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author Bloom, Joshua S.
Sathe, Laila
Munugala, Chetan
Jones, Eric M.
Gasperini, Molly
Lubock, Nathan B.
Yarza, Fauna
Thompson, Erin M.
Kovary, Kyle M.
Park, Jimin
Marquette, Dawn
Kay, Stephania
Lucas, Mark
Love, TreQuan
Booeshaghi, A. Sina
Brandenberg, Oliver F.
Guo, Longhua
Boocock, James
Hochman, Myles
Simpkins, Scott W.
Lin, Isabella
LaPierre, Nathan
Hong, Duke
Zhang, Yi
Oland, Gabriel
Choe, Bianca Judy
Chandrasekaran, Sukantha
Hilt, Evann E.
Butte, Manish J.
Damoiseaux, Robert
Kravit, Clifford
Cooper, Aaron R.
Yin, Yi
Pachter, Lior
Garner, Omai B.
Flint, Jonathan
Eskin, Eleazar
Luo, Chongyuan
Kosuri, Sriram
Kruglyak, Leonid
Arboleda, Valerie A.
author_facet Bloom, Joshua S.
Sathe, Laila
Munugala, Chetan
Jones, Eric M.
Gasperini, Molly
Lubock, Nathan B.
Yarza, Fauna
Thompson, Erin M.
Kovary, Kyle M.
Park, Jimin
Marquette, Dawn
Kay, Stephania
Lucas, Mark
Love, TreQuan
Booeshaghi, A. Sina
Brandenberg, Oliver F.
Guo, Longhua
Boocock, James
Hochman, Myles
Simpkins, Scott W.
Lin, Isabella
LaPierre, Nathan
Hong, Duke
Zhang, Yi
Oland, Gabriel
Choe, Bianca Judy
Chandrasekaran, Sukantha
Hilt, Evann E.
Butte, Manish J.
Damoiseaux, Robert
Kravit, Clifford
Cooper, Aaron R.
Yin, Yi
Pachter, Lior
Garner, Omai B.
Flint, Jonathan
Eskin, Eleazar
Luo, Chongyuan
Kosuri, Sriram
Kruglyak, Leonid
Arboleda, Valerie A.
author_sort Bloom, Joshua S.
collection PubMed
description The rapid spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is due to the high rates of transmission by individuals who are asymptomatic at the time of transmission(1,2). Frequent, widespread testing of the asymptomatic population for SARS-CoV-2 is essential to suppress viral transmission. Despite increases in testing capacity, multiple challenges remain in deploying traditional reverse transcription and quantitative PCR (RT-qPCR) tests at the scale required for population screening of asymptomatic individuals. We have developed SwabSeq, a high-throughput testing platform for SARS-CoV-2 that uses next-generation sequencing as a readout. SwabSeq employs sample-specific molecular barcodes to enable thousands of samples to be combined and simultaneously analyzed for the presence or absence of SARS-CoV-2 in a single run. Importantly, SwabSeq incorporates an in vitro RNA standard that mimics the viral amplicon, but can be distinguished by sequencing. This standard allows for end-point rather than quantitative PCR, improves quantitation, reduces requirements for automation and sample-to-sample normalization, enables purification-free detection, and gives better ability to call true negatives. After setting up SwabSeq in a high-complexity CLIA laboratory, we performed more than 80,000 tests for COVID-19 in less than two months, confirming in a real world setting that SwabSeq inexpensively delivers highly sensitive and specific results at scale, with a turn-around of less than 24 hours. Our clinical laboratory uses SwabSeq to test both nasal and saliva samples without RNA extraction, while maintaining analytical sensitivity comparable to or better than traditional RT-qPCR tests. Moving forward, SwabSeq can rapidly scale up testing to mitigate devastating spread of novel pathogens.
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spelling pubmed-74800602020-09-10 Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing Bloom, Joshua S. Sathe, Laila Munugala, Chetan Jones, Eric M. Gasperini, Molly Lubock, Nathan B. Yarza, Fauna Thompson, Erin M. Kovary, Kyle M. Park, Jimin Marquette, Dawn Kay, Stephania Lucas, Mark Love, TreQuan Booeshaghi, A. Sina Brandenberg, Oliver F. Guo, Longhua Boocock, James Hochman, Myles Simpkins, Scott W. Lin, Isabella LaPierre, Nathan Hong, Duke Zhang, Yi Oland, Gabriel Choe, Bianca Judy Chandrasekaran, Sukantha Hilt, Evann E. Butte, Manish J. Damoiseaux, Robert Kravit, Clifford Cooper, Aaron R. Yin, Yi Pachter, Lior Garner, Omai B. Flint, Jonathan Eskin, Eleazar Luo, Chongyuan Kosuri, Sriram Kruglyak, Leonid Arboleda, Valerie A. medRxiv Article The rapid spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is due to the high rates of transmission by individuals who are asymptomatic at the time of transmission(1,2). Frequent, widespread testing of the asymptomatic population for SARS-CoV-2 is essential to suppress viral transmission. Despite increases in testing capacity, multiple challenges remain in deploying traditional reverse transcription and quantitative PCR (RT-qPCR) tests at the scale required for population screening of asymptomatic individuals. We have developed SwabSeq, a high-throughput testing platform for SARS-CoV-2 that uses next-generation sequencing as a readout. SwabSeq employs sample-specific molecular barcodes to enable thousands of samples to be combined and simultaneously analyzed for the presence or absence of SARS-CoV-2 in a single run. Importantly, SwabSeq incorporates an in vitro RNA standard that mimics the viral amplicon, but can be distinguished by sequencing. This standard allows for end-point rather than quantitative PCR, improves quantitation, reduces requirements for automation and sample-to-sample normalization, enables purification-free detection, and gives better ability to call true negatives. After setting up SwabSeq in a high-complexity CLIA laboratory, we performed more than 80,000 tests for COVID-19 in less than two months, confirming in a real world setting that SwabSeq inexpensively delivers highly sensitive and specific results at scale, with a turn-around of less than 24 hours. Our clinical laboratory uses SwabSeq to test both nasal and saliva samples without RNA extraction, while maintaining analytical sensitivity comparable to or better than traditional RT-qPCR tests. Moving forward, SwabSeq can rapidly scale up testing to mitigate devastating spread of novel pathogens. Cold Spring Harbor Laboratory 2021-03-09 /pmc/articles/PMC7480060/ /pubmed/32909008 http://dx.doi.org/10.1101/2020.08.04.20167874 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Bloom, Joshua S.
Sathe, Laila
Munugala, Chetan
Jones, Eric M.
Gasperini, Molly
Lubock, Nathan B.
Yarza, Fauna
Thompson, Erin M.
Kovary, Kyle M.
Park, Jimin
Marquette, Dawn
Kay, Stephania
Lucas, Mark
Love, TreQuan
Booeshaghi, A. Sina
Brandenberg, Oliver F.
Guo, Longhua
Boocock, James
Hochman, Myles
Simpkins, Scott W.
Lin, Isabella
LaPierre, Nathan
Hong, Duke
Zhang, Yi
Oland, Gabriel
Choe, Bianca Judy
Chandrasekaran, Sukantha
Hilt, Evann E.
Butte, Manish J.
Damoiseaux, Robert
Kravit, Clifford
Cooper, Aaron R.
Yin, Yi
Pachter, Lior
Garner, Omai B.
Flint, Jonathan
Eskin, Eleazar
Luo, Chongyuan
Kosuri, Sriram
Kruglyak, Leonid
Arboleda, Valerie A.
Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing
title Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing
title_full Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing
title_fullStr Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing
title_full_unstemmed Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing
title_short Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing
title_sort swab-seq: a high-throughput platform for massively scaled up sars-cov-2 testing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480060/
https://www.ncbi.nlm.nih.gov/pubmed/32909008
http://dx.doi.org/10.1101/2020.08.04.20167874
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