Correction: Gorris et al. Detection and Diagnosis of Xylella fastidiosa by Specific Monoclonal Antibodies. Agronomy 2021, 11, 48
In the original publication [1], the explanation of Table 3 in Section 3, Section 3.4, and the title of that table were not correct. In addition, the information in Tables 4 and 5 was not complete and a sentence was missing. In Table 6, there were minor calculation mistakes; the diagnostic parameter...
| Autores principales: | , , , , , |
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| Formato: | draft |
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MDPI
2023
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| Materias: | |
| Acceso en línea: | https://hdl.handle.net/20.500.11939/8701 https://www.mdpi.com/2073-4395/13/7/1826 |
| _version_ | 1855492542643044352 |
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| author | Gorris, María T. Sanz, Antonio Penyalver, Ramón López, María M. Colomer, Mario Marco-Noales, Ester |
| author_browse | Colomer, Mario Gorris, María T. López, María M. Marco-Noales, Ester Penyalver, Ramón Sanz, Antonio |
| author_facet | Gorris, María T. Sanz, Antonio Penyalver, Ramón López, María M. Colomer, Mario Marco-Noales, Ester |
| author_sort | Gorris, María T. |
| collection | ReDivia |
| description | In the original publication [1], the explanation of Table 3 in Section 3, Section 3.4, and the title of that table were not correct. In addition, the information in Tables 4 and 5 was not complete and a sentence was missing. In Table 6, there were minor calculation mistakes; the diagnostic parameters of Cohen’s Kappa indices have been recalculated, and Reference [39] has been included; a related sentence and Reference [35] have been added to the Materials and Methods section. Finally, Reference [31] was not complete. All of this information has been corrected as follows. A correction has been made to Section 3.4, and it should read: Out of the 233 samples, all were analyzed with real-time PCR by Harper et al. [31], 231 were analyzed with real-time PCR by Francis et al. [32], and 218 were analyzed by using DAS-ELISA with MAb2 G1/PPD (developed in this study). The total number of positive (and negative) samples for each technique out of the 233 that were analyzed (Table 3) is shown in the contingency Tables 4 and 5: In Table 4, DAS-ELISA is compared with Harper’s PCR; in Table 5, DAS-ELISA is compared with Francis’ PCR. |
| format | draft |
| id | ReDivia8701 |
| institution | Instituto Valenciano de Investigaciones Agrarias (IVIA) |
| publishDate | 2023 |
| publishDateRange | 2023 |
| publishDateSort | 2023 |
| publisher | MDPI |
| publisherStr | MDPI |
| record_format | dspace |
| spelling | ReDivia87012025-04-25T14:49:18Z Correction: Gorris et al. Detection and Diagnosis of Xylella fastidiosa by Specific Monoclonal Antibodies. Agronomy 2021, 11, 48 Gorris, María T. Sanz, Antonio Penyalver, Ramón López, María M. Colomer, Mario Marco-Noales, Ester Detection H20 Plant diseases U30 Research methods Xylella fastidiosa Diagnosis Monoclonal antibodies PCR In the original publication [1], the explanation of Table 3 in Section 3, Section 3.4, and the title of that table were not correct. In addition, the information in Tables 4 and 5 was not complete and a sentence was missing. In Table 6, there were minor calculation mistakes; the diagnostic parameters of Cohen’s Kappa indices have been recalculated, and Reference [39] has been included; a related sentence and Reference [35] have been added to the Materials and Methods section. Finally, Reference [31] was not complete. All of this information has been corrected as follows. A correction has been made to Section 3.4, and it should read: Out of the 233 samples, all were analyzed with real-time PCR by Harper et al. [31], 231 were analyzed with real-time PCR by Francis et al. [32], and 218 were analyzed by using DAS-ELISA with MAb2 G1/PPD (developed in this study). The total number of positive (and negative) samples for each technique out of the 233 that were analyzed (Table 3) is shown in the contingency Tables 4 and 5: In Table 4, DAS-ELISA is compared with Harper’s PCR; in Table 5, DAS-ELISA is compared with Francis’ PCR. 2023-09-06T11:17:00Z 2023-09-06T11:17:00Z 2023 draft Gorris, M. T., Sanz, A., Peñalver, J., López, M. M., Colomer, M. & Marco-Noales, E. (2023). Correction: Gorris et al. Detection and Diagnosis of Xylella fastidiosa by Specific Monoclonal Antibodies. Agronomy 2021, 11, 48. Agronomy, 13(7), 1826. 2073-4395 https://hdl.handle.net/20.500.11939/8701 10.3390/agronomy13071826 https://www.mdpi.com/2073-4395/13/7/1826 Attribution-NonCommercial-NoDerivatives 4.0 Internacional http://creativecommons.org/licenses/by-nc-nd/4.0/ openAccess MDPI |
| spellingShingle | Detection H20 Plant diseases U30 Research methods Xylella fastidiosa Diagnosis Monoclonal antibodies PCR Gorris, María T. Sanz, Antonio Penyalver, Ramón López, María M. Colomer, Mario Marco-Noales, Ester Correction: Gorris et al. Detection and Diagnosis of Xylella fastidiosa by Specific Monoclonal Antibodies. Agronomy 2021, 11, 48 |
| title | Correction: Gorris et al. Detection and Diagnosis of Xylella fastidiosa by Specific Monoclonal Antibodies. Agronomy 2021, 11, 48 |
| title_full | Correction: Gorris et al. Detection and Diagnosis of Xylella fastidiosa by Specific Monoclonal Antibodies. Agronomy 2021, 11, 48 |
| title_fullStr | Correction: Gorris et al. Detection and Diagnosis of Xylella fastidiosa by Specific Monoclonal Antibodies. Agronomy 2021, 11, 48 |
| title_full_unstemmed | Correction: Gorris et al. Detection and Diagnosis of Xylella fastidiosa by Specific Monoclonal Antibodies. Agronomy 2021, 11, 48 |
| title_short | Correction: Gorris et al. Detection and Diagnosis of Xylella fastidiosa by Specific Monoclonal Antibodies. Agronomy 2021, 11, 48 |
| title_sort | correction gorris et al detection and diagnosis of xylella fastidiosa by specific monoclonal antibodies agronomy 2021 11 48 |
| topic | Detection H20 Plant diseases U30 Research methods Xylella fastidiosa Diagnosis Monoclonal antibodies PCR |
| url | https://hdl.handle.net/20.500.11939/8701 https://www.mdpi.com/2073-4395/13/7/1826 |
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