The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
FastTree 2 – Approximately Maximum-Likelihood Trees for Large Alignments
Open accessAbstract
BACKGROUND: We recently described FastTree, a tool for inferring phylogenies for alignments with up to hundreds of thousands of sequences. Here, we describe improvements to FastTree that improve its accuracy without sacrificing scalability. METHODOLOGY/PRINCIPAL FINDINGS: Where FastTree 1 used nearest-neighbor interchanges (NNIs) and the minimum-evolution criterion to improve the tree, FastTree 2 adds minimum-evolution subtree-pruning-regrafting (SPRs) and maximum-likelihood NNIs. FastTree 2 uses heuristics to restrict the search for better trees and estimates a rate of evolution for each site (the "CAT" approximation). Nevertheless, for both simulated and genuine alignments, FastTree 2 is slightly more accurate than a standard implementation of maximum-likelihood NNIs (PhyML 3 with default settings). Although FastTree 2 is not quite as accurate as methods that use maximum-likelihood SPRs, most of the splits that disagree are poorly supported, and for large alignments, FastTree 2 is 100-1,000 times faster. FastTree 2 inferred a topology and likelihood-based local support values for 237,882 distinct 16S ribosomal RNAs on a desktop computer in 22 hours and 5.8 gigabytes of memory. CONCLUSIONS/SIGNIFICANCE: FastTree 2 allows the inference of maximum-likelihood phylogenies for huge alignments. FastTree 2 is freely available at http://www.microbesonline.org/fasttree.
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
Figures
![Figure 1 Local support values for splits found by PhyML with SPR moves and/or FastTree. We examined local support values for the splits inferred by PhyML 3.0 with + SPRs on simulated alignments with 250 protein sequences. We classified PhyML's splits as correct and found by both PhyML and FastTree, correct but missed by FastTree, or incorrect. We show the distribution of support values for each class. The right-most bin includes the strongly supported splits (0.95 to 1.0), and the gray dashed line shows the uniform distribution. The support values are PhyML's minimum of the approximate likelihood ratio test [21] and SH-like [16], [17] local supports.](/paper-figures/8d86db71595b4c3189b248ede78bcc3f/fasttree-2-approximately-maximum-likelihood-trees-for-large-alignments-figure-1.jpg)


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?
The cited source says what the claim attributes to it.
In the citing paper
“Thus, the validation process for our methods is centered around the comparison of phylogenetic trees estimated from the alignment with FastTree 2.1 (ref. 34).”
From Improving microbial phylogeny with citizen science within a mass-market video game (2025) · cites this paper as [34]
In the citing paper
“On the other hand, FastTree was found to be much faster than RAxML and PhyML but reported lower likelihood scores for data sets with both small and large numbers of sequences (Guindon et al. 2010; Price et al. 2010; Liu et al. 2011).”
From Evaluating fast maximum likelihood-based phylogenetic programs using empirical phylogenomic data sets (2018) · cites this paper as Price et al. 2010
In the citing paper
“So far, these four programs have only been evaluated using simulated data (Guindon et al. 2010; Price et al. 2010; Liu et al. 2011), and empirical data sets with wide ranges of taxon numbers (e.g., up to 237,882 taxa in Price et al. [2010]) but relatively small numbers of genes (from ∼10 [Price et al. 2010; Liu et al. 2011; Chernomor et al. 2016] to ∼200 [Guindon et al. 2010; Money and Whelan 2012”
From Evaluating fast maximum likelihood-based phylogenetic programs using empirical phylogenomic data sets (2018) · cites this paper as Price et al. 2010
In the citing paper
“As a tradeoff, FastTree generates less accurate tree estimates than SPR-based ML methods (Price et al. 2010).”
From Evaluating fast maximum likelihood-based phylogenetic programs using empirical phylogenomic data sets (2018) · cites this paper as Price et al. 2010
In the citing paper
“For example, the recently developed FastTree program can be orders of magnitude faster than either PhyML or RAxML/ExaML (Price et al. 2010).”
From Evaluating fast maximum likelihood-based phylogenetic programs using empirical phylogenomic data sets (2018) · cites this paper as Price et al. 2010
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
The neighbor-joining method: a new method for reconstructing phylogenetic trees.
Saitou, N., & Nei, M. (1987) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a040454 · Cited by 59,959
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP
Felsenstein, J. (1985) · Evolution · doi:10.1111/j.1558-5646.1985.tb00420.x · Cited by 44,735
DeLong, E. R., DeLong, D. M., & Clarke-Pearson, D. L. (1988) · Biometrics · doi:10.2307/2531595 · Cited by 22,649
Guindon, S., Dufayard, J.-F., Lefort, V., Anisimova, M., Hordijk, W., & Gascuel, O. (2010) · Systematic Biology · doi:10.1093/sysbio/syq010 · Cited by 18,376
A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood
Guindon, S., & Gascuel, O. (2003) · Systematic Biology · doi:10.1080/10635150390235520 · Cited by 16,923
RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
Stamatakis, A. (2006) · Bioinformatics · doi:10.1093/bioinformatics/btl446 · Cited by 15,582
Evolutionary trees from DNA sequences: A maximum likelihood approach.
Felsenstein, J. (1981) · Journal of Molecular Evolution · doi:10.1007/bf01734359 · Cited by 14,571
Greengenes, a Chimera-Checked 16S rRNA Gene Database and Workbench Compatible with ARB
DeSantis, T. Z., Hugenholtz, P., Larsen, N., Rojas, M., Brodie, E. L., Keller, K., Huber, T., Dalevi, D., Hu, P., & Andersen, G. L. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.03006-05 · Cited by 10,891
A Rapid Bootstrap Algorithm for the RAxML Web Servers
Stamatakis, A., Hoover, P., & Rougemont, J. (2008) · Systematic Biology · doi:10.1080/10635150802429642 · Cited by 7,028
FastTree: Computing Large Minimum Evolution Trees with Profiles instead of a Distance Matrix
Price, M. N., Dehal, P. S., & Arkin, A. P. (2009) · Molecular Biology and Evolution · doi:10.1093/molbev/msp077 · Cited by 5,602
Self-citation
Cited by
Sorted by citations
Items 901–1,000 of 1,081
Varsani, A., & Krupovìč, M. (2016) · Virus Evolution · doi:10.1093/ve/vew037 · Cited by 134
Villaverde, T., Pokorny, L., Olsson, S., Barrado, M. R., Johnson, M. G., Gardner, E. M., Wickett, N. J., Molero, J., Riina, R., & Sanmartín, I. (2018) · New Phytologist · doi:10.1111/nph.15312 · Cited by 134
The impact of antimicrobials on gonococcal evolution
Sánchez-Busó, L., Golparian, D., Corander, J., Grad, Y. H., Ohnishi, M., Flemming, R., Parkhill, J., Bentley, S. D., Unemo, M., & Harris, S. R. (2019) · Nature Microbiology · doi:10.1038/s41564-019-0501-y · Cited by 134
Characterization of antibiotic resistance genes in the species of the rumen microbiota
Sabino, Y. N. V., Santana, M. F., Oyama, L. B., Godoy-Santos, F., Moreira, A. J. S., Huws, S., & Mantovani, H. C. (2019) · Nature Communications · doi:10.1038/s41467-019-13118-0 · Cited by 134
Maistrenko, O. M., Mende, D. R., Lütge, M., Hildebrand, F., Schmidt, T., Li, S. S., Rodrigues, J. F. M., von Mering, C., Coelho, L. P., Huerta‐Cepas, J., et al. (2020) · The ISME Journal · doi:10.1038/s41396-020-0600-z · Cited by 134
Concerted expansion and contraction of immune receptor gene repertoires in plant genomes
Ngou, B. P. M., Heal, R., Wyler, M., Schmid, M. W., & Jones, J. D. G. (2022) · Nature Plants · doi:10.1038/s41477-022-01260-5 · Cited by 134
Zhou, L., Qiu, W., Wang, J., Zhao, A., Zhou, C., Sun, T., Xiong, Z., Cao, P., Shen, W., Chen, J., et al. (2023) · Cell Host & Microbe · doi:10.1016/j.chom.2023.05.022 · Cited by 134
Evolution and host-specific adaptation ofPseudomonas aeruginosa
Weimann, A., Dinan, A. M., Ruis, C., Bernut, A., Pont, S., Brown, K., Ryan, J., Santos, L., Ellison, L., Ukor, E.-F., et al. (2024) · Science · doi:10.1126/science.adi0908 · Cited by 134
Emergence of human-adapted Salmonella enterica is linked to the Neolithization process
Key, F. M., Posth, C., Esquivel-Gomez, L. R., Hübler, R., Spyrou, M. A., Neumann, G. U., Furtwängler, A., Sabin, S., Burri, M., Wissgott, A., et al. (2020) · Nature Ecology & Evolution · doi:10.1038/s41559-020-1106-9 · Cited by 133
ITEP: An integrated toolkit for exploration of microbial pan-genomes
Benedict, M. N., Henriksen, J. R., Metcalf, W. W., Whitaker, R. J., & Price, N. D. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-8 · Cited by 133
Taxonomy of rhizobia and agrobacteria from the Rhizobiaceae family in light of genomics
Ormeño‐Orrillo, E., Servín-Garcidueñas, L. E., Rogel, M. A., González, V., Peralta, H., Mora, J., Martínez‐Romero, J., & Martínez‐Romero, E. (2014) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2014.12.002 · Cited by 133
Venkataraman, A., Rosenbaum, M. A., Perkins, S. D., Werner, J. J., & Angenent, L. T. (2011) · Energy & Environmental Science · doi:10.1039/c1ee01377g · Cited by 133
Gómez-Valero, L., Rusniok, C., Rolando, M., Néou, M., Ravault, D., Demirtas, J., Rouy, Z., Moore, R. J., Chen, H., Petty, N. K., et al. (2014) · Genome biology · doi:10.1186/preaccept-1086350395137407 · Cited by 133
Influence of early life exposure, host genetics and diet on the mouse gut microbiome and metabolome
Snijders, A. M., Langley, S. A., Kim, Y., Brislawn, C., Noecker, C. A., Zink, E., Fansler, S. J., Casey, C., Miller, D. R., Huang, Y., et al. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.221 · Cited by 133
Hutter, C. R., Lambert, S. M., & Wiens, J. J. (2017) · The American Naturalist · doi:10.1086/694319 · Cited by 133
Peng, R., Han, B., Cai, Q.-Q., Zuo, X.-Y., Xia, T., Chen, J., Feng, L.-N., Lim, J. Q., Chen, S., Zeng, M., et al. (2018) · Leukemia · doi:10.1038/s41375-018-0324-5 · Cited by 133
Wang, F., Dong, W., Zhao, Z., Wang, H., Wen-zheng, L., Chen, G., Wang, F., Zhao, Y., Huang, J. S., & Zhou, T. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.146383 · Cited by 133
Zhu, Q., Huang, S. W., González, A., McGrath, I., McDonald, D. T., Haiminen, N., Armstrong, G., Vázquez‐Baeza, Y., Yu, J., Kuczynski, J., et al. (2022) · mSystems · doi:10.1128/msystems.00167-22 · Cited by 133
Predicting butyrate- and propionate-forming bacteria of gut microbiota from sequencing data
Kircher, B., Woltemate, S., Gutzki, F. M., Schlüter, D., Geffers, R., Bähre, H., & Vital, M. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2149019 · Cited by 133
An accurate and efficient experimental approach for characterization of the complex oral microbiota
Zheng, W., Tsompana, M., Ruscitto, A., Sharma, A., Genco, R. J., Sun, Y., & Buck, M. J. (2015) · Microbiome · doi:10.1186/s40168-015-0110-9 · Cited by 132
Yergeau, É., Bell, T. H., Champagne, J., Maynard, C., Tardif, S., Tremblay, J., & Greer, C. W. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01436 · Cited by 132
Pterostilbene‐induced changes in gut microbiota composition in relation to obesity
Etxeberría, U., Hijona, E., Aguirre, L., Milagro, F. I., Bujanda, L., Rimando, A. M., Martínez, J. A., & Portillo, M. P. (2016) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201500906 · Cited by 132
Akiva, E., Copp, J. N., Tokuriki, N., & Babbitt, P. C. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1706849114 · Cited by 132
Smythe, A. B., Holovachov, O. V., & Kocot, K. M. (2019) · BMC Evolutionary Biology · doi:10.1186/s12862-019-1444-x · Cited by 132
Armaleo, D., Müller, O., Lutzoni, F. M., Andrésson, Ó. S., Blanc, G., Bode, H. B., Collart, F., Grande, F. D., Dietrich, F. S., Grigoriev, I. V., et al. (2019) · BMC Genomics · doi:10.1186/s12864-019-5629-x · Cited by 132
Secor, P. R., Burgener, E. B., Kinnersley, M. A., Jennings, L. K., Román-Cruz, V. C., Popescu, M. C., Belleghem, J. D. V., Haddock, N. L., Copeland, C., Michaels, L. A., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00244 · Cited by 132
The Urine Microbiome of Healthy Men and Women Differs by Urine Collection Method
Pohl, H. G., Groah, S. L., Pérez‐Losada, M., Ljungberg, I. H., Sprague, B. M., Chandal, N., Caldovic, L., & Hsieh, M. H. (2020) · International Neurourology Journal · doi:10.5213/inj.1938244.122 · Cited by 132
Epidemiological hypothesis testing using a phylogeographic and phylodynamic framework
Dellicour, S., Lequime, S., Vrancken, B., Gill, M. S., Bastide, P., Gangavarapu, K., Matteson, N. L., Tan, Y., du Plessis, L., Fisher, A. A., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-19122-z · Cited by 132
Strati, F., Pujolassos, M., Burrello, C., Giuffrè, M. R., Lattanzi, G., Caprioli, F., Troisi, J., & Facciotti, F. (2021) · Microbiome · doi:10.1186/s40168-020-00991-x · Cited by 132
Lehtimäki, J., Karkman, A., Laatikainen, T., Paalanen, L., von Hertzen, L., Haahtela, T., Hanski, I., & Ruokolainen, L. (2017) · Scientific Reports · doi:10.1038/srep45651 · Cited by 131
Fugmann, M., Breier, M., Rottenkolber, M., Banning, F., Ferrari, U., Sacco, V., Grallert, H., Parhofer, K. G., Seissler, J., Clavel, T., et al. (2015) · Scientific Reports · doi:10.1038/srep13212 · Cited by 131
Protist diversity along a salinity gradient in a coastal lagoon
Balzano, S., Abs, E., & Leterme, S. C. (2015) · Aquatic Microbial Ecology · doi:10.3354/ame01740 · Cited by 131
Landscape topography structures the soil microbiome in arctic polygonal tundra
Taş, N., Prestat, E., Shi, W., Wu, Y., Ulrich, C., Kneafsey, T. J., Tringe, S. G., Torn, M. S., Hubbard, S. S., & Jansson, J. K. (2018) · Nature Communications · doi:10.1038/s41467-018-03089-z · Cited by 131
Effects of Arsenic on Gut Microbiota and Its Biotransformation Genes in EarthwormMetaphire sieboldi
Wang, H., Zhu, D., Li, G., Zheng, F., Ding, J., O’Connor, P., Zhu, Y., & Xue, X.-M. (2019) · Environmental Science & Technology · doi:10.1021/acs.est.8b06695 · Cited by 131
The evolutionary origins of the cat attractant nepetalactone in catnip
Lichman, B. R., Godden, G. T., Hamilton, J. P., Palmer, L., Kamileen, M. O., Zhao, D., Vaillancourt, B., Wood, J. C., Sun, M., Kinser, T. J., et al. (2020) · Science Advances · doi:10.1126/sciadv.aba0721 · Cited by 131
Murphy, C. L., Biggerstaff, J., Eichhorn, A., Ewing, E., Shahan, R., Soriano, D., Stewart, S. N., VanMol, K., Walker, R., Walters, P., et al. (2021) · Environmental Microbiology · doi:10.1111/1462-2920.15614 · Cited by 131
A catalog of the diversity and ubiquity of bacterial microcompartments
Sutter, M., Melnicki, M. R., Schulz, F., Woyke, T., & Kerfeld, C. A. (2021) · Nature Communications · doi:10.1038/s41467-021-24126-4 · Cited by 131
Xiong, R., He, X., Gao, N., Li, Q. X., Qiu, Z., Hou, Y., & Shen, W. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.04165-23 · Cited by 131
Bacterial community structure and soil properties of a subarctic tundra soil in Council, Alaska
Kim, H. M., Jung, J. Y., Yergeau, É., Hwang, C. Y., Hinzman, L. D., Nam, S., Hong, S. G., Kim, O.-S., Chun, J., & Lee, Y. K. (2014) · FEMS Microbiology Ecology · doi:10.1111/1574-6941.12362 · Cited by 131
Pepe‐Ranney, C., Koechli, C., Potrafka, R. M., Andam, C. P., Eggleston, E. M., García‐Pichel, F., & Buckley, D. H. (2015) · The ISME Journal · doi:10.1038/ismej.2015.106 · Cited by 130
Ahmed, S. A., Awosika, J. A., Baldwin, C. D., Bishop‐Lilly, K. A., Biswas, B., Broomall, S. M., Chain, P., Chertkov, O., Chokoshvili, O., Coyne, S. R., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048228 · Cited by 130
Bacterioplankton Dynamics within a Large Anthropogenically Impacted Urban Estuary
Jeffries, T. C., Fontes, M. L. S., Harrison, D. P., van Dongen‐Vogels, V., Eyre, B. D., Ralph, P. J., & Seymour, J. R. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01438 · Cited by 130
Huang, A. C., Kautsar, S. A., Hong, Y. J., Medema, M. H., Bond, A. D., Tantillo, D. J., & Osbourn, A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1705567114 · Cited by 130
Long-term in situ permafrost thaw effects on bacterial communities and potential aerobic respiration
Monteux, S., Weedon, J. T., Blume‐Werry, G., Gavazov, K., Jassey, V. E. J., Johansson, M., Keuper, F., Olid, C., & Dorrepaal, E. (2018) · The ISME Journal · doi:10.1038/s41396-018-0176-z · Cited by 130
Masetti, G., Moshkelgosha, S., Köhling, H.-L., Covelli, D., Banga, J. P., Berchner‐Pfannschmidt, U., Horstmann, M., Díaz‐Cano, S. J., Goertz, G.-E., Plummer, S. F., et al. (2018) · Microbiome · doi:10.1186/s40168-018-0478-4 · Cited by 130
Quin, C., Estaki, M., Vollman, D. M., Barnett, J. A., Gill, S. K., & Gibson, D. L. (2018) · Scientific Reports · doi:10.1038/s41598-018-26423-3 · Cited by 130
Zhang, X., Tu, B., Dai, L., Lawson, P. A., Zheng, Z., Liu, L., Deng, Y., Zhang, H., & Cheng, L. (2018) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijsem.0.002966 · Cited by 130
Park, S., Lee, K., Kim, Y. O., Won, S., & Chun, J. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00834 · Cited by 130
An Integrated Metagenome Catalog Reveals New Insights into the Murine Gut Microbiome
Lesker, T. R., Raj, A. C. D., Gálvez, E. J. C., Lagkouvardos, I., Baines, J. F., Clavel, T., Sczyrba, A., McHardy, A. C., & Strowig, T. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.02.036 · Cited by 130
Zhang, C., Pan, J., Liu, Y., Duan, C., & Li, M. (2020) · Microbiome · doi:10.1186/s40168-020-00876-z · Cited by 130
Wang, C., Chen, D., Shen, J., Yuan, Q., Fan, F., Wei, W., Li, Y., & Wu, J. (2021) · Agriculture Ecosystems & Environment · doi:10.1016/j.agee.2020.107291 · Cited by 130
Diversity and distribution of viruses inhabiting the deepest ocean on Earth
Jian, H., Yi, Y., Wang, J., Hao, Y., Zhang, M., Wang, S., Meng, C., Zhang, Y., Jing, H., Wang, Y., et al. (2021) · The ISME Journal · doi:10.1038/s41396-021-00994-y · Cited by 130
Compendium of 530 metagenome-assembled bacterial and archaeal genomes from the polar Arctic Ocean
Royo‐Llonch, M., Sánchez, P., Ruiz‐González, C., Salazar, G., Pedrós‐Alió, C., Sebastián, M., Labadie, K., Paoli, L., Ibarbalz, F. M., Zinger, L., et al. (2021) · Nature Microbiology · doi:10.1038/s41564-021-00979-9 · Cited by 130
Human origins in a southern African palaeo-wetland and first migrations
Chan, E. K. F., Timmermann, A., Baldi, B. F., Moore, A. E., Lyons, R. J., Lee, S.-S., Kalsbeek, A. M. F., Petersen, D. C., Rautenbach, H., Förtsch, H. E. A., et al. (2019) · Nature · doi:10.1038/s41586-019-1714-1 · Cited by 130
16S rRNA gene high-throughput sequencing data mining of microbial diversity and interactions
Ju, F., & Zhang, T. (2015) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-015-6536-y · Cited by 129
Derakhshani, H., Tun, H. M., & Khafipour, E. (2015) · Journal of Basic Microbiology · doi:10.1002/jobm.201500420 · Cited by 129
Bletz, M. C., Archer, H. M., Harris, R. N., McKenzie, V. J., Rabemananjara, F. C. E., Rakotoarison, A., & Vences, M. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01530 · Cited by 129
Ecogenomics of virophages and their giant virus hosts assessed through time series metagenomics
Roux, S., Chan, L., Egan, R. S., Malmstrom, R. R., McMahon, K. D., & Sullivan, M. B. (2017) · Nature Communications · doi:10.1038/s41467-017-01086-2 · Cited by 129
Microbial life on a sand grain: from bulk sediment to single grains
Probandt, D., Eickhorst, T., Ellrott, A., Amann, R., & Knittel, K. (2017) · The ISME Journal · doi:10.1038/ismej.2017.197 · Cited by 129
Casting light on Asgardarchaeota metabolism in a sunlit microoxic niche
Bulzu, P., Andrei, A., Salcher, M. M., Mehrshad, M., Inoue, K., Kandori, H., Béjà, O., Ghai, R., & Banciu, H. L. (2019) · Nature Microbiology · doi:10.1038/s41564-019-0404-y · Cited by 129
Johnston, E. R., Hatt, J. K., He, Z., Wu, L., Guo, X. Y., Luo, Y., Schuur, E. A. G., Tiedje, J. M., Zhou, J. Z., & Konstantinidis, K. T. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1901307116 · Cited by 129
Janouškovec, J., Paskerova, G. G., Miroliubova, T. S., Mikhailov, K. V., Birley, T., Aleoshin, V. V., & Simdyanov, T. G. (2019) · eLife · doi:10.7554/elife.49662 · Cited by 129
Iroki: automatic customization and visualization of phylogenetic trees
Moore, R. M., Harrison, A. O., McAllister, S. M., Polson, S. W., & Wommack, K. E. (2020) · PeerJ · doi:10.7717/peerj.8584 · Cited by 129
Emmenegger, B., Massoni, J., Pestalozzi, C. M., Bortfeld‐Miller, M., Maier, B. A., & Vorholt, J. A. (2023) · Nature Communications · doi:10.1038/s41467-023-43793-z · Cited by 129
A suberized exodermis is required for tomato drought tolerance
Cantó‐Pastor, A., Kajala, K., Shaar‐Moshe, L., Manzano, C., Timilsena, P. R., Bellis, D. D., Gray, S. B., Holbein, J., Yang, H., Mohammad, S., et al. (2024) · Nature Plants · doi:10.1038/s41477-023-01567-x · Cited by 129
Genomes of multicellular algal sisters to land plants illuminate signaling network evolution
Feng, X., Zheng, J., Irisarri, I., Yu, H., Zheng, B., Ali, Z. M., de Vries, S., Keller, J., Fürst‐Jansen, J. M. R., Dadras, A., et al. (2024) · Nature Genetics · doi:10.1038/s41588-024-01737-3 · Cited by 129
Kautz, S., Rubin, B. E. R., Russell, J. A., & Moreau, C. S. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.03107-12 · Cited by 128
Microbiomic differences in tumor and paired-normal tissue in head and neck squamous cell carcinomas
Wang, H., Funchain, P., Bebek, G., Altemus, J. B., Zhang, H., Niazi, F., Peterson, C., Lee, W. T., Burkey, B. B., & Eng, C. (2017) · Genome Medicine · doi:10.1186/s13073-017-0405-5 · Cited by 128
Wood Ash Induced pH Changes Strongly Affect Soil Bacterial Numbers and Community Composition
Bang‐Andreasen, T., Nielsen, J. T., Voříšková, J., Heise, J., Rønn, R., Kjøller, R., Hansen, H. C. B., & Jacobsen, C. S. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01400 · Cited by 128
Towards a balanced view of the bacterial tree of life
Schulz, F., Eloe‐Fadrosh, E. A., Bowers, R. M., Jarett, J. K., Nielsen, T., Ivanova, N., Kyrpides, N. C., & Woyke, T. (2017) · Microbiome · doi:10.1186/s40168-017-0360-9 · Cited by 128
Context-specific emergence and growth of the SARS-CoV-2 Delta variant
McCrone, J. T., Hill, V., Bajaj, S., Pena, R. E., Lambert, B. C., Inward, R. P. D., Bhatt, S., Volz, E., Ruis, C., Dellicour, S., et al. (2022) · Nature · doi:10.1038/s41586-022-05200-3 · Cited by 128
The hyphal-specific toxin candidalysin promotes fungal gut commensalism
Liang, S.-H., Sircaik, S., Dainis, J. P., Kakade, P., Penumutchu, S., McDonough, L. D., Chen, Y.-H., Frazer, C., Schille, T. B., Allert, S., et al. (2024) · Nature · doi:10.1038/s41586-024-07142-4 · Cited by 128
Allali, I., Delgado, S., Marrón, P. I., Astudillo, A., Yeh, J. J., Ghazal, H., Amzazi, S., Keku, T. O., & Azcárate-Peril, M. A. (2015) · Gut Microbes · doi:10.1080/19490976.2015.1039223 · Cited by 127
Lagkouvardos, I., Kläring, K., Heinzmann, S. S., Platz, S., Scholz, B., Engel, K., Schmitt‐Kopplin, P., Haller, D., Rohn, S., Skurk, T., et al. (2015) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201500125 · Cited by 127
Oceanographic structure drives the assembly processes of microbial eukaryotic communities
Monier, A., Comte, J., Babin, M., Forest, A., Matsuoka, A., & Lovejoy, C. (2014) · The ISME Journal · doi:10.1038/ismej.2014.197 · Cited by 127
Sun, H., Shi, B., Bai, Y., & Wang, D. (2013) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2013.11.017 · Cited by 127
Lateral Gene Transfer Dynamics in the Ancient Bacterial Genus Streptomyces
McDonald, B. R., & Currie, C. R. (2017) · mBio · doi:10.1128/mbio.00644-17 · Cited by 127
Pan-genome analyses of model fungal species
McCarthy, C. G. P., & Fitzpatrick, D. A. (2019) · Microbial Genomics · doi:10.1099/mgen.0.000243 · Cited by 127
Evolutionary Patterns of Thylakoid Architecture in Cyanobacteria
Mareš, J., Strunecký, O., Bučinská, L., & Wiedermannová, J. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00277 · Cited by 127
Hale, V. L., Jeraldo, P., Chen, J., Mundy, M. B., Yao, J. Z., Priya, S., Keeney, G., Lyke, K. J., Ridlon, J. M., White, B. A., et al. (2018) · Genome Medicine · doi:10.1186/s13073-018-0586-6 · Cited by 127
Ozer, E. A., Nnah, E., Didelot, X., Whitaker, R. J., & Hauser, A. R. (2019) · Genome Biology and Evolution · doi:10.1093/gbe/evz119 · Cited by 127
Romdhane, S., Spor, A., Busset, H., Falchetto, L., Martin, J. G. C., Bizouard, F., Bru, D., Breuil, M., Philippot, L., & Cordeau, S. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01618 · Cited by 127
Wang, L., Zhao, L., Zhang, X., Zhang, Q., Jia, Y., Wang, G., Li, S., Tian, D., Li, W., & Yang, S. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1910229116 · Cited by 127
Ouyang, Y., & Norton, J. M. (2019) · Applied and Environmental Microbiology · doi:10.1128/aem.02278-19 · Cited by 127
Wang, Y., Wang, K., Huang, L., Dong, P., Wang, S., Chen, H., Lu, Z., Hou, D., & Zhang, D. (2020) · Microbiome · doi:10.1186/s40168-020-00879-w · Cited by 127
Undinarchaeota illuminate DPANN phylogeny and the impact of gene transfer on archaeal evolution
Dombrowski, N., Williams, T. A., Sun, J., Woodcroft, B. J., Lee, J.-H., Minh, B. Q., Rinke, C., & Spang, A. (2020) · Nature Communications · doi:10.1038/s41467-020-17408-w · Cited by 127
Yan, Q., Li, S., Yan, Q., Huo, X., Wang, C., Wang, X., Sun, Y., Zhao, W., Yu, Z., Zhang, Y., et al. (2024) · Cell · doi:10.1016/j.cell.2024.04.043 · Cited by 127
Multiple independent origins of apicomplexan-like parasites
Mathur, V., Kolísko, M., Hehenberger, E., Irwin, N. A. T., Leander, B. S., Kristmundsson, Á., Freeman, M. A., & Keeling, P. J. (2019) · Current Biology · doi:10.1016/j.cub.2019.07.019 · Cited by 126
Ininbergs, K., Bay, G., Rasmussen, U., Wardle, D. A., & Nilsson, M. (2011) · New Phytologist · doi:10.1111/j.1469-8137.2011.03809.x · Cited by 126
Evolutionary informatics: unifying knowledge about the diversity of life
Parr, C. S., Guralnick, R., Cellinese, N., & Page, R. (2011) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2011.11.001 · Cited by 126
Naveed, M., Herath, L., Møldrup, P., Arthur, E., Nicolaisen, M., Nørgaard, T., Ferré, T. P. A., & de Jonge, L. W. (2016) · Applied Soil Ecology · doi:10.1016/j.apsoil.2016.03.004 · Cited by 126
Mancuso, F. P., D’hondt, S., Willems, A., Airoldi, L., & Clerck, O. D. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00476 · Cited by 126
Microhabitat heterogeneity across leaves and flower organs promotes bacterial diversity
Junker, R. R., & Keller, A. (2015) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiv097 · Cited by 126
Gut microbiota of dung beetles correspond to dietary specializations of adults and larvae
Shukla, S. P., Sanders, J. G., Byrne, M. J., & Pierce, N. E. (2016) · Molecular Ecology · doi:10.1111/mec.13901 · Cited by 126
Novel SCC mec type XIII (9A) identified in an ST152 methicillin-resistant Staphylococcus aureus
Baig, S., Johannesen, T. B., Overballe‐Petersen, S., Larsen, J., Larsen, A. R., & Stegger, M. (2018) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2018.03.013 · Cited by 126
Flórez, L. V., Scherlach, K., Miller, I. J., Rodrigues, A. L., Kwan, J. C., Hertweck, C., & Kaltenpoth, M. (2018) · Nature Communications · doi:10.1038/s41467-018-04955-6 · Cited by 126
Hidden in plain sight—highly abundant and diverse planktonic freshwater Chloroflexi
Mehrshad, M., Salcher, M. M., Okazaki, Y., Nakano, S., Šimek, K., Andrei, A., & Ghai, R. (2018) · Microbiome · doi:10.1186/s40168-018-0563-8 · Cited by 126
Shotgun Metagenomics of a Water Kefir Fermentation Ecosystem Reveals a Novel Oenococcus Species
Verce, M., De Vuyst, L., & Weckx, S. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00479 · Cited by 121
The individual-specific and diverse nature of the preterm infant microbiota
Barrett, E., Kerr, C., Murphy, K., O'Sullivan, O., Ryan, C. A., Dempsey, E. M., Murphy, B. P., O'Toole, P. W., Cotter, P. D., Fitzgerald, G. F., et al. (2013) · Archives of Disease in Childhood - Fetal and Neonatal Edition · doi:10.1136/archdischild-2012-303035 · Cited by 120
Genomic factors shape carbon and nitrogen metabolic niche breadth across Saccharomycotina yeasts
Opulente, D. A., LaBella, A. L., Harrison, M.-C., Wolters, J. F., Liu, C., Li, Y., Kominek, J., Steenwyk, J. L., Stoneman, H. R., VanDenAvond, J., et al. (2024) · Science · doi:10.1126/science.adj4503 · Cited by 121
Metadata
- Authors
- Price, M. N., Dehal, P. S., & Arkin, A. P.
- Affiliations
- Lawrence Berkeley National Laboratory (US)
- Corresponding author
- Price, Morgan N.
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2010-03-10
- Volume
- 5
- Issue
- 3
- Pages
- e9490
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC2835736
- OpenAlex
- W2031611770
- Cited by
- 14,894
- References
- 37
- Citations by year
- 2026: 1298 · 2025: 1543 · 2024: 1657 · 2023: 1486 · 2022: 1676 · 2021: 1651 · 2020: 1363 · 2019: 1013 · 2018: 776 · 2017: 686 · 2016: 521 · 2015: 415 · 2014: 309 · 2013: 256 · 2012: 133
- FWCI
- 63.80
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS ONE (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- eScholarship (California Digital Library) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by)
- Figshare (submittedVersion, cc-by)
- Funders
- U.S. Department of Energy (-AC02-05CH11231, 05CH11231, DE AC02 05CH11231, DE-AC02-)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fractal and DNA sequence analysis
- Keywords
- phylogenetic inference, maximum likelihood phylogeny, nearest neighbor interchange, cat model, 16S rRNA, phylogenetic accuracy, scalability
- MeSH terms
- Algorithms, Animals, Computers, Data Interpretation, Statistical, Genetic Techniques, Humans, Models, Genetic, Phylogeny, RNA, Ribosomal, 16S, Software, Likelihood Functions, Sequence Alignment, Databases, Protein
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