dc.contributor.author | de Puig, Helena | |
dc.contributor.author | Lee, Rose A. | |
dc.contributor.author | Najjar, Devora | |
dc.contributor.author | Tan, Xiao | |
dc.contributor.author | Soekensen, Luis R. | |
dc.contributor.author | Angenent-Mari, Nicolaas M. | |
dc.contributor.author | Donghia, Nina M. | |
dc.contributor.author | Weckman, Nicole E. | |
dc.contributor.author | Ory, Audrey | |
dc.contributor.author | Ng, Carlos F. | |
dc.contributor.author | Nguyen, Peter Q. | |
dc.contributor.author | Mao, Angelo S. | |
dc.contributor.author | Ferrante, Thomas C. | |
dc.contributor.author | Lansberry, Geoffrey | |
dc.contributor.author | Sallum, Hani | |
dc.contributor.author | Niemi, James | |
dc.contributor.author | Collins, James J. | |
dc.date.accessioned | 2021-08-10T21:36:34Z | |
dc.date.available | 2021-08-10T21:36:34Z | |
dc.date.issued | 2021-08 | |
dc.date.submitted | 2021-03 | |
dc.identifier.issn | 2375-2548 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/131169 | |
dc.description.abstract | The COVID-19 pandemic highlights the need for diagnostics that can be rapidly adapted and deployed in a variety of settings. Several SARS-CoV-2 variants have shown worrisome effects on vaccine and treatment efficacy, but no current point-of-care (POC) testing modality allows their specific identification. We have developed miSHERLOCK, a low-cost, CRISPR-based POC diagnostic platform that takes unprocessed patient saliva; extracts, purifies, and concentrates viral RNA; performs amplification and detection reactions; and provides fluorescent visual output with only three user actions and 1 hour from sample input to answer out. miSHERLOCK achieves highly sensitive multiplexed detection of SARS-CoV-2 and mutations associated with variants B.1.1.7, B.1.351, and P.1. Our modular system enables easy exchange of assays to address diverse user needs and can be rapidly reconfigured to detect different viruses and variants of concern. An adjunctive smartphone application enables output quantification, automated interpretation, and the possibility of remote, distributed result reporting. | en_US |
dc.publisher | American Association for the Advancement of Science | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1126/sciadv.abh2944 | en_US |
dc.rights | Creative Commons Attribution NonCommercial License 4.0 | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by-nc/4.0/ | en_US |
dc.source | Science Advances | en_US |
dc.title | Minimally instrumented SHERLOCK (miSHERLOCK) for CRISPR-based point-of-care diagnosis of SARS-CoV-2 and emerging variants | en_US |
dc.type | Article | en_US |
dc.identifier.citation | de Puig, Helena et al. "Minimally instrumented SHERLOCK (miSHERLOCK) for CRISPR-based point-of-care diagnosis of SARS-CoV-2 and emerging variants." Science Advances 7, 32 (August 2021): eabh2944. © 2021 The Authors | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Institute for Medical Engineering & Science | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biological Engineering | en_US |
dc.contributor.department | Abdul Latif Jameel Clinic for Machine Learning in Health | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Synthetic Biology Center | en_US |
dc.contributor.department | Harvard-MIT Program in Health Sciences and Technology | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Media Laboratory | en_US |
dc.relation.journal | Science Advances | en_US |
dc.eprint.version | Final published version | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.date.submission | 2021-08-09T12:09:56Z | |
mit.journal.volume | 7 | en_US |
mit.journal.issue | 32 | en_US |
mit.license | PUBLISHER_CC | |
mit.metadata.status | Complete | |