Serveur d'exploration MERS

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

The utility and perspectives of NGS-based methods in BSL-3 and BSL-4 laboratory - sequencing and analysis strategies.

Identifieur interne : 000A88 ( PubMed/Corpus ); précédent : 000A87; suivant : 000A89

The utility and perspectives of NGS-based methods in BSL-3 and BSL-4 laboratory - sequencing and analysis strategies.

Auteurs : Tomasz Wolkowicz

Source :

RBID : pubmed:29136087

English descriptors

Abstract

Modern diagnostics is in general based on molecular biology methods. Nowadays sequencing-based methods, especially whole genome sequencing, are becoming increasingly important. Implementation of such methods into routine diagnostic of highly dangerous pathogens, like Bacillus anthracis, Francisella tularensis, Yersinia pestis, Ebola virus, MERS, Lassa virus etc. would be very helpful. The best diagnostic strategy would be the metagenomic sequencing directly from the clinical sample. Implementation of majority of currently available WGS platforms inside the BSL-3 or 4 laboratory is impractical because of the size of the equipment and time consuming wet lab part (e.g. library preparation). Nowadays there is a possibility to implement pocket size MinION - real time whole genome sequencer into BSL-3 and 4 laboratory for rapid and precise diagnostic purposes.

DOI: 10.1093/bfgp/elx033
PubMed: 29136087

Links to Exploration step

pubmed:29136087

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">The utility and perspectives of NGS-based methods in BSL-3 and BSL-4 laboratory - sequencing and analysis strategies.</title>
<author>
<name sortKey="Wolkowicz, Tomasz" sort="Wolkowicz, Tomasz" uniqKey="Wolkowicz T" first="Tomasz" last="Wolkowicz">Tomasz Wolkowicz</name>
<affiliation>
<nlm:affiliation>National Institute of Public Health - NIH, Poland.</nlm:affiliation>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PubMed</idno>
<date when="2018">2018</date>
<idno type="RBID">pubmed:29136087</idno>
<idno type="pmid">29136087</idno>
<idno type="doi">10.1093/bfgp/elx033</idno>
<idno type="wicri:Area/PubMed/Corpus">000A88</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000A88</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en">The utility and perspectives of NGS-based methods in BSL-3 and BSL-4 laboratory - sequencing and analysis strategies.</title>
<author>
<name sortKey="Wolkowicz, Tomasz" sort="Wolkowicz, Tomasz" uniqKey="Wolkowicz T" first="Tomasz" last="Wolkowicz">Tomasz Wolkowicz</name>
<affiliation>
<nlm:affiliation>National Institute of Public Health - NIH, Poland.</nlm:affiliation>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Briefings in functional genomics</title>
<idno type="eISSN">2041-2657</idno>
<imprint>
<date when="2018" type="published">2018</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Animals</term>
<term>High-Throughput Nucleotide Sequencing (methods)</term>
<term>Humans</term>
<term>Laboratories</term>
<term>Molecular Diagnostic Techniques</term>
<term>Nanopores</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>High-Throughput Nucleotide Sequencing</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Humans</term>
<term>Laboratories</term>
<term>Molecular Diagnostic Techniques</term>
<term>Nanopores</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Modern diagnostics is in general based on molecular biology methods. Nowadays sequencing-based methods, especially whole genome sequencing, are becoming increasingly important. Implementation of such methods into routine diagnostic of highly dangerous pathogens, like Bacillus anthracis, Francisella tularensis, Yersinia pestis, Ebola virus, MERS, Lassa virus etc. would be very helpful. The best diagnostic strategy would be the metagenomic sequencing directly from the clinical sample. Implementation of majority of currently available WGS platforms inside the BSL-3 or 4 laboratory is impractical because of the size of the equipment and time consuming wet lab part (e.g. library preparation). Nowadays there is a possibility to implement pocket size MinION - real time whole genome sequencer into BSL-3 and 4 laboratory for rapid and precise diagnostic purposes.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">29136087</PMID>
<DateCompleted>
<Year>2019</Year>
<Month>06</Month>
<Day>07</Day>
</DateCompleted>
<DateRevised>
<Year>2020</Year>
<Month>04</Month>
<Day>03</Day>
</DateRevised>
<Article PubModel="Print">
<Journal>
<ISSN IssnType="Electronic">2041-2657</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>17</Volume>
<Issue>6</Issue>
<PubDate>
<Year>2018</Year>
<Month>11</Month>
<Day>26</Day>
</PubDate>
</JournalIssue>
<Title>Briefings in functional genomics</Title>
<ISOAbbreviation>Brief Funct Genomics</ISOAbbreviation>
</Journal>
<ArticleTitle>The utility and perspectives of NGS-based methods in BSL-3 and BSL-4 laboratory - sequencing and analysis strategies.</ArticleTitle>
<Pagination>
<MedlinePgn>471-476</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1093/bfgp/elx033</ELocationID>
<Abstract>
<AbstractText>Modern diagnostics is in general based on molecular biology methods. Nowadays sequencing-based methods, especially whole genome sequencing, are becoming increasingly important. Implementation of such methods into routine diagnostic of highly dangerous pathogens, like Bacillus anthracis, Francisella tularensis, Yersinia pestis, Ebola virus, MERS, Lassa virus etc. would be very helpful. The best diagnostic strategy would be the metagenomic sequencing directly from the clinical sample. Implementation of majority of currently available WGS platforms inside the BSL-3 or 4 laboratory is impractical because of the size of the equipment and time consuming wet lab part (e.g. library preparation). Nowadays there is a possibility to implement pocket size MinION - real time whole genome sequencer into BSL-3 and 4 laboratory for rapid and precise diagnostic purposes.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Wolkowicz</LastName>
<ForeName>Tomasz</ForeName>
<Initials>T</Initials>
<AffiliationInfo>
<Affiliation>National Institute of Public Health - NIH, Poland.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
<PublicationType UI="D016454">Review</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo>
<Country>England</Country>
<MedlineTA>Brief Funct Genomics</MedlineTA>
<NlmUniqueID>101528229</NlmUniqueID>
<ISSNLinking>2041-2649</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D059014" MajorTopicYN="N">High-Throughput Nucleotide Sequencing</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D007753" MajorTopicYN="Y">Laboratories</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D025202" MajorTopicYN="N">Molecular Diagnostic Techniques</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D058608" MajorTopicYN="N">Nanopores</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="pubmed">
<Year>2017</Year>
<Month>11</Month>
<Day>15</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2019</Year>
<Month>6</Month>
<Day>8</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2017</Year>
<Month>11</Month>
<Day>15</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">29136087</ArticleId>
<ArticleId IdType="pii">4616141</ArticleId>
<ArticleId IdType="doi">10.1093/bfgp/elx033</ArticleId>
<ArticleId IdType="pmc">PMC7109780</ArticleId>
</ArticleIdList>
<ReferenceList>
<Reference>
<Citation>BMC Genomics. 2014 Apr 16;15:288</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">24734872</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>J Infect Dis. 2011 Nov;204 Suppl 3:S776-84</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">21987750</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Genomics Proteomics Bioinformatics. 2015 Feb;13(1):4-16</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">25743089</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>PeerJ. 2016 Apr 05;4:e1752</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">27069781</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Philos Trans R Soc Lond B Biol Sci. 2017 May 26;372(1721):</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">28396469</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Proc Natl Acad Sci U S A. 1998 Feb 3;95(3):1224-9</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">9448313</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>J Clin Microbiol. 2011 Sep;49(9):3268-75</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">21715589</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Mol Cell Probes. 2007 Feb;21(1):12-6</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">16893624</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Euro Surveill. 2017 Jun 8;22(23):</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">28662764</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>FEMS Microbiol Lett. 2007 Jul;272(1):55-9</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">17490431</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:263-73</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">3472723</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Science. 2014 Sep 12;345(6202):1369-72</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">25214632</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Nat Commun. 2017 Feb 20;8:14515</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">28218240</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Investig Genet. 2010 Sep 01;1(1):5</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">21092340</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Bio Protoc. 2016 Nov 5;6(21):</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">28180136</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>PLoS Pathog. 2008 Nov;4(11):e1000212</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">19023410</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Genome Biol. 2014;15(11):519</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">25403361</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>NPJ Microgravity. 2016 Oct 20;2:16035</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">28725742</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>ISME J. 2012 Sep;6(9):1677-87</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">22297556</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):13770-3</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">8943010</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>J Infect Dis. 2007 Nov 15;196 Suppl 2:S199-204</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">17940950</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Microb Genom. 2016 Sep 8;2(9):e000085</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">28348876</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Genome Res. 2005 Oct;15(10):1451-5</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">16169926</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Nat Protoc. 2017 Jun;12(6):1261-1276</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">28538739</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Microbiol Immunol. 2004;48(4):263-9</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">15107536</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>J Infect Dis. 1999 Feb;179 Suppl 1:S164-9</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">9988180</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>J Infect Dis. 2011 Jul 15;204(2):200-8</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">21571728</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Sci Rep. 2017 Dec 21;7(1):18022</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">29269933</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Antiviral Res. 2004 Sep;63(3):209-15</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">15451189</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>J Biomol Tech. 2017 Apr;28(1):2-7</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">28337073</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>J Clin Microbiol. 2000 Nov;38(11):4180-5</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">11060087</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>BMC Genomics. 2014 Feb 04;15:96</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">24495417</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>J Clin Microbiol. 1994 Dec;32(12):2898-903</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">7883875</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>PLoS One. 2011;6(5):e19838</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">21603639</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463-7</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">271968</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Genome Biol. 2015 Sep 30;16:204</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">26420219</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>J Clin Microbiol. 2014 May;52(5):1529-39</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">24574292</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Science. 1998 Jul 17;281(5375):363, 365</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">9705713</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>J Appl Genet. 2011 Nov;52(4):413-35</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">21698376</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>J Clin Microbiol. 2002 Jul;40(7):2323-30</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">12089242</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>PLoS One. 2013 Sep 11;8(9):e74787</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">24040342</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Science. 2009 Jan 2;323(5910):133-8</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">19023044</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
<ReferenceList>
<Reference>
<Citation>Gene. 1994 Oct 11;148(1):1-6</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">7523248</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
</PubmedData>
</pubmed>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/MersV1/Data/PubMed/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000A88 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd -nk 000A88 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    MersV1
   |flux=    PubMed
   |étape=   Corpus
   |type=    RBID
   |clé=     pubmed:29136087
   |texte=   The utility and perspectives of NGS-based methods in BSL-3 and BSL-4 laboratory - sequencing and analysis strategies.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/RBID.i   -Sk "pubmed:29136087" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd   \
       | NlmPubMed2Wicri -a MersV1 

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Mon Apr 20 23:26:43 2020. Site generation: Sat Mar 27 09:06:09 2021