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dc.date.accessioned2018-01-02T15:00:07Z
dc.date.available2018-01-02T15:00:07Z
dc.date.created2016-09-26T19:17:38Z
dc.date.issued2016
dc.identifier.citationKocot, Kevin M. Struck, Torsten H Merkel, Julia Waits, Damien S. Todt, Christiane Bannock, Pamela M. Weese, David A. Cannon, Johanna T. Moroz, Leonid L. Lieb, Bernhard Halanych, Kenneth M. . Phylogenomics of Lophotrochozoa with consideration of systematic error. Systematic Biology. 2016, 66(2), 256-282
dc.identifier.urihttp://hdl.handle.net/10852/59477
dc.description.abstractAbstract.—Phylogenomic studies have improved understanding of deep metazoan phylogeny and show promise for resolving incongruences among analyses based on limited numbers of loci. One region of the animal tree that has been especially difficult to resolve, even with phylogenomic approaches, is relationships within Lophotrochozoa (the animal clade that includes molluscs, annelids, and flatworms among others). Lack of resolution in phylogenomic analyses could be due to insufficient phylogenetic signal, limitations in taxon and/or gene sampling, or systematic error. Here, we investigated why lophotrochozoan phylogeny has been such a difficult question to answer by identifying and reducing sources of systematic error. We supplemented existing data with 32 new transcriptomes spanning the diversity of Lophotrochozoa and constructed a new set of Lophotrochozoa-specific core orthologs. Of these, 638 orthologous groups (OGs) passed strict screening for paralogy using a tree-based approach. In order to reduce possible sources of systematic error, we calculated branch-length heterogeneity, evolutionary rate, percent missing data, compositional bias, and saturation for each OG and analyzed increasingly stricter subsets of only the most stringent (best) OGs for these five variables. Principal component analysis of the values for each factor examined for each OG revealed that compositional heterogeneity and average patristic distance contributed most to the variance observed along the first principal component while branch-length heterogeneity and, to a lesser extent, saturation contributed most to the variance observed along the second. Missing data did not strongly contribute to either. Additional sensitivity analyses examined effects of removing taxa with heterogeneous branch lengths, large amounts of missing data, and compositional heterogeneity. Although our analyses do not unambiguously resolve lophotrochozoan phylogeny, we advance the field by reducing the list of viable hypotheses. Moreover, our systematic approach for dissection of phylogenomic data can be applied to explore sources of incongruence and poor support in any phylogenomic data set. The final version of this research has been published in Systemic Biology. © 2016 Oxford University Pressen_US
dc.languageEN
dc.titlePhylogenomics of Lophotrochozoa with consideration of systematic erroren_US
dc.typeJournal articleen_US
dc.creator.authorKocot, Kevin M.
dc.creator.authorStruck, Torsten H
dc.creator.authorMerkel, Julia
dc.creator.authorWaits, Damien S.
dc.creator.authorTodt, Christiane
dc.creator.authorBannock, Pamela M.
dc.creator.authorWeese, David A.
dc.creator.authorCannon, Johanna T.
dc.creator.authorMoroz, Leonid L.
dc.creator.authorLieb, Bernhard
dc.creator.authorHalanych, Kenneth M.
cristin.unitcode185,28,8,0
cristin.unitnameSeksjon for forskning og samlinger
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2
dc.identifier.cristin1385891
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Systematic Biology&rft.volume=66&rft.spage=256&rft.date=2016
dc.identifier.jtitleSystematic Biology
dc.identifier.volume66
dc.identifier.issue2
dc.identifier.startpage256
dc.identifier.endpage282
dc.identifier.doihttp://dx.doi.org/10.1093/sysbio/syw079
dc.identifier.urnURN:NBN:no-62128
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1063-5157
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/59477/2/Kocot_SystBiol2016_inPress.pdf
dc.type.versionAcceptedVersion


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