The DOI matches its Crossref record; 59 of the 59 references it cites were found in a registry or an index.
Tracing the evolutionary history and global expansion of Candida auris using population genomic analyses
Open accessPreprint — published as 10.1128/mbio.03364-19 · Paper page
Abstract
Candida auris has emerged globally as a multidrug-resistant yeast that can spread via nosocomial transmission. An initial phylogenetic study of isolates from Japan, India, Pakistan, South Africa, and Venezuela revealed four populations (Clades I, II, III, and IV) corresponding to these geographic regions. Since this description, C. auris has been reported in over 30 additional countries. To trace this global emergence, we compared the genomes of 304 C. auris isolates from 19 countries on six continents. We found that four predominant clades persist across wide geographic locations. We observed phylogeographic mixing in most clades; Clade IV, with isolates mainly from South America, demonstrated the strongest phylogeographic substructure. C. auris isolates from two clades with opposite mating types were detected contemporaneously in a single healthcare facility in Kenya. We estimated a Bayesian molecular clock phylogeny and dated the origin of each clade within the last 339 years; outbreak-causing clusters from Clades I, III, and IV originated 34-35 years ago. We observed high rates of antifungal resistance in Clade I, including four isolates resistant to all three major classes of antifungals. Mutations that contribute to resistance varied between the clades, with Y132F in ERG11 as the most widespread mutation associated with azole resistance and S639P in FKS1 for echinocandin resistance. Copy number variants in ERG11 predominantly appeared in Clade III and were associated with fluconazole resistance. These results provide a global context for the phylogeography, population structure, and mechanisms associated with antifungal resistance in C. auris . Importance: In less than a decade, C. auris has emerged in healthcare settings worldwide; this species is capable of colonizing skin and causing outbreaks of invasive candidiasis. In contrast to other Candida species, C. auris is unique in its ability to spread via nosocomial transmission and its high rates of drug resistance. As part of the public health response, whole-genome sequencing has played a major role in characterizing transmission dynamics and detecting new C. auris introductions. Through a global collaboration, we assessed genome evolution of isolates of C. auris from 19 countries. Here, we described estimated timing of the expansion of each C. auris clade and of fluconazole resistance, characterized discrete phylogeographic population structure of each clade, and compared genome data to sensitivity measurements to describe how antifungal resistance mechanisms vary across the population. These efforts are critical for a sustained, robust public health response that effectively utilizes molecular epidemiology.
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?
The cited source says what the claim attributes to it.
In the citing paper
“Furthermore, C. auris clades display substantial genetic diversity and show distinct phenotypic traits, especially diminished susceptibilities to antifungal therapies (11–14).”
From Transcriptomics and Phenotyping Define Genetic Signatures Associated with Echinocandin Resistance in Candida auris (2022) · cites this paper as [13]
The cited source says what the claim attributes to it.
In the citing paper
“C. auris can show clinical resistance to all classes of antifungal drugs, including echinocandins that are usually recommended as first-line therapies for invasive candidiasis.”
From Transcriptomics and Phenotyping Define Genetic Signatures Associated with Echinocandin Resistance in Candida auris (2022) · cites this paper as [13]
The cited source says what the claim attributes to it.
In the citing paper
“This seems surprising as clade I as well as clade III isolates of C. auris display the lowest intraclade genetic diversities (13).”
From Transcriptomics and Phenotyping Define Genetic Signatures Associated with Echinocandin Resistance in Candida auris (2022) · cites this paper as [13]
In the citing paper
“C. auris isolates have been implicated in nosocomial outbreaks worldwide, with 5 distinct clades classified by region of independent emergence.”
From Clinical Efficacy and Safety of a Novel Antifungal, Fosmanogepix, in Patients with Candidemia Caused by Candida auris : Results from a Phase 2 Trial (2023) · cites this paper as [2]
In the citing paper
“Clade III isolates (found in South Africa) have also been detected in other countries, including Canada and the United States (2, 35).”
From Clinical Efficacy and Safety of a Novel Antifungal, Fosmanogepix, in Patients with Candidemia Caused by Candida auris : Results from a Phase 2 Trial (2023) · cites this paper as [2]
In the citing paper
“a notable proportion of C. auris clinical isolates have been observed to exhibit increased copy numbers of resistance-associated genes”
From Mutations in TAC1B : a Novel Genetic Determinant of Clinical Fluconazole Resistance in Candida auris (2020) · cites this paper as [27]
In the citing paper
“Interrogation of a data set consisting of whole-genome sequencing data for 304 globally distributed C. auris isolates representing each of the four major clades revealed 14 nonsynonymous TAC1B mutations and one deletion”
From Mutations in TAC1B : a Novel Genetic Determinant of Clinical Fluconazole Resistance in Candida auris (2020) · cites this paper as [27]
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
Fast and accurate short read alignment with Burrows-Wheeler transform
Li, H., & Durbin, R. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp324 · Cited by 58,607
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
Stamatakis, A. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu033 · Cited by 32,291
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
McKenna, A., Hanna, M., Banks, E., Sivachenko, A., Cibulskis, K., Kernytsky, A., Garimella, K., Altshuler, D., Gabriel, S., Daly, M., et al. (2010) · Genome Research · doi:10.1101/gr.107524.110 · Cited by 27,895
BEAST: Bayesian evolutionary analysis by sampling trees
Drummond, A. J., & Rambaut, A. (2007) · BMC Evolutionary Biology · doi:10.1186/1471-2148-7-214 · Cited by 13,104
Cingolani, P., Platts, A., Wang, L. L., Coon, M., Nguyen, T., Wang, L., Land, S. J., Lu, X., & Ruden, D. M. (2012) · Fly · doi:10.4161/fly.19695 · Cited by 11,816
Posterior summarization in Bayesian phylogenetics using tracer 1.7
Rambaut, A., Drummond, A. J., Xie, D., Baele, G., & Suchard, M. A. (2018) · Systematic Biology · doi:10.1093/sysbio/syy032 · Cited by 11,159
Aligning sequence reads, clone sequences and assembly con*gs with BWA-MEMPreprint
Li, H. (2014) · arXiv (Cornell University) · doi:10.6084/m9.figshare.963153.v1 · Cited by 5,155
Quality control and preprocessing of metagenomic datasets
Schmieder, R., & Edwards, R. A. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr026 · Cited by 5,119
Repbase Update, a database of eukaryotic repetitive elements
Jurka, J., Kapitonov, V. V., Pavlíček, A., Klonowski, P., Kohany, O., & Walichiewicz, J. (2005) · Cytogenetic and Genome Research · doi:10.1159/000084979 · Cited by 3,413
A high-performance computing toolset for relatedness and principal component analysis of SNP data
Zheng, X., Levine, D., Shen, J., Gogarten, S. M., Laurie, C. C., & Weir, B. S. (2012) · Bioinformatics · doi:10.1093/bioinformatics/bts606 · Cited by 2,510
Flagged first, then by citations
Cited by
Sorted by citations
Items 401–462 of 462
Candida auris — a New Pathogen of Nosocomial Infections
Chernenkaya, T. V. (2024) · Russian Sklifosovsky Journal Emergency Medical Care · doi:10.23934/2223-9022-2024-13-2-258-263
Candida auris: An Emerging Challenge in Clinical Mycology and Public Health in Latin America
Acosta-España, J. D., Maldonado, A., & Herrera-Yela, A. (2024) · Bionatura journal : · doi:10.70099/bj/2024.03.01.23
First Report of Candida auris Isolated from a Patient with Severe Pneumonia in Zhejiang, China
Chen, K., Zhu, Y., Shan, X., Shi, J., & Deng, H. (2024) · Jundishapur Journal of Microbiology · doi:10.5812/jjm-154207
Simulating a travel-related origin of Candida auris in New York–New Jersey
Verma, R. R., Kiegle, E., Keyel, A. C., Chaturvedi, S., & Chaturvedi, V. P. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.02065-24 · Cited by 1
Isolate Specific Transcriptome Changes Exerted by Isavuconazole Treatment in Candida auris
Balla, N., Kovács, F., Tóth, Z., Harmath, A., Bozó, A., Majoros, L., Kovács, R., & Jakab, Á. (2024) · Mycopathologia · doi:10.1007/s11046-024-00919-1
Construction of a drug sensitised Candida auris strainPreprint
Hassan, M., Furner-Pardoe, J., Chen, Y., Mason, A. J., Rahman, K. M., Sutton, J. M., Hind, C. K., & Panaretou, B. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.28.630619
Bohner, F. (2024) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.12031
Abu‐Helu, R., Tebbji, F., Bishawi, A. A., Baniodeh, H., Vincent, A. T., & Sellam, A. (2025) · Microbiology Resource Announcements · doi:10.1128/mra.01239-24
Barbian, H. J., Walblay, K., Kittner, A., Zelinski, C., Newcomer, E. P., Adil, H., Green, S. J., Valley, A. M., Kim, D. Y., Black, S. R., et al. (2025) · medRxiv · doi:10.1101/2025.06.25.25330301
Resistome and Resistance Mechanisms of Candidozyma Auris Clade IV: A Systematic Review
Bonilla-Caballero, M. A., Álvarez, G., & González, Á. F. (2025) · Current Tropical Medicine Reports · doi:10.1007/s40475-025-00353-3
Fungal Pathogenesis and Virulence in the Anthropocene: Multidimensional Impacts of Climate Change
Araújo, G. R. D. S., & Frasés, S. (2025) · Current Clinical Microbiology Reports · doi:10.1007/s40588-025-00252-1
Candida auris surveillance in the Military Health System: a multidrug-resistant threat
Brough, J. J., Ellis, G. C., Robinson, S. L., Kiley, J. L., Blaney, D. D., Dressner, M., Stam, J. A., Myers, J., Green, E., Wagner, M., et al. (2025) · Antimicrobial Stewardship & Healthcare Epidemiology · doi:10.1017/ash.2025.10204 · Cited by 1
Briefing: Candidozyma (Candida) auris
Kampmeier, S., & Kurzai, O. (2025) · Krankenhaushygiene up2date · doi:10.1055/a-2519-8657
Self-citationAyala, M., Jakamartana, A., Costa, R. M. D. S., Bednarek, J. M., Moreau, C. T., Cheung, C. K., & Brown, J. C. S. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.31.697249
Lee, S., Baritugo, K., Kim, H.-S., Lee, H., Ryu, S. W., Kim, S., Lee, C. H., Kim, Y. R., SHIN, J., Kim, J., et al. (2026) · Journal of Fungi · doi:10.3390/jof12010076 · Cited by 1
Özmerdiven, G. E., & İrvem, A. (2026) · Indian Journal of Medical Microbiology · doi:10.1016/j.ijmmb.2026.101065
Résistance aux antifongiques : détection, mécanismes et épidémiologie
Pasquier, G., & Charif, D. L. (2026) · Revue Francophone des Laboratoires · doi:10.1016/s1773-035x(26)76541-2
Seyer, A. (2026) · Cyprus Journal of Medical Sciences · doi:10.4274/cjms.2026.2025-153
Jordan, V. S., Perera, M., Unsworth, A., Basile, K., Halliday, C., & Chen, S. C.-A. (2026) · Future Microbiology · doi:10.1080/17460913.2026.2634539
García-Bustos, V. (2026) · Revista Iberoamericana de Micología · doi:10.1016/j.riam.2026.01.001
van Hofwegen, L. S., Hassnain, M., Balraadjsing, P. P. S., van Dijk, K., Hagen, F., Nizamoğlu, S., & Zaat, S. A. J. (2026) · Journal of Fungi · doi:10.3390/jof12030216
Antifungal drug resistance: Current mechanisms and future directions
Tang, M., Fan, L., Shen, L., & Xing, H. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-36518-8.00009-6
Kemmerich, K. K., Alves, L. R., de Almeida, J. N., Colombo, A. L., & Alves, L. R. (2026) · Journal of Medical Microbiology · doi:10.1099/jmm.0.002135
L'interaction Hsp90/co-chaperonnes : nouvelle cible pour le traitement des candidoses invasives
Rouges, C. (2023) · theses.fr (ABES) · doi:10.70675/40b24a3fz159ez4d8ez8a34zdd8ffa1c22fa
Harnessing random peptide mixtures to combat multidrug-resistant fungal infections
Adeoye, J. A., Belo, Y., Rocha, M. C., Hayby, H., Israyilova, A., Hayouka, Z., & Shlezinger, N. (2026) · mBio · doi:10.1128/mbio.00400-26
The Epidemiology and Infection Control of Candida Auris in Shanghai
Wei, M., Guo, J., Li, L., ZHU, J., Xue, Y., Chen, G., Yang, F., Wu, W., & Zhu, M. (2026) · Mycoses · doi:10.1111/myc.70176
Schnell, N. A., Sickbert-Bennett, E. E., & Weber, D. J. (2026) · Current Epidemiology Reports · doi:10.1007/s40471-026-00392-y
Pangenome and genome-scale essentiality in the emerging fungal pathogen Candidozyma aurisPreprint
Hale, J. J., Larkin, A., Rapala, J. R., Hurto, R. L., Zhao, G., Elson, B. E., Freddolino, L., Snitkin, E. S., & O’Meara, T. R. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.12.724661
Fungal Infections and Climate Change: Emerging Threats, Future Directions, and Clinical Implications
Chastain, D. B., George, M. E., Cluck, D. B., & Henao‐Martínez, A. F. (2026) · Springer eBooks · doi:10.1007/978-3-032-21237-5_15
Cao, J., Wang, X., Qin, C., Gu, D., Zhang, R., Zhou, H., & Li, R. (2026) · Virulence · doi:10.1080/21505594.2026.2667550
Galon, C. M., & Charlebois, D. A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.04.730223
WGS-Based Hypersurveillance of Dual-Clade Overlapping Candidozyma auris Outbreaks From 2021-2024Preprint
Hess, D., Massic, L., Siao, D. D., Siao, L., Martins, C., Dykema, P., Hua, C. N., Schneider, E., Southern, T., Hooser, S. V., et al. (2026) · Research Square · doi:10.21203/rs.3.rs-9898928/v1
Lamoth, F., & Kontoyiannis, D. P. (2026) · mBio · doi:10.1128/mbio.00750-26
Merber, R., Laczi, K., Bende, G., Kazinczi, E., Farkas, A., Maróti, G., Sinka, R., & Galgóczy, L. (2026) · Microbiology Spectrum · doi:10.1128/spectrum.00404-26
Şenol, F. F., Toraman, Z. A., Vural, U., Çelik, Z., Akkaya, Y., Çılkız, M., Erdin, B. N., Kırbağ, S., & Kılıç, İ. H. (2026) · Antibiotics · doi:10.3390/antibiotics15070692
Osama, D., Alsedawy, M., Hussein, M. S., Hassan, M. A., Elrefaey, S. M., & Tawfick, M. M. (2026) · Antonie van Leeuwenhoek · doi:10.1007/s10482-026-02393-9
Circulation of fluconazole-resistant Candida auris in Peru confirmed by genomic analysis
Gago, R. P., Núñez-Llanos, A., Céspedes-Román, C., Izarra, V., Hurtado, V., Padilla, C., Cáceres, O., & Lizárraga, W. C. (2026) · Memórias do Instituto Oswaldo Cruz · doi:10.1590/0074-02760260027
Lagojda, L., Chambers, D., Cantrell, A. J., Bastounis, A., Booth, A., van Leeuwen, E., Mirfenderesky, M., & Manuel, R. J. (2026) · NIHR Open Research · doi:10.3310/nihropenres.14366.1
Mboowa, G., Sserwadda, I., Kanyerezi, S., Kidenya, B. R., Jonani, B., & Musinguzi, B. (2026) · Frontiers in Bioinformatics · doi:10.3389/fbinf.2026.1896572
Spruijtenburg, B., Ünal, N., do Prado, C. M., Meis, J. F. G. M., Bingöl, O., Toyran, T., Akar, N., Ay, N., Gülen, T. A., Turunç, T., et al. (2026) · International Journal of Infectious Diseases · doi:10.1016/j.ijid.2026.109045
Resistance gene mutations and phylogenetic relationships in Candidozyma auris isolates from Russia
Oganesyan, E. G., Zhuk, A. S., Gusarova, K. V., Kovyrshin, S., Alekseevskaya, E. S., Orlova, O. E., Khostelidi, S. N., Kozlova, O. P., Любимова, А. В., Taraskina, A. E., et al. (2026) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2026.1929119
Parallel evolution under constraint shapes echinocandin resistance in Candida aurisPreprint
Cauldron, N. C., Dort, E. N., Weeks, G., Rogers, P. D., & Cuomo, C. A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.30.748140
Self-citationChancharussin, N., Jitmuang, A., Chakrabarti, A., & Chayakulkeeree, M. (2026) · Mycoses · doi:10.1111/myc.70222
Phan-Canh, T., Elbe‐Bürger, A., & Kuchler, K. (2026) · Trends in Microbiology · doi:10.1016/j.tim.2026.08.011
Clinical Practice Recommendations for the Treatment of Candida auris Infection in Korea
Lee, S.-Y., Ko, J., 김, 남., Kim, T. H., Park, J. W., Yoo, I. Y., Lee, M., Lee, S. G., Jung, T. R., Chong, Y. P., et al. (2026) · Infection and Chemotherapy · doi:10.3947/ic.2026.0109
Microbe snapshot – Candida auris
Helminiak, L., & Yang, S. (2026) · Clinical Microbiology Newsletter · doi:10.1016/j.clinmicnews.2026.09.001
Dabi, K. C., Haridas, H., Sayed, S. E. H., Talwar, V., & Gaind, R. (2026) · American Journal of Infection Control · doi:10.1016/j.ajic.2026.09.012
Non-albicans Candida Species: Epidemiology and Antifungal Resistance
Bosan, M. A., Durrani, A. D., Faiz, A., Farooqi, J. Q., & Jabeen, K. (2026) · Current Fungal Infection Reports · doi:10.1007/s12281-026-00542-1
Silva, I. G., Inácio, C. P., da Silva, V. P., Veras, D. L., dos Santos, F. A. B., Alves, L. C., dos Santos, M. J., Alves, M. A. R., Lima, J. M., Buonafina, M. D. S., et al. (2026) · Microbial Pathogenesis · doi:10.1016/j.micpath.2026.108851
Soni, A., Vrzoňová, R., Paulovičová, L., Bzducha‐Wróbel, A., & Farkaš, P. (2026) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2026.154672
Candidozyma auris ( Candida auris ) as a harbinger of novel fungal pathogens
Schuh, C., & Gokhale, C. S. (2026) · mSphere · doi:10.1128/msphere.00109-26
Majid, U., Bashir, G., Roohi, S., Ahangar, I. N., & Bhat, S. R. (2026) · Indian Journal of Medical Microbiology · doi:10.1016/j.ijmmb.2026.101313
Gifford, H., Pradhan, A., Caswall, B. A., Murphy, S. E., Leaves, I., Edmondson, M. B., Chakraborty, T., Wilson, D., Taori, S. K., Gow, N. A. R., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-76954-x · Cited by 1
Fayed, B. E. (2026) · Medical Sciences · doi:10.3390/medsci14060679
Perspective: Evolutionary Genetics Is the Backbone of Genomic Epidemiology in Fungal Pathogens
Matute, D. R. (2026) · Journal of Fungi · doi:10.3390/jof12100790
Ukolobi, O., Jacob, J. N., Akpo, M. O., Edo, G. I., Agbo, J. J., Orogu, J. O., Yousif, E., Jikah, A. N., Akpoghelie, P. O., Oghroro, E. E. A., et al. (2026) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/j.diagmicrobio.2026.117711
Otu, A. A., & Ibe, C. (2026) · Journal of Fungi · doi:10.3390/jof12110805
Kamau, E. T. (2026) · Journal of Clinical Microbiology · doi:10.1128/jcm.01106-26
Purine metabolism dysregulation as a multi-omics signature of fatal Candida auris infection
Bataineh, M. T. A., Barreiros, A. S., Sreedharan, S. P., Dash, N. R., Mudalagiriyappa, S., Alkhayyal, N., Al‐Omari, B., & Alnaqbi, H. (2026) · Mycology: An International Journal on Fungal Biology · doi:10.1080/21501203.2026.2735107
Metadata
- Authors
- Chow, N. A., Muñoz, J. F., Gade, L., Berkow, E., Li, X., Welsh, R. M., Forsberg, K., Lockhart, S. R., Adam, R., Alanio, A., Alastruey-Izquierdo, A., Althawadi, S., Belén Araúz, A., Ben-Ami, R., Bharat, A., Calvo, B., Desnos-Ollivier, M., Escandón, P., Gardam, D., Gunturu, R., Heath, C. H., Kurzai, O., Martin, R., Litvintseva, A. P., & Cuomo, C. A.
- Affiliations
- Centers for Disease Control and Prevention (US)
- Broad Institute (US)
- Aga Khan University Hospital Nairobi (KE)
- Centre National de la Recherche Scientifique (FR)
- King Faisal Specialist Hospital & Research Centre (SA)
- Public Health Agency of Canada (CA)
- Universidad del Zulia (VE)
- Instituto Nacional de Salud (CO)
- Fiona Stanley Hospital (AU)
- The University of Western Australia (AU)
- University of Würzburg (DE)
- Corresponding author
- Litvintseva, Anastasia P.
- Cuomo, Christina A.
- ORCID
- Chow, Nancy A.
- Muñoz, José F.
- Gade, Lalitha
- Berkow, Elizabeth
- Welsh, Rory M.
- Forsberg, Kaitlin
- Lockhart, Shawn R.
- Adam, Rodney
- Alanio, Alexandre
- Alastruey-Izquierdo, Ana
- Althawadi, Sahar
- Bharat, Amrita
- Escandón, Patricia
- Gardam, Dianne
- Heath, Christopher H.
- Kurzai, Oliver
- Martin, Ronny
- Litvintseva, Anastasia P.
- Cuomo, Christina A.
- Venue
- mBio
- Publisher
- openRxiv
- Published
- 2020-01-07
- Volume
- 11
- Issue
- 2
- Pages
- e03364-19
- ISSN
- 2150-7511 (ISSN-L)
- PMC
- PMC7188998
- OpenAlex
- W3020256411
- Cited by
- 463
- References
- 57
- Citations by year
- 2026: 76 · 2025: 86 · 2024: 81 · 2023: 80 · 2022: 64 · 2021: 52 · 2020: 24
- FWCI
- 7.21
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- mBio (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- PubMed Central (publishedVersion)
- UWA Profiles and Research Repository (UWA) (publishedVersion, other-oa)
- PubMed (publishedVersion)
- LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (submittedVersion, cc-by-nc-sa)
- eCommons - AKU (Aga Khan University) (submittedVersion)
- HAL (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Greater South Information System
- Funders
- U.S. Department of Health and Human Services (U19-AI110818)
- Canadian Institute for Advanced Research
- Broad Institute (U19AI110818)
- National Institutes of Health
- Centers for Disease Control and Prevention (U19AI110818)
- National Institute of Allergy and Infectious Diseases (U19AI110818)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Immunology and Microbiology › Microbiology › Yeasts and Rust Fungi Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Keywords
- Candida auris, evolutionary history, international expansion, phylogeography, fluconazole resistance, antifungal resistance, nosocomial transmission, invasive candidiasis, molecular epidemiology, population structure, whole genome sequencing
- MeSH terms
- Whole Genome Sequencing, Antifungal Agents, Azoles, Candida, Biological Evolution, Genes, Fungal, Genetics, Population, Humans, Mutation, Phylogeny, Fluconazole, Genome, Fungal, Molecular Epidemiology, Drug Resistance, Fungal, Echinocandins, Metagenomics, Candidiasis, Invasive, Phylogeography
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