mdh.sePublikasjoner
Endre søk
RefereraExporteraLink to record
Permanent link

Direct link
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
Automated recognition of retroviral sequences in genomic data - RetroTector©
Department of Neuroscience, Physiology, Uppsala University, Uppsala, Sweden.
Mälardalens högskola. Section of Virology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
Section of Virology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
Section of Virology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
2007 (engelsk)Inngår i: Nucleic Acids Research, ISSN 0305-1048, E-ISSN 1362-4962, Vol. 35, nr 15, s. 4964-4976Artikkel i tidsskrift (Fagfellevurdert) Published
Resurstyp
Text
Abstract [en]

Eukaryotic genomes contain many endogenous retroviral sequences (ERVs). ERVs are often severely mutated, therefore difficult to detect. A platform independent (Java) program package, RetroTector© (ReTe), was constructed. It has three basic modules: (i) detection of candidate long terminal repeats (LTRs), (ii) detection of chains of conserved retroviral motifs fulfilling distance constraints and (iii) attempted reconstruction of original retroviral protein sequences, combining alignment, codon statistics and properties of protein ends. Other features are prediction of additional open reading frames, automated database collection, graphical presentation and automatic classification. ReTe favors elements >1000-bp long due to its dependence on order of and distances between retroviral fragments. It detects single or low-copy-number elements. ReTe assigned a 'retroviral' score of 890-2827 to 10 exogenous retroviruses from seven genera, and accurately predicted their genes. In a simulated model, ReTe was robust against mutational decay. The human genome was analyzed in 1-2 days on a LINUX cluster. Retroviral sequences were detected in divergent vertebrate genomes. Most ReTe detected chains were coincident with Repeatmasker output and the HERVd database. ReTe did not report most of the volutionary old HERV-L related and MalR sequences, and is not yet tailored for single LTR detection. Nevertheless, ReTe rationally detects and annotates many retroviral sequences.

sted, utgiver, år, opplag, sider
2007. Vol. 35, nr 15, s. 4964-4976
Emneord [en]
amino acid sequence, article, automated pattern recognition, computer program, data base, endogenous retrovirus, gene cluster, genetic analysis, genetic code, genetic screening, long terminal repeat, nonhuman, nucleotide sequence, priority journal, protein motif, sensitivity and specificity, sequence analysis, viral genetics, Algorithms, Animals, Endogenous Retroviruses, Genome, Human, Genomics, Humans, Mutation, Reproducibility of Results, Retroviridae Proteins, Software, Terminal Repeat Sequences, Eukaryota
HSV kategori
Identifikatorer
URN: urn:nbn:se:mdh:diva-31744DOI: 10.1093/nar/gkm515ISI: 000249612300004Scopus ID: 2-s2.0-34548590461OAI: oai:DiVA.org:mdh-31744DiVA, id: diva2:933736
Tilgjengelig fra: 2016-06-07 Laget: 2016-06-07 Sist oppdatert: 2017-11-30bibliografisk kontrollert

Open Access i DiVA

Fulltekst mangler i DiVA

Andre lenker

Forlagets fulltekstScopus
Av organisasjonen
I samme tidsskrift
Nucleic Acids Research

Søk utenfor DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric

doi
urn-nbn
Totalt: 16 treff
RefereraExporteraLink to record
Permanent link

Direct link
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf