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Mutation effects predicted from sequence co-variation
Open accessAbstract
Many high-throughput experimental technologies have been developed to assess the effects of large numbers of mutations (variation) on phenotypes. However, designing functional assays for these methods is challenging, and systematic testing of all combinations is impossible, so robust methods to predict the effects of genetic variation are needed. Most prediction methods exploit evolutionary sequence conservation but do not consider the interdependencies of residues or bases. We present EVmutation, an unsupervised statistical method for predicting the effects of mutations that explicitly captures residue dependencies between positions. We validate EVmutation by comparing its predictions with outcomes of high-throughput mutagenesis experiments and measurements of human disease mutations and show that it outperforms methods that do not account for epistasis. EVmutation can be used to assess the quantitative effects of mutations in genes of any organism. We provide pre-computed predictions for ∼7,000 human proteins at http://evmutation.org/.
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“One of the major insights leveraged by AlphaFold 1,2 comes from the use of evolutionary covariations that can be extracted from large-scale multiple sequence alignments.[49][50][51][52][53][54]”
From AlphaFold and Implications for Intrinsically Disordered Proteins (2021) · cites this paper as [53]
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Cites
Berman, H. M. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.1.235 · Cited by 40,196
Matplotlib: a 2D graphics environment
Hunter, J. D. (2007) · Computing in Science & Engineering · doi:10.1109/mcse.2007.55 · Cited by 39,249
Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega
Sievers, F., Wilm, A., Dineen, D., Gibson, T., Karplus, K., Li, W.-Z., Lopez, R., McWilliam, H., Remmert, M., Söding, J., et al. (2011) · Molecular Systems Biology · doi:10.1038/msb.2011.75 · Cited by 15,576
pROC: an open-source package for R and S+ to analyze and compare ROC curves
Robin, X., Turck, N., Hainard, A., Tiberti, N., Lisacek, F., Sanchez, J.-C., & Müller, M. (2011) · BMC Bioinformatics · doi:10.1186/1471-2105-12-77 · Cited by 13,697
A method and server for predicting damaging missense mutations.
Adzhubei, I. A., Schmidt, S., Peshkin, L., Ramensky, V. E., Gerasimova, A., Bork, P., Kondrashov, A. S., & Sunyaev, S. R. (2010) · Nature Methods · doi:10.1038/nmeth0410-248 · Cited by 13,194
Information theory and statistical mechanics
Jaynes, E. T. (1957) · Physical Review · doi:10.1103/physrev.106.620 · Cited by 12,931
Analysis of protein-coding genetic variation in 60,706 humans
Exome Aggregation Consortium, Lek, M., Karczewski, K. J., Minikel, E. V., Samocha, K. E., Banks, E., Fennell, T., O’Donnell-Luria, A. H., Ware, J. S., Hill, A. J., et al. (2016) · Nature · doi:10.1038/nature19057 · Cited by 9,587
The NumPy Array: A Structure for Efficient Numerical Computation
van der Walt, S., Colbert, S. C., & Varoquaux, G. (2011) · Computing in Science & Engineering · doi:10.1109/mcse.2011.37 · Cited by 9,381
Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,951
Accelerated Profile HMM Searches
Eddy, S. R. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002195 · Cited by 6,975
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Cheung, N. J., & Yu, W. (2019) · BMC Bioinformatics · doi:10.1186/s12859-019-2984-1 · Cited by 9
Gandarilla-Pérez, C. A., Mergny, P., Weigt, M., & Bitbol, A. (2020) · Physical review. E · doi:10.1103/physreve.101.032413 · Cited by 8
Frederick, A. K., Thompson, S. L., Vakharia, Z. M., Cherney, M. M., Lei, H., Evenson, G. E., & Bowler, B. E. (2022) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2022.111819 · Cited by 8
Larrea, A., Jebari‐Benslaiman, S., García, U. G., Urteaga, A. S. J., Uribe, K. B., Benito‐Vicente, A., & Martı́n, C. (2023) · Current Atherosclerosis Reports · doi:10.1007/s11883-023-01154-7 · Cited by 12
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Kilian, M., & Bischofs, I. B. (2023) · Molecular Microbiology · doi:10.1111/mmi.15169 · Cited by 8
Zhang, H., Xin, M., Lin, L., Chen, C., Balestra, D., & Ding, Q. (2024) · Journal of Thrombosis and Haemostasis · doi:10.1016/j.jtha.2023.12.031 · Cited by 7
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Çelik, M. H., & Xie, X. (2025) · iScience · doi:10.1016/j.isci.2025.113495 · Cited by 7
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Wang, R., Gao, Y., Wang, W., Xue, B., & Cao, Y. (2025) · Chinese Journal of Chemistry · doi:10.1002/cjoc.70210 · Cited by 11
Ochoa, R., Laskowski, R. A., Thornton, J. M., & Cossio, P. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.636562 · Cited by 6
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Li, C., Luo, Y., Xie, Y., Zhang, Z., Liu, Y., Zou, L., & Xiao, F. (2023) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2023.12.031 · Cited by 8
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Zhang, Z., Li, Z., Wang, Q., Wu, H., Yang, M., Zhao, F., Tan, M., & Han, S. (2024) · Protein Science · doi:10.1002/pro.5211 · Cited by 7
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Joo, J., Lim, K., Yang, S., Kim, S.-H., Cocco, L., & Suh, P. (2021) · Advances in Biological Regulation · doi:10.1016/j.jbior.2021.100833 · Cited by 7
Behrendt, A., Golchin, P., Koenig, F., Mulnaes, D., Stalke, A., Dröge, C., Keitel, V., & Gohlke, H. (2022) · Hepatology Communications · doi:10.1002/hep4.2088 · Cited by 10
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Wang, X., Li, A., Li, X., & Cui, H. (2024) · Chemistry - A European Journal · doi:10.1002/chem.202303889 · Cited by 7
Wierbowski, S. D., Fragoza, R., Liang, S., & Yu, H. (2018) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2018.09.006 · Cited by 8
Těšínský, M., Šimčíková, D., & Heneberg, P. (2018) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2018.12.008 · Cited by 7
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Weinstein, E. N., & Marks, D. S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.31.231381 · Cited by 8
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Gurev, S. F., Youssef, N., Jain, N., Mehrotra, A., Leung, S. R. M., Jackson, A., & Marks, D. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.04.668549 · Cited by 10
Fan, Z., & Xu, Y. (2024) · Annals of Data Science · doi:10.1007/s40745-024-00530-7 · Cited by 6
Mychack, A., Evans, D., Gilles, T., James, M. J., & Walker, S. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2414696122 · Cited by 7
Ma, X., Zhu, K., Wang, K., Liao, W., Yang, X., Yu, W., Wang, W., & Han, F. (2025) · Marine Drugs · doi:10.3390/md23050198 · Cited by 6
Tremmel, R., Honoré, A., Park, Y., Zhou, Y.-T., Xiao, M., & Lauschke, V. (2025) · Pharmacogenomics (London) · doi:10.1080/14622416.2025.2504863 · Cited by 6
Kelm, M., Burkard, N., Hörner, M., Kollmann, C., Otto, C., Saravi, B., Seubert, A. C., Forchel, F., Kohler, T. N., Penner, M., et al. (2025) · Mucosal Immunology · doi:10.1016/j.mucimm.2025.08.003 · Cited by 6
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Gentile, I., Domingo, M. S., Zebell, S. G., Fitzgerald, B., & Lippman, Z. B. (2025) · Molecular Biology and Evolution · doi:10.1093/molbev/msaf294 · Cited by 6
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Gu, J., Su, X., Wang, J., Yu, Y., Li, Z., Mu, W., Xu, Y., & Nie, Y. (2026) · ACS Catalysis · doi:10.1021/acscatal.6c00035 · Cited by 6
Nagar, N., Tubiana, J., Loewenthal, G., Wolfson, H. J., Ben‐Tal, N., & Pupko, T. (2023) · Journal of Molecular Biology · doi:10.1016/j.jmb.2023.168155 · Cited by 7
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Bittrich, S., Schroeder, M., & Labudde, D. (2018) · PLoS ONE · doi:10.1371/journal.pone.0206369 · Cited by 4
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Robustness and stability of spin-glass ground states to perturbed interactions
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Uninterpretable interactions: epistasis as uncertaintyPreprint
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Qiu, J., Nechaev, D., & Rost, B. (2020) · BMC Bioinformatics · doi:10.1186/s12859-020-03759-0 · Cited by 5
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Zhou, X., Wei, K.-Y., Li, S., Shen, Q., Xue, Y., & Zheng, Y. (2025) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5c07983 · Cited by 4
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Wang, H., Ren, Z., Sun, J., Chen, Y., Bo, X., Xue, J., Gao, J., & Ni, M. (2024) · Briefings in Bioinformatics · doi:10.1093/bib/bbae579 · Cited by 5
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Metadata
- Authors
- Hopf, T. A., Ingraham, J. B., Poelwijk, F. J., Schärfe, C. P. I., Springer, M., Sander, C., & Marks, D. S.
- Affiliations
- Harvard University (US)
- Dana-Farber Cancer Institute (US)
- Corresponding author
- Marks, Debora S
- ORCID
- Venue
- Nature Biotechnology
- Published
- 2017-01-16
- Volume
- 35
- Issue
- 2
- Pages
- 128-135
- ISSN
- 0733-222X (ISSN-L)
- 1087-0156
- 1546-1696
- PMC
- PMC5383098
- OpenAlex
- W2245592118
- Cited by
- 775
- References
- 113
- Citations by year
- 2026: 85 · 2025: 115 · 2024: 106 · 2023: 83 · 2022: 86 · 2021: 100 · 2020: 54 · 2019: 60 · 2018: 50 · 2017: 34
- FWCI
- 35.85
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Biotechnology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- arXiv (Cornell University) (submittedVersion)
- Funders
- National Institute of General Medical Sciences (R01GM106303)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Keywords
- mutation effect prediction, epistasis, high-throughput mutagenesis, protein evolution
- MeSH terms
- Amino Acid Sequence, DNA Mutational Analysis, Epistasis, Genetic, Humans, Molecular Sequence Data, Mutation, Genetic Variation, Conserved Sequence, Evolution, Molecular, Proteome, High-Throughput Nucleotide Sequencing
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