<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tapia-Sidas DA</submitter><funding>CINVESTAV</funding><funding>Consejo Nacional de Ciencia y Tecnología, Mexico</funding><funding>Agencia Mexicana de Cooperación para el Desarrollo (AMEXCID), Secretaría de Relaciones Exteriores Mexico</funding><pagination>e0279681</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9879405</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(1)</volume><pubmed_abstract>The pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has affected millions of people worldwide. Public health strategies to reduce viral transmission are based on widespread diagnostic testing to detect and isolate contagious patients. Several reverse transcription (RT)-PCR tests, along with other SARS-CoV-2 diagnostic assays, are available to attempt to cover the global demand. Loop-mediated isothermal amplification (LAMP) based methods have been established as rapid, accurate, point of care diagnostic tests for viral infections; hence, they represent an excellent alternative for SARS-CoV-2 detection. The aim of this study was to develop and describe molecular detection systems for SARS-CoV-2 based on RT-LAMP. Recombinant DNA polymerase from Bacillus ste</pubmed_abstract><journal>PloS one</journal><pubmed_title>Starting from scratch: Step-by-step development of diagnostic tests for SARS-CoV-2 detection by RT-LAMP.</pubmed_title><pmcid>PMC9879405</pmcid><funding_grant_id>483659</funding_grant_id><funding_grant_id>2020-1, AMEXCID Mexico-Uruguay</funding_grant_id><funding_grant_id>754736</funding_grant_id><pubmed_authors>Vargas-Hernandez BY</pubmed_authors><pubmed_authors>Tapia-Sidas DA</pubmed_authors><pubmed_authors>Brieba LG</pubmed_authors><pubmed_authors>Lopez-Macias C</pubmed_authors><pubmed_authors>Xoconostle-Cazares B</pubmed_authors><pubmed_authors>Ruiz-Medrano R</pubmed_authors><pubmed_authors>Lira-Carmona R</pubmed_authors><pubmed_authors>Nunez-Munoz LA</pubmed_authors><pubmed_authors>Calderon-Perez B</pubmed_authors><pubmed_authors>Ferat-Osorio E</pubmed_authors><pubmed_authors>Gonzalez-Gonzalez R</pubmed_authors><pubmed_authors>Ramirez-Pool JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Starting from scratch: Step-by-step development of diagnostic tests for SARS-CoV-2 detection by RT-LAMP.</name><description>The pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has affected millions of people worldwide. Public health strategies to reduce viral transmission are based on widespread diagnostic testing to detect and isolate contagious patients. Several reverse transcription (RT)-PCR tests, along with other SARS-CoV-2 diagnostic assays, are available to attempt to cover the global demand. Loop-mediated isothermal amplification (LAMP) based methods have been established as rapid, accurate, point of care diagnostic tests for viral infections; hence, they represent an excellent alternative for SARS-CoV-2 detection. The aim of this study was to develop and describe molecular detection systems for SARS-CoV-2 based on RT-LAMP. Recombinant DNA polymerase from Bacillus ste</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2026-07-14T21:10:44.272Z</modification><creation>2025-04-06T08:17:59.874Z</creation></dates><accession>S-EPMC9879405</accession><cross_references><pubmed>36701313</pubmed><doi>10.1371/journal.pone.0279681</doi></cross_references></HashMap>