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NT 2.5b-m-s (Manzo et al. 2025)

NT 2.5b-m-s (Manzo et al. 2025) as evaluated in the cited comparison.

4 evaluations · 4 results

Overview

NT 2.5b-m-s (Manzo et al. 2025) as evaluated in the cited comparison.

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

Evaluations and results

4 evaluations · 4 results. Different protocols are not a single leaderboard.

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Exact evaluated configurations and original reported results
Tested configurationProtocol and datasetFindingEvidence and details
Configuration: NT 2.5b-m-s (Manzo et al. 2025)Protocol: Allelic reporter effect correlation in HeLa (Manzo et al. 2025 Table 1)
Dataset: HeLa regulatory variant reporter data (Manzo et al. 2025)
0.066 pearson-correlation
unitless · higher

Uncertainty: SE 0.027. Standard error as printed in brackets; its basis is not defined in the caption

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

NT 2.5b-m-s on HeLa reporter variant effects

regulatory-variant-20261009-protocol-manzo2025-hela-pearson

Aggregation: Not reported

Comparative Analysis of Deep Learning Models for Predicting Causative Regulatory Variants · Table 1 row 'NT 2.5b-m-s', column 'Hela (5241 SNPs)'
Configuration: NT 2.5b-m-s (Manzo et al. 2025)Protocol: Allelic reporter effect correlation in HepG2 (Manzo et al. 2025 Table 1)
Dataset: HepG2 regulatory variant reporter data (Manzo et al. 2025)
0.139 pearson-correlation
unitless · higher

Uncertainty: SE 0.027. Standard error as printed in brackets; its basis is not defined in the caption

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

NT 2.5b-m-s on HepG2 reporter variant effects

regulatory-variant-20261009-protocol-manzo2025-hepg2-pearson

Aggregation: Not reported

Comparative Analysis of Deep Learning Models for Predicting Causative Regulatory Variants · Table 1 row 'NT 2.5b-m-s', column 'HepG2 (16,255 SNPs)'
Configuration: NT 2.5b-m-s (Manzo et al. 2025)Protocol: Allelic reporter effect correlation in K562 (Manzo et al. 2025 Table 1)
Dataset: K562 regulatory variant reporter data (Manzo et al. 2025)
0.153 pearson-correlation
unitless · higher

Uncertainty: SE 0.055. Standard error as printed in brackets; its basis is not defined in the caption

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

NT 2.5b-m-s on K562 reporter variant effects

regulatory-variant-20261009-protocol-manzo2025-k562-pearson

Aggregation: Not reported

Comparative Analysis of Deep Learning Models for Predicting Causative Regulatory Variants · Table 1 row 'NT 2.5b-m-s', column 'K562 (19,321 SNPs)'
Configuration: NT 2.5b-m-s (Manzo et al. 2025)Protocol: Allelic reporter effect correlation in NPC (Manzo et al. 2025 Table 1)
Dataset: NPC regulatory variant reporter data (Manzo et al. 2025)
0.027 pearson-correlation
unitless · higher

Uncertainty: SE 0.001. Standard error as printed in brackets; its basis is not defined in the caption

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

NT 2.5b-m-s on NPC reporter variant effects

regulatory-variant-20261009-protocol-manzo2025-npc-pearson

Aggregation: Not reported

Comparative Analysis of Deep Learning Models for Predicting Causative Regulatory Variants · Table 1 row 'NT 2.5b-m-s', column 'NPC (14,042 SNPs)'

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Claims, original sources and review scope · Release 2026-10-10-6e93f504adfc
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Sources and history

Release 2026-10-10-6e93f504adfc · Record review: source checked

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Technical metadata and extraction receipts

Stable ID: regulatory-variant-20261009-config-manzo2025-nt-2-5b-m-s

areas
dna-genomes
contexts
research
method types
foundation_model
reported name
NT 2.5b-m-s (Manzo et al. 2025)
foundation model eligible
true
parameters
Fine-tuned per cell line for enhancer versus control classification on 1 kb sequences (Table 2); variant effect is the log2 ratio of alternative to reference scores
source locator
Table 1 row 'NT 2.5b-m-s'; Table 2
missing metadata
version: reason: unreported; note: The table prints only the label 'NT 2.5b-m-s'; no release or checkpoint identifier.
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