The DOI matches its Crossref record; 95 of the 95 references it cites were found in a registry or an index.
Improved prediction of fungal effector proteins from secretomes with EffectorP 2.0
Open accessAbstract
Summary: Plant‐pathogenic fungi secrete effector proteins to facilitate infection. We describe extensive improvements to EffectorP, the first machine learning classifier for fungal effector prediction. EffectorP 2.0 is now trained on a larger set of effectors and utilizes a different approach based on an ensemble of classifiers trained on different subsets of negative data, offering different views on classification. EffectorP 2.0 achieves an accuracy of 89%, compared with 82% for EffectorP 1.0 and 59.8% for a small size classifier. Important features for effector prediction appear to be protein size, protein net charge as well as the amino acids serine and cysteine. EffectorP 2.0 decreases the number of predicted effectors in secretomes of fungal plant symbionts and saprophytes by 40% when compared with EffectorP 1.0. However, EffectorP 1.0 retains value, and combining EffectorP 1.0 and 2.0 results in a stringent classifier with a low false positive rate of 9%. EffectorP 2.0 predicts significant enrichments of effectors in 12 of 13 sets of infection‐induced proteins from diverse fungal pathogens, whereas a small cysteine‐rich classifier detects enrichment in only seven of 13. EffectorP 2.0 will fast track the prioritization of high‐confidence effector candidates for functional validation and aid in improving our understanding of effector biology. EffectorP 2.0 is available at http://effectorp.csiro.au .
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.
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
A simple method for displaying the hydropathic character of a protein
Kyte, J., & Doolittle, R. F. (1982) · Journal of Molecular Biology · doi:10.1016/0022-2836(82)90515-0 · Cited by 22,843
The WEKA data mining software: an update
Hall, M., Frank, E., Holmes, G., Pfahringer, B., Reutemann, P., & Witten, I. H. (2009) · ACM SIGKDD Explorations Newsletter · doi:10.1145/1656274.1656278 · Cited by 17,750
Krogh, A., Larsson, B., von Heijne, G., & Sonnhammer, E. L. L. (2001) · Journal of Molecular Biology · doi:10.1006/jmbi.2000.4315 · Cited by 12,654
EMBOSS: the European molecular biology open software suite.
Rice, P., Longden, I., & Bleasby, A. (2000) · Trends in Genetics · doi:10.1016/s0168-9525(00)02024-2 · Cited by 9,466
SignalP 4.0: discriminating signal peptides from transmembrane regions
Petersen, T. N., Brunak, S., von Heijne, G., & Nielsen, H. (2011) · Nature Methods · doi:10.1038/nmeth.1701 · Cited by 8,847
Protein Identification and Analysis Tools on the ExPASy Server
Gasteiger, E., Hoogland, C., Gattiker, A., Duvaud, S., Wilkins, M. R., Appel, R. D., & Bairoch, A. (2005) · The Proteomics Protocols Handbook · doi:10.1385/1-59259-890-0:571 · Cited by 8,681
Improved Prediction of Signal Peptides: SignalP 3.0
Dyrløv Bendtsen, J., Nielsen, H., von Heijne, G., & Brunak, S. (2004) · Journal of Molecular Biology · doi:10.1016/j.jmb.2004.05.028 · Cited by 6,350
HMMER web server: interactive sequence similarity searching
Finn, R. D., Clements, J., & Eddy, S. R. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr367 · Cited by 5,952
High-throughput functional annotation and data mining with the Blast2GO suite
Gotz, S., Garcia-Gomez, J. M., Terol, J., Williams, T. D., Nagaraj, S. H., Nueda, M. J., Robles, M., Talon, M., Dopazo, J., & Conesa, A. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn176 · Cited by 4,423
Predicting Subcellular Localization of Proteins Based on their N-terminal Amino Acid Sequence
Emanuelsson, O., Nielsen, H., Brunak, S., & von Heijne, G. (2000) · Journal of Molecular Biology · doi:10.1006/jmbi.2000.3903 · Cited by 4,263
Goffeau, A., Barrell, B. G., Bussey, H., Davis, R. W., Dujon, B., Feldmann, H., Galibert, F., Hoheisel, J. D., Jacq, C., Johnston, M., et al. (1996) · Science · doi:10.1126/science.274.5287.546 · Cited by 4,263
Intrinsically disordered protein
Dunker, A. K., Lawson, J. D., Brown, C. J., Williams, R. M., Romero, P., Oh, J. S., Oldfield, C. J., Campen, A. M., Ratliff, C. M., Hipps, K. W., et al. (2001) · Journal of Molecular Graphics and Modelling · doi:10.1016/s1093-3263(00)00138-8 · Cited by 2,272
The Paleozoic Origin of Enzymatic Lignin Decomposition Reconstructed from 31 Fungal Genomes
Floudas, D., Binder, M., Riley, R., Barry, K., Blanchette, R. A., Henrissat, B., Martínez, A. T., Otillar, R., Spatafora, J. W., Yadav, J. S., et al. (2012) · Science · doi:10.1126/science.1221748 · Cited by 1,779
Comparative genomics reveals mobile pathogenicity chromosomes in Fusarium
Ma, L.-J., van der Does, H. C., Borkovich, K. A., Coleman, J. J., Daboussi, M.-J., Di Pietro, A., Dufresne, M., Freitag, M., Grabherr, M., Henrissat, B., et al. (2010) · Nature · doi:10.1038/nature08850 · Cited by 1,772
Self-citationThe genome sequence of the filamentous fungus Neurospora crassa
Galagan, J. E., Calvo, S. E., Borkovich, K. A., Selker, E. U., Read, N. D., Jaffe, D., FitzHugh, W., Ma, L.-J., Smirnov, S., Purcell, S., et al. (2003) · Nature · doi:10.1038/nature01554 · Cited by 1,670
The genome sequence of the rice blast fungus Magnaporthe grisea
Dean, R. A., Talbot, N. J., Ebbole, D. J., Farman, M. L., Mitchell, T. K., Orbach, M. J., Thon, M., Kulkarni, R., Xu, J.-R., Pan, H., et al. (2005) · Nature · doi:10.1038/nature03449 · Cited by 1,660
Intrinsically Disordered Proteins
Uversky, V. N. (2013) · Brenner's Encyclopedia of Genetics · doi:10.1016/b978-0-12-374984-0.01698-3 · Cited by 1,637
Fungal Effectors and Plant Susceptibility
Lo Presti, L., Lanver, D., Schweizer, G., Tanaka, S., Liang, L., Tollot, M., Zuccaro, A., Reissmann, S., & Kahmann, R. (2015) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-043014-114623 · Cited by 1,249
Genome sequencing and analysis of Aspergillus oryzae
Machida, M., Asai, K., Sano, M., Tanaka, T., Kumagai, T., Terai, G., Kusumoto, K.-I., Arima, T., Akita, O., Kashiwagi, Y., et al. (2005) · Nature · doi:10.1038/nature04300 · Cited by 1,245
Insights from the genome of the biotrophic fungal plant pathogen Ustilago maydis
Kämper, J., Kahmann, R., Bölker, M., Ma, L.-J., Brefort, T., Saville, B. J., Banuett, F., Kronstad, J. W., Gold, S. E., Müller, O., et al. (2006) · Nature · doi:10.1038/nature05248 · Cited by 1,208
Mycorrhizal Genomics Initiative Consortium, Kohler, A., Kuo, A., Nagy, L. G., Morin, E., Barry, K. W., Buscot, F., Canbäck, B., Choi, C., Cichocki, N., et al. (2015) · Nature Genetics · doi:10.1038/ng.3223 · Cited by 1,060
Genome sequence and gene compaction of the eukaryote parasite Encephalitozoon cuniculi
Katinka, M. D., Duprat, S., Cornillot, E., Méténier, G., Thomarat, F., Prensier, G., Barbe, V., Peyretaillade, E., Brottier, P., Wincker, P., et al. (2001) · Nature · doi:10.1038/35106579 · Cited by 1,058
The genome of Laccaria bicolor provides insights into mycorrhizal symbiosis
Martin, F., Aerts, A., Ahrén, D., Brun, A., Danchin, E. G. J., Duchaussoy, F., Gibon, J., Kohler, A., Lindquist, E., Pereda, V., et al. (2008) · Nature · doi:10.1038/nature06556 · Cited by 1,053
O'Connell, R. J., Thon, M. R., Hacquard, S., Amyotte, S. G., Kleemann, J., Torres, M. F., Damm, U., Buiate, E. A., Epstein, L., Alkan, N., et al. (2012) · Nature Genetics · doi:10.1038/ng.2372 · Cited by 1,047
Genomic Analysis of the Necrotrophic Fungal Pathogens Sclerotinia sclerotiorum and Botrytis cinerea
Amselem, J., Cuomo, C. A., van Kan, J. A. L., Viaud, M., Benito, E. P., Couloux, A., Coutinho, P. M., de Vries, R. P., Dyer, P. S., Fillinger, S., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002230 · Cited by 1,040
Plant Cell Wall–Degrading Enzymes and Their Secretion in Plant-Pathogenic Fungi
Kubicek, C. P., Starr, T. L., & Glass, N. L. (2014) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-102313-045831 · Cited by 945
Cuomo, C. A., Güldener, U., Xu, J.-R., Trail, F., Turgeon, B. G., Di Pietro, A., Walton, J. D., Ma, L.-J., Baker, S. E., Rep, M., et al. (2007) · Science · doi:10.1126/science.1143708 · Cited by 897
A Catalogue of the Effector Secretome of Plant Pathogenic Oomycetes
Kamoun, S. (2006) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.44.070505.143436 · Cited by 828
Genome Expansion and Gene Loss in Powdery Mildew Fungi Reveal Tradeoffs in Extreme Parasitism
Spanu, P. D., Abbott, J. C., Amselem, J., Burgis, T. A., Soanes, D. M., Stüber, K., Loren van Themaat, E. V., Brown, J. K. M., Butcher, S. A., Gurr, S. J., et al. (2010) · Science · doi:10.1126/science.1194573 · Cited by 812
The diploid genome sequence of Candida albicans
Jones, T., Federspiel, N. A., Chibana, H., Dungan, J., Kalman, S., Magee, B. B., Newport, G., Thorstenson, Y. R., Agabian, N., Magee, P. T., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401648101 · Cited by 768
Obligate biotrophy features unraveled by the genomic analysis of rust fungi
Duplessis, S., Cuomo, C. A., Lin, Y.-C., Aerts, A., Tisserant, E., Veneault-Fourrey, C., Joly, D. L., Hacquard, S., Amselem, J., Cantarel, B. L., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1019315108 · Cited by 729
Self-citationA review of wheat diseases—a field perspective
Figueroa, M., Hammond‐Kosack, K. E., & Solomon, P. S. (2018) · Molecular Plant Pathology · doi:10.1111/mpp.12618 · Cited by 718
Surface and inside volumes in globular proteins
JANIN, J. (1979) · Nature · doi:10.1038/277491a0 · Cited by 714
Fauch, E., J-L, S. R., & Pliska (1983) · Chimie thérapeutique · Cited by 699
The Genome of the Basidiomycetous Yeast and Human Pathogen Cryptococcus neoformans
Loftus, B. J., Fung, E., Roncaglia, P., Rowley, D., Amedeo, P., Bruno, D., Vamathevan, J., Miranda, M., Anderson, I. J., Fraser, J. A., et al. (2005) · Science · doi:10.1126/science.1103773 · Cited by 694
Gao, Q., Jin, K., Ying, S.-H., Zhang, Y., Xiao, G., Shang, Y., Duan, Z., Hu, X., Xie, X.-Q., Zhou, G., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1001264 · Cited by 671
Building text classifiers using positive and unlabeled examples
Liu, B., Dai, Y., Li, X., Lee, W. S., & Yu, P. S. (2004) · Third IEEE International Conference on Data Mining · doi:10.1109/icdm.2003.1250918 · Cited by 667
Goodwin, S. B., Ben M'Barek, S., Dhillon, B., Wittenberg, A. H. J., Crane, C. F., Hane, J. K., Foster, A. J., Van der Lee, T. A. J., Grimwood, J., Aerts, A., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002070 · Cited by 607
Analysis of protein-protein interaction sites using surface patches 1 1Edited by G.Von Heijne
Jones, S., & Thornton, J. M. (1997) · Journal of Molecular Biology · doi:10.1006/jmbi.1997.1234 · Cited by 602
The characterization of amino acid sequences in proteins by statistical methods
Zimmerman, J. M., Eliezer, N., & Simha, R. (1968) · Journal of Theoretical Biology · doi:10.1016/0022-5193(68)90069-6 · Cited by 552
Comparative Genomics Yields Insights into Niche Adaptation of Plant Vascular Wilt Pathogens
Klosterman, S. J., Subbarao, K. V., Kang, S., Veronese, P., Gold, S. E., Thomma, B. P. H. J., Chen, Z., Henrissat, B., Lee, Y.-H., Park, J., et al. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002137 · Cited by 543
Rouxel, T., Grandaubert, J., Hane, J. K., Hoede, C., van de Wouw, A. P., Couloux, A., Dominguez, V., Anthouard, V., Bally, P., Bourras, S., et al. (2011) · Nature Communications · doi:10.1038/ncomms1189 · Cited by 525
Genome sequence of the lignocellulose-bioconverting and xylose-fermenting yeast Pichia stipitis
Jeffries, T. W., Grigoriev, I. V., Grimwood, J., Laplaza, J. M., Aerts, A., Salamov, A., Schmutz, J., Lindquist, E., Dehal, P., Shapiro, H., et al. (2007) · Nature Biotechnology · doi:10.1038/nbt1290 · Cited by 494
LOCALIZER: subcellular localization prediction of both plant and effector proteins in the plant cell
Sperschneider, J., Catanzariti, A.-M., DeBoer, K., Petre, B., Gardiner, D. M., Singh, K. B., Dodds, P. N., & Taylor, J. M. (2017) · Scientific Reports · doi:10.1038/srep44598 · Cited by 466
Self-citationHaustorially Expressed Secreted Proteins from Flax Rust Are Highly Enriched for Avirulence Elicitors
Catanzariti, A.-M., Dodds, P. N., Lawrence, G. J., Ayliffe, M. A., & Ellis, J. G. (2005) · The Plant Cell · doi:10.1105/tpc.105.035980 · Cited by 459
Self-citationZheng, P., Xia, Y., Xiao, G., Xiong, C., Hu, X., Zhang, S., Zheng, H., Huang, Y., Zhou, Y., Wang, S., et al. (2011) · Genome Biology · doi:10.1186/gb-2011-12-11-r116 · Cited by 454
Xu, J., Saunders, C. W., Hu, P., Grant, R. A., Boekhout, T., Kuramae, E. E., Kronstad, J. W., DeAngelis, Y. M., Reeder, N. L., Johnstone, K. R., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706756104 · Cited by 431
Stajich, J. E., Wilke, S. K., Ahrén, D., Au, C. H., Birren, B. W., Borodovsky, M., Burns, C., Canbäck, B., Casselton, L. A., Cheng, C. K., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1003391107 · Cited by 430
A multi-omic map of the lipid-producing yeast Rhodosporidium toruloides
Zhu, Z., Zhang, S., Liu, H., Shen, H., Lin, X., Yang, F., Zhou, Y. J., Jin, G., Ye, M., Zou, H., et al. (2012) · Nature Communications · doi:10.1038/ncomms2112 · Cited by 430
Composition Profiler: a tool for discovery and visualization of amino acid composition differences
Vacic, V., Uversky, V. N., Dunker, A. K., & Lonardi, S. (2007) · BMC Bioinformatics · doi:10.1186/1471-2105-8-211 · Cited by 428
E ffector P: predicting fungal effector proteins from secretomes using machine learning
Sperschneider, J., Gardiner, D. M., Dodds, P. N., Tini, F., Covarelli, L., Singh, K. B., Manners, J. M., & Taylor, J. M. (2016) · New Phytologist · doi:10.1111/nph.13794 · Cited by 419
Self-citationMorin, E., Kohler, A., Baker, A. R., Foulongne-Oriol, M., Lombard, V., Nagye, L. G., Ohm, R. A., Patyshakuliyeva, A., Brun, A., Aerts, A. L., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1206847109 · Cited by 394
Vleeshouwers, V. G. A. A., & Oliver, R. P. (2014) · Molecular Plant-Microbe Interactions® · doi:10.1094/mpmi-10-13-0313-ia · Cited by 389
Kleemann, J., Rincon-Rivera, L. J., Takahara, H., Neumann, U., van Themaat, E. V. L., van der Does, H. C., Hacquard, S., Stüber, K., Will, I., Schmalenbach, W., et al. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002643 · Cited by 378
Mosquera, G., Giraldo, M. C., Khang, C. H., Coughlan, S., & Valent, B. (2009) · The Plant Cell · doi:10.1105/tpc.107.055228 · Cited by 372
Janbon, G., Ormerod, K. L., Paulet, D., Byrnes, E. J., Yadav, V., Chatterjee, G., Mullapudi, N., Hon, C.-C., Billmyre, R. B., Brunel, F., et al. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004261 · Cited by 371
Andersen, M. R., Salazar, M. P., Schaap, P. J., van de Vondervoort, P. J. I., Culley, D., Thykaer, J., Frisvad, J. C., Nielsen, K. F., Albang, R., Albermann, K., et al. (2011) · Genome Research · doi:10.1101/gr.112169.110 · Cited by 362
Filamentous pathogen effector functions: of pathogens, hosts and microbiomes
Rovenich, H., Boshoven, J. C., & Thomma, B. P. (2014) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2014.05.001 · Cited by 288
de Wit, P. J. G. M., van der Burgt, A., Ökmen, B., Stergiopoulos, I., Abd-Elsalam, K. A., Aerts, A. L., Bahkali, A. H., Beenen, H. G., Chettri, P., Cox, M. P., et al. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1003088 · Cited by 285
Hane, J. K., Lowe, R. G. T., Solomon, P. S., Tan, K.-C., Schoch, C. L., Spatafora, J. W., Crous, P. W., Kodira, C., Birren, B. W., Galagan, J. E., et al. (2007) · The Plant Cell · doi:10.1105/tpc.107.052829 · Cited by 262
Crop Yields and Global Food Security. Will Yield Increase Continue to Feed the World?
van Ittersum, M. K. (2016) · European Review of Agricultural Economics · doi:10.1093/erae/jbv034 · Cited by 262
The wheat powdery mildew genome shows the unique evolution of an obligate biotroph
Wicker, T., Oberhaensli, S., Parlange, F., Buchmann, J. P., Shatalina, M., Roffler, S., Ben-David, R., Doležel, J., Šimková, H., Schulze-Lefert, P., et al. (2013) · Nature Genetics · doi:10.1038/ng.2704 · Cited by 247
Structure and evolution of barley powdery mildew effector candidates
Pedersen, C., van Themaat, E. V. L., McGuffin, L. J., Abbott, J. C., Burgis, T. A., Barton, G., Bindschedler, L. V., Lu, X., Maekawa, T., Weßling, R., et al. (2012) · BMC Genomics · doi:10.1186/1471-2164-13-694 · Cited by 243
Loss of AvrSr50 by somatic exchange in stem rust leads to virulence for Sr50 resistance in wheat
Chen, J., Upadhyaya, N. M., Ortiz, D., Sperschneider, J., Li, F., Bouton, C., Breen, S., Dong, C., Xu, B., Zhang, X., et al. (2017) · Science · doi:10.1126/science.aao4810 · Cited by 239
Self-citationde Guillen, K., Ortiz-Vallejo, D., Gracy, J., Fournier, E., Kroj, T., & Padilla, A. (2015) · PLOS Pathogens · doi:10.1371/journal.ppat.1005228 · Cited by 235
Urban, M., Cuzick, A., Rutherford, K., Irvine, A., Pedro, H., Pant, R., Sadanadan, V., Khamari, L., Billal, S., Mohanty, S., et al. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkw1089 · Cited by 231
Variation in the AvrSr35 gene determines Sr35 resistance against wheat stem rust race Ug99
Salcedo, A., Rutter, W., Wang, S., Akhunova, A., Bolus, S., Chao, S., Anderson, N., De Soto, M. F., Rouse, M., Szabo, L., et al. (2017) · Science · doi:10.1126/science.aao7294 · Cited by 222
ApoplastP : prediction of effectors and plant proteins in the apoplast using machine learning
Sperschneider, J., Dodds, P. N., Singh, K. B., & Taylor, J. M. (2018) · New Phytologist · doi:10.1111/nph.14946 · Cited by 198
Self-citationCantu, D., Govindarajulu, M., Kozik, A., Wang, M., Chen, X., Kojima, K. K., Jurka, J., Michelmore, R. W., & Dubcovsky, J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024230 · Cited by 187
ZHAN, J., LINDE, C. C., JÜRGENS, T., MERZ, U., STEINEBRUNNER, F., & McDONALD, B. A. (2005) · Molecular Ecology · doi:10.1111/j.1365-294x.2005.02638.x · Cited by 187
Advances and Challenges in Computational Prediction of Effectors from Plant Pathogenic Fungi
Sperschneider, J., Dodds, P. N., Gardiner, D. M., Manners, J. M., Singh, K. B., & Taylor, J. M. (2015) · PLOS Pathogens · doi:10.1371/journal.ppat.1004806 · Cited by 176
Self-citationÜnal, C. M., & Steinert, M. (2014) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00015-14 · Cited by 175
Comparative Genomic Analysis of Human Fungal Pathogens Causing Paracoccidioidomycosis
Desjardins, C. A., Champion, M. D., Holder, J. W., Muszewska, A., Goldberg, J., Bailão, A. M., Brigido, M. M., Ferreira, M. E. D. S., Garcia, A. M., Grynberg, M., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002345 · Cited by 174
Petre, B., Saunders, D. G. O., Sklenar, J., Lorrain, C., Win, J., Duplessis, S., & Kamoun, S. (2015) · Molecular Plant-Microbe Interactions® · doi:10.1094/mpmi-01-15-0003-r · Cited by 170
Manning, V. A., Pandelova, I., Dhillon, B., Wilhelm, L. J., Goodwin, S. B., Berlin, A. M., Figueroa, M., Freitag, M., Hane, J. K., Henrissat, B., et al. (2013) · G3 Genes|Genomes|Genetics · doi:10.1534/g3.112.004044 · Cited by 168
Laurie, J. D., Ali, S., Linning, R., Mannhaupt, G., Wong, P., Güldener, U., Münsterkötter, M., Moore, R., Kahmann, R., Bakkeren, G., et al. (2012) · The Plant Cell · doi:10.1105/tpc.112.097261 · Cited by 165
New Phytologist– an evolving host for mycorrhizal research
Martin, F. M., & Slater, H. (2007) · New Phytologist · doi:10.1111/j.1469-8137.2007.02058.x · Cited by 150
Genomics of wood-degrading fungi
Ohm, R. A., Riley, R. W., Salamov, A. A., Min, B., Choi, I., & Grigoriev, I. V. (2014) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2014.05.001 · Cited by 147
Plant pathogens as a source of diverse enzymes for lignocellulose digestion
Gibson, D. M., King, B. C., Hayes, M. L., & Bergstrom, G. C. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2011.04.002 · Cited by 146
Panwar, V., McCALLUM, B. D., & Bakkeren, G. (2012) · The Plant Journal · doi:10.1111/tpj.12047 · Cited by 141
Genomic Survey of the Non-Cultivatable Opportunistic Human Pathogen, Enterocytozoon bieneusi
Akiyoshi, D. E., Morrison, H. G., Lei, S., Feng, X., Zhang, Q., Corradi, N., Mayanja‐Kizza, H., Tumwine, J. K., Keeling, P. J., Weiss, L. M., et al. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000261 · Cited by 140
The genome sequence and effector complement of the flax rust pathogen Melampsora lini
Nemri, A., Saunders, D. G. O., Anderson, C., Upadhyaya, N. M., Win, J., Lawrence, G. J., Jones, D. A., Kamoun, S., Ellis, J. G., & Dodds, P. N. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00098 · Cited by 138
Self-citationKettles, G. J., Bayón, C., Canning, G., Rudd, J. J., & Kanyuka, K. (2016) · New Phytologist · doi:10.1111/nph.14215 · Cited by 108
Upadhyaya, N. M., Garnica, D. P., Karaoglu, H., Sperschneider, J., Nemri, A., Xu, B., Mago, R., Cuomo, C. A., Rathjen, J. P., Park, R., et al. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00759 · Cited by 105
Self-citationTollot, M., Daniela, A., Becker, C., Altmüller, J., Dutheil, J. Y., Wegner, C., & Kahmann, R. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005697 · Cited by 100
Morita, T., Koike, H., Koyama, Y., Hagiwara, H., Ito, E., Fukuoka, T., Imura, T., Machida, M., & Kitamoto, D. (2013) · Genome Announcements · doi:10.1128/genomea.00064-13 · Cited by 75
Sella, L., Gazzetti, K., Faoro, F., Odorizzi, S., D'Ovidio, R., Schäfer, W., & Favaron, F. (2013) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2012.12.008 · Cited by 74
Sperschneider, J., Williams, A., Hane, J. K., Singh, K. B., & Taylor, J. M. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.01168 · Cited by 72
Self-citationMesarich, C. H., Ökmen, B., Rövenich, H., Griffiths, S. A., Wang, C., Jashni, M. K., Mihajlovski, A., Collemare, J., Hunziker, L., Deng, C. H., et al. (2017) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-05-17-0114-fi · Cited by 69
Transposable Element Dynamics among Asymbiotic and Ectomycorrhizal Amanita Fungi
Hess, J., Skrede, I., Wolfe, B. E., LaButti, K. M., Ohm, R. A., Grigoriev, I. V., & Pringle, A. (2014) · Genome Biology and Evolution · doi:10.1093/gbe/evu121 · Cited by 62
Gervais, J., Plissonneau, C., Linglin, J., Meyer, M., Labadie, K., Cruaud, C., Fudal, I., Rouxel, T., & Balesdent, M. (2016) · Molecular Plant Pathology · doi:10.1111/mpp.12464 · Cited by 59
Lorenz, S., Guenther, M., Grumaz, C., Rupp, S., Zibek, S., & Sohn, K. (2014) · Genome Announcements · doi:10.1128/genomea.00053-14 · Cited by 51
A molecular perspective: biology of the emerging pathogen Batrachochytrium dendrobatidis
Rosenblum, E., Fisher, M. C., James, T., Stajich, J., Longcore, J., Gentry, L., & Poorten, T. J. (2009) · Diseases of Aquatic Organisms · doi:10.3354/dao02179 · Cited by 35
Penselin, D., Münsterkötter, M., Kirsten, S., Felder, M., Taudien, S., Platzer, M., Ashelford, K. E., Paskiewicz, K. H., Harrison, R. J., Hughes, D., et al. (2016) · BMC Genomics · doi:10.1186/s12864-016-3299-5 · Cited by 35
Beliën, T., Campenhout, S. V., Acker, M. V., Robben, J., Courtin, C. M., Delcour, J. A., & Volckaert, G. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.00442-07 · Cited by 34
Metadata
- Authors
- Sperschneider, J., Dodds, P. N., Gardiner, D. M., Singh, K. B., & Taylor, J. M.
- Venue
- Molecular Plant Pathology
- Publisher
- Wiley
- Published
- 2018-05-11
- Volume
- 19
- Issue
- 9
- Pages
- 2094-2110
- ISSN
- 1364-3703 (ISSN-L)
- 1464-6722
- OpenAlex
- W2787339353
- Cited by
- 403
- References
- 95
- FWCI
- 17.19
- Type
- journal article
- Language
- en
- Open access
- green
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.