rewirebio.iobenchmarks
Contested result

MUpro and ThermoNet: Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new dataset reverses the order

  • Low severity
  • Not yet reviewed
  • Ordering reversal
  • Different tasks across studies

Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new dataset ranks ThermoNet above MUpro in 9 of 9 comparisons; other studies rank MUpro above ThermoNet in 5 of 6.

An automatic lead, not a finding of error. The results below are shown as published, everywhere on the site, until a reviewer decides otherwise.

Which studies agree

Transfer learning to leverage larger… ranks MUpro above ThermoNet in 5 of its 6 comparisons and ThermoNet higher in 1. Predicting protein stability changes… ranks ThermoNet above MUpro in all 9 comparisons that are not ties (1 is a tie).

Papers grouped by which system they rank higher: MUpro or ThermoNetRank MUpro higher: Transfer learning to leverage larger…. Rank ThermoNet higher: Predicting protein stability changes… (disagrees). Mixed: none.Rank MUpro higherMixedRank ThermoNet higherTransfer learningto leverage larger…Transfer learning to leverage larger datasets for improved prediction of protein stability changesPredicting proteinstability changes…Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new dataset
  • Rank MUpro higher (1): Transfer learning to leverage larger…
  • Rank ThermoNet higher (1): Predicting protein stability changes… (disagrees)
  • Mixed (0): none

Each paper sits where at least two thirds of its comparisons point; Mixed means neither model reaches two thirds. The larger, outlined dot is the paper that disagrees.

Comparisons in which each paper scores MUpro or ThermoNet higherPredicting protein stability changes… (disagrees): MUpro higher in 0, ThermoNet higher in 9, 1 tie. Transfer learning to leverage larger…: MUpro higher in 5, ThermoNet higher in 1, 0 ties.Disagrees: Predicting protein stability changes…Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new dataset1 tie19 ThermoNet higher9Transfer learning to leverage larger…Transfer learning to leverage larger datasets for improved prediction of protein stability changes5 MUpro higher51 ThermoNet higher1
MUpro higherTieThermoNet higherNumbers are counts of comparisons; the outlined bar is the paper that disagrees.
Comparisons in Predicting protein stability changes… (10)
ProtocolDatasetMetricMUproThermoNetHigher
S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)S669: 669 single-point variants from ThermoMutDB in proteins under 25% identity to S2648 and VariBench, with reverse variantsMAE (S669, 669 direct variants), kilocalorie-per-mole1.211.17ThermoNet
S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)S669: 669 single-point variants from ThermoMutDB in proteins under 25% identity to S2648 and VariBench, with reverse variantsMAE (S669, 669 reverse variants), kilocalorie-per-mole1.961.23ThermoNet
S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)S669: 669 single-point variants from ThermoMutDB in proteins under 25% identity to S2648 and VariBench, with reverse variantsMAE (S669, all 1,338 direct and reverse variants), kilocalorie-per-mole1.581.2ThermoNet
S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)S669: 669 single-point variants from ThermoMutDB in proteins under 25% identity to S2648 and VariBench, with reverse variantsPearson (S669, 669 direct variants), unitless0.250.39ThermoNet
S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)S669: 669 single-point variants from ThermoMutDB in proteins under 25% identity to S2648 and VariBench, with reverse variantsPearson (S669, 669 reverse variants), unitless0.20.38ThermoNet
S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)S669: 669 single-point variants from ThermoMutDB in proteins under 25% identity to S2648 and VariBench, with reverse variantsPearson (S669, all 1,338 direct and reverse variants), unitless0.320.51ThermoNet
S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)S669: 669 single-point variants from ThermoMutDB in proteins under 25% identity to S2648 and VariBench, with reverse variantsPearson (S669, antisymmetry, direct versus reverse predictions (perfect antisymmetry is -1, so lower is better)), unitless-0.32-0.85ThermoNet
S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)S669: 669 single-point variants from ThermoMutDB in proteins under 25% identity to S2648 and VariBench, with reverse variantsRMSE (S669, 669 direct variants), kilocalorie-per-mole1.611.62Tie
S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)S669: 669 single-point variants from ThermoMutDB in proteins under 25% identity to S2648 and VariBench, with reverse variantsRMSE (S669, 669 reverse variants), kilocalorie-per-mole2.381.66ThermoNet
S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)S669: 669 single-point variants from ThermoMutDB in proteins under 25% identity to S2648 and VariBench, with reverse variantsRMSE (S669, all 1,338 direct and reverse variants), kilocalorie-per-mole2.031.64ThermoNet
Comparisons in Transfer learning to leverage larger… (6)

What disagrees

Other studies
rank MUpro above ThermoNet in 5 of 6 comparisons
This study
ranks ThermoNet above MUpro in 9 of 9 comparisons
Compared
MUpro, ThermoNet
Study that disagrees
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new dataset
Other studies
Transfer learning to leverage larger datasets for improved prediction of protein stability changes
Rule
Ordering reversal; different tasks across studies
Model identity
Matched across studies partly through links not yet reviewed

The compared numbers

Each value links to its result record and source. Compare values within one protocol; the rule compares rankings, not raw values across protocols.

In the study that disagrees (18)
StudyToolProtocol or benchmarkMetricValue
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetMUpro (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)Pearson (S669, antisymmetry, direct versus reverse predictions (perfect antisymmetry is -1, so lower is better))–0.32
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetMUpro (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)MAE (S669, 669 direct variants)1.21
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetMUpro (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)Pearson (S669, 669 direct variants)0.25
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetMUpro (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)MAE (S669, 669 reverse variants)1.96
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetMUpro (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)Pearson (S669, 669 reverse variants)0.2
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetMUpro (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)RMSE (S669, 669 reverse variants)2.38
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetMUpro (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)MAE (S669, all 1,338 direct and reverse variants)1.58
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetMUpro (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)Pearson (S669, all 1,338 direct and reverse variants)0.32
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetMUpro (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)RMSE (S669, all 1,338 direct and reverse variants)2.03
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetThermoNet (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)Pearson (S669, antisymmetry, direct versus reverse predictions (perfect antisymmetry is -1, so lower is better))–0.85
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetThermoNet (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)MAE (S669, 669 direct variants)1.17
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetThermoNet (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)Pearson (S669, 669 direct variants)0.39
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetThermoNet (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)MAE (S669, 669 reverse variants)1.23
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetThermoNet (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)Pearson (S669, 669 reverse variants)0.38
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetThermoNet (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)RMSE (S669, 669 reverse variants)1.66
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetThermoNet (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)MAE (S669, all 1,338 direct and reverse variants)1.2
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetThermoNet (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)Pearson (S669, all 1,338 direct and reverse variants)0.51
Predicting protein stability changes upon single-point mutation: a thorough comparison of the available tools on a new datasetThermoNet (Pancotti et al. 2022)S669 direct and reverse ddG prediction (Pancotti et al. 2022 Table 1)RMSE (S669, all 1,338 direct and reverse variants)1.64
In the other studies (12)
StudyToolProtocol or benchmarkMetricValue
Transfer learning to leverage larger datasets for improved prediction of protein stability changesMUPRO (Dieckhaus et al. 2024)Fireprot homologue-free split ddG prediction (Dieckhaus et al. 2024 Table 2)Pearson (Fireprot homologue-free split)0.58
Transfer learning to leverage larger datasets for improved prediction of protein stability changesMUPRO (Dieckhaus et al. 2024)Fireprot homologue-free split ddG prediction (Dieckhaus et al. 2024 Table 2)RMSE (Fireprot homologue-free split)1.54
Transfer learning to leverage larger datasets for improved prediction of protein stability changesMUPRO (Dieckhaus et al. 2024)Fireprot homologue-free split ddG prediction (Dieckhaus et al. 2024 Table 2)Spearman (Fireprot homologue-free split)0.57
Transfer learning to leverage larger datasets for improved prediction of protein stability changesMUPRO (Dieckhaus et al. 2024)Megascale held-out test split ddG prediction (Dieckhaus et al. 2024 Table 2)Pearson (Megascale held-out test split)0.31
Transfer learning to leverage larger datasets for improved prediction of protein stability changesMUPRO (Dieckhaus et al. 2024)Megascale held-out test split ddG prediction (Dieckhaus et al. 2024 Table 2)RMSE (Megascale held-out test split)1.08
Transfer learning to leverage larger datasets for improved prediction of protein stability changesMUPRO (Dieckhaus et al. 2024)Megascale held-out test split ddG prediction (Dieckhaus et al. 2024 Table 2)Spearman (Megascale held-out test split)0.29
Transfer learning to leverage larger datasets for improved prediction of protein stability changesThermoNet (Dieckhaus et al. 2024)Fireprot homologue-free split ddG prediction (Dieckhaus et al. 2024 Table 2)Pearson (Fireprot homologue-free split)0.37
Transfer learning to leverage larger datasets for improved prediction of protein stability changesThermoNet (Dieckhaus et al. 2024)Fireprot homologue-free split ddG prediction (Dieckhaus et al. 2024 Table 2)RMSE (Fireprot homologue-free split)1.99
Transfer learning to leverage larger datasets for improved prediction of protein stability changesThermoNet (Dieckhaus et al. 2024)Fireprot homologue-free split ddG prediction (Dieckhaus et al. 2024 Table 2)Spearman (Fireprot homologue-free split)0.36
Transfer learning to leverage larger datasets for improved prediction of protein stability changesThermoNet (Dieckhaus et al. 2024)Megascale held-out test split ddG prediction (Dieckhaus et al. 2024 Table 2)Pearson (Megascale held-out test split)0.33
Transfer learning to leverage larger datasets for improved prediction of protein stability changesThermoNet (Dieckhaus et al. 2024)Megascale held-out test split ddG prediction (Dieckhaus et al. 2024 Table 2)RMSE (Megascale held-out test split)1.2
Transfer learning to leverage larger datasets for improved prediction of protein stability changesThermoNet (Dieckhaus et al. 2024)Megascale held-out test split ddG prediction (Dieckhaus et al. 2024 Table 2)Spearman (Megascale held-out test split)0.27

Follow-up

Current state: Not yet reviewed.

No one has reviewed this finding yet.

How to help resolve this

If you know why these studies disagree, for example a different population, metric or preprocessing step, or you have a corrected value, tell us through the contribution form. A reviewer checks every submission against its source before anything changes, and the step is added to the follow-up above.

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