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dc.contributor.authorSanchez-Garcia, Marisol
dc.contributor.authorJumpponen, Ari
dc.contributor.authorAmend, Anthony S.
dc.contributor.authorde Sousa, Filipe
dc.contributor.authorEbersberger, Ingo
dc.contributor.authorDe Wit, Pierre
dc.contributor.authorNilsson, R. Henrik
dc.contributor.authorBengtsson-Palme, Johan
dc.contributor.authorRyberg, Martin
dc.contributor.authorHartmann, Martin
dc.contributor.authorBranco, Sara
dc.contributor.authorWang, Zheng
dc.contributor.authorGodhe, Anna
dc.contributor.authorVeldre, Vilmar
dc.contributor.authorVik, Unni
dc.contributor.authorEriksson, K. Martin
dc.contributor.authorSanli, Kemal
dc.contributor.authorBertrand, Yann J. K.
dc.contributor.authorAbarenkov, Kessy
dc.contributor.authorKristiansson, Erik
dc.contributor.authorUnterseher, Martin
dc.date.accessioned2021-12-10T09:50:49Z
dc.date.available2021-12-10T09:50:49Z
dc.date.issued2013
dc.identifier.citationBengtsson-Palme J., Ryberg M., Hartmann M., Branco S., Wang Z., Godhe A., De Wit P., Sanchez-Garcia M., Ebersberger I., de Sousa F., et al., "Improved software detection and extraction of ITS1 and ITS2 from ribosomal ITS sequences of fungi and other eukaryotes for analysis of environmental sequencing data", METHODS IN ECOLOGY AND EVOLUTION, cilt.4, sa.10, ss.914-919, 2013
dc.identifier.issn2041-210X
dc.identifier.othervv_1032021
dc.identifier.otherav_1682c30d-9338-4670-8f9e-4303e3595486
dc.identifier.urihttp://hdl.handle.net/20.500.12627/168605
dc.identifier.urihttps://doi.org/10.1111/2041-210x.12073
dc.identifier.urihttps://avesis.istanbul.edu.tr/api/publication/1682c30d-9338-4670-8f9e-4303e3595486/file
dc.description.abstractThe nuclear ribosomal internal transcribed spacer (ITS) region is the primary choice for molecular identification of fungi. Its two highly variable spacers (ITS1 and ITS2) are usually species specific, whereas the intercalary 5.8S gene is highly conserved. For sequence clustering and blast searches, it is often advantageous to rely on either one of the variable spacers but not the conserved 5.8S gene. To identify and extract ITS1 and ITS2 from large taxonomic and environmental data sets is, however, often difficult, and many ITS sequences are incorrectly delimited in the public sequence databases.
dc.language.isoeng
dc.subjectMühendislik ve Teknoloji
dc.subjectEcology
dc.subjectEcology, Evolution, Behavior and Systematics
dc.subjectEKOLOJİ
dc.subjectÇevre / Ekoloji
dc.subjectTarım ve Çevre Bilimleri (AGE)
dc.subjectTarımsal Bilimler
dc.subjectÇevre Mühendisliği
dc.subjectÇevre Teknolojisi
dc.subjectEkoloji ve Kirlenme
dc.subjectLife Sciences
dc.subjectPhysical Sciences
dc.subjectEcological Modeling
dc.titleImproved software detection and extraction of ITS1 and ITS2 from ribosomal ITS sequences of fungi and other eukaryotes for analysis of environmental sequencing data
dc.typeMakale
dc.relation.journalMETHODS IN ECOLOGY AND EVOLUTION
dc.contributor.departmentUniversity Of Leeds , ,
dc.identifier.volume4
dc.identifier.issue10
dc.identifier.startpage914
dc.identifier.endpage919
dc.contributor.firstauthorID2685974


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