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{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/7574920","sourcedb":"PMC","sourceid":"7574920","source_url":"https://www.ncbi.nlm.nih.gov/pmc/7574920","text":"SUPPLEMENTARY MATERIALS\nstm.sciencemag.org/cgi/content/full/scitranslmed.abc7075/DC1\nMaterials and Methods\nFig. S1. Design of the study.\nFig. S2. Comparison of the RT-LAMP assay with CT values from RT-qPCR using primer sets E-Sarbeco and N-Sarbeco.\nFig. S3. Comparison of the RT-LAMP assay using primer set 1a-A with CT values from RT-qPCR using primer set E-Sarbeco.\nFig. S4. Analysis of LAMP-sequencing reads.\nFig. S5. Sample classification with LAMP-sequencing.\nFig. S6. RNA stability and detection limit of the RT-LAMP assay in pharyngeal swab specimens with IVT RNA.\nFig. S7. Swab–to–RT-LAMP assay titration of positive COVID-19 specimens.\nTable S1. Sequences of primers and amplicons used in this study.\nTable S2. Sensitivity and specificity of the RT-LAMP test from Fig. 3B.\nTable S3. Sensitivity and specificity of the RT-LAMP test from Fig. 5B.\nTable S4. Primers used for LAMP-sequencing.\nTable S5. Overview of time requirements for various sample handling steps.\nData File S1. Raw data for figs. 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