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Nematode small subunit phylogeny correlates with alignment parameters. Systematic Biology 55 (2006)

by A B Smythe, M J Sanderson, S A Nadler
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Parsimony and Model-Based Analyses of Indels in Avian Nuclear Genes Reveal Congruent and Incongruent Phylogenetic Signals

by Tamaki Yuri, Rebecca T. Kimball, John Harshman, Rauri C. K. Bowie, Michael J. Braun, Jena L. Chojnowski, Kin-lan Han, Shannon J. Hackett, Christopher J. Huddleston, William S. Moore, Sushma Reddy, Frederick H. Sheldon, David W. Steadman, Christopher C. Witt, Edward L. Braun , 2013
"... biology ..."
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Guidelines for Authors

by Presentation Of Articles, Hermes Science Publications
"... This document comprising guidelines for authors, is divided into three sections. The editor kindly requests that authors respect these guidelines. This abstract should be no longer than ten lines. An abstract in French should also be given. Both are written in Times New Roman 9pt on 11pt, italic, wi ..."
Abstract - Cited by 1 (0 self) - Add to MetaCart
This document comprising guidelines for authors, is divided into three sections. The editor kindly requests that authors respect these guidelines. This abstract should be no longer than ten lines. An abstract in French should also be given. Both are written in Times New Roman 9pt on 11pt, italic, with a space of 3pt in between each subsection. RSUM: L'ensemble des consignes rassembles ci-dessous s'organise en trois rubriques. La rdaction remercie les auteurs pour le strict respect qu'ils accorderont ces dispositions. La taille de ce rsum ne doit pas dpasser une dizaine de lignes. Il est composer en Times corps 9 italique, interlign 11 points. Un rsum en anglais doit l'accompagner. KEY WORDS: a maximum of six significant words should be chosen in English and in French and presented as key words MOTS-CLS: un maximum de six mots significatifs, en franais et en anglais, doivent tre isols sous forme de mots-cls 122 Title of journal. Volume X -- No. X/2000 1.
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...hylogenetic tree inference was given special attention, because different approaches to constructing and using multiple alignments have been shown to have substantial effects on nematode phylogenies (=-=Smythe et al. 2006-=-). The resulting molecular phylogenetic hypotheses are compared with classical proposals of relationships and previously published hypotheses based on molecular data. MATERIALS AND METHODS PCR and seq...

Class Enoplea Inglis 1983 (3 subclasses) 8 Subclass Enoplia Pearse 1942 (2 superorders) Superorder Enoplica Hodda 2007 (5 orders) 9

by Order Enoplida Filipjev Suborder, Suborder Enoplina Chitwood, Chitwood Superfamilies
"... Recent Nematoda includes 3 classes, 31 orders, 267 families, 2829 genera and 24,783 species, with fossil taxa represented in 2 genera by 10 species. There are 7 genera and 7 species known only as fossils. 2. Rudolphi (1808) is most often cited as the author of the accepted name of the phylum, which ..."
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Recent Nematoda includes 3 classes, 31 orders, 267 families, 2829 genera and 24,783 species, with fossil taxa represented in 2 genera by 10 species. There are 7 genera and 7 species known only as fossils. 2. Rudolphi (1808) is most often cited as the author of the accepted name of the phylum, which is Nematoda. The first holophyletic diagnosis at Phylum rank used the name "Nemates " (Cobb 1932). The latter name has never been in wide use, and the competing claims of the two names have been discussed extensively (Chitwood 1957, 1958, Dougherty 1958a, 1958b). Following the principle outlined below, Cobb (1932) is cited as authority because his use is specifically as a phylum. 3. The evolutionary affinities of Nematoda have long been controversial (see discussion in Hodda 2007). The most recent molecular evidence has favoured affinities first with Nematomorpha, then with decreasing relationships to Kinorhyncha, Priapulida and Loricifera within a superphylum Ecdysozoa (Aguinaldo et al. 1997, Dunn et al. 2008). However, significant unresolved differences between phylogenies hypothesised using different taxa, assumptions, methods and lines of evidence remain. 4. Unless indicated otherwise, the classification follows Hodda (2007). The higher classification of the phylum has been interpreted in many ways, with consequent changes in the hierarchical level of many names (Hodda 2007). Above the level of the genus nematode classification has been—and continues to be—volatile. Particularly, analyses of accumulating molecular data have produced only broadly similar phylogenies,
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...ps remains dependent on the genes and taxa selected as well as the methods of alignment and analysis (De Ley & Blaxter 2004, Hodda 2007, Holterman et al. 2006, Meldal et al. 2007, Nadler et al. 2007, =-=Smythe et al. 2006-=-, Van Megen et al. 2009). The present classification continues the tradition of regarding branch points in nematode phylogeny that are ambiguous, unsupported or differ between studies as polytomies (H...

Article Parsimony and Model-Based Analyses of Indels in Avian Nuclear Genes Reveal Congruent and Incongruent Phylogenetic Signals

by Tamaki Yuri, Rebecca T. Kimball, John Harshman, Rauri C. K. Bowie, Michael J. Braun, Jena L. Chojnowski, Kin-lan Han, Shannon J. Hackett, Christopher J. Huddleston, William S. Moore, Sushma Reddy, Frederick H. Sheldon, David W. Steadman, Christopher C. Witt, Edward L. Braun , 2013
"... biology ..."
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DO1:10.1080/10635150701618527 Molecular Phylogenetics of the Lizard Genus Microlophus (SquamataiTropiduridae): Aligning and Retrieving Indel Signal from Nuclear Introns

by Edgar Benavides, Rebecca Baum, David Mcclellan, Jack W. Sites
"... Abstract. — We use a multigene data set (the mitochondrial locus and nine nuclear gene regions) to test phylogenetic relation-ships in the South American "lava lizards " (genus Microlophus) and describe a strategy for aligning noncoding sequences that accounts for differences in tempo and ..."
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Abstract. — We use a multigene data set (the mitochondrial locus and nine nuclear gene regions) to test phylogenetic relation-ships in the South American "lava lizards " (genus Microlophus) and describe a strategy for aligning noncoding sequences that accounts for differences in tempo and class of mutational events. We focus on seven nuclear introns that vary in size and frequency of multibase length mutations (i.e., indels) and present a manual alignment strategy that incorporates insertions and deletions (indels) for each intron. Our method is based on mechanistic explanations of intron evolution that does not require a guide tree. We also use a progressive alignment algorithm (Probabilistic Alignment Kit; PRANK) and distinguishes insertions from deletions and avoids the "gapcost " conundrum. We describe an approach to selecting a guide tree purged of ambiguously aligned regions and use this to refine PRANK performance. We show that although manual alignment is successful in finding repeat motifs and the most obvious indels, some regions can only be subjectively aligned, and there are limits to the size and complexity of a data matrix for which this approach can be taken. PRANK alignments identified more parsimony-informative indels while simultaneously increasing nucleotide identity in conserved sequence blocks flanking the indel regions. When comparing manual and PRANK with two widely used methods (CLUSTAL, MUSCLE) for the alignment of the most length-variable intron, only PRANK recovered a tree congruent at deeper nodes with the combined data tree inferred from all nuclear gene regions. We take this concordance as an objective function of alignment quality and present a strongly supported phylogenetic hypothesis for Microlophus relationships. From this hypothesis we show that
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...mbined data tree (hereinafter the "combined" tree; see below). Our goal is not to provide an intensively "bench-marked" baseline on optimal alignment parameters (see instead, Terry and Whiting, 2005; =-=Smythe et al., 2007-=-), but rather to qualitatively evaluate tree topology and nodal support in the manual and PRANK-aligned sequences. We chose the Cryba intron because its sequence complexity features: (1) "orphan" sequ...

Documentation

by Christian Arnold, Luke Matthews, Charles Nunn
"... 2 This document provides additional information for the 10kTrees Project. If you have questions or comments, feel free to contact me, Christian Arnold (carnold@fas.harvard.edu). I will be happy to answer any questions related to this project as well as questions related to the web-implementation. ..."
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2 This document provides additional information for the 10kTrees Project. If you have questions or comments, feel free to contact me, Christian Arnold (carnold@fas.harvard.edu). I will be happy to answer any questions related to this project as well as questions related to the web-implementation.
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...g -distance1 kmer20_4). As it has been repeatedly demonstrated thatsalignment quality may have a substantial impact on the inferred tree (Kjer 1995; Morrison andsEllis 1997; Ogden and Rosenberg 2006; =-=Smythe et al. 2006-=-; Talavera and Castresana 2007), weseliminated poorly aligned positions and divergent regions of the alignment using the programsGblocks (Castresana 2002) with the settings -b5=h, -t=d, and -b2=0.6 * ...

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