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...

Full description

Saved in:
Bibliographic Details
Published inGenomics (San Diego, Calif.) Vol. 112; no. 6; pp. 5204 - 5213
Main Authors Wang, Rui, Hozumi, Yuta, Yin, Changchuan, Wei, Guo-Wei
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.11.2020
Subjects
Online AccessGet full text

Cover

Loading…
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.
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
BookMark eNqNkUtvEzEURi1URNPCL0CqsuxmBr8fi1aqUh6ViroBtpbjuRMcTezWdiL13-OSUgELysoLf-e71z5H6CCmCAi9JbgnmMh36_5-BTH1FFPcY9Njql-gGcHadFpyeYBmWGvdKcHZIToqZY0xNkzTV-iQUSOlFmqGTj9vq6shxTJPcb64-XZ12REzH4JbxVRq8PPq8gpqeY1ejm4q8ObxPEZfP7z_svjUXd98vFpcXHeeG1o7xxkQ7TQVS8eEM0JgR0bAymNKhRJMiqVwHPhIB8YE53R0QkmhHQii2MiO0fm-93a73MDgIdbsJnubw8ble5tcsH_exPDdrtLOKtEmaN4KTh8LcrrbQql2E4qHaXIR0rZYypWSbbL4nygXRlEiVYue_L7W0z6_frIF2D7gcyolw_gUIdg--LJr-9OXffBlsbHNV6PMX5QPex_tbWF6hj3bs9B07AJkW3yA6GEIGXy1Qwr_5H8AGhav5A
CitedBy_id crossref_primary_10_1007_s00203_023_03579_9
crossref_primary_10_1016_j_diagmicrobio_2021_115540
crossref_primary_10_5144_0256_4947_2022_147
crossref_primary_10_7189_jogh_11_03038
crossref_primary_10_1016_j_bios_2022_114101
crossref_primary_10_1080_21655979_2021_1987821
crossref_primary_10_1016_j_jphotobiol_2022_112545
crossref_primary_10_1371_journal_pone_0279428
crossref_primary_10_3390_covid1010004
crossref_primary_10_3390_v12101095
crossref_primary_10_1007_s00521_024_10428_3
crossref_primary_10_3389_fcimb_2022_799678
crossref_primary_10_1099_jgv_0_001584
crossref_primary_10_1016_j_omega_2023_102898
crossref_primary_10_1136_bmjgh_2020_004408
crossref_primary_10_1371_journal_pone_0278061
crossref_primary_10_1016_j_scitotenv_2022_157546
crossref_primary_10_5812_jjm_122889
crossref_primary_10_1021_acsomega_1c04024
crossref_primary_10_1186_s13643_023_02377_0
crossref_primary_10_1016_j_envres_2021_111849
crossref_primary_10_1111_jam_15571
crossref_primary_10_1016_j_virusres_2022_199016
crossref_primary_10_1128_JCM_00075_21
crossref_primary_10_1038_s41598_021_00496_z
crossref_primary_10_2147_JMDH_S455396
crossref_primary_10_1159_000515417
crossref_primary_10_1016_j_scitotenv_2024_175138
crossref_primary_10_3390_pathogens11050516
crossref_primary_10_1111_eci_13706
crossref_primary_10_24171_j_phrp_2022_0183
crossref_primary_10_32604_cmc_2021_015355
crossref_primary_10_1002_jmv_27418
crossref_primary_10_3390_biology11020178
crossref_primary_10_1021_acsomega_2c06786
crossref_primary_10_1016_j_compbiomed_2022_105659
crossref_primary_10_1155_2022_7130061
crossref_primary_10_35341_afet_977488
crossref_primary_10_5582_ddt_2022_01092
crossref_primary_10_1038_s41467_021_21996_6
crossref_primary_10_1016_j_virusres_2021_198398
crossref_primary_10_1109_TNNLS_2023_3290188
crossref_primary_10_1126_sciadv_abn3481
crossref_primary_10_3389_fmicb_2021_637202
crossref_primary_10_1159_000517269
crossref_primary_10_1080_16078454_2021_1950898
crossref_primary_10_1007_s12559_020_09790_w
crossref_primary_10_3390_v14061316
crossref_primary_10_1097_SLA_0000000000005176
crossref_primary_10_1093_comjnl_bxae058
crossref_primary_10_1111_1751_7915_14027
crossref_primary_10_1371_journal_pone_0297081
crossref_primary_10_3390_bios11070238
crossref_primary_10_1016_j_ab_2022_114803
crossref_primary_10_1016_j_susmat_2022_e00397
crossref_primary_10_3390_diagnostics11071270
crossref_primary_10_1016_j_psep_2021_06_043
crossref_primary_10_1021_acsomega_1c06093
crossref_primary_10_1128_Spectrum_01494_21
crossref_primary_10_1016_j_bios_2022_114032
crossref_primary_10_1080_09540091_2024_2365334
crossref_primary_10_3389_fmed_2022_1034682
crossref_primary_10_1007_s12033_022_00570_5
crossref_primary_10_1093_emph_eoac013
crossref_primary_10_1111_1751_7915_14031
crossref_primary_10_1109_TCBB_2022_3165395
crossref_primary_10_1093_bib_bbad046
crossref_primary_10_1007_s10910_023_01512_5
crossref_primary_10_1038_s41598_023_42348_y
crossref_primary_10_1007_s42399_021_01059_z
crossref_primary_10_3389_fmed_2022_815389
crossref_primary_10_1128_spectrum_02654_23
crossref_primary_10_1016_j_jmoldx_2022_04_003
crossref_primary_10_3389_fmmed_2022_917201
crossref_primary_10_1039_D2CP00469K
crossref_primary_10_1016_j_heliyon_2022_e11130
crossref_primary_10_3390_life14060735
crossref_primary_10_3390_tropicalmed9020050
crossref_primary_10_1016_j_diagmicrobio_2022_115860
crossref_primary_10_1186_s12879_024_10345_9
crossref_primary_10_2144_btn_2021_0063
crossref_primary_10_1038_s41598_023_41086_5
crossref_primary_10_1093_nar_gkab895
crossref_primary_10_3390_ijms232214110
crossref_primary_10_1093_femsmc_xtad004
crossref_primary_10_2139_ssrn_3951700
crossref_primary_10_1007_s10114_022_2326_5
crossref_primary_10_1021_acsomega_1c01625
crossref_primary_10_1093_bib_bbac024
crossref_primary_10_3389_fpubh_2021_708476
crossref_primary_10_7717_peerj_11232
crossref_primary_10_2166_wh_2021_133
crossref_primary_10_3389_fpubh_2021_626697
crossref_primary_10_7759_cureus_16206
crossref_primary_10_3389_fimmu_2022_847617
crossref_primary_10_1021_acsinfecdis_1c00557
crossref_primary_10_1038_s41374_021_00663_w
crossref_primary_10_7717_peerj_13522
crossref_primary_10_1371_journal_pone_0264785
crossref_primary_10_3389_fcimb_2021_653616
crossref_primary_10_1557_s43579_021_00146_5
crossref_primary_10_1186_s13104_021_05722_5
crossref_primary_10_1016_j_ygeno_2021_07_020
crossref_primary_10_3389_fnut_2022_992733
crossref_primary_10_17066_tpdrd_1138538
crossref_primary_10_3389_fcimb_2021_741147
crossref_primary_10_3390_v13122474
crossref_primary_10_3892_etm_2022_11197
crossref_primary_10_1016_j_ebiom_2021_103540
crossref_primary_10_3390_pathogens10091088
crossref_primary_10_1093_bib_bbae465
crossref_primary_10_1186_s12985_022_01784_4
crossref_primary_10_1016_j_idcr_2021_e01233
crossref_primary_10_1051_e3sconf_202129203076
crossref_primary_10_2903_j_efsa_2021_6459
crossref_primary_10_1155_2022_4510900
crossref_primary_10_1038_s41598_022_13995_4
crossref_primary_10_4103_mjhs_mjhs_14_22
crossref_primary_10_1016_j_scitotenv_2021_147829
crossref_primary_10_1002_jmv_27510
crossref_primary_10_23736_S1825_859X_21_00122_5
crossref_primary_10_1128_jcm_00600_22
crossref_primary_10_3390_ijms24109072
crossref_primary_10_3390_v16071141
crossref_primary_10_1016_j_genrep_2021_101378
crossref_primary_10_1016_j_jmoldx_2021_12_007
crossref_primary_10_1128_JCM_03278_20
crossref_primary_10_3390_molecules26082383
crossref_primary_10_1128_JCM_02369_20
crossref_primary_10_3389_fmicb_2023_1217567
crossref_primary_10_1177_2632010X221075584
crossref_primary_10_1590_1678_4324_2023220591
crossref_primary_10_1080_08927022_2021_2016741
crossref_primary_10_1002_jcla_24242
crossref_primary_10_3390_diagnostics12010147
crossref_primary_10_1016_j_biomaterials_2023_122312
crossref_primary_10_3390_biomedicines10092329
crossref_primary_10_1021_acs_chemrev_1c00965
crossref_primary_10_1039_D3SC06961C
crossref_primary_10_1128_spectrum_00761_23
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
ContentType Journal Article
Copyright 2020 Elsevier Inc.
Copyright © 2020 Elsevier Inc. All rights reserved.
2020 Elsevier Inc. All rights reserved. 2020 Elsevier Inc.
Copyright_xml – notice: 2020 Elsevier Inc.
– notice: Copyright © 2020 Elsevier Inc. All rights reserved.
– notice: 2020 Elsevier Inc. All rights reserved. 2020 Elsevier Inc.
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
7S9
L.6
5PM
DOI 10.1016/j.ygeno.2020.09.028
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
AGRICOLA
AGRICOLA - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
AGRICOLA
AGRICOLA - Academic
DatabaseTitleList MEDLINE


AGRICOLA
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Engineering
Chemistry
Biology
EISSN 1089-8646
EndPage 5213
ExternalDocumentID PMC7502284
32966857
10_1016_j_ygeno_2020_09_028
S0888754320306546
Genre Research Support, U.S. Gov't, Non-P.H.S
Journal Article
Research Support, N.I.H., Extramural
GrantInformation_xml – fundername: NIGMS NIH HHS
  grantid: R01 GM126189
GroupedDBID ---
--K
--M
-DZ
-~X
.55
.GJ
.~1
0R~
0SF
1B1
1RT
1~.
1~5
29H
4.4
457
4G.
53G
5GY
5VS
6I.
7-5
71M
8P~
9JM
AACTN
AAEDT
AAEDW
AAFTH
AAIAV
AAIKJ
AAKOC
AALRI
AAOAW
AAQFI
AAXUO
AAYOK
ABEFU
ABFNM
ABFRF
ABGSF
ABJNI
ABLJU
ABMAC
ABUDA
ABVKL
ABXDB
ABYKQ
ACDAQ
ACGFO
ACGFS
ACRLP
ADBBV
ADEZE
ADFGL
ADMUD
ADUVX
AEBSH
AEFWE
AEHWI
AEKER
AENEX
AEXQZ
AFKWA
AFTJW
AFXIZ
AGHFR
AGRDE
AGUBO
AGYEJ
AHHHB
AHPSJ
AI.
AIEXJ
AIKHN
AITUG
AJBFU
AJOXV
ALMA_UNASSIGNED_HOLDINGS
AMFUW
AMRAJ
AXJTR
BAWUL
BKOJK
BLXMC
CAG
COF
CS3
DIK
DM4
DOVZS
DU5
E3Z
EBS
EFBJH
EFLBG
EJD
EO8
EO9
EP2
EP3
F5P
FDB
FEDTE
FGOYB
FIRID
FNPLU
FYGXN
G-2
G-Q
GBLVA
GROUPED_DOAJ
HLW
HVGLF
HZ~
IHE
IXB
J1W
K-O
KOM
L7B
LG5
LX2
M41
MO0
N9A
NCXOZ
O-L
O9-
OAUVE
OK1
OZT
P-8
P-9
P2P
PC.
Q38
RIG
ROL
RPZ
SBG
SCC
SDF
SDG
SDP
SES
SEW
SPCBC
SSU
SSZ
T5K
TN5
TR2
VH1
WUQ
X7M
XPP
XSW
ZA5
ZGI
ZMT
ZU3
ZXP
~G-
~KM
AAFWJ
AAHBH
AATTM
AAXKI
AAYWO
AAYXX
ABWVN
ACRPL
ACVFH
ADCNI
ADNMO
ADVLN
AEIPS
AEUPX
AFJKZ
AFPKN
AFPUW
AGCQF
AGRNS
AIGII
AIIUN
AKBMS
AKRWK
AKYEP
ANKPU
APXCP
BNPGV
CITATION
SSH
CGR
CUY
CVF
ECM
EIF
NPM
7X8
7S9
EFKBS
L.6
5PM
ID FETCH-LOGICAL-c492t-a43e18a825ba35a9550a1fe07c022575365b5a4e4f2d335442fa57658ae5173f3
IEDL.DBID IXB
ISSN 0888-7543
1089-8646
IngestDate Thu Aug 21 18:19:20 EDT 2025
Tue Aug 05 09:34:05 EDT 2025
Fri Jul 11 16:16:55 EDT 2025
Thu Apr 03 07:08:32 EDT 2025
Tue Jul 01 01:48:25 EDT 2025
Thu Apr 24 23:06:45 EDT 2025
Fri Feb 23 02:45:02 EST 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 6
Language English
License Copyright © 2020 Elsevier Inc. All rights reserved.
Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c492t-a43e18a825ba35a9550a1fe07c022575365b5a4e4f2d335442fa57658ae5173f3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://pubmed.ncbi.nlm.nih.gov/PMC7502284
PMID 32966857
PQID 2445972167
PQPubID 23479
PageCount 10
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_7502284
proquest_miscellaneous_2477635454
proquest_miscellaneous_2445972167
pubmed_primary_32966857
crossref_primary_10_1016_j_ygeno_2020_09_028
crossref_citationtrail_10_1016_j_ygeno_2020_09_028
elsevier_sciencedirect_doi_10_1016_j_ygeno_2020_09_028
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2020-11-01
PublicationDateYYYYMMDD 2020-11-01
PublicationDate_xml – month: 11
  year: 2020
  text: 2020-11-01
  day: 01
PublicationDecade 2020
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Genomics (San Diego, Calif.)
PublicationTitleAlternate Genomics
PublicationYear 2020
Publisher Elsevier Inc
Publisher_xml – name: Elsevier Inc
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.
SSID ssj0009382
Score 2.6377633
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...
SourceID pubmedcentral
proquest
pubmed
crossref
elsevier
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 5204
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
URI https://dx.doi.org/10.1016/j.ygeno.2020.09.028
https://www.ncbi.nlm.nih.gov/pubmed/32966857
https://www.proquest.com/docview/2445972167
https://www.proquest.com/docview/2477635454
https://pubmed.ncbi.nlm.nih.gov/PMC7502284
Volume 112
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LT-MwEB7xEGL3gKAsLK8qSBz2QLaJH3kcoYAKCDjwUG-Wk9iiCKXVtj1w4bcztpNCF9QDxyTjKJ6xx9_E428ADkIa6YhqQz5IM5_RIvKlYaBVAc1zRmUR2tIJV9dR555ddHl3Dtr1WRiTVln5fufTrbeu7rQqbbYGvV7rFucHgm1GSWCrnxvabcoSe4ive_xOvEttwSgj7BvpmnnI5ni9GCJUDBJJYMlOTUn2r1enz-jz_yTKD6vS2SqsVHDSO3JfvAZzqmzAkisw-dKA5XZdz60BPz9QD67Dn6ux24Qfev3Sa988nJ_4YeoVLvMO3-a5HPHhL7g_O71rd_yqaoKfs5SMfMmoChOJkV8mKZcphiAy1CqIc1yuEZzRiGdcMsU0KSjljBEtMejgiVQcDabpBiyU_VL9Bo8lBdGh5nGYxywNAvPDSEdFKknGDC3-FpBaWyKvKMVNZYtnUeeOPQmrYmFULIJUoIq34HDSaOAYNWaLR7UZxNTAEOjzZzfcr40mUNNmH0SWqj8eCkQ03JIWxbNkYkPVxzh2ctMZevK1lGCMmHBsHU8NgYmAoeyeflL2Hi11N-IzgoBg-7ud2oEf5sodhtyFhdG_sdpDVDTKmjD_9zVswuLR-WXnumknwRuxYgpC
linkProvider Elsevier
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LT-MwEB6xoBVwQNBd3o8gcdgDURM_kuYIBdRCyx4WUG-Wk9iiCKWItgf-PWM7Ke2CeuAajyNn_PomHn8fwElIIx1RbcgHaeozmke-NAy0KqBZxqjMQyud0L2NWvfsusd7C9Cs7sKYtMpy7Xdrul2tyyf10pv1l36__g_nB4JtRklg1c-jH7CEaCA2-g3t3vkH8y61ilHG2jfmFfWQTfJ6M0yoGCWSwLKdGk32r7enz_Dz_yzKqW3pah3WSjzpnbkmb8CCKmrw0ylMvtVguVkJutVgdYp78Bf86Y7dKfzQGxRe8-9D-8IPEy93qXf4Ns8liQ9_w_3V5V2z5ZeyCX7GEjLyJaMqbEgM_VJJuUwwBpGhVkGc4X6N6IxGPOWSKaZJTilnjGiJUQdvSMWxxzTdhMViUKht8FgjJzrUPA6zmCVBYP4Y6ShPJEmZ4cXfAVJ5S2Qlp7iRtngWVfLYk7AuFsbFIkgEungHTieVXhylxnzzqOoGMTMyBC768yseV50m0NPmIEQWajAeCoQ03LIWxfNsYsPVxzh-5Jbr6ElrKcEgscGxdjwzBCYGhrN7tqToP1rubgRoBBHB7nc_6giWW3fdjui0b2_2YMWUuJuR-7A4eh2rA4RIo_TQToF3dwMK1Q
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Mutations+on+COVID-19+diagnostic+targets&rft.jtitle=Genomics+%28San+Diego%2C+Calif.%29&rft.au=Wang%2C+Rui&rft.au=Hozumi%2C+Yuta&rft.au=Yin%2C+Changchuan&rft.au=Wei%2C+Guo-Wei&rft.date=2020-11-01&rft.issn=1089-8646&rft.eissn=1089-8646&rft.volume=112&rft.issue=6&rft.spage=5204&rft_id=info:doi/10.1016%2Fj.ygeno.2020.09.028&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0888-7543&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0888-7543&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0888-7543&client=summon