InstaNovo
algorithm · Transformer (AR)
Knapsack beam search
| Kind | algorithm |
| Deep learning | yes |
| Acquisition | DDA |
| Family | Transformer (AR) |
Code
Live stars, open issues and last-push figures are on the Code activity chart.
Data
What the papers describing this method trained it on and reported its results on, as each paper states it. A version is named only where the paper names one.
Trained on
- Nine-species benchmark (InstaNovo split) · 2025 peer-reviewed
- Nine-species benchmark (original (DeepNovo, 2017)) · 2023 preprint, 2025 peer-reviewed
- ProteomeTools (Parts I-III) · 2023 preprint, 2025 peer-reviewed
- ProteomeTools (all-confidence (InstaNovo)) · 2023 preprint
- ProteomeTools (high-confidence (InstaNovo)) · 2023 preprint, 2025 peer-reviewed
Evaluated on
- High-throughput MS-based immunopeptidomics (as deposited) · 2023 preprint, 2025 peer-reviewed
- High-throughput proteomics of the 26 medically most important elapids and vipers from sub-Saharan Africa (as deposited) · 2023 preprint, 2025 peer-reviewed
- InstaNovo enables diffusion-powered de novo peptide identification in large scale proteomics experiments (as deposited) · 2023 preprint, 2025 peer-reviewed
- Longitudinal evaluation of biomarkers in wound fluids of venous leg ulcers treated with a protease-modulating wound dressing (as deposited) · 2023 preprint, 2025 peer-reviewed
- Nine-species benchmark (InstaNovo split) · 2023 preprint, 2025 peer-reviewed
- Nine-species benchmark (original (DeepNovo, 2017)) · 2023 preprint, 2025 peer-reviewed
- ProteomeTools (all-confidence (InstaNovo)) · 2023 preprint, 2025 peer-reviewed
- ProteomeTools (high-confidence (InstaNovo)) · 2023 preprint, 2025 peer-reviewed
- Supplementary Data for “Comprehensive evaluation of peptide de novo sequencing tools for monoclonal antibody assembly” (as deposited) · 2023 preprint, 2025 peer-reviewed
Deposited
Benchmarks
- denovo_benchmarks: median peptide-level average precision 0.853 over 86 datasets, median rank 2 of 15 (version 1.2.2).
Both are mass-based matches on the tool’s most recent run. What these numbers mean.
Own results (2)
Tables from this method’s own papers that report it alone, on each of its evaluation sets, with no other method in the table. Standardised like the comparisons: every value on a 0-1 scale, the measure and then the evaluation set across.
Supplementary Table 2
De novo peptide sequencing with InstaNovo: Accurate, database-free peptide identification for large scale proteomics experiments, page 58: InstaNovo evaluation results on all datasets. Confidence intervals are calculated as ±1.96 × se_B where se_B is a bootstrap standard error estimated from 10,000 replicates.*We do not calculate bootstrap standard errors for the ProteomeTools datasets because their size makes it prohibitively costly but also implies the standard errors would be very small.
| a dataset per evaluation set | Amino acid precision | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HeLa single-shot | Immunopeptidomics | Candidatus Scalindua brodae | Snake venoms | Nanobodies | Wound exudates | HeLa degradome | Herceptin | Saccharomyces cerevisiae | HC-PT | AC-PT | Mean | |
| InstaNovo | 0.609 | 0.778 | 0.815 | 0.396 | 0.597 | 0.411 | 0.798 | 0.659 | 0.695 | 0.687 | 0.794 | 0.658 |
| a dataset per evaluation set | Amino acid accuracy | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HeLa single-shot | Immunopeptidomics | Candidatus Scalindua brodae | Snake venoms | Nanobodies | Wound exudates | HeLa degradome | Herceptin | Saccharomyces cerevisiae | HC-PT | AC-PT | Mean | |
| InstaNovo | 0.608 | 0.779 | 0.815 | 0.398 | 0.595 | 0.406 | 0.798 | 0.658 | 0.664 | 0.685 | 0.794 | 0.655 |
| a dataset per evaluation set | Peptide accuracy | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HeLa single-shot | Immunopeptidomics | Candidatus Scalindua brodae | Snake venoms | Nanobodies | Wound exudates | HeLa degradome | Herceptin | Saccharomyces cerevisiae | HC-PT | AC-PT | Mean | |
| InstaNovo | 0.503 | 0.581 | 0.724 | 0.196 | 0.447 | 0.225 | 0.695 | 0.494 | 0.533 | 0.573 | 0.685 | 0.514 |
| a dataset per evaluation set | Peptide AUC | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HeLa single-shot | Immunopeptidomics | Candidatus Scalindua brodae | Snake venoms | Nanobodies | Wound exudates | HeLa degradome | Herceptin | Saccharomyces cerevisiae | HC-PT | AC-PT | Mean | |
| InstaNovo | 0.465 | 0.532 | 0.697 | 0.167 | 0.412 | 0.190 | 0.676 | 0.472 | 0.497 | 0.550 | 0.666 | 0.490 |
A table of the paper's OWN results: it names one method and compares nothing, so it is recorded as own results rather than as a comparison. 'Exc. Yeast' is measured ON yeast: it names the leave-one-out setup in which the model is trained on the other eight species. The paper: 'the models were trained on nine-species excluding yeast, and then evaluated on yeast' (p. 8), and 'For Yeast, we use the splits as defined in DeepNovo and PointNovo'. Fig. 2d's caption reads 'accuracy … on the high-resolution nine-species dataset excluding yeast' before saying 'evaluated on yeast', which invites the opposite reading.
Extended Data Table 2
InstaNovo enables diffusion-powered de novo peptide sequencing in large-scale proteomics experiments, page 24: InstaNovo evaluation results on all datasets
| a dataset per evaluation set | Amino acid precision | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HeLa single-shot | Immunopeptidomics | Candidatus Scalindua brodae | Snake venoms | Nanobodies | Wound exudates | HeLa degradome | Herceptin | Saccharomyces cerevisiae | Bacillus subtilis | Mus musculus | HC-PT | |
| InstaNovo | 0.609 | 0.778 | 0.815 | 0.396 | 0.597 | 0.411 | 0.798 | 0.659 | 0.709 | 0.762 | 0.695 | 0.687 |
| a dataset per evaluation set | Amino acid precision | |
|---|---|---|
| AC-PT | Mean | |
| InstaNovo | 0.794 | 0.670 |
| a dataset per evaluation set | Amino acid accuracy | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HeLa single-shot | Immunopeptidomics | Candidatus Scalindua brodae | Snake venoms | Nanobodies | Wound exudates | HeLa degradome | Herceptin | Saccharomyces cerevisiae | Bacillus subtilis | Mus musculus | HC-PT | |
| InstaNovo | 0.608 | 0.779 | 0.815 | 0.398 | 0.595 | 0.406 | 0.798 | 0.658 | 0.626 | 0.721 | 0.692 | 0.685 |
| a dataset per evaluation set | Amino acid accuracy | |
|---|---|---|
| AC-PT | Mean | |
| InstaNovo | 0.794 | 0.660 |
| a dataset per evaluation set | Peptide accuracy | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HeLa single-shot | Immunopeptidomics | Candidatus Scalindua brodae | Snake venoms | Nanobodies | Wound exudates | HeLa degradome | Herceptin | Saccharomyces cerevisiae | Bacillus subtilis | Mus musculus | HC-PT | |
| InstaNovo | 0.503 | 0.581 | 0.724 | 0.196 | 0.447 | 0.225 | 0.695 | 0.494 | 0.559 | 0.624 | 0.466 | 0.573 |
| a dataset per evaluation set | Peptide accuracy | |
|---|---|---|
| AC-PT | Mean | |
| InstaNovo | 0.685 | 0.521 |
| a dataset per evaluation set | Peptide AUC | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HeLa single-shot | Immunopeptidomics | Candidatus Scalindua brodae | Snake venoms | Nanobodies | Wound exudates | HeLa degradome | Herceptin | Saccharomyces cerevisiae | Bacillus subtilis | Mus musculus | HC-PT | |
| InstaNovo | 0.465 | 0.532 | 0.697 | 0.167 | 0.412 | 0.190 | 0.676 | 0.472 | 0.528 | 0.595 | 0.428 | 0.550 |
| a dataset per evaluation set | Peptide AUC | |
|---|---|---|
| AC-PT | Mean | |
| InstaNovo | 0.666 | 0.491 |
Read from an IMAGE: the page has no text layer for this table, and GLM-OCR and PaddleOCR-VL, read independently, agree on every cell.
Compared against in other papers (12)
44 tables from 12 papers that report this method as a baseline, newest first. The caveats of the comparisons above hold twice over: each paper ran, retrained or quoted this method its own way, so its number here is that paper’s claim, not a measurement of the method. Where a paper says which it did, the word follows the method’s name.
ScopeNovo: a De Novo Peptide Sequencing Method Using Spectrum-Spectrum Similarity to Refine the Prediction Accuracy (2026) · 2 tables
Table 1 (Nine-species · revised (build not stated))
ScopeNovo: a De Novo Peptide Sequencing Method Using Spectrum-Spectrum Similarity to Refine the Prediction Accuracy, page 5: Comparison of de novo peptide sequencing methods on 9-species-V1 and 9-species-V2 benchmarks. For ScopeNovo we report two operating regimes: Setting 1 (External Library, spectrum-consistency reranking against a curated external spectral library), which characterizes the upper-bound performance attainable when high-quality external spectral resources are available; and Setting 2 (Self-Constructed Library), in which the reference library is bootstrapped entirely from high-confidence in-batch de novo predictions on the test data itself, placing ScopeNovo under the same resource assumptions as the baselines and yielding a direct comparison. In each column, the best value among the baselines and ScopeNovo (Setting 2) is in bold; ScopeNovo (Setting 1) is reported separately for reference and excluded from the bold comparison.
|
Nine-species benchmark revised (build not stated) |
Amino acid precision | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Bacillus subtilis | Candidatus Thiodiazotropha endoloripes | Apis mellifera | Homo sapiens | Methanosarcina mazei | Mus musculus | Vigna mungo | Solanum lycopersicum | Saccharomyces cerevisiae | Average | |
| Casanovo | 0.923 | 0.787 | 0.776 | 0.856 | 0.828 | 0.806 | 0.854 | 0.874 | 0.865 | 0.881 |
| Casanovo V2 | 0.843 | 0.799 | 0.788 | 0.865 | 0.836 | 0.813 | 0.867 | 0.882 | 0.875 | 0.865 |
| InstaNovo | 0.852 | 0.751 | 0.799 | 0.847 | 0.848 | 0.634 | 0.894 | 0.864 | 0.877 | 0.850 |
| ContraNovo | 0.863 | 0.802 | 0.817 | 0.909 | 0.864 | 0.830 | 0.903 | 0.881 | 0.883 | 0.865 |
| AdaNovo | 0.792 | 0.816 | 0.756 | 0.800 | 0.804 | 0.757 | 0.759 | 0.831 | 0.801 | 0.794 |
| RankNovo | 0.836 | 0.836 | 0.891 | 0.836 | 0.879 | 0.920 | 0.896 | 0.893 | 0.879 | 0.880 |
| π-PrimeNovo | 0.874 | 0.806 | 0.824 | 0.870 | 0.869 | 0.808 | 0.921 | 0.885 | 0.891 | 0.866 |
| ScopeNovo Setting 1 | 0.885 | 0.822 | 0.839 | 0.884 | 0.882 | 0.841 | 0.931 | 0.897 | 0.900 | 0.885 |
| ScopeNovo Setting 2 | 0.877 | 0.814 | 0.829 | 0.879 | 0.874 | 0.821 | 0.926 | 0.889 | 0.892 | 0.868 |
|
Nine-species benchmark revised (build not stated) |
Peptide accuracy | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Bacillus subtilis | Candidatus Thiodiazotropha endoloripes | Apis mellifera | Homo sapiens | Methanosarcina mazei | Mus musculus | Vigna mungo | Solanum lycopersicum | Saccharomyces cerevisiae | Average | |
| Casanovo | 0.687 | 0.522 | 0.579 | 0.662 | 0.656 | 0.522 | 0.645 | 0.730 | 0.738 | 0.682 |
| Casanovo V2 | 0.693 | 0.532 | 0.587 | 0.670 | 0.661 | 0.531 | 0.654 | 0.737 | 0.743 | 0.683 |
| InstaNovo | 0.704 | 0.512 | 0.625 | 0.670 | 0.666 | 0.504 | 0.679 | 0.721 | 0.758 | 0.698 |
| ContraNovo | 0.709 | 0.533 | 0.615 | 0.759 | 0.698 | 0.567 | 0.722 | 0.729 | 0.725 | 0.701 |
| AdaNovo | 0.636 | 0.624 | 0.597 | 0.590 | 0.641 | 0.472 | 0.538 | 0.693 | 0.653 | 0.635 |
| RankNovo | 0.713 | 0.603 | 0.617 | 0.717 | 0.712 | 0.559 | 0.744 | 0.724 | 0.680 | 0.682 |
| π-PrimeNovo | 0.712 | 0.572 | 0.612 | 0.710 | 0.714 | 0.548 | 0.766 | 0.719 | 0.684 | 0.697 |
| ScopeNovo Setting 1 | 0.748 | 0.664 | 0.669 | 0.762 | 0.772 | 0.664 | 0.816 | 0.771 | 0.702 | 0.737 |
| ScopeNovo Setting 2 | 0.728 | 0.619 | 0.641 | 0.750 | 0.743 | 0.611 | 0.788 | 0.745 | 0.691 | 0.716 |
The paper bolds the best of the baselines and ScopeNovo (Setting 2) only: 'ScopeNovo (Setting 1) is reported separately for reference and excluded from the bold comparison.' Bold and underline here rank every row, Setting 1 included; the paper's own marks were checked against its rule, and match it.
Table 1 (Nine-species · original (DeepNovo, 2017))
ScopeNovo: a De Novo Peptide Sequencing Method Using Spectrum-Spectrum Similarity to Refine the Prediction Accuracy, page 5: Comparison of de novo peptide sequencing methods on 9-species-V1 and 9-species-V2 benchmarks. For ScopeNovo we report two operating regimes: Setting 1 (External Library, spectrum-consistency reranking against a curated external spectral library), which characterizes the upper-bound performance attainable when high-quality external spectral resources are available; and Setting 2 (Self-Constructed Library), in which the reference library is bootstrapped entirely from high-confidence in-batch de novo predictions on the test data itself, placing ScopeNovo under the same resource assumptions as the baselines and yielding a direct comparison. In each column, the best value among the baselines and ScopeNovo (Setting 2) is in bold; ScopeNovo (Setting 1) is reported separately for reference and excluded from the bold comparison.
|
Nine-species benchmark original (DeepNovo, 2017) |
Amino acid precision | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Bacillus subtilis | Candidatus Thiodiazotropha endoloripes | Apis mellifera | Homo sapiens | Methanosarcina mazei | Mus musculus | Vigna mungo | Solanum lycopersicum | Saccharomyces cerevisiae | Average | |
| Casanovo | 0.788 | 0.676 | 0.708 | 0.676 | 0.754 | 0.765 | 0.761 | 0.792 | 0.756 | 0.743 |
| Casanovo V2 | 0.801 | 0.687 | 0.721 | 0.687 | 0.767 | 0.774 | 0.768 | 0.802 | 0.768 | 0.754 |
| InstaNovo | 0.802 | 0.656 | 0.718 | 0.691 | 0.756 | 0.742 | 0.794 | 0.774 | 0.767 | 0.745 |
| ContraNovo | 0.828 | 0.700 | 0.764 | 0.778 | 0.798 | 0.803 | 0.804 | 0.812 | 0.787 | 0.785 |
| AdaNovo | 0.858 | 0.798 | 0.767 | 0.690 | 0.804 | 0.778 | 0.878 | 0.818 | 0.791 | 0.798 |
| RankNovo | 0.807 | 0.771 | 0.880 | 0.784 | 0.838 | 0.823 | 0.876 | 0.846 | 0.828 | 0.827 |
| π-PrimeNovo | 0.840 | 0.715 | 0.767 | 0.725 | 0.799 | 0.797 | 0.823 | 0.822 | 0.795 | 0.789 |
| ScopeNovo Setting 1 | 0.849 | 0.715 | 0.778 | 0.729 | 0.811 | 0.809 | 0.816 | 0.825 | 0.796 | 0.797 |
| ScopeNovo Setting 2 | 0.844 | 0.722 | 0.774 | 0.732 | 0.806 | 0.809 | 0.829 | 0.828 | 0.798 | 0.795 |
|
Nine-species benchmark original (DeepNovo, 2017) |
Peptide accuracy | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Bacillus subtilis | Candidatus Thiodiazotropha endoloripes | Apis mellifera | Homo sapiens | Methanosarcina mazei | Mus musculus | Vigna mungo | Solanum lycopersicum | Saccharomyces cerevisiae | Average | |
| Casanovo | 0.621 | 0.437 | 0.494 | 0.446 | 0.568 | 0.485 | 0.593 | 0.622 | 0.601 | 0.551 |
| Casanovo V2 | 0.630 | 0.445 | 0.504 | 0.455 | 0.579 | 0.493 | 0.600 | 0.629 | 0.607 | 0.559 |
| InstaNovo | 0.652 | 0.459 | 0.535 | 0.515 | 0.595 | 0.525 | 0.635 | 0.635 | 0.618 | 0.582 |
| ContraNovo | 0.688 | 0.486 | 0.580 | 0.625 | 0.633 | 0.574 | 0.678 | 0.674 | 0.673 | 0.628 |
| AdaNovo | 0.753 | 0.638 | 0.620 | 0.494 | 0.671 | 0.546 | 0.797 | 0.684 | 0.660 | 0.660 |
| RankNovo | 0.765 | 0.592 | 0.642 | 0.621 | 0.688 | 0.595 | 0.765 | 0.720 | 0.726 | 0.687 |
| π-PrimeNovo | 0.725 | 0.532 | 0.602 | 0.575 | 0.654 | 0.572 | 0.701 | 0.701 | 0.703 | 0.650 |
| ScopeNovo Setting 1 | 0.789 | 0.610 | 0.665 | 0.628 | 0.731 | 0.660 | 0.755 | 0.752 | 0.744 | 0.711 |
| ScopeNovo Setting 2 | 0.749 | 0.572 | 0.643 | 0.624 | 0.690 | 0.637 | 0.733 | 0.732 | 0.721 | 0.684 |
The paper bolds the best of the baselines and ScopeNovo (Setting 2) only: 'ScopeNovo (Setting 1) is reported separately for reference and excluded from the bold comparison.' Bold and underline here rank every row, Setting 1 included; the paper's own marks were checked against its rule, and match it.
dIon: Fragmentation-Based Invariance for Self-Supervised Learning of Tandem Mass Spectra (2026) · 3 tables
Table 26
dIon: Fragmentation-Based Invariance for Self-Supervised Learning of Tandem Mass Spectra, page 33: Complete MSKB-final de novo results, including amino-acid metrics and the dIoninitialized models fine-tuned with a 1,000-peak cap. Within each training regime, scratch and dIon initialization use an identical end-to-end training protocol.
|
Casanovo digestion enzyme bias data as deposited |
Amino acid precision | Amino acid recall | Peptide precision at coverage 1 |
|---|---|---|---|
| dIon from scratch, end-to-end; trained on MSKB-final | 0.895 | 0.895 | 0.747 |
| dIon init., end-to-end; trained on MSKB-final | 0.927 | 0.926 | 0.802 |
| dIon init., end-to-end, 1,000 peaks; trained on MSKB-final | 0.935 | 0.934 | 0.822 |
| dIon from scratch, end-to-end; trained on DNL-v1 | 0.933 | 0.934 | 0.819 |
| dIon init., end-to-end; trained on DNL-v1 | 0.945 | 0.945 | 0.842 |
| dIon init., end-to-end, 1,000 peaks; trained on DNL-v1 | 0.949 | 0.949 | 0.856 |
| Casanovo 5.2.1 · released | 0.911 | 0.912 | 0.783 |
| InstaNovo 1.2.2 · released | 0.961 | 0.961 | 0.916 |
MSKB-final, rows grouped by training corpus as in Table 1. InstaNovo 1.2.2 is printed in grey with an asterisk because it 'is documented as training on MassIVE-KB v1, the source corpus of this test set', so its numbers are not a held-out evaluation.
In the paper: column amino acid precision: the original table bolded dIon init., end-to-end, 1,000 peaks; trained on DNL-v1 (0.949).
In the paper: column peptide precision at coverage 1: the original table bolded dIon init., end-to-end, 1,000 peaks; trained on DNL-v1 (0.856).
In the paper: column amino acid recall: the original table bolded dIon init., end-to-end, 1,000 peaks; trained on DNL-v1 (0.949).
Table25
dIon: Fragmentation-Based Invariance for Self-Supervised Learning of Tandem Mass Spectra, page 32: Per-species peptide precision at full coverage on the Kingdoms de novo test set (deterministic run-disjoint split, at most 100k spectra per species).
| The Proteome Landscape of the Kingdoms of Life | Peptide precision at coverage 1 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Akkermansia muciniphila | Arabidopsis thaliana (callus) | Arabidopsis thaliana (root) | Arabidopsis thaliana (sprout) | Bacillus subtilis | Bacteroides fragilis | Bacteroides thetaiotaomicron | Bacteroides uniformis | Bacteroides vulgatus | Bifidobacterium adolescentis | Bifidobacterium longum subsp. longum | Blautia obeum | |
| dIon init.; DNL-v1, 200 peaks | 0.584 | 0.617 | 0.620 | 0.652 | 0.559 | 0.631 | 0.607 | 0.632 | 0.612 | 0.563 | 0.525 | 0.606 |
| dIon from scratch; DNL-v1, 200 peaks | 0.535 | 0.573 | 0.574 | 0.605 | 0.527 | 0.583 | 0.561 | 0.585 | 0.562 | 0.519 | 0.487 | 0.554 |
| Casanovo 5.2.1 · released | 0.487 | 0.528 | 0.510 | 0.537 | 0.506 | 0.505 | 0.493 | 0.512 | 0.491 | 0.471 | 0.451 | 0.502 |
| InstaNovo 1.2.2 · released | 0.546 | 0.586 | 0.581 | 0.620 | 0.546 | 0.574 | 0.554 | 0.576 | 0.554 | 0.537 | 0.503 | 0.572 |
| The Proteome Landscape of the Kingdoms of Life | Peptide precision at coverage 1 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Bos taurus | Caenorhabditis elegans | Canis lupus | Chlamydomonas reinhardtii | Chromera velia | Clostridium bolteae | Clostridium perfringens | Clostridium saccharolyticum | Collinsella aerofaciens | Coprococcus comes | Cricetulus griseus | Danio rerio | |
| dIon init.; DNL-v1, 200 peaks | 0.672 | 0.633 | 0.631 | 0.537 | 0.535 | 0.587 | 0.642 | 0.608 | 0.570 | 0.612 | 0.551 | 0.603 |
| dIon from scratch; DNL-v1, 200 peaks | 0.617 | 0.584 | 0.576 | 0.504 | 0.492 | 0.534 | 0.594 | 0.556 | 0.525 | 0.560 | 0.500 | 0.554 |
| Casanovo 5.2.1 · released | 0.540 | 0.519 | 0.504 | 0.476 | 0.450 | 0.485 | 0.538 | 0.502 | 0.475 | 0.500 | 0.451 | 0.485 |
| InstaNovo 1.2.2 · released | 0.649 | 0.600 | 0.607 | 0.520 | 0.519 | 0.553 | 0.600 | 0.570 | 0.538 | 0.569 | 0.545 | 0.575 |
| The Proteome Landscape of the Kingdoms of Life | Peptide precision at coverage 1 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Dictyostelium discoideum | Didelphis didelphinae | Dorea formicigenerans | Drosophila melanogaster | Eggerthella lenta | Emiliania huxleyi | Escherichia coli | Eubacterium rectale | Fusarium oxysporum | Fusobacterium nucleatum subsp. nucleatum | Gallus gallus | Glycine max | |
| dIon init.; DNL-v1, 200 peaks | 0.622 | 0.645 | 0.555 | 0.640 | 0.519 | 0.560 | 0.619 | 0.564 | 0.494 | 0.641 | 0.659 | 0.608 |
| dIon from scratch; DNL-v1, 200 peaks | 0.566 | 0.589 | 0.514 | 0.586 | 0.462 | 0.515 | 0.567 | 0.516 | 0.457 | 0.594 | 0.607 | 0.561 |
| Casanovo 5.2.1 · released | 0.476 | 0.508 | 0.485 | 0.501 | 0.408 | 0.449 | 0.495 | 0.467 | 0.438 | 0.538 | 0.528 | 0.494 |
| InstaNovo 1.2.2 · released | 0.569 | 0.611 | 0.530 | 0.596 | 0.482 | 0.530 | 0.573 | 0.521 | 0.476 | 0.599 | 0.622 | 0.573 |
| The Proteome Landscape of the Kingdoms of Life | Peptide precision at coverage 1 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Gossypium hirsutum | Guillardia theta | Haloarcula marismortui | Halobacterium sp. | Homo sapiens | Lactobacillus paracasei | Mus musculus | Mycoplasma intracellular | Neurospora crassa | Odoribacter splanchnicus | Oryctolagus cuniculus | Oryzias melastigma | |
| dIon init.; DNL-v1, 200 peaks | 0.607 | 0.579 | 0.652 | 0.556 | 0.679 | 0.586 | 0.611 | 0.761 | 0.553 | 0.598 | 0.648 | 0.593 |
| dIon from scratch; DNL-v1, 200 peaks | 0.560 | 0.533 | 0.616 | 0.522 | 0.624 | 0.541 | 0.555 | 0.698 | 0.511 | 0.552 | 0.582 | 0.539 |
| Casanovo 5.2.1 · released | 0.504 | 0.472 | 0.581 | 0.489 | 0.543 | 0.489 | 0.479 | 0.636 | 0.461 | 0.500 | 0.497 | 0.471 |
| InstaNovo 1.2.2 · released | 0.575 | 0.550 | 0.589 | 0.518 | 0.662 | 0.554 | 0.596 | 0.743 | 0.522 | 0.551 | 0.611 | 0.557 |
| The Proteome Landscape of the Kingdoms of Life | Peptide precision at coverage 1 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Parabacteroides distasonis | Parabacteroides merdae | Phaeodactylum tricornutum | Porphyra umbilicalis | Prevotella copri | Rattus norvegicus | Roseburia intestinalis | Ruminococcus bromii | Ruminococcus gnavus | Ruminococcus torques | Saccharomyces cerevisiae | Stentor coeruleus | |
| dIon init.; DNL-v1, 200 peaks | 0.637 | 0.627 | 0.555 | 0.617 | 0.646 | 0.580 | 0.522 | 0.595 | 0.623 | 0.649 | 0.650 | 0.615 |
| dIon from scratch; DNL-v1, 200 peaks | 0.585 | 0.577 | 0.511 | 0.574 | 0.598 | 0.531 | 0.476 | 0.549 | 0.573 | 0.600 | 0.602 | 0.562 |
| Casanovo 5.2.1 · released | 0.523 | 0.520 | 0.457 | 0.497 | 0.537 | 0.482 | 0.445 | 0.505 | 0.505 | 0.530 | 0.517 | 0.486 |
| InstaNovo 1.2.2 · released | 0.588 | 0.577 | 0.532 | 0.583 | 0.599 | 0.580 | 0.497 | 0.562 | 0.578 | 0.604 | 0.602 | 0.572 |
| The Proteome Landscape of the Kingdoms of Life | Peptide precision at coverage 1 | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Streptococcus parasanguinis | Sulfolobus solfataricus | Sus scrofa | Symbiodinium microadriaticum | Synechocystis nigrescens | Tardigrade | Thalassiosira pseudonana | Triticum aestivum | Veillonella parvula | Vitis vinifera | |
| dIon init.; DNL-v1, 200 peaks | 0.627 | 0.567 | 0.577 | 0.551 | 0.652 | 0.618 | 0.562 | 0.616 | 0.554 | 0.581 |
| dIon from scratch; DNL-v1, 200 peaks | 0.577 | 0.514 | 0.525 | 0.510 | 0.615 | 0.564 | 0.515 | 0.569 | 0.509 | 0.543 |
| Casanovo 5.2.1 · released | 0.518 | 0.473 | 0.462 | 0.477 | 0.577 | 0.493 | 0.454 | 0.488 | 0.454 | 0.510 |
| InstaNovo 1.2.2 · released | 0.583 | 0.543 | 0.572 | 0.546 | 0.633 | 0.578 | 0.531 | 0.577 | 0.511 | 0.559 |
Peptide precision at full coverage per species of dIon's Kingdoms de novo test split. The 'Spectra' column, the number of test spectra per species, is not recorded as a measurement.
Table1 (Kingdoms de novo)
dIon: Fragmentation-Based Invariance for Self-Supervised Learning of Tandem Mass Spectra, page 7: De novo sequencing on the Kingdoms de novo (all 70 species) and MSKB-final test sets. Within each training regime, scratch and dIon initialization use an identical end-to-end training protocol.
| The Proteome Landscape of the Kingdoms of Life | Peptide precision at coverage 1 |
|---|---|
| Kingdoms | |
| dIon from scratch, end-to-end; trained on MSKB-final | 0.449 |
| dIon init., end-to-end; trained on MSKB-final | 0.533 |
| dIon from scratch, end-to-end; trained on DNL-v1 | 0.554 |
| dIon init., end-to-end; trained on DNL-v1 | 0.602 |
| Casanovo 5.2.1 · released | 0.492 |
| InstaNovo 1.2.2 · released | 0.570 |
Peptide precision here is at FULL coverage, unanswered spectra counted wrong, which is Casanovo's precision at coverage 1. Rows are grouped by training corpus, recorded in each variant. InstaNovo 1.2.2 has no MSKB-final value: it 'was trained on MassIVE-KB v1, the source of this test set'.
GyroNovo: Error-Guided Fragment Imputation with Mass-Aware Attention for De Novo Peptide Sequencing (2026) · 6 tables
Table2 (Seven-species)
GyroNovo: Error-Guided Fragment Imputation with Mass-Aware Attention for De Novo Peptide Sequencing, page 7: PTM-levelperformanceontheNine-Species,SevenSpecies, and HC-PT datasets. Best results are shown in bold.
|
Seven-species benchmark NovoBench split |
Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo · quoted | 0.391 | 0.373 |
| PointNovo · quoted | 0.117 | 0.094 |
| InstaNovo · quoted | 0.126 | 0.115 |
| Casanovo · quoted | 0.360 | 0.251 |
| AdaNovo · quoted | 0.448 | 0.321 |
| LIPNovo · quoted | 0.604 | 0.498 |
| LIPNovo+ · quoted | 0.648 | 0.561 |
| LIPNovo reproduced · retrained | 0.602 | 0.500 |
| GyroNovo | 0.665 | 0.565 |
Table2 (Nine-species)
GyroNovo: Error-Guided Fragment Imputation with Mass-Aware Attention for De Novo Peptide Sequencing, page 7: PTM-levelperformanceontheNine-Species,SevenSpecies, and HC-PT datasets. Best results are shown in bold.
| Nine-species benchmark | Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo · quoted | 0.576 | 0.529 |
| PointNovo · quoted | 0.629 | 0.546 |
| InstaNovo · quoted | 0.443 | 0.294 |
| Casanovo · quoted | 0.706 | 0.566 |
| AdaNovo · quoted | 0.652 | 0.570 |
| LIPNovo · quoted | 0.765 | 0.656 |
| LIPNovo+ · quoted | 0.801 | 0.678 |
| LIPNovo reproduced · retrained | 0.773 | 0.646 |
| GyroNovo | 0.815 | 0.731 |
Table2 (HC-PT)
GyroNovo: Error-Guided Fragment Imputation with Mass-Aware Attention for De Novo Peptide Sequencing, page 7: PTM-levelperformanceontheNine-Species,SevenSpecies, and HC-PT datasets. Best results are shown in bold.
|
ProteomeTools HC-PT (NovoBench) |
Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo · quoted | 0.626 | 0.615 |
| PointNovo · quoted | 0.676 | 0.740 |
| InstaNovo · quoted | 0.350 | 0.261 |
| Casanovo · quoted | 0.501 | 0.460 |
| AdaNovo · quoted | 0.552 | 0.482 |
| LIPNovo · quoted | 0.732 | 0.745 |
| LIPNovo+ · quoted | 0.757 | 0.805 |
| LIPNovo reproduced · retrained | 0.690 | 0.762 |
| GyroNovo | 0.790 | 0.817 |
Table1 (Seven-species)
GyroNovo: Error-Guided Fragment Imputation with Mass-Aware Attention for De Novo Peptide Sequencing, page 7: Amino-acid- and peptide-level performance on the Nine-Species, Seven-Species, and HC-PT datasets. Best results are shown in bold.
|
Seven-species benchmark NovoBench split |
Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| DeepNovo · quoted | 0.492 | 0.433 | 0.204 | 0.136 |
| PointNovo · quoted | 0.196 | 0.169 | 0.022 | 0.007 |
| Casanovo · quoted | 0.322 | 0.327 | 0.119 | 0.084 |
| AdaNovo · quoted | 0.379 | 0.385 | 0.174 | 0.135 |
| InstaNovo · quoted | 0.192 | 0.176 | 0.031 | 0.009 |
| LIPNovo · quoted | 0.557 | 0.560 | 0.327 | 0.281 |
| LIPNovo+ · quoted | 0.619 | 0.622 | 0.383 | 0.337 |
| LIPNovo reproduced · retrained | 0.553 | 0.554 | 0.325 | 0.270 |
| GyroNovo | 0.632 | 0.635 | 0.421 | 0.378 |
Table1 (Nine-species)
GyroNovo: Error-Guided Fragment Imputation with Mass-Aware Attention for De Novo Peptide Sequencing, page 7: Amino-acid- and peptide-level performance on the Nine-Species, Seven-Species, and HC-PT datasets. Best results are shown in bold.
| Nine-species benchmark | Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| PEAKS · quoted | 0.748 | 0.428 | ||
| DeepNovo · quoted | 0.696 | 0.638 | 0.428 | 0.376 |
| PointNovo · quoted | 0.740 | 0.671 | 0.480 | 0.436 |
| Casanovo · quoted | 0.697 | 0.696 | 0.481 | 0.439 |
| AdaNovo · quoted | 0.698 | 0.709 | 0.505 | 0.469 |
| InstaNovo · quoted | 0.420 | 0.395 | 0.164 | 0.123 |
| LIPNovo · quoted | 0.797 | 0.797 | 0.582 | 0.547 |
| LIPNovo+ · quoted | 0.831 | 0.831 | 0.637 | 0.612 |
| LIPNovo reproduced · retrained | 0.794 | 0.796 | 0.583 | 0.549 |
| GyroNovo | 0.848 | 0.848 | 0.674 | 0.646 |
Table1 (HC-PT)
GyroNovo: Error-Guided Fragment Imputation with Mass-Aware Attention for De Novo Peptide Sequencing, page 7: Amino-acid- and peptide-level performance on the Nine-Species, Seven-Species, and HC-PT datasets. Best results are shown in bold.
|
ProteomeTools HC-PT (NovoBench) |
Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| DeepNovo · quoted | 0.531 | 0.534 | 0.313 | 0.255 |
| PointNovo · quoted | 0.623 | 0.622 | 0.419 | 0.373 |
| Casanovo · quoted | 0.442 | 0.453 | 0.211 | 0.177 |
| AdaNovo · quoted | 0.442 | 0.451 | 0.212 | 0.178 |
| InstaNovo · quoted | 0.289 | 0.285 | 0.057 | 0.034 |
| LIPNovo · quoted | 0.637 | 0.643 | 0.458 | 0.427 |
| LIPNovo+ · quoted | 0.698 | 0.694 | 0.519 | 0.490 |
| LIPNovo reproduced · retrained | 0.653 | 0.654 | 0.469 | 0.438 |
| GyroNovo | 0.704 | 0.702 | 0.532 | 0.502 |
Learning from tandem mass spectra at scale with a self-supervised foundation model for proteomics (2026) · 2 tables
Table S13
Learning from tandem mass spectra at scale with a self-supervised foundation model for proteomics, page 84: Peptide recall across the biological validation datasets for the de novo sequencing InstaNovo-FM and InstaNovo model variant benchmarks. The best model per dataset is in bold. We abbreviate “InstaNovo (FM size matched)” to “IN (FM-SM)” to conserve page space.
| a dataset per evaluation set | Peptide recall | |||||
|---|---|---|---|---|---|---|
| HeLa degradome | Candidatus Scalindua brodae | Snake venoms | HeLa single-shot | Nanobodies | Wound exudates | |
| InstaNovo-FM fine-tuned | 0.821 | 0.740 | 0.230 | 0.662 | 0.528 | 0.366 |
| InstaNovo-FM from scratch | 0.819 | 0.747 | 0.239 | 0.657 | 0.522 | 0.354 |
| InstaNovo-FM frozen | 0.775 | 0.726 | 0.156 | 0.577 | 0.474 | 0.266 |
| InstaNovo | 0.821 | 0.756 | 0.219 | 0.652 | 0.520 | 0.345 |
| InstaNovo FM size matched | 0.823 | 0.748 | 0.226 | 0.650 | 0.516 | 0.362 |
No accession is printed for the six validation sets. They are mapped from the Methods, which call them InstaNovo's application datasets minus 'the Immuno and Herceptin datasets': GluC is InstaNovo's 'HeLa GluC degradome', TPL Antibodies its nanobodies, and Hela QC, by elimination, its HeLa single-shot set.
Table S12
Learning from tandem mass spectra at scale with a self-supervised foundation model for proteomics, page 84: Peptide recall across the biological validation datasets for the de novo sequencing benchmark. The best model per dataset is in bold.
| a dataset per evaluation set | Peptide recall | |||||
|---|---|---|---|---|---|---|
| HeLa degradome | Candidatus Scalindua brodae | Snake venoms | HeLa single-shot | Nanobodies | Wound exudates | |
| InstaNovo-FM fine-tuned | 0.821 | 0.740 | 0.230 | 0.662 | 0.528 | 0.366 |
| InstaNovo v1.2 | 0.868 | 0.764 | 0.227 | 0.708 | 0.517 | 0.431 |
| Casanovo | 0.767 | 0.743 | 0.217 | 0.531 | 0.465 | 0.262 |
| XuanjiNovo | 0.808 | 0.741 | 0.233 | 0.673 | 0.529 | 0.466 |
No accession is printed for the six validation sets. They are mapped from the Methods, which call them InstaNovo's application datasets minus 'the Immuno and Herceptin datasets': GluC is InstaNovo's 'HeLa GluC degradome', TPL Antibodies its nanobodies, and Hela QC, by elimination, its HeLa single-shot set.
Prime-DiffNovo: Accurate Peptide De Novo Sequencing via Non-autoregressive Generation and Diffusion Refinement (2026) · 2 tables
Table 1 (Nine-species · revised (build not stated))
Prime-DiffNovo: Accurate Peptide De Novo Sequencing via Non-autoregressive Generation and Diffusion Refinement, page 8: Peptide accuracy comparison of different de novo peptide sequencing methods across nine species on two benchmark datasets.
|
Nine-species benchmark revised (build not stated) |
Peptide accuracy | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Apis mellifera | Bacillus subtilis | Candidatus Thiodiazotropha endoloripes | Homo sapiens | Methanosarcina mazei | Mus musculus | Saccharomyces cerevisiae | Solanum lycopersicum | Vigna mungo | Weighted average | |
| InstaNovo v1.1 | 0.625 | 0.704 | 0.512 | 0.670 | 0.666 | 0.504 | 0.758 | 0.721 | 0.679 | 0.698 |
| InstaNovo+ v1.1 | 0.646 | 0.731 | 0.545 | 0.687 | 0.691 | 0.523 | 0.779 | 0.743 | 0.704 | 0.723 |
| π-PrimeNovo | 0.602 | 0.702 | 0.549 | 0.704 | 0.681 | 0.537 | 0.671 | 0.699 | 0.731 | 0.682 |
| Prime-DiffNovo | 0.658 | 0.751 | 0.581 | 0.733 | 0.717 | 0.566 | 0.817 | 0.771 | 0.748 | 0.749 |
Table 1 (Nine-species · original (DeepNovo, 2017))
Prime-DiffNovo: Accurate Peptide De Novo Sequencing via Non-autoregressive Generation and Diffusion Refinement, page 8: Peptide accuracy comparison of different de novo peptide sequencing methods across nine species on two benchmark datasets.
|
Nine-species benchmark original (DeepNovo, 2017) |
Peptide accuracy | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Apis mellifera | Bacillus subtilis | Candidatus Thiodiazotropha endoloripes | Homo sapiens | Methanosarcina mazei | Mus musculus | Saccharomyces cerevisiae | Solanum lycopersicum | Vigna mungo | Weighted average | |
| InstaNovo v1.1 | 0.526 | 0.629 | 0.444 | 0.506 | 0.571 | 0.509 | 0.602 | 0.615 | 0.613 | 0.565 |
| InstaNovo+ v1.1 | 0.555 | 0.662 | 0.475 | 0.516 | 0.596 | 0.525 | 0.634 | 0.642 | 0.662 | 0.593 |
| π-PrimeNovo | 0.592 | 0.697 | 0.511 | 0.566 | 0.627 | 0.558 | 0.688 | 0.679 | 0.678 | 0.630 |
| Prime-DiffNovo | 0.607 | 0.716 | 0.526 | 0.572 | 0.644 | 0.566 | 0.698 | 0.690 | 0.709 | 0.645 |
Discrete Diffusion with Physical Mass Constraints for De Novo Peptide Sequencing (2026) · 6 tables
Table2 (Seven-species)
Discrete Diffusion with Physical Mass Constraints for De Novo Peptide Sequencing, page 7: Comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in PTM-level performance.
|
Seven-species benchmark NovoBench split |
Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo · retrained | 0.391 | 0.373 |
| PointNovo · retrained | 0.117 | 0.094 |
| InstaNovo · retrained | 0.126 | 0.115 |
| Casanovo · retrained | 0.360 | 0.251 |
| AdaNovo · retrained | 0.448 | 0.321 |
| π-HelixNovo · retrained | 0.473 | 0.366 |
| LIPNovo · retrained | 0.604 | 0.498 |
| PhysNovo | 0.654 | 0.549 |
Table2 (Nine-species)
Discrete Diffusion with Physical Mass Constraints for De Novo Peptide Sequencing, page 7: Comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in PTM-level performance.
|
Nine-species benchmark revised (balanced) |
Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo · retrained | 0.576 | 0.529 |
| PointNovo · retrained | 0.629 | 0.546 |
| InstaNovo · retrained | 0.443 | 0.294 |
| Casanovo · retrained | 0.706 | 0.566 |
| AdaNovo · retrained | 0.652 | 0.570 |
| π-HelixNovo · retrained | 0.680 | 0.598 |
| LIPNovo · retrained | 0.765 | 0.656 |
| PhysNovo | 0.793 | 0.686 |
Table2 (HC-PT)
Discrete Diffusion with Physical Mass Constraints for De Novo Peptide Sequencing, page 7: Comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in PTM-level performance.
|
ProteomeTools HC-PT (NovoBench) |
Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo · retrained | 0.626 | 0.615 |
| PointNovo · retrained | 0.676 | 0.740 |
| InstaNovo · retrained | 0.350 | 0.261 |
| Casanovo · retrained | 0.501 | 0.460 |
| AdaNovo · retrained | 0.552 | 0.482 |
| π-HelixNovo · retrained | 0.568 | 0.667 |
| LIPNovo · retrained | 0.732 | 0.745 |
| PhysNovo | 0.763 | 0.770 |
Table1 (Seven-species)
Discrete Diffusion with Physical Mass Constraints for De Novo Peptide Sequencing, page 7: Comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in amino acid-level and peptidelevel performance. The best results are marked in bold, and the second best are underlined.
|
Seven-species benchmark NovoBench split |
Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| DeepNovo · retrained | 0.492 | 0.433 | 0.204 | 0.136 |
| PointNovo · retrained | 0.196 | 0.169 | 0.022 | 0.007 |
| InstaNovo · retrained | 0.192 | 0.176 | 0.031 | 0.009 |
| Casanovo · retrained | 0.322 | 0.327 | 0.119 | 0.084 |
| AdaNovo · retrained | 0.379 | 0.385 | 0.174 | 0.135 |
| π-HelixNovo · retrained | 0.481 | 0.472 | 0.234 | 0.173 |
| LIPNovo · retrained | 0.557 | 0.560 | 0.327 | 0.281 |
| ReNovo | 0.512 | 0.514 | 0.278 | 0.228 |
| PhysNovo | 0.568 | 0.569 | 0.346 | 0.290 |
Table1 (Nine-species)
Discrete Diffusion with Physical Mass Constraints for De Novo Peptide Sequencing, page 7: Comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in amino acid-level and peptidelevel performance. The best results are marked in bold, and the second best are underlined.
|
Nine-species benchmark revised (balanced) |
Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| PEAKS | 0.748 | 0.428 | ||
| DeepNovo · retrained | 0.696 | 0.638 | 0.428 | 0.376 |
| PointNovo · retrained | 0.740 | 0.671 | 0.480 | 0.436 |
| InstaNovo · retrained | 0.420 | 0.395 | 0.164 | 0.123 |
| Casanovo · retrained | 0.697 | 0.696 | 0.481 | 0.439 |
| AdaNovo · retrained | 0.698 | 0.709 | 0.505 | 0.469 |
| π-HelixNovo · retrained | 0.765 | 0.758 | 0.517 | 0.453 |
| LIPNovo · retrained | 0.797 | 0.797 | 0.582 | 0.547 |
| π-PrimeNovo | 0.790 | |||
| ReNovo | 0.770 | 0.769 | 0.568 | 0.528 |
| PhysNovo | 0.815 | 0.814 | 0.588 | 0.553 |
Table1 (HC-PT)
Discrete Diffusion with Physical Mass Constraints for De Novo Peptide Sequencing, page 7: Comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in amino acid-level and peptidelevel performance. The best results are marked in bold, and the second best are underlined.
|
ProteomeTools HC-PT (NovoBench) |
Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| DeepNovo · retrained | 0.531 | 0.534 | 0.313 | 0.255 |
| PointNovo · retrained | 0.623 | 0.622 | 0.419 | 0.373 |
| InstaNovo · retrained | 0.289 | 0.285 | 0.057 | 0.034 |
| Casanovo · retrained | 0.442 | 0.453 | 0.211 | 0.177 |
| AdaNovo · retrained | 0.442 | 0.451 | 0.212 | 0.178 |
| π-HelixNovo · retrained | 0.588 | 0.582 | 0.356 | 0.318 |
| LIPNovo · retrained | 0.637 | 0.643 | 0.458 | 0.427 |
| ReNovo | 0.651 | 0.648 | 0.467 | 0.436 |
| PhysNovo | 0.649 | 0.652 | 0.473 | 0.444 |
MemNovo: Look Back at the Spectrum for Balanced De Novo Peptide Sequencing from Mass Spectrometry (2026) · 2 tables
Table 6
MemNovo: Look Back at the Spectrum for Balanced De Novo Peptide Sequencing from Mass Spectrometry, page 10: Complete four-metric comparison on the Nine Species benchmark for InstaNovo and InstaNovo + MemNovo.
|
Nine-species benchmark revised (balanced) |
Amino acid precision | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Bacillus subtilis | Saccharomyces cerevisiae | Methanosarcina mazei | Apis mellifera | Solanum lycopersicum | Vigna mungo | Homo sapiens | Mus musculus | Candidatus Thiodiazotropha endoloripes | Average | |
| InstaNovo | 0.7307 | 0.7665 | 0.7410 | 0.6740 | 0.7862 | 0.7851 | 0.7186 | 0.6767 | 0.6242 | 0.7226 |
| MemNovo on InstaNovo | 0.7372 | 0.7798 | 0.7383 | 0.6775 | 0.7945 | 0.7912 | 0.7314 | 0.6739 | 0.6433 | 0.7308 |
|
Nine-species benchmark revised (balanced) |
Amino acid recall | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Bacillus subtilis | Saccharomyces cerevisiae | Methanosarcina mazei | Apis mellifera | Solanum lycopersicum | Vigna mungo | Homo sapiens | Mus musculus | Candidatus Thiodiazotropha endoloripes | Average | |
| InstaNovo | 0.7124 | 0.7482 | 0.7281 | 0.6542 | 0.7710 | 0.7623 | 0.7010 | 0.6608 | 0.6028 | 0.7045 |
| MemNovo on InstaNovo | 0.7109 | 0.7441 | 0.7334 | 0.6590 | 0.7704 | 0.7553 | 0.6990 | 0.6686 | 0.6053 | 0.7051 |
|
Nine-species benchmark revised (balanced) |
Peptide precision | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Bacillus subtilis | Saccharomyces cerevisiae | Methanosarcina mazei | Apis mellifera | Solanum lycopersicum | Vigna mungo | Homo sapiens | Mus musculus | Candidatus Thiodiazotropha endoloripes | Average | |
| InstaNovo | 0.6366 | 0.6877 | 0.6096 | 0.5526 | 0.6904 | 0.6425 | 0.6138 | 0.4922 | 0.4660 | 0.5991 |
| MemNovo on InstaNovo | 0.6357 | 0.6925 | 0.6036 | 0.5477 | 0.6904 | 0.6419 | 0.6146 | 0.4843 | 0.4698 | 0.5978 |
|
Nine-species benchmark revised (balanced) |
Peptide recall | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Bacillus subtilis | Saccharomyces cerevisiae | Methanosarcina mazei | Apis mellifera | Solanum lycopersicum | Vigna mungo | Homo sapiens | Mus musculus | Candidatus Thiodiazotropha endoloripes | Average | |
| InstaNovo | 0.6249 | 0.6772 | 0.5997 | 0.5384 | 0.6821 | 0.6293 | 0.6031 | 0.4823 | 0.4555 | 0.5881 |
| MemNovo on InstaNovo | 0.6259 | 0.6780 | 0.6015 | 0.5408 | 0.6824 | 0.6303 | 0.6026 | 0.4834 | 0.4567 | 0.5891 |
Table2
MemNovo: Look Back at the Spectrum for Balanced De Novo Peptide Sequencing from Mass Spectrometry, page 7: Performance comparison on the Nine Species benchmark. We report amino acid precision (AA) and peptide precision (Pep.) for each method. For Casanovo and InstaNovo, we additionally show results with MemNovo applied and the corresponding relative improvement (Rel. Imp.). Best results for each species are shown in bold. Results marked with † are reported from original publications, which may use different model versions and evaluation protocols; direct numerical comparison with our evaluation should be interpreted with caution.
|
Nine-species benchmark revised (balanced) |
Amino acid precision | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Mus musculus | Homo sapiens | Saccharomyces cerevisiae | Methanosarcina mazei | Apis mellifera | Solanum lycopersicum | Vigna mungo | Bacillus subtilis | Candidatus Thiodiazotropha endoloripes | Average | |
| DeepNovo · quoted | 0.6230 | 0.6100 | 0.7500 | 0.6940 | 0.6300 | 0.7310 | 0.6790 | 0.7420 | 0.6020 | 0.6734 |
| PointNovo · quoted | 0.6260 | 0.6060 | 0.7790 | 0.7120 | 0.6440 | 0.7330 | 0.7300 | 0.7680 | 0.5890 | 0.6874 |
| Casanovo | 0.6352 | 0.6885 | 0.7672 | 0.7253 | 0.6730 | 0.7302 | 0.7446 | 0.7701 | 0.6895 | 0.7137 |
| AdaNovo · quoted | 0.6460 | 0.6180 | 0.7930 | 0.7280 | 0.6500 | 0.7400 | 0.7190 | 0.7390 | 0.6420 | 0.6972 |
| InstaNovo | 0.7351 | 0.7934 | 0.8447 | 0.8214 | 0.7754 | 0.8181 | 0.8450 | 0.8367 | 0.7631 | 0.8037 |
| MemNovo on Casanovo | 0.6524 | 0.7031 | 0.7688 | 0.7287 | 0.7749 | 0.7442 | 0.7469 | 0.7941 | 0.7055 | 0.7354 |
| MemNovo on InstaNovo | 0.7614 | 0.8130 | 0.8553 | 0.8350 | 0.7934 | 0.8324 | 0.8566 | 0.8504 | 0.7912 | 0.8210 |
|
Nine-species benchmark revised (balanced) |
Peptide precision | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Mus musculus | Homo sapiens | Saccharomyces cerevisiae | Methanosarcina mazei | Apis mellifera | Solanum lycopersicum | Vigna mungo | Bacillus subtilis | Candidatus Thiodiazotropha endoloripes | Average | |
| DeepNovo · quoted | 0.2860 | 0.2930 | 0.4620 | 0.4220 | 0.3300 | 0.4540 | 0.4360 | 0.4490 | 0.2530 | 0.3761 |
| PointNovo · quoted | 0.3550 | 0.3510 | 0.5340 | 0.4780 | 0.3960 | 0.5130 | 0.5110 | 0.5180 | 0.2980 | 0.4393 |
| Casanovo | 0.2404 | 0.3105 | 0.4089 | 0.3254 | 0.2875 | 0.3873 | 0.3314 | 0.3585 | 0.2274 | 0.3197 |
| AdaNovo · quoted | 0.4670 | 0.3730 | 0.5930 | 0.4960 | 0.4310 | 0.5300 | 0.5460 | 0.5280 | 0.3720 | 0.4818 |
| InstaNovo | 0.3485 | 0.4562 | 0.5559 | 0.4927 | 0.4318 | 0.5116 | 0.5177 | 0.5185 | 0.3435 | 0.4640 |
| MemNovo on Casanovo | 0.3372 | 0.4541 | 0.4968 | 0.4295 | 0.5226 | 0.5250 | 0.3530 | 0.5309 | 0.3529 | 0.4447 |
| MemNovo on InstaNovo | 0.3522 | 0.4675 | 0.5981 | 0.5051 | 0.4419 | 0.5305 | 0.5481 | 0.5298 | 0.3668 | 0.4822 |
LIPNovo+: Self-Reflective Latent Imputation for Robust De Novo Peptide Sequencing (2026) · 6 tables
Table3 (Seven-species)
LIPNovo+: Self-Reflective Latent Imputation for Robust De Novo Peptide Sequencing, page 16: Comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in PTM-level performance. The best and second-best results are marked in bold and underline, respectively.
|
Seven-species benchmark NovoBench split |
Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo | 0.391 | 0.373 |
| PointNovo | 0.117 | 0.094 |
| InstaNovo | 0.126 | 0.115 |
| Casanovo · retrained | 0.360 | 0.251 |
| AdaNovo | 0.448 | 0.321 |
| π-HelixNovo | 0.473 | 0.366 |
| SearchNovo | 0.472 | 0.447 |
| Casanovo retrained · retrained | 0.368 | 0.292 |
| LIPNovo | 0.604 | 0.498 |
| LIPNovo+ | 0.648 | 0.561 |
Table3 (Nine-species)
LIPNovo+: Self-Reflective Latent Imputation for Robust De Novo Peptide Sequencing, page 16: Comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in PTM-level performance. The best and second-best results are marked in bold and underline, respectively.
| Nine-species benchmark | Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo | 0.576 | 0.529 |
| PointNovo | 0.629 | 0.546 |
| InstaNovo | 0.443 | 0.294 |
| Casanovo · retrained | 0.706 | 0.566 |
| AdaNovo | 0.652 | 0.570 |
| π-HelixNovo | 0.680 | 0.598 |
| SearchNovo | 0.764 | 0.599 |
| Casanovo retrained · retrained | 0.755 | 0.601 |
| LIPNovo | 0.765 | 0.656 |
| LIPNovo+ | 0.801 | 0.678 |
Table3 (HC-PT)
LIPNovo+: Self-Reflective Latent Imputation for Robust De Novo Peptide Sequencing, page 16: Comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in PTM-level performance. The best and second-best results are marked in bold and underline, respectively.
|
ProteomeTools HC-PT (NovoBench) |
Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo | 0.626 | 0.615 |
| PointNovo | 0.676 | 0.740 |
| InstaNovo | 0.350 | 0.261 |
| Casanovo · retrained | 0.501 | 0.460 |
| AdaNovo | 0.552 | 0.482 |
| π-HelixNovo | 0.568 | 0.667 |
| SearchNovo | 0.715 | 0.772 |
| Casanovo retrained · retrained | 0.550 | 0.582 |
| LIPNovo | 0.732 | 0.745 |
| LIPNovo+ | 0.757 | 0.805 |
In the paper: column ptm recall: the original table underlined SearchNovo (0.772), LIPNovo (0.745).
Table2 (Seven-species)
LIPNovo+: Self-Reflective Latent Imputation for Robust De Novo Peptide Sequencing, page 15: Comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in amino acid-level and peptide-level performance. The best and second-best results are marked in bold and underline, respectively.
|
Seven-species benchmark NovoBench split |
Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| DeepNovo | 0.492 | 0.433 | 0.204 | 0.136 |
| PointNovo | 0.196 | 0.169 | 0.022 | 0.007 |
| Casanovo · retrained | 0.322 | 0.327 | 0.119 | 0.084 |
| AdaNovo | 0.379 | 0.385 | 0.174 | 0.135 |
| π-HelixNovo | 0.481 | 0.472 | 0.234 | 0.173 |
| InstaNovo | 0.192 | 0.176 | 0.031 | 0.009 |
| SearchNovo | 0.489 | 0.488 | 0.259 | 0.174 |
| ReNovo | 0.512 | 0.514 | 0.278 | 0.228 |
| DiffuNovo | 0.437 | 0.435 | 0.193 | 0.162 |
| Casanovo retrained · retrained | 0.357 | 0.366 | 0.159 | 0.119 |
| LIPNovo | 0.557 | 0.560 | 0.327 | 0.281 |
| LIPNovo+ | 0.619 | 0.622 | 0.383 | 0.337 |
Table2 (Nine-species)
LIPNovo+: Self-Reflective Latent Imputation for Robust De Novo Peptide Sequencing, page 15: Comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in amino acid-level and peptide-level performance. The best and second-best results are marked in bold and underline, respectively.
| Nine-species benchmark | Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| PEAKS | 0.748 | 0.428 | ||
| DeepNovo | 0.696 | 0.638 | 0.428 | 0.376 |
| PointNovo | 0.740 | 0.671 | 0.480 | 0.436 |
| Casanovo · retrained | 0.697 | 0.696 | 0.481 | 0.439 |
| AdaNovo | 0.698 | 0.709 | 0.505 | 0.469 |
| π-HelixNovo | 0.765 | 0.758 | 0.517 | 0.453 |
| InstaNovo | 0.420 | 0.395 | 0.164 | 0.123 |
| SearchNovo | 0.748 | 0.746 | 0.550 | 0.489 |
| ReNovo | 0.770 | 0.769 | 0.568 | 0.528 |
| DiffuNovo | 0.791 | 0.789 | 0.565 | 0.536 |
| Casanovo retrained · retrained | 0.741 | 0.740 | 0.529 | 0.493 |
| LIPNovo | 0.797 | 0.797 | 0.582 | 0.547 |
| LIPNovo+ | 0.831 | 0.831 | 0.637 | 0.612 |
Table2 (HC-PT)
LIPNovo+: Self-Reflective Latent Imputation for Robust De Novo Peptide Sequencing, page 15: Comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in amino acid-level and peptide-level performance. The best and second-best results are marked in bold and underline, respectively.
|
ProteomeTools HC-PT (NovoBench) |
Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| DeepNovo | 0.531 | 0.534 | 0.313 | 0.255 |
| PointNovo | 0.623 | 0.622 | 0.419 | 0.373 |
| Casanovo · retrained | 0.442 | 0.453 | 0.211 | 0.177 |
| AdaNovo | 0.442 | 0.451 | 0.212 | 0.178 |
| π-HelixNovo | 0.588 | 0.582 | 0.356 | 0.318 |
| InstaNovo | 0.289 | 0.285 | 0.057 | 0.034 |
| SearchNovo | 0.652 | 0.658 | 0.447 | 0.413 |
| ReNovo | 0.651 | 0.648 | 0.467 | 0.436 |
| DiffuNovo | 0.654 | 0.654 | 0.458 | 0.434 |
| Casanovo retrained · retrained | 0.525 | 0.530 | 0.324 | 0.290 |
| LIPNovo | 0.637 | 0.643 | 0.458 | 0.427 |
| LIPNovo+ | 0.698 | 0.694 | 0.519 | 0.490 |
In the paper: column amino acid precision: the original table underlined LIPNovo (0.637).
CausalNovo: Advancing De Novo Peptide Sequencing via a Causality-Informed Framework (2026) · 6 tables
Table2 (Seven-species)
CausalNovo: Advancing De Novo Peptide Sequencing via a Causality-Informed Framework, page 6: Comparison with state-of-the-art models in PTM-level performance. † denotes our retrained results, and others are given by NovoBench. The best is marked in bold.
|
Seven-species benchmark NovoBench split |
Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo · quoted | 0.391 | 0.373 |
| PointNovo · quoted | 0.117 | 0.094 |
| InstaNovo · quoted | 0.126 | 0.115 |
| SearchNovo · quoted | 0.472 | 0.447 |
| Casanovo · quoted | 0.360 | 0.251 |
| Casanovo · retrained | 0.368 | 0.292 |
| CausalNovo on †CasaNovo | 0.503 | 0.422 |
| AdaNovo · quoted | 0.448 | 0.321 |
| AdaNovo · retrained | 0.430 | 0.356 |
| CausalNovo on †AdaNovo | 0.469 | 0.398 |
| π-HelixNovo · quoted | 0.473 | 0.366 |
| π-HelixNovo · retrained | 0.362 | 0.370 |
| CausalNovo on †π-HelixNovo | 0.513 | 0.427 |
Table2 (Nine-species)
CausalNovo: Advancing De Novo Peptide Sequencing via a Causality-Informed Framework, page 6: Comparison with state-of-the-art models in PTM-level performance. † denotes our retrained results, and others are given by NovoBench. The best is marked in bold.
| Nine-species benchmark | Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo · quoted | 0.576 | 0.529 |
| PointNovo · quoted | 0.629 | 0.546 |
| InstaNovo · quoted | 0.443 | 0.294 |
| SearchNovo · quoted | 0.764 | 0.599 |
| Casanovo · quoted | 0.706 | 0.566 |
| Casanovo · retrained | 0.755 | 0.601 |
| CausalNovo on †CasaNovo | 0.791 | 0.608 |
| AdaNovo · quoted | 0.652 | 0.570 |
| AdaNovo · retrained | 0.678 | 0.552 |
| CausalNovo on †AdaNovo | 0.769 | 0.607 |
| π-HelixNovo · quoted | 0.680 | 0.598 |
| π-HelixNovo · retrained | 0.723 | 0.593 |
| CausalNovo on †π-HelixNovo | 0.731 | 0.616 |
Table2 (HC-PT)
CausalNovo: Advancing De Novo Peptide Sequencing via a Causality-Informed Framework, page 6: Comparison with state-of-the-art models in PTM-level performance. † denotes our retrained results, and others are given by NovoBench. The best is marked in bold.
|
ProteomeTools HC-PT (NovoBench) |
Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo · quoted | 0.626 | 0.615 |
| PointNovo · quoted | 0.676 | 0.740 |
| InstaNovo · quoted | 0.350 | 0.261 |
| SearchNovo · quoted | 0.715 | 0.772 |
| Casanovo · quoted | 0.501 | 0.460 |
| Casanovo · retrained | 0.550 | 0.582 |
| CausalNovo on †CasaNovo | 0.671 | 0.741 |
| AdaNovo · quoted | 0.552 | 0.482 |
| AdaNovo · retrained | 0.562 | 0.532 |
| CausalNovo on †AdaNovo | 0.652 | 0.743 |
| π-HelixNovo · quoted | 0.568 | 0.667 |
| π-HelixNovo · retrained | 0.632 | 0.566 |
| CausalNovo on †π-HelixNovo | 0.737 | 0.746 |
Table1 (Seven-species)
CausalNovo: Advancing De Novo Peptide Sequencing via a Causality-Informed Framework, page 6: Comparison with state-of-the-art models in amino acid-level and peptide-level performance. † denotes our retrained results, and others are provided by NovoBench. The best results are marked in bold, and the second-best results are underlined.
|
Seven-species benchmark NovoBench split |
Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| DeepNovo · quoted | 0.492 | 0.433 | 0.204 | 0.136 |
| PointNovo · quoted | 0.196 | 0.169 | 0.022 | 0.007 |
| InstaNovo · quoted | 0.192 | 0.176 | 0.031 | 0.009 |
| SearchNovo · quoted | 0.489 | 0.488 | 0.259 | 0.174 |
| Casanovo · quoted | 0.322 | 0.327 | 0.119 | 0.084 |
| Casanovo · retrained | 0.357 | 0.366 | 0.159 | 0.119 |
| CausalNovo on †CasaNovo | 0.477 | 0.478 | 0.245 | 0.200 |
| AdaNovo · quoted | 0.379 | 0.385 | 0.174 | 0.135 |
| AdaNovo · retrained | 0.403 | 0.405 | 0.189 | 0.149 |
| CausalNovo on †AdaNovo | 0.453 | 0.453 | 0.233 | 0.192 |
| π-HelixNovo · quoted | 0.481 | 0.472 | 0.234 | 0.173 |
| π-HelixNovo · retrained | 0.465 | 0.462 | 0.218 | 0.156 |
| CausalNovo on †π-HelixNovo | 0.536 | 0.534 | 0.282 | 0.229 |
Table1 (Nine-species)
CausalNovo: Advancing De Novo Peptide Sequencing via a Causality-Informed Framework, page 6: Comparison with state-of-the-art models in amino acid-level and peptide-level performance. † denotes our retrained results, and others are provided by NovoBench. The best results are marked in bold, and the second-best results are underlined.
| Nine-species benchmark | Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| PEAKS · quoted | 0.748 | 0.428 | ||
| DeepNovo · quoted | 0.696 | 0.638 | 0.428 | 0.376 |
| PointNovo · quoted | 0.740 | 0.671 | 0.480 | 0.436 |
| InstaNovo · quoted | 0.420 | 0.395 | 0.164 | 0.123 |
| SearchNovo · quoted | 0.748 | 0.746 | 0.550 | 0.489 |
| Casanovo · quoted | 0.697 | 0.696 | 0.481 | 0.439 |
| Casanovo · retrained | 0.741 | 0.740 | 0.529 | 0.493 |
| CausalNovo on †CasaNovo | 0.765 | 0.766 | 0.564 | 0.528 |
| AdaNovo · quoted | 0.698 | 0.709 | 0.505 | 0.469 |
| AdaNovo · retrained | 0.681 | 0.681 | 0.473 | 0.439 |
| CausalNovo on †AdaNovo | 0.744 | 0.746 | 0.542 | 0.507 |
| π-HelixNovo · quoted | 0.765 | 0.758 | 0.517 | 0.453 |
| π-HelixNovo · retrained | 0.765 | 0.752 | 0.509 | 0.431 |
| CausalNovo on †π-HelixNovo | 0.787 | 0.784 | 0.543 | 0.483 |
Table1 (HC-PT)
CausalNovo: Advancing De Novo Peptide Sequencing via a Causality-Informed Framework, page 6: Comparison with state-of-the-art models in amino acid-level and peptide-level performance. † denotes our retrained results, and others are provided by NovoBench. The best results are marked in bold, and the second-best results are underlined.
|
ProteomeTools HC-PT (NovoBench) |
Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| DeepNovo · quoted | 0.531 | 0.534 | 0.313 | 0.255 |
| PointNovo · quoted | 0.623 | 0.622 | 0.419 | 0.373 |
| InstaNovo · quoted | 0.289 | 0.285 | 0.057 | 0.034 |
| SearchNovo · quoted | 0.652 | 0.658 | 0.447 | 0.413 |
| Casanovo · quoted | 0.442 | 0.453 | 0.211 | 0.177 |
| Casanovo · retrained | 0.525 | 0.530 | 0.324 | 0.290 |
| CausalNovo on †CasaNovo | 0.635 | 0.639 | 0.459 | 0.426 |
| AdaNovo · quoted | 0.442 | 0.451 | 0.212 | 0.178 |
| AdaNovo · retrained | 0.492 | 0.496 | 0.289 | 0.254 |
| CausalNovo on †AdaNovo | 0.634 | 0.637 | 0.453 | 0.420 |
| π-HelixNovo · quoted | 0.588 | 0.582 | 0.356 | 0.318 |
| π-HelixNovo · retrained | 0.532 | 0.537 | 0.301 | 0.261 |
| CausalNovo on †π-HelixNovo | 0.656 | 0.658 | 0.450 | 0.415 |
Bidirectional Representations Augmented Autoregressive Biological Sequence Generation (2025) · 1 table
Table1
Bidirectional Representations Augmented Autoregressive Biological Sequence Generation, page 8: Comparison of the performance of CROSSNOVO and baseline methods on the 9-species-v1 test set.
The same table is also printed in Bidirectional Representations Augmented Autoregressive Biological Sequence Generation (Table1, page 8).
|
Nine-species benchmark original (DeepNovo, 2017) |
Amino acid precision | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Mus musculus | Homo sapiens | Saccharomyces cerevisiae | Methanosarcina mazei | Apis mellifera | Solanum lycopersicum | Vigna mungo | Bacillus subtilis | Candidatus Thiodiazotropha endoloripes | Average | |
| PEAKS | 0.600 | 0.639 | 0.748 | 0.673 | 0.633 | 0.728 | 0.644 | 0.719 | 0.586 | 0.663 |
| π-PrimeNovo | 0.784 | 0.729 | 0.802 | 0.801 | 0.763 | 0.815 | 0.822 | 0.846 | 0.734 | 0.788 |
| DeepNovo | 0.623 | 0.610 | 0.750 | 0.694 | 0.630 | 0.731 | 0.679 | 0.742 | 0.602 | 0.673 |
| PointNovo | 0.626 | 0.606 | 0.779 | 0.712 | 0.644 | 0.733 | 0.730 | 0.768 | 0.589 | 0.687 |
| Casanovo | 0.689 | 0.586 | 0.684 | 0.679 | 0.629 | 0.721 | 0.668 | 0.749 | 0.603 | 0.667 |
| InstaNovo | 0.703 | 0.636 | 0.691 | 0.712 | 0.660 | 0.732 | 0.711 | 0.739 | 0.619 | 0.689 |
| Casanovo V2 | 0.760 | 0.676 | 0.752 | 0.755 | 0.706 | 0.785 | 0.748 | 0.790 | 0.681 | 0.739 |
| π-HelixNovo | 0.765 | 0.665 | 0.768 | 0.784 | 0.757 | 0.721 | 0.793 | 0.816 | 0.681 | 0.750 |
| ContraNovo | 0.798 | 0.771 | 0.797 | 0.799 | 0.745 | 0.810 | 0.807 | 0.828 | 0.711 | 0.785 |
| CrossNovo | 0.816 | 0.800 | 0.814 | 0.826 | 0.785 | 0.830 | 0.831 | 0.856 | 0.740 | 0.811 |
|
Nine-species benchmark original (DeepNovo, 2017) |
Peptide recall | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Mus musculus | Homo sapiens | Saccharomyces cerevisiae | Methanosarcina mazei | Apis mellifera | Solanum lycopersicum | Vigna mungo | Bacillus subtilis | Candidatus Thiodiazotropha endoloripes | Average | |
| PEAKS | 0.197 | 0.277 | 0.428 | 0.356 | 0.287 | 0.403 | 0.362 | 0.387 | 0.203 | 0.322 |
| π-PrimeNovo | 0.567 | 0.574 | 0.697 | 0.650 | 0.603 | 0.697 | 0.702 | 0.721 | 0.531 | 0.638 |
| DeepNovo | 0.286 | 0.293 | 0.462 | 0.422 | 0.330 | 0.454 | 0.436 | 0.449 | 0.253 | 0.376 |
| PointNovo | 0.355 | 0.351 | 0.534 | 0.478 | 0.396 | 0.513 | 0.511 | 0.518 | 0.298 | 0.439 |
| Casanovo | 0.426 | 0.341 | 0.490 | 0.478 | 0.406 | 0.521 | 0.506 | 0.537 | 0.330 | 0.448 |
| InstaNovo | 0.471 | 0.455 | 0.559 | 0.528 | 0.466 | 0.732 | 0.564 | 0.576 | 0.416 | 0.530 |
| Casanovo V2 | 0.483 | 0.446 | 0.599 | 0.557 | 0.493 | 0.618 | 0.589 | 0.622 | 0.446 | 0.539 |
| π-HelixNovo | 0.483 | 0.392 | 0.568 | 0.560 | 0.473 | 0.560 | 0.623 | 0.596 | 0.388 | 0.517 |
| ContraNovo | 0.567 | 0.622 | 0.674 | 0.630 | 0.576 | 0.672 | 0.677 | 0.688 | 0.486 | 0.621 |
| CrossNovo | 0.596 | 0.661 | 0.698 | 0.660 | 0.610 | 0.695 | 0.716 | 0.726 | 0.518 | 0.654 |
In the paper: column peptide recall, Mouse: the original table only underlined ContraNovo (Contra.) (0.567); π-PrimeNovo (Prime.) (0.567) ties with it and is underlined here too.
In the paper: column peptide recall, Tomato: the original table bolded π-PrimeNovo (Prime.) (0.697), InstaNovo (Insta) (0.732) and underlined CrossNovo (Ours) (0.695).
Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing (2025) · 6 tables
Table2 (Seven-species)
Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing, page 6: Empirical comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in PTM-level performance. † denotes our retrained results, and other results are given by NovoBench. The best results are marked in bold.
The same table is also printed in Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing (Table2, page 6).
|
Seven-species benchmark NovoBench split |
Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo · quoted | 0.391 | 0.373 |
| PointNovo · quoted | 0.117 | 0.094 |
| InstaNovo · quoted | 0.126 | 0.115 |
| Casanovo · quoted | 0.360 | 0.251 |
| AdaNovo · quoted | 0.448 | 0.321 |
| AdaNovo · retrained | 0.430 | 0.356 |
| π-HelixNovo · quoted | 0.473 | 0.366 |
| π-HelixNovo · retrained | 0.362 | 0.370 |
| Casanovo · retrained | 0.368 | 0.292 |
| LIPNovo | 0.604 | 0.498 |
Table2 (Nine-species)
Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing, page 6: Empirical comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in PTM-level performance. † denotes our retrained results, and other results are given by NovoBench. The best results are marked in bold.
The same table is also printed in Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing (Table2, page 6).
| Nine-species benchmark | Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo · quoted | 0.576 | 0.529 |
| PointNovo · quoted | 0.629 | 0.546 |
| InstaNovo · quoted | 0.443 | 0.294 |
| Casanovo · quoted | 0.706 | 0.566 |
| AdaNovo · quoted | 0.652 | 0.570 |
| AdaNovo · retrained | 0.678 | 0.552 |
| π-HelixNovo · quoted | 0.680 | 0.598 |
| π-HelixNovo · retrained | 0.723 | 0.593 |
| Casanovo · retrained | 0.755 | 0.601 |
| LIPNovo | 0.765 | 0.656 |
Table2 (HC-PT)
Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing, page 6: Empirical comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in PTM-level performance. † denotes our retrained results, and other results are given by NovoBench. The best results are marked in bold.
The same table is also printed in Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing (Table2, page 6).
|
ProteomeTools HC-PT (NovoBench) |
Ptm precision | Ptm recall |
|---|---|---|
| DeepNovo · quoted | 0.626 | 0.615 |
| PointNovo · quoted | 0.676 | 0.740 |
| InstaNovo · quoted | 0.350 | 0.261 |
| Casanovo · quoted | 0.501 | 0.460 |
| AdaNovo · quoted | 0.552 | 0.482 |
| AdaNovo · retrained | 0.562 | 0.532 |
| π-HelixNovo · quoted | 0.568 | 0.667 |
| π-HelixNovo · retrained | 0.632 | 0.566 |
| Casanovo · retrained | 0.550 | 0.582 |
| LIPNovo | 0.732 | 0.745 |
Table1 (Seven-species)
Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing, page 6: Empirical comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in amino acid-level and peptide-level performance. † denotes our retrained results, and other results are provided by NovoBench. The best is marked in bold.
The same table is also printed in Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing (Table1, page 6).
|
Seven-species benchmark NovoBench split |
Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| DeepNovo · quoted | 0.492 | 0.433 | 0.204 | 0.136 |
| PointNovo · quoted | 0.196 | 0.169 | 0.022 | 0.007 |
| InstaNovo · quoted | 0.192 | 0.176 | 0.031 | 0.009 |
| Casanovo · quoted | 0.322 | 0.327 | 0.119 | 0.084 |
| AdaNovo · quoted | 0.379 | 0.385 | 0.174 | 0.135 |
| AdaNovo · retrained | 0.403 | 0.405 | 0.189 | 0.149 |
| π-HelixNovo · quoted | 0.481 | 0.472 | 0.234 | 0.173 |
| π-HelixNovo · retrained | 0.465 | 0.462 | 0.218 | 0.156 |
| Casanovo · retrained | 0.357 | 0.366 | 0.159 | 0.119 |
| LIPNovo | 0.557 | 0.560 | 0.327 | 0.281 |
Table1 (Nine-species)
Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing, page 6: Empirical comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in amino acid-level and peptide-level performance. † denotes our retrained results, and other results are provided by NovoBench. The best is marked in bold.
The same table is also printed in Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing (Table1, page 6).
| Nine-species benchmark | Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| PEAKS · quoted | 0.748 | 0.428 | ||
| DeepNovo · quoted | 0.696 | 0.638 | 0.428 | 0.376 |
| PointNovo · quoted | 0.740 | 0.671 | 0.480 | 0.436 |
| InstaNovo · quoted | 0.420 | 0.395 | 0.164 | 0.123 |
| Casanovo · quoted | 0.697 | 0.696 | 0.481 | 0.439 |
| AdaNovo · quoted | 0.698 | 0.709 | 0.505 | 0.469 |
| AdaNovo · retrained | 0.681 | 0.681 | 0.473 | 0.439 |
| π-HelixNovo · quoted | 0.765 | 0.758 | 0.517 | 0.453 |
| π-HelixNovo · retrained | 0.765 | 0.752 | 0.509 | 0.431 |
| Casanovo · retrained | 0.741 | 0.740 | 0.529 | 0.493 |
| LIPNovo | 0.797 | 0.797 | 0.582 | 0.547 |
In the paper: column amino acid precision: the original table only underlined π-HelixNovo (π-HelixNovo† (Yang et al., 2024)) (0.765); π-HelixNovo (π-HelixNovo (Yang et al., 2024)) (0.765) ties with it and is underlined here too.
Table1 (HC-PT)
Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing, page 6: Empirical comparison with state-of-the-art methods on Nine-species, Seven-species, and HC-PT datasets in amino acid-level and peptide-level performance. † denotes our retrained results, and other results are provided by NovoBench. The best is marked in bold.
The same table is also printed in Latent Imputation before Prediction: A New Computational Paradigm for De Novo Peptide Sequencing (Table1, page 6).
|
ProteomeTools HC-PT (NovoBench) |
Amino acid precision | Amino acid recall | Peptide precision | Peptide AUC |
|---|---|---|---|---|
| DeepNovo · quoted | 0.531 | 0.534 | 0.313 | 0.255 |
| PointNovo · quoted | 0.623 | 0.622 | 0.419 | 0.373 |
| InstaNovo · quoted | 0.289 | 0.285 | 0.057 | 0.034 |
| Casanovo · quoted | 0.442 | 0.453 | 0.211 | 0.177 |
| AdaNovo · quoted | 0.442 | 0.451 | 0.212 | 0.178 |
| AdaNovo · retrained | 0.492 | 0.496 | 0.289 | 0.254 |
| π-HelixNovo · quoted | 0.588 | 0.582 | 0.356 | 0.318 |
| π-HelixNovo · retrained | 0.532 | 0.537 | 0.301 | 0.261 |
| Casanovo · retrained | 0.525 | 0.530 | 0.324 | 0.290 |
| LIPNovo | 0.637 | 0.643 | 0.458 | 0.427 |
Curriculum Learning for Biological Sequence Prediction: The Case of De Novo Peptide Sequencing (2025) · 2 tables
Table6 (Nine-species)
Curriculum Learning for Biological Sequence Prediction: The Case of De Novo Peptide Sequencing, page 18: Performance comparison on the NovoBench benchmark (yeast test species). Scores for models marked with * are quoted from the NovoBench paper or original publications. CV denotes cross-validation results from the original PrimeNovo paper. “–” indicates data not available.
The same table is also printed in Curriculum Learning for Biological Sequence Prediction: The Case of De Novo Peptide Sequencing (Table6, page 18).
| Nine-species benchmark | Peptide precision |
|---|---|
| Saccharomyces cerevisiae | |
| Casanovo · quoted | 0.48 |
| InstaNovo · quoted | 0.53 |
| AdaNovo · quoted | 0.50 |
| π-HelixNovo · quoted | 0.52 |
| SearchNovo · quoted | 0.55 |
| π-PrimeNovo CV · quoted | 0.58 |
| Casanovo pretrained · released | 0.60 |
| π-PrimeNovo | 0.70 |
| RefineNovo | 0.71 |
Table6 (HC-PT)
Curriculum Learning for Biological Sequence Prediction: The Case of De Novo Peptide Sequencing, page 18: Performance comparison on the NovoBench benchmark (yeast test species). Scores for models marked with * are quoted from the NovoBench paper or original publications. CV denotes cross-validation results from the original PrimeNovo paper. “–” indicates data not available.
The same table is also printed in Curriculum Learning for Biological Sequence Prediction: The Case of De Novo Peptide Sequencing (Table6, page 18).
|
ProteomeTools HC-PT (NovoBench) |
Peptide precision |
|---|---|
| Casanovo · quoted | 0.21 |
| InstaNovo · quoted | 0.57 |
| AdaNovo · quoted | 0.21 |
| π-HelixNovo · quoted | 0.21 |
| SearchNovo · quoted | 0.45 |
| π-PrimeNovo | 0.85 |
| RefineNovo | 0.88 |
Papers describing it (2)
- De novo peptide sequencing with InstaNovo: Accurate, database-free peptide identification for large scale proteomics experiments (2023, bioRxiv, preprint)
- InstaNovo enables diffusion-powered de novo peptide sequencing in large-scale proteomics experiments (2025, Nature Machine Intelligence, peer-reviewed)
Papers using it (6)
Applications and evaluations that ran this method. They are not counted among its authors below.
- Can we Confidently Sequence the „Peptide Dark Matter“? Reaching a Consensus for De Novo Peptide Sequencing (2026, Proceedings of the 38th European Peptide Symposium, presentation)
- INSearch: AI-native framework for large scale proteomic database search via contrastive joint embeddings and transformer-based scoring function (2026, thesis)
- Sparse Autoencoders for Interpretability of InstaNovo (2026, thesis)
- Generalizable Direct Protein Sequencing With InstaNexus (2026, Molecular & Cellular Proteomics, peer-reviewed)
- Generalizable direct protein sequencing with InstaNexus (2025, bioRxiv, preprint)
- Advancing De Novo Glycopeptide Sequencing with InstaNovo in Glycoproteomics (2025, thesis)