Learning protein fitness models from evolutionary and assay-labeled data
Machine learning-based models of protein fitness typically learn from either unlabeled, evolutionarily related sequences or variant sequences with experimentally measured labels. For regimes where only limited experimental data are available, recent work has suggested methods for combining both sour...
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| Veröffentlicht in: | Nature biotechnology Jg. 40; H. 7; S. 1114 - 1122 |
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| Hauptverfasser: | , , , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
New York
Nature Publishing Group US
01.07.2022
Nature Publishing Group Springer Nature |
| Schlagworte: | |
| ISSN: | 1087-0156, 1546-1696, 1546-1696 |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | Machine learning-based models of protein fitness typically learn from either unlabeled, evolutionarily related sequences or variant sequences with experimentally measured labels. For regimes where only limited experimental data are available, recent work has suggested methods for combining both sources of information. Toward that goal, we propose a simple combination approach that is competitive with, and on average outperforms more sophisticated methods. Our approach uses ridge regression on site-specific amino acid features combined with one probability density feature from modeling the evolutionary data. Within this approach, we find that a variational autoencoder-based probability density model showed the best overall performance, although any evolutionary density model can be used. Moreover, our analysis highlights the importance of systematic evaluations and sufficient baselines.
A simple machine learning algorithm combines evolutionary and experimental data for improved protein fitness prediction. |
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| Bibliographie: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 AC52-07NA27344 USDOE Office of Science (SC), Biological and Environmental Research (BER) |
| ISSN: | 1087-0156 1546-1696 1546-1696 |
| DOI: | 10.1038/s41587-021-01146-5 |