Mutations on COVID-19 diagnostic targets
Effective, sensitive, and reliable diagnostic reagents are of paramount importance for combating the ongoing coronavirus disease 2019 (COVID-19) pandemic when there is neither a preventive vaccine nor a specific drug available for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It will...
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Published in | Genomics (San Diego, Calif.) Vol. 112; no. 6; pp. 5204 - 5213 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.11.2020
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Subjects | |
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Abstract | Effective, sensitive, and reliable diagnostic reagents are of paramount importance for combating the ongoing coronavirus disease 2019 (COVID-19) pandemic when there is neither a preventive vaccine nor a specific drug available for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It will cause a large number of false-positive and false-negative tests if currently used diagnostic reagents are undermined. Based on genotyping of 31,421 SARS-CoV-2 genome samples collected up to July 23, 2020, we reveal that essentially all of the current COVID-19 diagnostic targets have undergone mutations. We further show that SARS-CoV-2 has the most mutations on the targets of various nucleocapsid (N) gene primers and probes, which have been widely used around the world to diagnose COVID-19. To understand whether SARS-CoV-2 genes have mutated unevenly, we have computed the mutation rate and mutation h-index of all SARS-CoV-2 genes, indicating that the N gene is one of the most non-conservative genes in the SARS-CoV-2 genome. We show that due to human immune response induced APOBEC mRNA (C > T) editing, diagnostic targets should also be selected to avoid cytidines. Our findings might enable optimally selecting the conservative SARS-CoV-2 genes and proteins for the design and development of COVID-19 diagnostic reagents, prophylactic vaccines, and therapeutic medicines.
Interactive real-time online Mutation Tracker.
•Essentially all of the current COVID-19 diagnostic targets have undergone mutations.•SARS-CoV-2 nucleocapsid (N) gene primers and probes have the most mutations.•It would be better to select diagnostic targets avoiding cytidines. |
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AbstractList | Effective, sensitive, and reliable diagnostic reagents are of paramount importance for combating the ongoing coronavirus disease 2019 (COVID-19) pandemic when there is neither a preventive vaccine nor a specific drug available for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It will cause a large number of false-positive and false-negative tests if currently used diagnostic reagents are undermined. Based on genotyping of 31,421 SARS-CoV-2 genome samples collected up to July 23, 2020, we reveal that essentially all of the current COVID-19 diagnostic targets have undergone mutations. We further show that SARS-CoV-2 has the most mutations on the targets of various nucleocapsid (N) gene primers and probes, which have been widely used around the world to diagnose COVID-19. To understand whether SARS-CoV-2 genes have mutated unevenly, we have computed the mutation rate and mutation h-index of all SARS-CoV-2 genes, indicating that the N gene is one of the most non-conservative genes in the SARS-CoV-2 genome. We show that due to human immune response induced APOBEC mRNA (C > T) editing, diagnostic targets should also be selected to avoid cytidines. Our findings might enable optimally selecting the conservative SARS-CoV-2 genes and proteins for the design and development of COVID-19 diagnostic reagents, prophylactic vaccines, and therapeutic medicines. AVAILABILITY: Interactive real-time online Mutation Tracker. Effective, sensitive, and reliable diagnostic reagents are of paramount importance for combating the ongoing coronavirus disease 2019 (COVID-19) pandemic when there is neither a preventive vaccine nor a specific drug available for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It will cause a large number of false-positive and false-negative tests if currently used diagnostic reagents are undermined. Based on genotyping of 31,421 SARS-CoV-2 genome samples collected up to July 23, 2020, we reveal that essentially all of the current COVID-19 diagnostic targets have undergone mutations. We further show that SARS-CoV-2 has the most mutations on the targets of various nucleocapsid (N) gene primers and probes, which have been widely used around the world to diagnose COVID-19. To understand whether SARS-CoV-2 genes have mutated unevenly, we have computed the mutation rate and mutation h-index of all SARS-CoV-2 genes, indicating that the N gene is one of the most non-conservative genes in the SARS-CoV-2 genome. We show that due to human immune response induced APOBEC mRNA (C > T) editing, diagnostic targets should also be selected to avoid cytidines. Our findings might enable optimally selecting the conservative SARS-CoV-2 genes and proteins for the design and development of COVID-19 diagnostic reagents, prophylactic vaccines, and therapeutic medicines. Interactive real-time online Mutation Tracker. •Essentially all of the current COVID-19 diagnostic targets have undergone mutations.•SARS-CoV-2 nucleocapsid (N) gene primers and probes have the most mutations.•It would be better to select diagnostic targets avoiding cytidines. • Essentially all of the current COVID-19 diagnostic targets have undergone mutations. • SARS-CoV-2 nucleocapsid (N) gene primers and probes have the most mutations. • It would be better to select diagnostic targets avoiding cytidines. Effective, sensitive, and reliable diagnostic reagents are of paramount importance for combating the ongoing coronavirus disease 2019 (COVID-19) pandemic when there is neither a preventive vaccine nor a specific drug available for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It will cause a large number of false-positive and false-negative tests if currently used diagnostic reagents are undermined. Based on genotyping of 31,421 SARS-CoV-2 genome samples collected up to July 23, 2020, we reveal that essentially all of the current COVID-19 diagnostic targets have undergone mutations. We further show that SARS-CoV-2 has the most mutations on the targets of various nucleocapsid (N) gene primers and probes, which have been widely used around the world to diagnose COVID-19. To understand whether SARS-CoV-2 genes have mutated unevenly, we have computed the mutation rate and mutation h-index of all SARS-CoV-2 genes, indicating that the N gene is one of the most non-conservative genes in the SARS-CoV-2 genome. We show that due to human immune response induced APOBEC mRNA (C > T) editing, diagnostic targets should also be selected to avoid cytidines. Our findings might enable optimally selecting the conservative SARS-CoV-2 genes and proteins for the design and development of COVID-19 diagnostic reagents, prophylactic vaccines, and therapeutic medicines.Interactive real-time online Mutation Tracker. Effective, sensitive, and reliable diagnostic reagents are of paramount importance for combating the ongoing coronavirus disease 2019 (COVID-19) pandemic when there is neither a preventive vaccine nor a specific drug available for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It will cause a large number of false-positive and false-negative tests if currently used diagnostic reagents are undermined. Based on genotyping of 31,421 SARS-CoV-2 genome samples collected up to July 23, 2020, we reveal that essentially all of the current COVID-19 diagnostic targets have undergone mutations. We further show that SARS-CoV-2 has the most mutations on the targets of various nucleocapsid (N) gene primers and probes, which have been widely used around the world to diagnose COVID-19. To understand whether SARS-CoV-2 genes have mutated unevenly, we have computed the mutation rate and mutation h-index of all SARS-CoV-2 genes, indicating that the N gene is one of the most non-conservative genes in the SARS-CoV-2 genome. We show that due to human immune response induced APOBEC mRNA (C > T) editing, diagnostic targets should also be selected to avoid cytidines. Our findings might enable optimally selecting the conservative SARS-CoV-2 genes and proteins for the design and development of COVID-19 diagnostic reagents, prophylactic vaccines, and therapeutic medicines. AVAILABILITY: Interactive real-time online Mutation Tracker.Effective, sensitive, and reliable diagnostic reagents are of paramount importance for combating the ongoing coronavirus disease 2019 (COVID-19) pandemic when there is neither a preventive vaccine nor a specific drug available for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It will cause a large number of false-positive and false-negative tests if currently used diagnostic reagents are undermined. Based on genotyping of 31,421 SARS-CoV-2 genome samples collected up to July 23, 2020, we reveal that essentially all of the current COVID-19 diagnostic targets have undergone mutations. We further show that SARS-CoV-2 has the most mutations on the targets of various nucleocapsid (N) gene primers and probes, which have been widely used around the world to diagnose COVID-19. To understand whether SARS-CoV-2 genes have mutated unevenly, we have computed the mutation rate and mutation h-index of all SARS-CoV-2 genes, indicating that the N gene is one of the most non-conservative genes in the SARS-CoV-2 genome. We show that due to human immune response induced APOBEC mRNA (C > T) editing, diagnostic targets should also be selected to avoid cytidines. Our findings might enable optimally selecting the conservative SARS-CoV-2 genes and proteins for the design and development of COVID-19 diagnostic reagents, prophylactic vaccines, and therapeutic medicines. AVAILABILITY: Interactive real-time online Mutation Tracker. |
Author | Hozumi, Yuta Wei, Guo-Wei Yin, Changchuan Wang, Rui |
Author_xml | – sequence: 1 givenname: Rui surname: Wang fullname: Wang, Rui organization: Department of Mathematics, Michigan State University, MI 48824, USA – sequence: 2 givenname: Yuta surname: Hozumi fullname: Hozumi, Yuta organization: Department of Mathematics, Michigan State University, MI 48824, USA – sequence: 3 givenname: Changchuan surname: Yin fullname: Yin, Changchuan email: cyin1@uic.edu organization: Department of Mathematics, Statistics, and Computer Science, University of Illinois at Chicago, Chicago, IL 60607, USA – sequence: 4 givenname: Guo-Wei surname: Wei fullname: Wei, Guo-Wei email: wei@math.msu.edu organization: Department of Mathematics, Michigan State University, MI 48824, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32966857$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1021/bi962590c 10.2807/1560-7917.ES.2020.25.3.2000045 10.1016/j.virusres.2014.10.008 10.1002/0471250953.bi0313s48 10.1021/acsnano.0c02624 10.1128/JCM.00557-20 10.1098/rsos.200636 10.1016/j.cell.2020.06.040 10.1038/s41586-020-2008-3 10.1126/science.1100658 10.1038/234034a0 10.2807/1560-7917.ES.2020.25.9.2000152 10.1007/s00018-016-2299-6 10.2807/1560-7917.ES.2017.22.13.30494 10.1128/JCM.00310-20 |
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References | (bb0055) 2020 Allawi, SantaLucia (bb0080) 1997; 36 Sevajol, Subissi, Decroly, Canard, Imbert (bb0075) 2014; 194 Levandowsky, Winter (bb0095) 1971; 234 Bishop, Holmes, Sheehy, Malim (bb0060) 2004; 305 Sanjuán, Domingo-Calap (bb0065) 2016; 73 Sievers, Higgins (bb0090) 2014; 48 Wang, Hozumi, Yin, Wei (bb0100) 2020 Wu, Zhao, Yu, Chen, Wang, Song, Hu, Tao, Tian, Pei (bb0015) 2020; 579 Jung, Park, Moon, Ku, Beak, Kim, Park, Park, Lee, Byeon (bb0030) 2020; 6 Nalla, Casto, Huang, Perchetti, Sampoleo, Shrestha, Wei, Zhu, Jerome, Greninger (bb0045) 2020; 58 Vogels, Brito, Wyllie, Fauver, Ott, Kalinich, Petrone, Landry, Foxman, Grubaugh (bb0040) 2020; 5 Udugama, Kadhiresan, Kozlowski, Malekjahani, Osborne, Li, Chen, Mubareka, Gubbay, Chan (bb0025) 2020; 14 WHO (bb0005) 2020 Pfefferle, Reucher, Nörz, Lütgehetmann (bb0035) 2020; 25 Chan, Yip, To, Tang, Wong, Leung, Fung, Ng, Zou, Tsoi (bb0010) 2020; 58 Corman, Landt, Kaiser, Molenkamp, Meijer, Chu, Bleicker, Brünink, Schneider, Schmidt (bb0020) 2020; 25 Khan, Cheung (bb0105) 2020; 7 Shirato, Nao, Katano, Takayama, Saito, Kato, Katoh, Sakata, Nakatsu, Mori (bb0050) 2020; 2020 Grubaugh, Hanage, Rasmussen (bb0070) 2020; 182 Shu, McCauley (bb0085) 2017; 22 Sievers (10.1016/j.ygeno.2020.09.028_bb0090) 2014; 48 Bishop (10.1016/j.ygeno.2020.09.028_bb0060) 2004; 305 Sanjuán (10.1016/j.ygeno.2020.09.028_bb0065) 2016; 73 Levandowsky (10.1016/j.ygeno.2020.09.028_bb0095) 1971; 234 Khan (10.1016/j.ygeno.2020.09.028_bb0105) 2020; 7 Corman (10.1016/j.ygeno.2020.09.028_bb0020) 2020; 25 Wang (10.1016/j.ygeno.2020.09.028_bb0100) 2020 Grubaugh (10.1016/j.ygeno.2020.09.028_bb0070) 2020; 182 Jung (10.1016/j.ygeno.2020.09.028_bb0030) 2020; 6 Chan (10.1016/j.ygeno.2020.09.028_bb0010) 2020; 58 Shirato (10.1016/j.ygeno.2020.09.028_bb0050) 2020; 2020 Nalla (10.1016/j.ygeno.2020.09.028_bb0045) 2020; 58 Wu (10.1016/j.ygeno.2020.09.028_bb0015) 2020; 579 Sevajol (10.1016/j.ygeno.2020.09.028_bb0075) 2014; 194 Allawi (10.1016/j.ygeno.2020.09.028_bb0080) 1997; 36 Vogels (10.1016/j.ygeno.2020.09.028_bb0040) 2020; 5 Pfefferle (10.1016/j.ygeno.2020.09.028_bb0035) 2020; 25 Shu (10.1016/j.ygeno.2020.09.028_bb0085) 2017; 22 WHO (10.1016/j.ygeno.2020.09.028_bb0005) 2020 Udugama (10.1016/j.ygeno.2020.09.028_bb0025) 2020; 14 |
References_xml | – volume: 58 year: 2020 ident: bb0045 article-title: Comparative performance of SARS-CoV-2 detection assays using seven different primer/probe sets and one assay kit publication-title: J. Clin. Microbiol. – year: 2020 ident: bb0005 article-title: Coronavirus Disease 2019 (COVID-19) Situation Report-185 Coronavirus Disease (COVID-2019) Situation Reports – volume: 58 year: 2020 ident: bb0010 article-title: Improved molecular diagnosis of COVID-19 by the novel, highly sensitive and specific COVID-19-rdrp/hel real-time reverse transcription-PCR assay validated in vitro and with clinical specimens publication-title: J. Clin. Microbiol. – volume: 25 year: 2020 ident: bb0020 article-title: Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR publication-title: Eurosurveillance – volume: 22 year: 2017 ident: bb0085 article-title: Gisaid: global initiative on sharing all influenza data–from vision to reality publication-title: Eurosurveillance – year: 2020 ident: bb0055 article-title: Chinese Firm to Replace Clinical Laboratory Test Kits after Spanish Health Authorities Report Tests from Chinas Shenzen Bioeasy Were Only 30% Accurate – volume: 234 start-page: 34 year: 1971 end-page: 35 ident: bb0095 article-title: Distance between sets publication-title: Nature – volume: 194 start-page: 90 year: 2014 end-page: 99 ident: bb0075 article-title: Insights into RNA synthesis, capping, and proofreading mechanisms of SARS-coronavirus publication-title: Virus Res. – volume: 6 start-page: 2513 year: 2020 end-page: 2523 ident: bb0030 article-title: Comparative analysis of primer-probe sets for the laboratory confirmation of SARS-CoV-2 publication-title: BioRxiv – volume: 5 start-page: 1299 year: 2020 end-page: 1305 ident: bb0040 article-title: Analytical sensitivity and efficiency comparisons of SARS-CoV-2 RT-PCR assays publication-title: medRxiv – volume: 579 start-page: 265 year: 2020 end-page: 269 ident: bb0015 article-title: A new coronavirus associated with human respiratory disease in China publication-title: Nature – volume: 14 start-page: 3822 year: 2020 end-page: 3835 ident: bb0025 article-title: Diagnosing COVID-19: the disease and tools for detection publication-title: ACS Nano – volume: 48 start-page: 3 year: 2014 end-page: 13 ident: bb0090 article-title: Clustal omega publication-title: Curr. Protoc. Bioinformatics – volume: 2020 year: 2020 ident: bb0050 article-title: Development of genetic diagnostic methods for novel coronavirus 2019 (nCoV-2019) in Japan publication-title: Jpn. J. Infect. Dis. – volume: 182 start-page: 794 year: 2020 end-page: 795 ident: bb0070 article-title: Making sense of mutation: what D614G means for the COVID-19 pandemic remains unclear publication-title: Cell – year: 2020 ident: bb0100 article-title: Mutations on COVID-19 diagnostic targets publication-title: arXiv preprint – volume: 73 start-page: 4433 year: 2016 end-page: 4448 ident: bb0065 article-title: Mechanisms of viral mutation publication-title: Cell. Mol. Life Sci. – volume: 7 year: 2020 ident: bb0105 article-title: Presence of mismatches between diagnostic PCR assays and coronavirus SARS-CoV-2 genome publication-title: R. Soc. Open Sci. – volume: 25 start-page: 2000152 year: 2020 ident: bb0035 article-title: Evaluation of a quantitative RT-PCR assay for the detection of the emerging coronavirus SARS-CoV-2 using a high throughput system publication-title: Eurosurveillance – volume: 36 start-page: 10581 year: 1997 end-page: 10594 ident: bb0080 article-title: Thermodynamics and NMR of internal G.T mismatches in DNA publication-title: Biochemistry – volume: 305 start-page: 645 year: 2004 ident: bb0060 article-title: APOBEC-mediated editing of viral RNA publication-title: Science – volume: 36 start-page: 10581 issue: 34 year: 1997 ident: 10.1016/j.ygeno.2020.09.028_bb0080 article-title: Thermodynamics and NMR of internal G.T mismatches in DNA publication-title: Biochemistry doi: 10.1021/bi962590c – volume: 25 issue: 3 year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0020 article-title: Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR publication-title: Eurosurveillance doi: 10.2807/1560-7917.ES.2020.25.3.2000045 – volume: 194 start-page: 90 year: 2014 ident: 10.1016/j.ygeno.2020.09.028_bb0075 article-title: Insights into RNA synthesis, capping, and proofreading mechanisms of SARS-coronavirus publication-title: Virus Res. doi: 10.1016/j.virusres.2014.10.008 – volume: 48 start-page: 3 issue: 1 year: 2014 ident: 10.1016/j.ygeno.2020.09.028_bb0090 article-title: Clustal omega publication-title: Curr. Protoc. Bioinformatics doi: 10.1002/0471250953.bi0313s48 – volume: 14 start-page: 3822 issue: 4 year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0025 article-title: Diagnosing COVID-19: the disease and tools for detection publication-title: ACS Nano doi: 10.1021/acsnano.0c02624 – volume: 58 issue: 6 year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0045 article-title: Comparative performance of SARS-CoV-2 detection assays using seven different primer/probe sets and one assay kit publication-title: J. Clin. Microbiol. doi: 10.1128/JCM.00557-20 – year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0100 article-title: Mutations on COVID-19 diagnostic targets publication-title: arXiv preprint – volume: 7 issue: 6 year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0105 article-title: Presence of mismatches between diagnostic PCR assays and coronavirus SARS-CoV-2 genome publication-title: R. Soc. Open Sci. doi: 10.1098/rsos.200636 – volume: 182 start-page: 794 issue: 4 year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0070 article-title: Making sense of mutation: what D614G means for the COVID-19 pandemic remains unclear publication-title: Cell doi: 10.1016/j.cell.2020.06.040 – volume: 6 start-page: 2513 issue: 9 year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0030 article-title: Comparative analysis of primer-probe sets for the laboratory confirmation of SARS-CoV-2 publication-title: BioRxiv – volume: 579 start-page: 265 issue: 7798 year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0015 article-title: A new coronavirus associated with human respiratory disease in China publication-title: Nature doi: 10.1038/s41586-020-2008-3 – volume: 305 start-page: 645 issue: 5684 year: 2004 ident: 10.1016/j.ygeno.2020.09.028_bb0060 article-title: APOBEC-mediated editing of viral RNA publication-title: Science doi: 10.1126/science.1100658 – year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0005 – volume: 234 start-page: 34 issue: 5323 year: 1971 ident: 10.1016/j.ygeno.2020.09.028_bb0095 article-title: Distance between sets publication-title: Nature doi: 10.1038/234034a0 – volume: 25 start-page: 2000152 issue: 9 year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0035 article-title: Evaluation of a quantitative RT-PCR assay for the detection of the emerging coronavirus SARS-CoV-2 using a high throughput system publication-title: Eurosurveillance doi: 10.2807/1560-7917.ES.2020.25.9.2000152 – volume: 73 start-page: 4433 issue: 23 year: 2016 ident: 10.1016/j.ygeno.2020.09.028_bb0065 article-title: Mechanisms of viral mutation publication-title: Cell. Mol. Life Sci. doi: 10.1007/s00018-016-2299-6 – volume: 5 start-page: 1299 year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0040 article-title: Analytical sensitivity and efficiency comparisons of SARS-CoV-2 RT-PCR assays publication-title: medRxiv – volume: 22 issue: 13 year: 2017 ident: 10.1016/j.ygeno.2020.09.028_bb0085 article-title: Gisaid: global initiative on sharing all influenza data–from vision to reality publication-title: Eurosurveillance doi: 10.2807/1560-7917.ES.2017.22.13.30494 – volume: 58 issue: 5 year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0010 article-title: Improved molecular diagnosis of COVID-19 by the novel, highly sensitive and specific COVID-19-rdrp/hel real-time reverse transcription-PCR assay validated in vitro and with clinical specimens publication-title: J. Clin. Microbiol. doi: 10.1128/JCM.00310-20 – volume: 2020 year: 2020 ident: 10.1016/j.ygeno.2020.09.028_bb0050 article-title: Development of genetic diagnostic methods for novel coronavirus 2019 (nCoV-2019) in Japan publication-title: Jpn. J. Infect. Dis. |
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Snippet | Effective, sensitive, and reliable diagnostic reagents are of paramount importance for combating the ongoing coronavirus disease 2019 (COVID-19) pandemic when... • Essentially all of the current COVID-19 diagnostic targets have undergone mutations. • SARS-CoV-2 nucleocapsid (N) gene primers and probes have the most... |
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SubjectTerms | Coronavirus Envelope Proteins - genetics COVID-19 - virology COVID-19 infection COVID-19 Testing DNA Primers genes genotyping Genotyping Techniques Humans immune response messenger RNA Mutation mutation rate nucleocapsid Original pandemic Polymorphism, Single Nucleotide proteins SARS-CoV-2 - genetics SARS-CoV-2 - isolation & purification Severe acute respiratory syndrome coronavirus 2 therapeutics vaccines |
Title | Mutations on COVID-19 diagnostic targets |
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