FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2168234145> ?p ?o ?g. }

• W2168234145 endingPage "1184" @default.
• W2168234145 startingPage "1175" @default.
• W2168234145 abstract "In considering the best possible solutions for answering phylogenetic questions from genomic sequences, we have chosen a strategy that we suggest is superior to others that have gone previously. We have ignored multigene families and instead have used single-gene families. This minimizes the inadvertent analysis of paralogs. We have employed strict data controls and have reasoned that if a protein is not capable of recovering the uncontroversial parts of a phylogenetic tree, then why should we use it for the more controversial parts? We have sliced and diced the data in as many ways as possible in order to uncover the signals in that data. Using this strategy, we have tested two controversial hypotheses concerning eukaryotic phylogenetic relationships: the placement of arthropoda and nematodes and the relationships of animals, plants, and fungi. We have constructed phylogenetic trees from 780 single-gene families from 10 completed genomes and amalgamated these into a single supertree. We have also carried out a total evidence analysis on the only universally distributed protein families that can accurately reconstruct the uncontroversial parts of the phylogenetic tree: a total of five families. In doing so, we ignore the majority of single-gene families that are universally distributed as they do not have the appropriate signals to recover the uncontroversial parts of the tree. We have also ignored every protein that has ever been used previously to address this issue, simply because none of them meet our strict criteria. Using these data controls, site stripping, and multiple analyses, 24 out of 26 analyses strongly support the grouping of vertebrates with arthropods (Coelomata hypothesis) and plants with animals. In the other two analyses, the data were ambivalent. The latter finding overturns an 11-year theory of Eukaryotic evolution; the first confirms what has already been said by others. In the light of this new tree, we re-analyze the evolution of intron gain and loss in the rpL14 gene and find that it is much more compatible with the hypothesis presented here than with the Opisthokonta hypothesis." @default.
• W2168234145 created "2016-06-24" @default.
• W2168234145 creator A5013249079 @default.
• W2168234145 creator A5037761875 @default.
• W2168234145 creator A5061955804 @default.
• W2168234145 date "2005-02-09" @default.
• W2168234145 modified "2023-10-12" @default.
• W2168234145 title "The Opisthokonta and the Ecdysozoa May Not Be Clades: Stronger Support for the Grouping of Plant and Animal than for Animal and Fungi and Stronger Support for the Coelomata than Ecdysozoa" @default.
• W2168234145 cites W1553872548 @default.
• W2168234145 cites W1577837202 @default.
• W2168234145 cites W1582956895 @default.
• W2168234145 cites W1975060999 @default.
• W2168234145 cites W1985970813 @default.
• W2168234145 cites W1988608815 @default.
• W2168234145 cites W1991049526 @default.
• W2168234145 cites W1992800126 @default.
• W2168234145 cites W1999681000 @default.
• W2168234145 cites W2000818024 @default.
• W2168234145 cites W2003281178 @default.
• W2168234145 cites W2010879590 @default.
• W2168234145 cites W2017519756 @default.
• W2168234145 cites W2029482176 @default.
• W2168234145 cites W2030966943 @default.
• W2168234145 cites W2032559209 @default.
• W2168234145 cites W2039191677 @default.
• W2168234145 cites W2040438092 @default.
• W2168234145 cites W2055465755 @default.
• W2168234145 cites W2059383371 @default.
• W2168234145 cites W2060665252 @default.
• W2168234145 cites W2065664697 @default.
• W2168234145 cites W2068225247 @default.
• W2168234145 cites W2082096918 @default.
• W2168234145 cites W2082801059 @default.
• W2168234145 cites W2084653357 @default.
• W2168234145 cites W2091714047 @default.
• W2168234145 cites W2105462635 @default.
• W2168234145 cites W2106882534 @default.
• W2168234145 cites W2107190860 @default.
• W2168234145 cites W2115641289 @default.
• W2168234145 cites W2121317739 @default.
• W2168234145 cites W2123172705 @default.
• W2168234145 cites W2128919173 @default.
• W2168234145 cites W2131484804 @default.
• W2168234145 cites W2134057866 @default.
• W2168234145 cites W2137464835 @default.
• W2168234145 cites W2145913429 @default.
• W2168234145 cites W2158133863 @default.
• W2168234145 cites W2158714788 @default.
• W2168234145 cites W2159718078 @default.
• W2168234145 cites W2161444534 @default.
• W2168234145 cites W2162160001 @default.
• W2168234145 cites W2166126882 @default.
• W2168234145 cites W2170991287 @default.
• W2168234145 cites W2170996473 @default.
• W2168234145 cites W2171516003 @default.
• W2168234145 cites W2583187415 @default.
• W2168234145 doi "https://doi.org/10.1093/molbev/msi102" @default.
• W2168234145 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15703245" @default.
• W2168234145 hasPublicationYear "2005" @default.
• W2168234145 type Work @default.
• W2168234145 sameAs 2168234145 @default.
• W2168234145 citedByCount "170" @default.
• W2168234145 countsByYear W21682341452012 @default.
• W2168234145 countsByYear W21682341452013 @default.
• W2168234145 countsByYear W21682341452014 @default.
• W2168234145 countsByYear W21682341452015 @default.
• W2168234145 countsByYear W21682341452016 @default.
• W2168234145 countsByYear W21682341452017 @default.
• W2168234145 countsByYear W21682341452018 @default.
• W2168234145 countsByYear W21682341452019 @default.
• W2168234145 countsByYear W21682341452021 @default.
• W2168234145 crossrefType "journal-article" @default.
• W2168234145 hasAuthorship W2168234145A5013249079 @default.
• W2168234145 hasAuthorship W2168234145A5037761875 @default.
• W2168234145 hasAuthorship W2168234145A5061955804 @default.
• W2168234145 hasBestOaLocation W21682341451 @default.
• W2168234145 hasConcept C104317684 @default.
• W2168234145 hasConcept C113174947 @default.
• W2168234145 hasConcept C124388736 @default.
• W2168234145 hasConcept C134306372 @default.
• W2168234145 hasConcept C141231307 @default.
• W2168234145 hasConcept C193252679 @default.
• W2168234145 hasConcept C26619641 @default.
• W2168234145 hasConcept C33923547 @default.
• W2168234145 hasConcept C44465124 @default.
• W2168234145 hasConcept C54355233 @default.
• W2168234145 hasConcept C55919133 @default.
• W2168234145 hasConcept C70343354 @default.
• W2168234145 hasConcept C78458016 @default.
• W2168234145 hasConcept C86803240 @default.
• W2168234145 hasConcept C90132467 @default.
• W2168234145 hasConceptScore W2168234145C104317684 @default.
• W2168234145 hasConceptScore W2168234145C113174947 @default.
• W2168234145 hasConceptScore W2168234145C124388736 @default.
• W2168234145 hasConceptScore W2168234145C134306372 @default.
• W2168234145 hasConceptScore W2168234145C141231307 @default.
• W2168234145 hasConceptScore W2168234145C193252679 @default.
• W2168234145 hasConceptScore W2168234145C26619641 @default.

• next