<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(1)</volume><submitter>Bokelmann L</submitter><funding>Funding was provided by the Max Planck Society, the NOMIS foundation and the ImmunoDeficiencyCenter Leipzig</funding><pubmed_abstract>Efforts to contain the spread of SARS-CoV-2 have spurred the need for reliable, rapid, and cost-effective diagnostic methods which can be applied to large numbers of people. However, current standard protocols for the detection of viral nucleic acids while sensitive, require a high level of automation and sophisticated laboratory equipment to achieve throughputs that allow whole communities to be tested on a regular basis. Here we present Cap-iLAMP (capture and improved loop-mediated isothermal amplification) which combines a hybridization capture-based RNA extraction of gargle lavage samples with an improved colorimetric RT-LAMP assay and smartphone-based color scoring. Cap-iLAMP is compatible with point-of-care testing and enables the detection of SARS-CoV-2 positive samples in less than</pubmed_abstract><journal>Nature communications</journal><pagination>1467</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7935920</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Point-of-care bulk testing for SARS-CoV-2 by combining hybridization capture with improved colorimetric LAMP.</pubmed_title><pmcid>PMC7935920</pmcid><pubmed_authors>Nickel O</pubmed_authors><pubmed_authors>Riesenberg S</pubmed_authors><pubmed_authors>Maricic T</pubmed_authors><pubmed_authors>Borte S</pubmed_authors><pubmed_authors>Meyer M</pubmed_authors><pubmed_authors>Paabo S</pubmed_authors><pubmed_authors>Bokelmann L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Point-of-care bulk testing for SARS-CoV-2 by combining hybridization capture with improved colorimetric LAMP.</name><description>Efforts to contain the spread of SARS-CoV-2 have spurred the need for reliable, rapid, and cost-effective diagnostic methods which can be applied to large numbers of people. However, current standard protocols for the detection of viral nucleic acids while sensitive, require a high level of automation and sophisticated laboratory equipment to achieve throughputs that allow whole communities to be tested on a regular basis. Here we present Cap-iLAMP (capture and improved loop-mediated isothermal amplification) which combines a hybridization capture-based RNA extraction of gargle lavage samples with an improved colorimetric RT-LAMP assay and smartphone-based color scoring. Cap-iLAMP is compatible with point-of-care testing and enables the detection of SARS-CoV-2 positive samples in less than</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-22T02:08:55.265Z</modification><creation>2025-04-05T20:12:18.715Z</creation></dates><accession>S-EPMC7935920</accession><cross_references><pubmed>33674580</pubmed><doi>10.1038/s41467-021-21627-0</doi></cross_references></HashMap>