Serveur d'exploration SRAS

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.

Heterogeneity detector: finding heterogeneous positions in Phred/Phrap assemblies.

Identifieur interne : 002E18 ( PubMed/Corpus ); précédent : 002E17; suivant : 002E19

Heterogeneity detector: finding heterogeneous positions in Phred/Phrap assemblies.

Auteurs : W H Lee ; V B Vega

Source :

RBID : pubmed:15130927

English descriptors

Abstract

A modification to Phred and program to detect heterogeneous positions, which is particularly useful in the identification of mutations and other abnormalities in Phred/Phrap genome assemblies.

DOI: 10.1093/bioinformatics/bth301
PubMed: 15130927

Links to Exploration step

pubmed:15130927

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Heterogeneity detector: finding heterogeneous positions in Phred/Phrap assemblies.</title>
<author>
<name sortKey="Lee, W H" sort="Lee, W H" uniqKey="Lee W" first="W H" last="Lee">W H Lee</name>
<affiliation>
<nlm:affiliation>Genome Institute of Singapore, Information and Mathematical Sciences, Singapore, 138672, Singapore. leewhc@gis.a-star.edu.sg</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Vega, V B" sort="Vega, V B" uniqKey="Vega V" first="V B" last="Vega">V B Vega</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PubMed</idno>
<date when="2004">2004</date>
<idno type="RBID">pubmed:15130927</idno>
<idno type="pmid">15130927</idno>
<idno type="doi">10.1093/bioinformatics/bth301</idno>
<idno type="wicri:Area/PubMed/Corpus">002E18</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">002E18</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en">Heterogeneity detector: finding heterogeneous positions in Phred/Phrap assemblies.</title>
<author>
<name sortKey="Lee, W H" sort="Lee, W H" uniqKey="Lee W" first="W H" last="Lee">W H Lee</name>
<affiliation>
<nlm:affiliation>Genome Institute of Singapore, Information and Mathematical Sciences, Singapore, 138672, Singapore. leewhc@gis.a-star.edu.sg</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Vega, V B" sort="Vega, V B" uniqKey="Vega V" first="V B" last="Vega">V B Vega</name>
</author>
</analytic>
<series>
<title level="j">Bioinformatics (Oxford, England)</title>
<idno type="ISSN">1367-4803</idno>
<imprint>
<date when="2004" type="published">2004</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Algorithms</term>
<term>Base Pair Mismatch</term>
<term>Consensus Sequence</term>
<term>DNA Mutational Analysis (methods)</term>
<term>Genetic Heterogeneity</term>
<term>SARS Virus (genetics)</term>
<term>Sequence Alignment (methods)</term>
<term>Sequence Analysis, DNA (methods)</term>
<term>Sequence Homology, Nucleic Acid</term>
<term>Software</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>DNA Mutational Analysis</term>
<term>Sequence Alignment</term>
<term>Sequence Analysis, DNA</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Algorithms</term>
<term>Base Pair Mismatch</term>
<term>Consensus Sequence</term>
<term>Genetic Heterogeneity</term>
<term>Sequence Homology, Nucleic Acid</term>
<term>Software</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">A modification to Phred and program to detect heterogeneous positions, which is particularly useful in the identification of mutations and other abnormalities in Phred/Phrap genome assemblies.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">15130927</PMID>
<DateCompleted>
<Year>2005</Year>
<Month>02</Month>
<Day>10</Day>
</DateCompleted>
<DateRevised>
<Year>2019</Year>
<Month>12</Month>
<Day>10</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Print">1367-4803</ISSN>
<JournalIssue CitedMedium="Print">
<Volume>20</Volume>
<Issue>16</Issue>
<PubDate>
<Year>2004</Year>
<Month>Nov</Month>
<Day>01</Day>
</PubDate>
</JournalIssue>
<Title>Bioinformatics (Oxford, England)</Title>
<ISOAbbreviation>Bioinformatics</ISOAbbreviation>
</Journal>
<ArticleTitle>Heterogeneity detector: finding heterogeneous positions in Phred/Phrap assemblies.</ArticleTitle>
<Pagination>
<MedlinePgn>2863-4</MedlinePgn>
</Pagination>
<Abstract>
<AbstractText Label="UNLABELLED">A modification to Phred and program to detect heterogeneous positions, which is particularly useful in the identification of mutations and other abnormalities in Phred/Phrap genome assemblies.</AbstractText>
<AbstractText Label="AVAILABILITY" NlmCategory="BACKGROUND">The package is made available at http://glscompute.gis.a-star.edu.sg/~charlie/DHetero.html</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Lee</LastName>
<ForeName>W H</ForeName>
<Initials>WH</Initials>
<AffiliationInfo>
<Affiliation>Genome Institute of Singapore, Information and Mathematical Sciences, Singapore, 138672, Singapore. leewhc@gis.a-star.edu.sg</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Vega</LastName>
<ForeName>V B</ForeName>
<Initials>VB</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D003160">Comparative Study</PublicationType>
<PublicationType UI="D023362">Evaluation Study</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2004</Year>
<Month>05</Month>
<Day>06</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>England</Country>
<MedlineTA>Bioinformatics</MedlineTA>
<NlmUniqueID>9808944</NlmUniqueID>
<ISSNLinking>1367-4803</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000465" MajorTopicYN="Y">Algorithms</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D020137" MajorTopicYN="N">Base Pair Mismatch</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016384" MajorTopicYN="N">Consensus Sequence</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D004252" MajorTopicYN="N">DNA Mutational Analysis</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018740" MajorTopicYN="Y">Genetic Heterogeneity</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D045473" MajorTopicYN="N">SARS Virus</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016415" MajorTopicYN="N">Sequence Alignment</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D017422" MajorTopicYN="N">Sequence Analysis, DNA</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D012689" MajorTopicYN="N">Sequence Homology, Nucleic Acid</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D012984" MajorTopicYN="Y">Software</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="pubmed">
<Year>2004</Year>
<Month>5</Month>
<Day>8</Day>
<Hour>5</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2005</Year>
<Month>2</Month>
<Day>11</Day>
<Hour>9</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2004</Year>
<Month>5</Month>
<Day>8</Day>
<Hour>5</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">15130927</ArticleId>
<ArticleId IdType="doi">10.1093/bioinformatics/bth301</ArticleId>
<ArticleId IdType="pii">bth301</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/SrasV1/Data/PubMed/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002E18 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd -nk 002E18 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    SrasV1
   |flux=    PubMed
   |étape=   Corpus
   |type=    RBID
   |clé=     pubmed:15130927
   |texte=   Heterogeneity detector: finding heterogeneous positions in Phred/Phrap assemblies.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/RBID.i   -Sk "pubmed:15130927" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd   \
       | NlmPubMed2Wicri -a SrasV1 

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Tue Apr 28 14:49:16 2020. Site generation: Sat Mar 27 22:06:49 2021