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From phylogenetics to phylogenomics: the evolutionary relationships of insect endosymbiotic gamma-Proteobacteria as a test case. Syst Biol (2007)

by I Comas, A Moya, F Gonzalez-Candelas
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Gabaldón T: PhylomeDB: a database for genome-wide collections of gene phylogenies

by Jaime Huerta-cepas, Anibal Bueno, Joaquín Dopazo, Toni Gabaldón - Nucleic Acids Res
"... gene phylogenies ..."
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gene phylogenies
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...ons, the availability of complete phylomes can be exploited to map duplication and speciation events and thus infer orthology relationships (3), to determine the evolutionary relationships among taxa =-=(4)-=- and even to reconstruct ancestral metabolisms (5). Although some databases provide automatically derived and curated phylogenies (6–9), these follow a family-based approach, since they first group th...

Optimal Data Partitioning and a Test Case for RayFinned Fishes (Actinopterygii) Based on Ten Nuclear Loci' Syst Biol 57(4

by Chenhong Li, Guoqing Lu, Guillermo Orti, Genomics Commons, Chenhong Li, Guoqing Lu , 2008
"... This Article is brought to you for free and open access by the Department of Biology at ..."
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This Article is brought to you for free and open access by the Department of Biology at
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...etic loci often result in well-resolved and highly supported phylogenetic hypotheses (e.g., Rokas et al., 2003a, 2003b, 2005; Philippe et al., 2005; McMahon and Sanderson, 2006; Baurain et al., 2007; =-=Comas et al., 2007-=-). In spite of this success and initial optimism about the phylogenomic approach (Gee, 2003; Rokas et al., 2003b), large and complex data sets also exacerbate many unresolved methodological challenges...

A GENOME-SCALE APPROACH TO PHYLOGENY OF RAY- FINNED FISH (ACTINOPTERYGII) AND MOLECULAR SYSTEMATICS OF CLUPEIFORMES

by Systematics Of Clupeiformes, Chenhong Li, Chenhong Li, Ph. D, Chenhong Li , 2007
"... Part of the Life Sciences Commons This Article is brought to you for free and open access by the Biological Sciences, School of at DigitalCommons@University of Nebraska- Lincoln. It has been accepted for inclusion in Dissertations and Theses in Biological Sciences by an authorized administrator of D ..."
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Part of the Life Sciences Commons This Article is brought to you for free and open access by the Biological Sciences, School of at DigitalCommons@University of Nebraska- Lincoln. It has been accepted for inclusion in Dissertations and Theses in Biological Sciences by an authorized administrator of DigitalCommons@University of Nebraska- Lincoln. Li, Chenhong, "A Genome-scale Approach to Phylogeny of Ray-finned Fish (Actinopterygii) and Molecular Systematics of
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...ygians andsthe non-monophyly of perciforms.s32s3.2. BackgroundsIn the light of genomic era, phylogenetic studies using multilocus sequence datasbecome increasingly popular (e.g. Baurain et al., 2007; =-=Comas et al., 2007-=-; McMahonsand Sanderson, 2006; Rokas et al., 2005; Rokas et al., 2003b). The large number ofscharacters and the independent phylogenetic evidences from the multilocus data oftensresulted in well-resol...

RESEARCH ARTICLE Reconstructing genome trees of prokaryotes using overlapping genes

by Chih-hsien Cheng, Chung-han Yang, Hsien-tai Chiu, Chin Lung Lu
"... Background: Overlapping genes (OGs) are defined as adjacent genes whose coding sequences overlap partially or entirely. In fact, they are ubiquitous in microbial genomes and more conserved between species than nonoverlapping genes. Based on this property, we have previously implemented a web server, ..."
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Background: Overlapping genes (OGs) are defined as adjacent genes whose coding sequences overlap partially or entirely. In fact, they are ubiquitous in microbial genomes and more conserved between species than nonoverlapping genes. Based on this property, we have previously implemented a web server, named OGtree, that allows the user to reconstruct genome trees of some prokaryotes according to their pairwise OG distances. By analogy to the analyses of gene content and gene order, the OG distance between two genomes we defined was based on a measure of combining OG content (i.e., the normalized number of shared orthologous OG pairs) and OG order (i.e., the normalized OG breakpoint distance) in their whole genomes. A shortcoming of using the concept of breakpoints to define the OG distance is its inability to analyze the OG distance of multi-chromosomal genomes. In addition, the amount of overlapping coding sequences between some distantly related prokaryotic genomes may be limited so that it is hard to find enough OGs to properly evaluate their pairwise OG distances. Results: In this study, we therefore define a new OG order distance that is based on more biologically accurate rearrangements (e.g., reversals, transpositions and translocations) rather than breakpoints and that is applicable to both uni-chromosomal and multi-chromosomal genomes. In addition, we expand the term “gene ” to include both its coding sequence and regulatory regions so that two adjacent genes whose coding sequences or regulatory
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...21 genomes of Proteobacteria, which consist of one a-Proteobacteria, three b-Proteobacteria and 17 g-Proteobacteria, as the testing dataset (Table 1). This dataset was previously used by Comas et al. =-=[21]-=- for their phylogenomic study on the monophyletic origin of insect endosymbionts from theCheng et al. BMC Bioinformatics 2010, 11:102 http://www.biomedcentral.com/1471-2105/11/102 Page 3 of 11 Table ...

Statistics and Truth in Phylogenomics

by Sudhir Kumar, Alan J. Filipski, Fabia U. Battistuzzi, Sergei L. Kosakovsky Pond, Koichiro Tamura
"... Phylogenomics refers to the inference of historical relationships among species using genome-scale sequence data and to the use of phylogenetic analysis to infer protein function in multigene families. With rapidly decreasing sequencing costs, phylogenomics is becoming synonymous with evolutionary a ..."
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Phylogenomics refers to the inference of historical relationships among species using genome-scale sequence data and to the use of phylogenetic analysis to infer protein function in multigene families. With rapidly decreasing sequencing costs, phylogenomics is becoming synonymous with evolutionary analysis of genome-scale and taxonomically densely sampled data sets. In phylogenetic inference applications,thistranslatesintoverylargedatasets that yield evolutionary and functional inferences with extremely small variances and high statistical confidence (P value). However, reports of highly significant P values are increasing even for contrasting phylogenetic hypotheses depending on the evolutionary model and inference method used, making it difficult to establish true relationships. We argue that the assessment of the robustness of results to biological factors, that may systematically mislead (bias) the outcomes of statistical estimation, will be a key to avoiding incorrect phylogenomic inferences. In fact, there is a need for increased emphasis on the magnitude of differences (effect sizes) in addition to the P values of the statistical test of the null hypothesis. On the other hand, the amount of sequence data available will likely always remain inadequate for some phylogenomic applications, for example, those involving episodic positive selection at individual codon positions and in specific lineages. Again, a focus on effect size and biological relevance, rather than the P value, may be warranted. Here, we present a theoretical overview and discuss practical aspects of the interplay between effect sizes, bias, and P values as it relates to the statistical inference of evolutionary truth in phylogenomics. Key words: molecular evolution, statistical inference, phylogenetics, evolutionary tree, statistical bias, variance.
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...a. The problem then becomes how to tell whether alternative phylogenies that are detected from these reduced data sets reflect actual gene histories or simply artifact and bias (Bapteste et al. 2005; =-=Comas et al. 2007-=-; Ané 2011; Blair and Murphy 2011). With 466 horizontally transferred genes estimated to be up to 60% of a genome depending on the species included in the analyses and the methods used to identify the...

BMC Evolutionary Biology BioMed Central

by Santiago Castillo-ramírez, Víctor González
"... ..."
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...the rest of the families [5]. More recently, it was found that only three out of 200 orthologous genes manifested the topology of the species tree, while 29% of the data set rejected the species tree =-=[11]-=-. In the case of Alphaproteobacteria, around 77% of the gene trees inferred from SGF manifested no significant differences with the proposed supertree, which was inferred from all the gene trees, and ...

RESEARCH ARTICLE Open Access

by unknown authors
"... Multiple origins of endosymbiosis within the ..."
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Multiple origins of endosymbiosis within the
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...ed to overcome these difficulties (Additional file 1). They are based mainly on the concatenation of a large number of genes through the whole genome [37-39], the supertree and the consensus approach =-=[37]-=-, exclusion of amino acids (FYMINK: phenylalanine, tyrosine, methionine, isoleucine, asparagine and lysine) most affected by nucleotide bias [37], modifications of sequence evolution models [11,12,36,...

unknown title

by Jaime Huerta-cepas, Salvador Capella-gutierrez, Leszek P. Pryszcz, Ivan Denisov , 2010
"... PhylomeDB v3.0: an expanding repository of genome-wide collections of trees, alignments and phylogeny-based orthology and paralogy predictions ..."
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PhylomeDB v3.0: an expanding repository of genome-wide collections of trees, alignments and phylogeny-based orthology and paralogy predictions
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...analysis of phylomes has proven to be very powerful in addressing a variety of questions, including the reconstruction of ancestral metabolisms (12), the evaluation of alternative species phylogenies =-=(13,14)-=-, the identification of horizontal gene transfers (15), the inference of functional implications of massive waves of gene duplications (6,16) and the detection of orthology and paralogy relationships ...

Animal evolution

by unknown authors
"... nt a c ..."
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...logical solution since at least 8000 randomly selected characters are required to obtain reasonable support for ancient diversifications (Rokas et al., 2003b). Ows and Evolution 67 (2013) 223–233 229(=-=Comas et al., 2007-=-; Swofford, 1991). In this study, we used the partitioning of a large alignment to test the effect of gene sampling on the higher-level metazoan eticphylogeny and assess the validity of the random-gen...

A Consistent Phylogenetic Backbone for the Fungi

by Kerstin Voigt, Arndt Von Haeseler, Associate Andrew Roger
"... The kingdom of fungi provides model organisms for biotechnology, cell biology, genetics, and life sciences in general. Only when their phylogenetic relationships are stably resolved, can individual results from fungal research be integrated into a holistic picture of biology. However, and despite re ..."
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The kingdom of fungi provides model organisms for biotechnology, cell biology, genetics, and life sciences in general. Only when their phylogenetic relationships are stably resolved, can individual results from fungal research be integrated into a holistic picture of biology. However, and despite recent progress, many deep relationships within the fungi remain unclear. Here, we present the first phylogenomic study of an entire eukaryotic kingdom that uses a consistency criterion to strengthen phylogenetic conclusions. We reason that branches (splits) recovered with independent data and different tree reconstruction methods are likely to reflect true evolutionary relationships. Two complementary phylogenomic data sets based on 99 fungal genomes and 109 fungal expressed sequence tag (EST) sets analyzed with four different tree reconstruction methods shed light from different angles on the fungal tree of life. Eleven additional data sets address specifically the phylogenetic position of Blastocladiomycota, Ustilaginomycotina, and Dothideomycetes, respectively. The combined evidence from the resulting trees supports the deep-level stability of the fungal groups toward a comprehensive natural system of the fungi. In addition, our analysis reveals methodologically interesting aspects. Enrichment for EST encoded data—a common practice in phylogenomic analyses—introduces a strong bias toward slowly evolving and functionally correlated genes. Consequently, the generalization of phylogenomic data sets as collections of randomly
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....g., Jeffroy et al. 2006). Phylogenomic analyses (Delsuc et al. 2005; Telford 2007) use the phylogenetic signal integrated over many genes as a proxy for the species phylogeny (Gatesy and Baker 2005; =-=Comas et al. 2007-=-). It is hoped that this approach reduces the influence of gene-specific signals (noise) and accentuates the phylogenetic signal generated by the evolutionary relationships of the species. Correspondi...

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