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VAPiD: a lightweight cross-platform viral annotation pipeline and identification tool to facilitate virus genome submissions to NCBI GenBank

Identifieur interne : 000144 ( Pmc/Checkpoint ); précédent : 000143; suivant : 000145

VAPiD: a lightweight cross-platform viral annotation pipeline and identification tool to facilitate virus genome submissions to NCBI GenBank

Auteurs : Ryan C. Shean [États-Unis] ; Negar Makhsous [États-Unis] ; Graham D. Stoddard [États-Unis] ; Michelle J. Lin [États-Unis] ; Alexander L. Greninger [États-Unis]

Source :

RBID : PMC:6343335

Abstract

Background

With sequencing technologies becoming cheaper and easier to use, more groups are able to obtain whole genome sequences of viruses of public health and scientific importance. Submission of genomic data to NCBI GenBank is a requirement prior to publication and plays a critical role in making scientific data publicly available. GenBank currently has automatic prokaryotic and eukaryotic genome annotation pipelines but has no viral annotation pipeline beyond influenza virus. Annotation and submission of viral genome sequence is a non-trivial task, especially for groups that do not routinely interact with GenBank for data submissions.

Results

We present Viral Annotation Pipeline and iDentification (VAPiD), a portable and lightweight command-line tool for annotation and GenBank deposition of viral genomes. VAPiD supports annotation of nearly all unsegmented viral genomes. The pipeline has been validated on human immunodeficiency virus, human parainfluenza virus 1–4, human metapneumovirus, human coronaviruses (229E/OC43/NL63/HKU1/SARS/MERS), human enteroviruses/rhinoviruses, measles virus, mumps virus, Hepatitis A-E Virus, Chikungunya virus, dengue virus, and West Nile virus, as well the human polyomaviruses BK/JC/MCV, human adenoviruses, and human papillomaviruses. The program can handle individual or batch submissions of different viruses to GenBank and correctly annotates multiple viruses, including those that contain ribosomal slippage or RNA editing without prior knowledge of the virus to be annotated. VAPiD is programmed in Python and is compatible with Windows, Linux, and Mac OS systems.

Conclusions

We have created a portable, lightweight, user-friendly, internet-enabled, open-source, command-line genome annotation and submission package to facilitate virus genome submissions to NCBI GenBank. Instructions for downloading and installing VAPiD can be found at https://github.com/rcs333/VAPiD.


Url:
DOI: 10.1186/s12859-019-2606-y
PubMed: 30674273
PubMed Central: 6343335


Affiliations:


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PMC:6343335

Le document en format XML

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<p id="Par1">With sequencing technologies becoming cheaper and easier to use, more groups are able to obtain whole genome sequences of viruses of public health and scientific importance. Submission of genomic data to NCBI GenBank is a requirement prior to publication and plays a critical role in making scientific data publicly available. GenBank currently has automatic prokaryotic and eukaryotic genome annotation pipelines but has no viral annotation pipeline beyond influenza virus. Annotation and submission of viral genome sequence is a non-trivial task, especially for groups that do not routinely interact with GenBank for data submissions.</p>
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<p id="Par2">We present Viral Annotation Pipeline and iDentification (VAPiD), a portable and lightweight command-line tool for annotation and GenBank deposition of viral genomes. VAPiD supports annotation of nearly all unsegmented viral genomes. The pipeline has been validated on human immunodeficiency virus, human parainfluenza virus 1–4, human metapneumovirus, human coronaviruses (229E/OC43/NL63/HKU1/SARS/MERS), human enteroviruses/rhinoviruses, measles virus, mumps virus, Hepatitis A-E Virus, Chikungunya virus, dengue virus, and West Nile virus, as well the human polyomaviruses BK/JC/MCV, human adenoviruses, and human papillomaviruses. The program can handle individual or batch submissions of different viruses to GenBank and correctly annotates multiple viruses, including those that contain ribosomal slippage or RNA editing without prior knowledge of the virus to be annotated. VAPiD is programmed in Python and is compatible with Windows, Linux, and Mac OS systems.</p>
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</TEI>
<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">BMC Bioinformatics</journal-id>
<journal-id journal-id-type="iso-abbrev">BMC Bioinformatics</journal-id>
<journal-title-group>
<journal-title>BMC Bioinformatics</journal-title>
</journal-title-group>
<issn pub-type="epub">1471-2105</issn>
<publisher>
<publisher-name>BioMed Central</publisher-name>
<publisher-loc>London</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">30674273</article-id>
<article-id pub-id-type="pmc">6343335</article-id>
<article-id pub-id-type="publisher-id">2606</article-id>
<article-id pub-id-type="doi">10.1186/s12859-019-2606-y</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Software</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>VAPiD: a lightweight cross-platform viral annotation pipeline and identification tool to facilitate virus genome submissions to NCBI GenBank</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Shean</surname>
<given-names>Ryan C.</given-names>
</name>
<address>
<email>rcs333@uw.edu</email>
</address>
<xref ref-type="aff" rid="Aff1">1</xref>
<xref ref-type="aff" rid="Aff2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Makhsous</surname>
<given-names>Negar</given-names>
</name>
<address>
<email>negarm@uw.edu</email>
</address>
<xref ref-type="aff" rid="Aff1">1</xref>
<xref ref-type="aff" rid="Aff2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Stoddard</surname>
<given-names>Graham D.</given-names>
</name>
<address>
<email>gds6@uw.edu</email>
</address>
<xref ref-type="aff" rid="Aff3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Lin</surname>
<given-names>Michelle J.</given-names>
</name>
<address>
<email>mjlin@uw.edu</email>
</address>
<xref ref-type="aff" rid="Aff1">1</xref>
<xref ref-type="aff" rid="Aff2">2</xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0002-7443-0527</contrib-id>
<name>
<surname>Greninger</surname>
<given-names>Alexander L.</given-names>
</name>
<address>
<email>agrening@uw.edu</email>
</address>
<xref ref-type="aff" rid="Aff1">1</xref>
<xref ref-type="aff" rid="Aff2">2</xref>
</contrib>
<aff id="Aff1">
<label>1</label>
<institution-wrap>
<institution-id institution-id-type="ISNI">0000000122986657</institution-id>
<institution-id institution-id-type="GRID">grid.34477.33</institution-id>
<institution>Department of Laboratory Medicine,</institution>
<institution>University of Washington,</institution>
</institution-wrap>
Seattle, WA USA</aff>
<aff id="Aff2">
<label>2</label>
<institution-wrap>
<institution-id institution-id-type="ISNI">0000 0001 2180 1622</institution-id>
<institution-id institution-id-type="GRID">grid.270240.3</institution-id>
<institution>Vaccine and Infectious Disease Division,</institution>
<institution>Fred Hutchinson Cancer Research Center,</institution>
</institution-wrap>
Seattle, WA USA</aff>
<aff id="Aff3">
<label>3</label>
<institution-wrap>
<institution-id institution-id-type="ISNI">0000000122986657</institution-id>
<institution-id institution-id-type="GRID">grid.34477.33</institution-id>
<institution>Department of Neurobiology,</institution>
<institution>University of Washington,</institution>
</institution-wrap>
Seattle, WA USA</aff>
</contrib-group>
<pub-date pub-type="epub">
<day>23</day>
<month>1</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>23</day>
<month>1</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="collection">
<year>2019</year>
</pub-date>
<volume>20</volume>
<elocation-id>48</elocation-id>
<history>
<date date-type="received">
<day>14</day>
<month>5</month>
<year>2018</year>
</date>
<date date-type="accepted">
<day>4</day>
<month>1</month>
<year>2019</year>
</date>
</history>
<permissions>
<copyright-statement>© The Author(s). 2019</copyright-statement>
<license license-type="OpenAccess">
<license-p>
<bold>Open Access</bold>
This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (
<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (
<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/publicdomain/zero/1.0/">http://creativecommons.org/publicdomain/zero/1.0/</ext-link>
) applies to the data made available in this article, unless otherwise stated.</license-p>
</license>
</permissions>
<abstract id="Abs1">
<sec>
<title>Background</title>
<p id="Par1">With sequencing technologies becoming cheaper and easier to use, more groups are able to obtain whole genome sequences of viruses of public health and scientific importance. Submission of genomic data to NCBI GenBank is a requirement prior to publication and plays a critical role in making scientific data publicly available. GenBank currently has automatic prokaryotic and eukaryotic genome annotation pipelines but has no viral annotation pipeline beyond influenza virus. Annotation and submission of viral genome sequence is a non-trivial task, especially for groups that do not routinely interact with GenBank for data submissions.</p>
</sec>
<sec>
<title>Results</title>
<p id="Par2">We present Viral Annotation Pipeline and iDentification (VAPiD), a portable and lightweight command-line tool for annotation and GenBank deposition of viral genomes. VAPiD supports annotation of nearly all unsegmented viral genomes. The pipeline has been validated on human immunodeficiency virus, human parainfluenza virus 1–4, human metapneumovirus, human coronaviruses (229E/OC43/NL63/HKU1/SARS/MERS), human enteroviruses/rhinoviruses, measles virus, mumps virus, Hepatitis A-E Virus, Chikungunya virus, dengue virus, and West Nile virus, as well the human polyomaviruses BK/JC/MCV, human adenoviruses, and human papillomaviruses. The program can handle individual or batch submissions of different viruses to GenBank and correctly annotates multiple viruses, including those that contain ribosomal slippage or RNA editing without prior knowledge of the virus to be annotated. VAPiD is programmed in Python and is compatible with Windows, Linux, and Mac OS systems.</p>
</sec>
<sec>
<title>Conclusions</title>
<p id="Par3">We have created a portable, lightweight, user-friendly, internet-enabled, open-source, command-line genome annotation and submission package to facilitate virus genome submissions to NCBI GenBank. Instructions for downloading and installing VAPiD can be found at
<ext-link ext-link-type="uri" xlink:href="https://github.com/rcs333/VAPiD">https://github.com/rcs333/VAPiD</ext-link>
.</p>
</sec>
</abstract>
<kwd-group xml:lang="en">
<title>Keywords</title>
<kwd>Viral annotation</kwd>
<kwd>Viral genomics</kwd>
<kwd>Virus sequence</kwd>
<kwd>Data submission</kwd>
<kwd>NCBI</kwd>
<kwd>GenBank</kwd>
<kwd>VAPiD</kwd>
</kwd-group>
<custom-meta-group>
<custom-meta>
<meta-name>issue-copyright-statement</meta-name>
<meta-value>© The Author(s) 2019</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
</pmc>
<affiliations>
<list>
<country>
<li>États-Unis</li>
</country>
<region>
<li>Washington (État)</li>
</region>
</list>
<tree>
<country name="États-Unis">
<region name="Washington (État)">
<name sortKey="Shean, Ryan C" sort="Shean, Ryan C" uniqKey="Shean R" first="Ryan C." last="Shean">Ryan C. Shean</name>
</region>
<name sortKey="Greninger, Alexander L" sort="Greninger, Alexander L" uniqKey="Greninger A" first="Alexander L." last="Greninger">Alexander L. Greninger</name>
<name sortKey="Greninger, Alexander L" sort="Greninger, Alexander L" uniqKey="Greninger A" first="Alexander L." last="Greninger">Alexander L. Greninger</name>
<name sortKey="Lin, Michelle J" sort="Lin, Michelle J" uniqKey="Lin M" first="Michelle J." last="Lin">Michelle J. Lin</name>
<name sortKey="Lin, Michelle J" sort="Lin, Michelle J" uniqKey="Lin M" first="Michelle J." last="Lin">Michelle J. Lin</name>
<name sortKey="Makhsous, Negar" sort="Makhsous, Negar" uniqKey="Makhsous N" first="Negar" last="Makhsous">Negar Makhsous</name>
<name sortKey="Makhsous, Negar" sort="Makhsous, Negar" uniqKey="Makhsous N" first="Negar" last="Makhsous">Negar Makhsous</name>
<name sortKey="Shean, Ryan C" sort="Shean, Ryan C" uniqKey="Shean R" first="Ryan C." last="Shean">Ryan C. Shean</name>
<name sortKey="Stoddard, Graham D" sort="Stoddard, Graham D" uniqKey="Stoddard G" first="Graham D." last="Stoddard">Graham D. Stoddard</name>
</country>
</tree>
</affiliations>
</record>

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