The DOI matches its Crossref record; 61 of the 62 references it cites were found in a registry or an index.
A genome-wide view of the spectrum of spontaneous mutations in yeast.
Open accessAbstract
The mutation process ultimately defines the genetic features of all populations and, hence, has a bearing on a wide range of issues involving evolutionary genetics, inheritance, and genetic disorders, including the predisposition to cancer. Nevertheless, formidable technical barriers have constrained our understanding of the rate at which mutations arise and the molecular spectrum of their effects. Here, we report on the use of complete-genome sequencing in the characterization of spontaneously arising mutations in the yeast Saccharomyces cerevisiae. Our results confirm some findings previously obtained by indirect methods but also yield numerous unexpected findings, in particular a very high rate of point mutation and skewed distribution of base-substitution types in the mitochondrion, a very high rate of segmental duplication and deletion in the nuclear genome, and substantial deviations in the mutational profile among various model organisms.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“If we were to assume a per base mutation rate similar to that of haploid yeasts (estimated at 0.33 10-9 per base per generation) (Lynch et al., 2008), each generation one would expect 0.0041 mutations in the genome (0.33 10-9 × 12,3 106 bases in the genome = 4.1 10-3).”
From Genome Comparisons of Candida glabrata Serial Clinical Isolates Reveal Patterns of Genetic Variation in Infecting Clonal Populations (2019) · cites this paper as Lynch et al., 2008
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Genome sequencing in microfabricated high-density picolitre reactors
Margulies, M., Egholm, M., Altman, W. E., Attiya, S., Bader, J. S., Bemben, L. A., Berka, J., Braverman, M. S., Chen, Y.-J., Chen, Z., et al. (2005) · Nature · doi:10.1038/nature03959 · Cited by 7,693
The Neutral Theory of Molecular Evolution
Kimura, M. (1979) · Scientific American · doi:10.1038/scientificamerican1179-98 · Cited by 7,687
The Neutral Theory of Molecular Evolution
Kimura, M. (1983) · Cambridge University Press eBooks · doi:10.1017/cbo9780511623486 · Cited by 6,300
Friedberg, E. C., Walker, G. C., Siede, W., Wood, R. D., Schultz, R. A., & Ellenberger, T. (2005) · doi:10.1128/9781555816704 · Cited by 5,683
Drake, J. W., Charlesworth, B., Charlesworth, D., & Crow, J. F. (1998) · Genetics · doi:10.1093/genetics/148.4.1667 · Cited by 1,932
Strand, M. K., Prolla, T. A., Liskay, R. M., & Petes, T. D. (1993) · Nature · doi:10.1038/365274a0 · Cited by 1,090
The origins, patterns and implications of human spontaneous mutation
Crow, J. F. (2000) · Nature Reviews Genetics · doi:10.1038/35049558 · Cited by 928
Mutation Pressure and the Evolution of Organelle Genomic Architecture
Lynch, M., Koskella, B. L., & Schaack, S. (2006) · Science · doi:10.1126/science.1118884 · Cited by 597
Characteristic genome rearrangements in experimental evolution of Saccharomyces cerevisiae
Dunham, M. J., Badrane, H., Ferea, T., Adams, J., Brown, P. O., Rosenzweig, F., & Botstein, D. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.242624799 · Cited by 564
Widespread aneuploidy revealed by DNA microarray expression profiling
Hughes, T. R., Roberts, C. J., Dai, H. A., Jones, A. R., Meyer, M. R., Slade, D., Burchard, J., Dow, S., Ward, T. R., Kidd, M. J., et al. (2000) · Nature Genetics · doi:10.1038/77116 · Cited by 482
Flagged first, then by citations
1 of the 62 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- M Lynch The Origins of Genomic Architecture (Sinauer, Sunderland, MA, 2007).
- 10.1128/mcb.12.6.2749-2757.1992 · DOI
Cited by
Sorted by citations
Items 301–400 of 708
Small inverted repeats drive mitochondrial genome evolution in Lake Baikal sponges.
Lavrov, D., Maikova, O., Pett, W., & Belikov, S. (2012) · Gene · doi:10.1016/j.gene.2012.05.039 · Cited by 31
Accelerated adaptive laboratory evolution: A tool for evolutionary biotechnology
Declerck, L., Bouchon, F., Demeester, W., Guidi, C., & Mey, M. D. (2025) · Biotechnology Advances · doi:10.1016/j.biotechadv.2025.108741 · Cited by 32
Lawrie, D. S., Petrov, D. A., & Messer, P. W. (2011) · Genome Biology and Evolution · doi:10.1093/gbe/evr032 · Cited by 31
Are Nonsynonymous Transversions Generally More Deleterious than Nonsynonymous Transitions?
Zou, Z., & Zhang, J. (2020) · Molecular Biology and Evolution · doi:10.1093/molbev/msaa200 · Cited by 32
Do organellar genomes function as long-term redox damage sensors?
Wright, A. F., Murphy, M. P., & Turnbull, D. M. (2009) · Trends in Genetics · doi:10.1016/j.tig.2009.04.006 · Cited by 29
Distinct adaptive mechanisms drive recovery from aneuploidy caused by loss of the Ulp2 SUMO protease
Ryu, H., López‐Giráldez, F., Knight, J., Hwang, S. S., Renner, C., Kreft, S. G., & Hochstrasser, M. (2018) · Nature Communications · doi:10.1038/s41467-018-07836-0 · Cited by 29
GENETIC VARIATION AND DNA REPLICATION TIMING, OR WHY IS THERE LATE REPLICATING DNA?
Herrick, J. (2011) · Evolution · doi:10.1111/j.1558-5646.2011.01407.x · Cited by 30
Li, J., Jew, B., Zhan, L., Hwang, S., Coppola, G., Freimer, N. B., & Sul, J. H. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007556 · Cited by 29
Universally high transcript error rates in bacteria
Li, W., & Lynch, M. (2020) · eLife · doi:10.7554/elife.54898 · Cited by 32
The natural diversity and ecology of fission yeast
Jeffares, D. C. (2017) · Yeast · doi:10.1002/yea.3293 · Cited by 29
Molecular signatures of aneuploidy-driven adaptive evolution
Kaya, A., Mariotti, M., Tyshkovskiy, A., Zhou, X., Hulke, M. L., Ma, S., Gerashchenko, M. V., Koren, A., & Gladyshev, V. N. (2020) · Nature Communications · doi:10.1038/s41467-019-13669-2 · Cited by 29
The Spatiotemporal Program of Replication in the Genome of Lachancea kluyveri
Agier, N., Romano, O. M., Touzain, F., Lagomarsino, M. C., & Fischer, G. (2013) · Genome Biology and Evolution · doi:10.1093/gbe/evt014 · Cited by 29
Selective Advantages of a Parasexual Cycle for the YeastCandida albicans
Zhang, N., Magee, B. B., Magee, P. T., Holland, B. R., Rodrigues, E., Holmes, A. R., Cannon, R. D., & Schmid, J. (2015) · Genetics · doi:10.1534/genetics.115.177170 · Cited by 31
The Human Mutation Rate Is Increasing, Even As It Slows
Thomas, G. W. C., & Hahn, M. W. (2013) · Molecular Biology and Evolution · doi:10.1093/molbev/mst218 · Cited by 27
Menie, M. A. W. O., Sarraf, M. A., Pestow, R., & Fernandes, H. B. F. (2017) · Evolutionary Psychological Science · doi:10.1007/s40806-017-0084-x · Cited by 26
Avecilla, G., Chuong, J. N., Li, F., Sherlock, G., Gresham, D., & Ram, Y. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001633 · Cited by 34
Adaptive deletion in resistance gene duplications in the malaria vector Anopheles gambiae
Assogba, B. S., Alout, H., Koffi, A. A., Pennetier, C., Djogbénou, L., Makoundou, P., Weill, M., & Labbé, P. (2018) · Evolutionary Applications · doi:10.1111/eva.12619 · Cited by 26
Similar Relative Mutation Rates in the Three Genetic Compartments of Mesostigma and Chlamydomonas
Hua, J., Smith, D. R., Borza, T., & Lee, R. W. (2011) · Protist · doi:10.1016/j.protis.2011.04.003 · Cited by 27
Loss of Heterozygosity and Base Mutation Rates Vary AmongSaccharomyces cerevisiaeHybrid Strains
Pankajam, A. V., Dash, S., Saifudeen, A., Dutta, A., & Nishant, K. T. (2020) · G3 Genes Genomes Genetics · doi:10.1534/g3.120.401551 · Cited by 29
Guo, X., Zhang, M., Gao, Y., Cao, G., Yang, Y., Lü, D., & Li, W. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-09626-0 · Cited by 28
Noor, M. A. F. (2008) · Molecular Biology and Evolution · doi:10.1093/molbev/msn186 · Cited by 27
Spontaneous mutation rates come into focus in Escherichia coli
Williams, A. B. (2014) · DNA repair · doi:10.1016/j.dnarep.2014.09.009 · Cited by 28
TRINS: a method for gene modification by randomized tandem repeat insertions
Kipnis, Y., Dellus-Gur, E., & Tawfik, D. S. (2012) · Protein Engineering Design and Selection · doi:10.1093/protein/gzs023 · Cited by 26
The evolution of genetic architectures underlying quantitative traits
Rajon, É., & Plotkin, J. B. (2013) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2013.1552 · Cited by 30
Evolution of a Record-Setting AT-Rich Genome: Indel Mutation, Recombination, and Substitution Bias
Nguyen, D., Wu, B.-J., Xiao, S., & Hao, W.-L. (2020) · Genome Biology and Evolution · doi:10.1093/gbe/evaa202 · Cited by 20
Adaptation dynamics between copy-number and point mutations
Tomanek, I., & Guet, C. C. (2022) · eLife · doi:10.7554/elife.82240 · Cited by 28
Making the right connections: biological networks in the light of evolution
Cg, K., & Pinney, J. W. (2009) · BioEssays · doi:10.1002/bies.200900043 · Cited by 27
Jeon, J., Choi, J., Lee, G.-W., Dean, R. A., & Lee, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065416 · Cited by 25
The Strength of Selection Against the Yeast Prion [PSI+]
Joanna Masel, A., & Griswold, C. K. (2009) · Genetics · doi:10.1534/genetics.108.100297 · Cited by 25
Chen, S., Ren, F., Zhang, L., Liu, Y., Chen, X., Li, Y., Zhang, L., Zhu, B., Zeng, P., Li, Z., et al. (2018) · Molecular Plant · doi:10.1016/j.molp.2018.04.009 · Cited by 26
Accelerated rates of large-scale mutations in the presence of copper and nickelPreprint
Chain, F. J. J., Flynn, J. M., Bull, J. K., & Cristescu, M. E. (2018) · Genome Research · doi:10.1101/gr.234724.118 · Cited by 24
Fitness Effects of Spontaneous Mutations in Picoeukaryotic Marine Green Algae
Krasovec, M., Eyre‐Walker, A., Grimsley, N. H., Salmeron, C., Pecqueur, D., Piganeau, G., & Sanchez-Brosseau, S. (2016) · G3 Genes Genomes Genetics · doi:10.1534/g3.116.029769 · Cited by 24
Mutagenic mechanisms of cancer-associated DNA polymerase ϵ alleles
Herzog, M., Alonso‐Perez, E., Salguero, I., Warringer, J., Adams, D. J., Jackson, S. P., & Puddu, F. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab160 · Cited by 22
Stoletzki, N. (2011) · BMC Evolutionary Biology · doi:10.1186/1471-2148-11-93 · Cited by 24
Zanders, S. E., Ma, X., RoyChoudhury, A., Hernandez, R. D., Demogines, A., Barker, B., Gu, Z., Bustamante, C. D., & Alani, E. (2010) · Genetics · doi:10.1534/genetics.110.120105 · Cited by 24
Limited Mutation-Rate Variation Within the Paramecium aurelia Species Complex
Long, H., Doak, T. G., & Lynch, M. (2018) · G3 Genes Genomes Genetics · doi:10.1534/g3.118.200420 · Cited by 24
Dooner, H. K., Wang, Q., Huang, J. T., Li, Y., He, L., Xiong, W., & Du, C. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1903809116 · Cited by 24
The dynamics of loss of heterozygosity events in genomes
Dutta, A., & Schacherer, J. (2025) · EMBO Reports · doi:10.1038/s44319-024-00353-w · Cited by 27
Stirling, P. C., Shen, Y., Corbett, R., Jones, S. J. M., & Hieter, P. (2013) · Genetics · doi:10.1534/genetics.113.159806 · Cited by 23
Phillips, M. A., Steenwyk, J. L., Shen, X., & Rokas, A. (2021) · Genome Biology and Evolution · doi:10.1093/gbe/evab219 · Cited by 21
Genome-Wide Mutation Rate Response to pH Change in the Coral Reef Pathogen Vibrio shilonii AK1
Strauss, C., Long, H., Patterson, C. E., Te, R., & Lynch, M. (2017) · mBio · doi:10.1128/mbio.01021-17 · Cited by 23
Nascent RNA folding mitigates transcription-associated mutagenesisPreprint
Chen, X., Yang, J., & Zhang, J. (2015) · Genome Research · doi:10.1101/gr.195164.115 · Cited by 22
Shor, E., Schuyler, J., & Perlin, D. S. (2019) · mBio · doi:10.1128/mbio.00120-19 · Cited by 19
The role of gene copy number variation in antimicrobial resistance in human fungal pathogens
Jay, A., Jordan, D., Gerstein, A. C., & Landry, C. R. (2025) · npj Antimicrobials and Resistance · doi:10.1038/s44259-024-00072-1 · Cited by 29
Rajeh, A. A., Lv, J., & Lin, Z. (2018) · BMC Genomics · doi:10.1186/s12864-018-4683-0 · Cited by 23
Pfeifer, S. P. (2020) · Springer eBooks · doi:10.1007/978-3-030-60181-2_3 · Cited by 21
Primo, V. A., Rezvani, Y., Farrell, A., Murphy, C. Q., Lou, J., Vajdi, A., Marth, G. T., Zarringhalam, K., & Gubbels, M. (2021) · mSystems · doi:10.1128/msystems.01196-21 · Cited by 22
A Model for Genome Size Evolution
Fischer, S., Bernard, S., Beslon, G., & Knibbe, C. (2014) · Bulletin of Mathematical Biology · doi:10.1007/s11538-014-9997-8 · Cited by 22
Mozhayskiy, V., & Tagkopoulos, I. (2012) · BMC Bioinformatics · doi:10.1186/1471-2105-13-s10-s13 · Cited by 23
Genome-wide survey of post-meiotic segregation during yeast recombination
Mancera, E., Bourgon, R., Huber, W. K., & Steinmetz, L. M. (2011) · Genome biology · doi:10.1186/gb-2011-12-4-r36 · Cited by 22
The repeatability of genome-wide mutation rate and spectrum estimates
Behringer, M. G., & Hall, D. W. (2016) · Current Genetics · doi:10.1007/s00294-016-0573-7 · Cited by 22
Dillon, M. M., & Cooper, V. S. (2016) · Genetics · doi:10.1534/genetics.116.193060 · Cited by 22
The Proteomic Constraint and Its Role in Molecular Evolution
Massey, S. E. (2008) · Molecular Biology and Evolution · doi:10.1093/molbev/msn210 · Cited by 23
The Emergence of Canalization and Evolvability in an Open-Ended, Interactive Evolutionary System
Huizinga, J., Stanley, K. O., & Clune, J. (2018) · Artificial Life · doi:10.1162/artl_a_00263 · Cited by 22
Aneuploidy Can Be an Evolutionary Diversion on the Path to Adaptation
Kohanovski, I., Pontz, M., Zande, P. V., Selmecki, A. M., Dahan, O., Pilpel, Y., Yona, A. H., & Ram, Y. (2024) · Molecular Biology and Evolution · doi:10.1093/molbev/msae052 · Cited by 23
Ibáñez, C., Pérez‐Torrado, R., Chiva, R., Guillamón, J. M., Barrio, E., & Querol, A. (2013) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2013.10.023 · Cited by 21
Babbitt, G. A., & Cotter, C. R. (2010) · Genome Biology and Evolution · doi:10.1093/gbe/evq081 · Cited by 21
A Recent Whole-Genome Duplication Divides Populations of a Globally Distributed Microsporidian
Williams, T. A., Nakjang, S., Campbell, S. E., Freeman, M. A., Eydal, M., Moore, K., Hirt, R. P., Embley, T. M., & Williams, B. (2016) · Molecular Biology and Evolution · doi:10.1093/molbev/msw083 · Cited by 23
Procedures for the Storage of Microorganisms
She, R. C., & Petti, C. A. (2015) · ASM Press eBooks · doi:10.1128/9781555817381.ch11 · Cited by 21
Simple sequence repeat variation in the Daphnia pulex genome
Sung, W., Tucker, A. E., Bergeron, R. D., Lynch, M., & Thomas, W. K. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-691 · Cited by 21
Wride, D. A., Pourmand, N., Bray, W. M., Kosarchuk, J. J., Nisam, S. C., Quan, T. K., Berkeley, R. F., Katzman, S. J., Hartzog, G. A., Dobkin, C., et al. (2014) · Molecular BioSystems · doi:10.1039/c4mb00146j · Cited by 18
Kan, S., Liao, X., & Wu, Z. (2022) · Genes · doi:10.3390/genes13061036 · Cited by 20
Diversity of the cell-wall associated genomic island of the archaeon Haloquadratum walsbyi
Martín-Cuadrado, A.-B., Pašić, L., & Rodríguez‐Valera, F. (2015) · BMC Genomics · doi:10.1186/s12864-015-1794-8 · Cited by 19
Neutrality and epistasis in program space
Renzullo, J., Weimer, W. R., Moses, M. E., & Forrest, S. (2018) · doi:10.1145/3194810.3194812 · Cited by 20
Multispecies pangenomes reveal a pervasive influence of population size on structural variation
Edwards, S. V., Fang, B., Khost, D. E., Kolyfetis, G. E., Cheek, R. G., DeRaad, D. A., Chen, N. X., Fitzpatrick, J. W., McCormack, J. E., Funk, W. C., et al. (2025) · Science · doi:10.1126/science.adw1931 · Cited by 29
Liu, K., & Wessler, S. R. (2017) · Mobile DNA · doi:10.1186/s13100-016-0084-6 · Cited by 19
Epigenetic regulation of nuclear processes in fungal plant pathogens
Kramer, H. M., Cook, D. E., Seidl, M. F., & Thomma, B. P. H. J. (2023) · PLoS Pathogens · doi:10.1371/journal.ppat.1011525 · Cited by 19
Mascher, M., Gerlach, N., Gahrtz, M., Bucher, M., Scholz, U., & Dresselhaus, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096782 · Cited by 19
Huefner, N. D., Mizuno, Y., Weil, C. F., Korf, I. F., & Britt, A. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.07.011 · Cited by 19
Watanabe, Y., Takahashi, A., Itoh, M., & Takano‐Shimizu, T. (2008) · Genetics · doi:10.1534/genetics.108.093385 · Cited by 19
Simulated Evolution of Protein-Protein Interaction Networks with Realistic Topology
Peterson, G. J., Pressé, S., Peterson, K. S., & Dill, K. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039052 · Cited by 19
Short tandem repeats bind transcription factors to tune eukaryotic gene expressionPreprint
Horton, C. A., Alexandari, A. M., Hayes, M. G. B., Marklund, E., Schaepe, J. M., Aditham, A. K., Shah, N., Shrikumar, A., Afek, A., Greenleaf, W. J., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.24.493321 · Cited by 20
Dissecting genetic and environmental mutation signatures with model organisms
Segovia, R., Tam, A., & Stirling, P. C. (2015) · Trends in Genetics · doi:10.1016/j.tig.2015.04.001 · Cited by 20
Selection in a growing colony biases results of mutation accumulation experiments
Mahilkar, A., Raj, N., Kemkar, S., & Saini, S. (2022) · Scientific Reports · doi:10.1038/s41598-022-19928-5 · Cited by 21
Iranawati, F., Jung, H., Chand, V., Hurwood, D. A., & Mather, P. B. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms130910807 · Cited by 18
Population Differentiation Within Anisogramma anomala in North America
Muehlbauer, M., Tobia, J., Honig, J., Zhang, N., Hillman, B. I., Gold, K. M., & Molnar, T. J. (2018) · Phytopathology · doi:10.1094/phyto-06-18-0209-r · Cited by 18
The Startling Role of Mismatch Repair in Trinucleotide Repeat Expansions
Richard, G. (2021) · Cells · doi:10.3390/cells10051019 · Cited by 18
Rancati, G. I., & Pavelka, N. (2013) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2013.01.009 · Cited by 18
Muver, a computational framework for accurately calling accumulated mutations
Burkholder, A., Lujan, S. A., Lavender, C. A., Grimm, S. A., Kunkel, T. A., & Fargo, D. C. (2018) · BMC Genomics · doi:10.1186/s12864-018-4753-3 · Cited by 18
Xiong, K., Lancaster, A. K., Siegal, M. L., & Masel, J. (2019) · Nature Communications · doi:10.1038/s41467-019-10388-6 · Cited by 17
Low Spontaneous Mutation Rate in Complex Multicellular Eukaryotes with a Haploid–Diploid Life Cycle
Krasovec, M., Hoshino, M., Zheng, M. H., Lipinska, A. P., & Coelho, S. M. (2023) · Molecular Biology and Evolution · doi:10.1093/molbev/msad105 · Cited by 17
Peña, T. A., Villarreal, P. D., Agier, N., Chiara, M. D., Barría, T., Urbina, K., Villarroel, C. A., Santos, A. R. O., Rosa, C. A., Nespolo, R. F., et al. (2024) · PLoS Genetics · doi:10.1371/journal.pgen.1011396 · Cited by 18
Gene Duplications in the Genomes of Staphylococci and Enterococci
Sánchez-Herrero, J. F., Bernabeu, M., Prieto, A., Hüttener, M., & Juárez, A. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.00160 · Cited by 17
Silva, W. T. A. F., Otto, S. P., & Immler, S. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009581 · Cited by 18
Thierry, A., Khanna, V., Créno, S., Lafontaine, I., Ma, L., Bouchier, C., & Dujon, B. (2015) · Nature Communications · doi:10.1038/ncomms7154 · Cited by 19
Katju, V., Farslow, J. C., & Bergthorsson, U. (2009) · Genome biology · doi:10.1186/gb-2009-10-7-r75 · Cited by 16
The Glyphosate-Based Herbicide Roundup Does Not Elevate Genome-Wide Mutagenesis ofEscherichia coli
Tincher, C., Long, H., Behringer, M. G., Walker, N. B., & Lynch, M. (2017) · G3 Genes Genomes Genetics · doi:10.1534/g3.117.300133 · Cited by 17
Radzvilavicius, A. L. (2016) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2016.05.037 · Cited by 18
Kovalchuk, I. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803309-8.00001-x · Cited by 17
Shcherbakov, V. P. (2010) · Biology Direct · doi:10.1186/1745-6150-5-14 · Cited by 17
The Genotype–Phenotype Maps of Systems Biology and Quantitative Genetics: Distinct and Complementary
Landry, C. R., & Rifkin, S. A. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-3567-9_17 · Cited by 16
Evolution of Codon Usage Bias in Diatoms
Krasovec, M., & Filatov, D. A. (2019) · Genes · doi:10.3390/genes10110894 · Cited by 16
ON THE FINDABILITY OF GENOTYPES
McCandlish, D. M. (2013) · Evolution · doi:10.1111/evo.12128 · Cited by 15
Rates of Mutations and Transcript Errors in the Foodborne PathogenSalmonella entericasubsp.enterica
Pan, J., Li, W., Ni, J., Wu, K., Konigsberg, I. R., Rivera, C. E., Tincher, C., Gregory, C., Zhou, X., Doak, T. G., et al. (2022) · Molecular Biology and Evolution · doi:10.1093/molbev/msac081 · Cited by 15
Recent insights into the evolution of mutation rates in yeast
Melde, R. H., Bao, K. H., & Sharp, N. P. (2022) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2022.101953 · Cited by 14
Macías, L. G., Flores, M. G., Adam, A. C., Rodríguez, M. E., Querol, A., Barrio, E., Lopes, C. A., & Pérez‐Torrado, R. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009872 · Cited by 15
Extremely Rare Polymorphisms in Saccharomyces cerevisiae Allow Inference of the Mutational Spectrum
Zhu, Y. O., Sherlock, G., & Petrov, D. A. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006455 · Cited by 14
Estimation of the Genome-Wide Mutation Rate and Spectrum in the Archaeal Species Haloferax volcanii
Küçükyıldırım, S., Behringer, M. G., Williams, E. M., Doak, T. G., & Lynch, M. (2020) · Genetics · doi:10.1534/genetics.120.303299 · Cited by 17
Recommendations for improving statistical inference in population genomicsPreprint
Johri, P., Aquadro, C. F., Beaumont, M., Charlesworth, B., Excoffier, L., Eyre‐Walker, A., Keightley, P. D., Lynch, M., McVean, G., Payseur, B. A., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.27.466171 · Cited by 13
Mitochondrial Genome Sequences of the Emerging Fungal Pathogen Candida auris
Misas, E., Chow, N. A., Gómez, O. M., Muñoz, J. F., McEwen, J. G., Litvintseva, A. P., & Clay, O. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.560332 · Cited by 13
Metadata
- Authors
- Lynch, M., Sung, W., Morris, K., Coffey, N., Landry, C. R., Dopman, E. B., Dickinson, W. J., Okamoto, K., Kulkarni, S., Hartl, D. L., & Thomas, W. K.
- Affiliations
- Indiana University Bloomington (US)
- University of New Hampshire (US)
- Harvard University (US)
- University of Utah (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2008-07-08
- Volume
- 105
- Issue
- 27
- Pages
- 9272-9277
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC2453693
- OpenAlex
- W2145406188
- Cited by
- 708
- References
- 62
- Citations by year
- 2026: 16 · 2025: 23 · 2024: 24 · 2023: 34 · 2022: 29 · 2021: 56 · 2020: 35 · 2019: 39 · 2018: 42 · 2017: 40 · 2016: 44 · 2015: 46 · 2014: 47 · 2013: 51 · 2012: 42
- FWCI
- 18.53
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- Natural Sciences and Engineering Research Council of Canada
- National Institute of General Medical Sciences (GM 36827, R01GM068465, R01GM036827, GM068465)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- spontaneous mutation, mutation spectrum, Saccharomyces cerevisiae, point mutations, mitochondrial mutations, segmental duplication, deletion, mutation rate
- MeSH terms
- Base Sequence, Cell Division, DNA, Mitochondrial, Mutation, Nucleotides, Ploidies, Saccharomyces cerevisiae, Chromosomes, Fungal, Genome, Fungal, Microsatellite Repeats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review