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dc.contributor.authorMetsky, Hayden C
dc.contributor.authorWelch, Nicole L
dc.contributor.authorPillai, Priya P
dc.contributor.authorHaradhvala, Nicholas J
dc.contributor.authorRumker, Laurie
dc.contributor.authorMantena, Sreekar
dc.contributor.authorZhang, Yibin B
dc.contributor.authorYang, David K
dc.contributor.authorAckerman, Cheri M
dc.contributor.authorWeller, Juliane
dc.contributor.authorBlainey, Paul C
dc.contributor.authorMyhrvold, Cameron
dc.contributor.authorMitzenmacher, Michael
dc.contributor.authorSabeti, Pardis C
dc.date.accessioned2023-01-30T14:00:23Z
dc.date.available2023-01-30T14:00:23Z
dc.date.issued2022
dc.identifier.urihttps://hdl.handle.net/1721.1/147774
dc.description.abstract<jats:title>Abstract</jats:title><jats:p>Design of nucleic acid-based viral diagnostics typically follows heuristic rules and, to contend with viral variation, focuses on a genome’s conserved regions. A design process could, instead, directly optimize diagnostic effectiveness using a learned model of sensitivity for targets and their variants. Toward that goal, we screen 19,209 diagnostic–target pairs, concentrated on CRISPR-based diagnostics, and train a deep neural network to accurately predict diagnostic readout. We join this model with combinatorial optimization to maximize sensitivity over the full spectrum of a virus’s genomic variation. We introduce Activity-informed Design with All-inclusive Patrolling of Targets (ADAPT), a system for automated design, and use it to design diagnostics for 1,933 vertebrate-infecting viral species within 2 hours for most species and within 24 hours for all but three. We experimentally show that ADAPT’s designs are sensitive and specific to the lineage level and permit lower limits of detection, across a virus’s variation, than the outputs of standard design techniques. Our strategy could facilitate a proactive resource of assays for detecting pathogens.</jats:p>en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionof10.1038/S41587-022-01213-5en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNatureen_US
dc.titleDesigning sensitive viral diagnostics with machine learningen_US
dc.typeArticleen_US
dc.identifier.citationMetsky, Hayden C, Welch, Nicole L, Pillai, Priya P, Haradhvala, Nicholas J, Rumker, Laurie et al. 2022. "Designing sensitive viral diagnostics with machine learning." Nature Biotechnology, 40 (7).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.relation.journalNature Biotechnologyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2023-01-30T13:52:20Z
dspace.orderedauthorsMetsky, HC; Welch, NL; Pillai, PP; Haradhvala, NJ; Rumker, L; Mantena, S; Zhang, YB; Yang, DK; Ackerman, CM; Weller, J; Blainey, PC; Myhrvold, C; Mitzenmacher, M; Sabeti, PCen_US
dspace.date.submission2023-01-30T13:52:26Z
mit.journal.volume40en_US
mit.journal.issue7en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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