recall curve on Human genome lncRNA test chromosomes 20 and 21.

SegmentNT human genome annotation lncRNA auPRC: lncRNA: per-nucleotide annotation (auPRC) · Human genome lncRNA test chromosomes 20 and 21 (SegmentNT human genome annotation split)

Evidence origin: Author-reported evaluation. Numerical source review does not establish independent reproduction.

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3, lncRNA column; primary article Sec16–17

Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds.

All comparison limitations (5)
  • Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds.
  • Table names the v1 backbone NTv1 human; 2.5B; Sec17 describes NT v1 2.5B 1000G. Preserve exact table label and methods context.
  • Source excludes homologous test genes but not homologous distal regulatory elements, which may inflate those region scores.
  • Input lengths and training setups differ. Architecture baselines are newly trained from random initialization, not original pretrained checkpoint results.
  • No aggregation across genomic elements or metrics. Split manifests and checkpoint revisions remain unextracted.

Automated source review: 2026-09-23.

No unavailable values; missing scores remain labelled and are never plotted as zero.

Showing 12 of 21 matching rows.

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Author-reported evaluations
21

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

Coverage is derived from release 2026-09-23-2b89723c6dd9. 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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Evidence table

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1 evidence row matching the loaded filters

Claims, original sources and review scope · Release 2026-09-23-2b89723c6dd9
Property and statementOriginal source and locationReview and provenance
Relationship: part of
segmentnt-human-genome-annotation-2025
Individual claims
SegmentNT supplementary information: complete Tables 2 and 3

Original source ↗

Supplementary Table 3, lncRNA column; primary article Sec16–17

Version: Published supplementary information to s41592-025-02881-2; SHA-256 pinned snapshot
Retrieved: 2026-09-23T11:23:43.985410+00:00

source checked

automated source review · 2026-09-23

Audit details

Primary-source transcription with no human sign-off and no independent reproduction.

Field: links:part_of:segmentnt-human-genome-annotation-2025

Claim: segmentnt-supplement-2025-association-lncrna-auprc

Source artifact SHA-256: c4ad23a62ab161a464fe789e5dd167cf2bfe9f43a91a9c3fb1261b99a5594b0f

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

Inspected artifact

Sources and history

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Release 2026-09-23-2b89723c6dd9 · Record review: source checked

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Technical metadata and extraction receipts

Stable ID: segmentnt-supplement-2025-task-lncrna-auprc

areas
genomics
tasks
lncRNA: per-nucleotide annotation (auPRC)
metric
Area under precision-recall curve
metric direction
higher
dataset
Human genome lncRNA test chromosomes 20 and 21
protocol
Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.
source locator
Supplementary Table 3, lncRNA column; primary article Sec16–17
comparison panels
id: segmentnt-supplement-2025-panel-lncrna-auprc; title: SegmentNT human genome annotation lncRNA auPRC: lncRNA: per-nucleotide annotation (auPRC); protocol id: segmentnt-supplement-2025-task-lncrna-auprc; dataset id: segmentnt-supplement-2025-dataset-human-genome-lncrna-test-chromosomes-20-and-21; metric: auprc; unit: dimensionless; direction: higher; result ids: segmentnt-supplement-2025-result-bpnet-arch-lncrna-auprc-auprc; segmentnt-supplement-2025-result-bpnet-arch-large-lncrna-auprc-auprc; segmentnt-supplement-2025-result-spliceai-arch-lncrna-auprc-auprc; segmentnt-supplement-2025-result-spliceai-arch-large-lncrna-auprc-auprc; segmentnt-supplement-2025-result-spliceai-arch-extra-large-lncrna-auprc-auprc; segmentnt-supplement-2025-result-unet-lncrna-auprc-auprc; segmentnt-supplement-2025-result-unet-1024-embedding-lncrna-auprc-auprc; segmentnt-supplement-2025-result-unet-large-lncrna-auprc-auprc; segmentnt-supplement-2025-result-random-init-only-head-lncrna-auprc-auprc; segmentnt-supplement-2025-result-random-init-lncrna-auprc-auprc; segmentnt-supplement-2025-result-segmentnt-3kb-only-head-lncrna-auprc-auprc; segmentnt-supplement-2025-result-segmentnt-3kb-ntv1-human-2-5b-lncrna-auprc-auprc; segmentnt-supplement-2025-result-segmentnt-3kb-lncrna-auprc-auprc; segmentnt-supplement-2025-result-segmentnt-3kb-single-task-x14-lncrna-auprc-auprc; segmentnt-supplement-2025-result-segmentnt-10kb-lncrna-auprc-auprc; segmentnt-supplement-2025-result-segmentnt-20kb-lncrna-auprc-auprc; segmentnt-supplement-2025-result-segmentnt-30kb-lncrna-auprc-auprc; segmentnt-supplement-2025-result-segmentenformer-30kb-lncrna-auprc-auprc; segmentnt-supplement-2025-result-segmentenformer-196kb-lncrna-auprc-auprc; segmentnt-supplement-2025-result-segmentborzoi-30kb-lncrna-auprc-auprc; segmentnt-supplement-2025-result-segmentborzoi-524kb-lncrna-auprc-auprc; source ids: coverage-segmentnt-2025-supplement; source locator: Supplementary Table 3, lncRNA column; primary article Sec16–17; context: Every method SegmentNT human genome annotation reports on lncRNA: per-nucleotide annotation (auPRC), scored with Area under precision-recall curve on Human genome lncRNA test chromosomes 20 and 21.; caveats: Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds.; Table names the v1 backbone NTv1 human; 2.5B; Sec17 describes NT v1 2.5B 1000G. Preserve exact table label and methods context.; Source excludes homologous test genes but not homologous distal regulatory elements, which may inflate those region scores.; Input lengths and training setups differ. Architecture baselines are newly trained from random initialization, not original pretrained checkpoint results.; No aggregation across genomic elements or metrics. Split manifests and checkpoint revisions remain unextracted.; review: method: automated_source_review; date: 2026-09-23
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