<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9</volume><submitter>Khan M</submitter><pubmed_abstract>Early blight (EB), caused by the pathogen &lt;i>Alternaria solani&lt;/i>, is a major threat to global potato and tomato production. Early and accurate diagnosis of this disease is therefore important. In this study, we conducted a loop-mediated isothermal amplification (LAMP) assay, as well as conventional polymerase chain reaction (PCR), nested PCR, and quantitative real-time PCR (RT-qPCR) assays to determine which of these techniques was less time consuming, more sensitive, and more accurate. We based our assays on sequence-characterized amplified regions of the &lt;i>histidine kinase&lt;/i> gene with an accession number (FJ424058). The LAMP assay provided more rapid and accurate results, amplifying the target pathogen in less than 60 min at 63°C, with 10-fold greater sensitivity than conventional P</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>2089</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6129767</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Comparative Evaluation of the LAMP Assay and PCR-Based Assays for the Rapid Detection of &lt;i>Alternaria solani&lt;/i>.</pubmed_title><pmcid>PMC6129767</pmcid><pubmed_authors>Weng Q</pubmed_authors><pubmed_authors>Chen Q</pubmed_authors><pubmed_authors>Khan M</pubmed_authors><pubmed_authors>Wang R</pubmed_authors><pubmed_authors>Liu P</pubmed_authors><pubmed_authors>Li B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparative Evaluation of the LAMP Assay and PCR-Based Assays for the Rapid Detection of &lt;i>Alternaria solani&lt;/i>.</name><description>Early blight (EB), caused by the pathogen &lt;i>Alternaria solani&lt;/i>, is a major threat to global potato and tomato production. Early and accurate diagnosis of this disease is therefore important. In this study, we conducted a loop-mediated isothermal amplification (LAMP) assay, as well as conventional polymerase chain reaction (PCR), nested PCR, and quantitative real-time PCR (RT-qPCR) assays to determine which of these techniques was less time consuming, more sensitive, and more accurate. We based our assays on sequence-characterized amplified regions of the &lt;i>histidine kinase&lt;/i> gene with an accession number (FJ424058). The LAMP assay provided more rapid and accurate results, amplifying the target pathogen in less than 60 min at 63°C, with 10-fold greater sensitivity than conventional P</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2026-04-08T01:45:02.349Z</modification><creation>2019-03-26T23:56:35Z</creation></dates><accession>S-EPMC6129767</accession><cross_references><pubmed>30233554</pubmed><doi>10.3389/fmicb.2018.02089</doi></cross_references></HashMap>