| scholarly article | Q13442814 |
| P2093 | author name string | Graybeal A | |
| P433 | issue | 1 | |
| P921 | main subject | phylogenetics | Q171184 |
| P304 | page(s) | 9-17 | |
| P577 | publication date | 1998-03-01 | |
| P1433 | published in | Systematic Biology | Q7663761 |
| P1476 | title | Is it better to add taxa or characters to a difficult phylogenetic problem? | |
| P478 | volume | 47 |
| Q28741438 | 43 genes support the lungfish-coelacanth grouping related to the closest living relative of tetrapods with the Bayesian method under the coalescence model |
| Q34497199 | A comprehensive phylogeny of birds (Aves) using targeted next-generation DNA sequencing |
| Q55129585 | A congruent phylogenomic signal places eukaryotes within the Archaea. |
| Q57267411 | A contribution to sedentary polychaete phylogeny using 18S rRNA sequence data |
| Q34137153 | A molecular phylogeny of anseriformes based on mitochondrial DNA analysis |
| Q54046568 | A new look at the phylogeny of coelurosauria (Dlnosauria: Theropoda) |
| Q43295689 | A new subfamilial and tribal classification of the pantropical flowering plant family Annonaceae informed by molecular phylogenetics |
| Q34596401 | A nuclear phylogeny of the Florideophyceae (Rhodophyta) inferred from combined EF2, small subunit and large subunit ribosomal DNA: establishing the new red algal subclass Corallinophycidae |
| Q28764043 | A phylogenomic study of human, dog, and mouse |
| Q13416674 | A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes |
| Q39730939 | A tree of geese: A phylogenomic perspective on the evolutionary history of True Geese |
| Q33283910 | Added resolution among ordinal level relationships of tapeworms (Platyhelminthes: Cestoda) with complete small and large subunit nuclear ribosomal RNA genes |
| Q34391778 | An archaeal origin of eukaryotes supports only two primary domains of life |
| Q33595617 | An evaluation of phylogenetic informativeness profiles and the molecular phylogeny of diplazontinae (Hymenoptera, Ichneumonidae). |
| Q24805107 | An improved probability mapping approach to assess genome mosaicism |
| Q33737018 | Analysis of long branch extraction and long branch shortening |
| Q57228021 | Ancestral range reconstruction of Galliformes: the effects of topology and taxon sampling |
| Q24805410 | Ancient flowering plants: DNA sequences and angiosperm classification |
| Q29618182 | Angiosperm phylogeny inferred from multiple genes as a tool for comparative biology |
| Q35095185 | Archaeal "dark matter" and the origin of eukaryotes |
| Q91644502 | Architectural instability, inverted skews and mitochondrial phylogenomics of Isopoda: outgroup choice affects the long-branch attraction artefacts |
| Q21146722 | Are 100 enough? Inferring acanthomorph teleost phylogeny using Anchored Hybrid Enrichment |
| Q33417945 | Assessing what is needed to resolve a molecular phylogeny: simulations and empirical data from emydid turtles |
| Q34462017 | Asynchronous colonization of Madagascar by the four endemic clades of primates, tenrecs, carnivores, and rodents as inferred from nuclear genes |
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| Q39831653 | Biases of tree-independent-character-subsampling methods |
| Q41450268 | Biogeographical and phylogenetic origins of African fig species (Ficus section Galoglychia). |
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| Q28766710 | Bushes in the tree of life |
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| Q38367980 | Can quartet analyses combining maximum likelihood estimation and Hennigian logic overcome long branch attraction in phylogenomic sequence data? |
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| Q30581659 | Circumscription and phylogeny of the Laurales: evidence from molecular and morphological data |
| Q28649717 | Circumstances in which parsimony but not compatibility will be provably misleading |
| Q99573053 | Clade stability and the addition of data: A case study from erigonine spiders (Araneae: Linyphiidae, Erigoninae) |
| Q56268379 | Cladistic analysis of the fire ants of the Solenopsis saevissima species-group (Hymenoptera: Formicidae) |
| Q40909237 | Coalescence vs. concatenation: Sophisticated analyses vs. first principles applied to rooting the angiosperms |
| Q35066377 | Coalescent species delimitation in milksnakes (genus Lampropeltis) and impacts on phylogenetic comparative analyses. |
| Q35176069 | Combining bioinformatics and phylogenetics to identify large sets of single-copy orthologous genes (COSII) for comparative, evolutionary and systematic studies: a test case in the euasterid plant clade |
| Q34498320 | Combining phylogenomic and supermatrix approaches, and a time-calibrated phylogeny for squamate reptiles (lizards and snakes) based on 52 genes and 4162 species |
| Q30978520 | Complete mitochondrial genome sequences of the South american and the Australian lungfish: testing of the phylogenetic performance of mitochondrial data sets for phylogenetic problems in tetrapod relationships |
| Q46273817 | Comprehensive phylogeny of acariform mites (Acariformes) provides insights on the origin of the four-legged mites (Eriophyoidea), a long branch. |
| Q24676723 | Conflict between datasets and phylogeny of centipedes: an analysis based on seven genes and morphology |
| Q30919244 | Conflicting phylogenies of balsaminoid families and the polytomy in Ericales: combining data in a Bayesian framework |
| Q45402006 | Congruence between nuclear and mitochondrial genes in Demospongiae: a new hypothesis for relationships within the G4 clade (Porifera: Demospongiae). |
| Q28752680 | Congruence of morphologically-defined genera with molecular phylogenies |
| Q92651873 | Congruence, fossils and the evolutionary tree of rodents and lagomorphs |
| Q33845478 | Contributions of plant molecular systematics to studies of molecular evolution |
| Q56784873 | Convergent evolution and character correlation in burrowing reptiles: towards a resolution of squamate relationships |
| Q21283831 | Convergent evolution, habitat shifts and variable diversification rates in the ovenbird-woodcreeper family (Furnariidae) |
| Q34472543 | Cytochrome b and Bayesian inference of whale phylogeny |
| Q116673322 | DNA Barcodes Combined with Multilocus Data of Representative Taxa Can Generate Reliable Higher-Level Phylogenies |
| Q28748783 | Data mining approach identifies research priorities and data requirements for resolving the red algal tree of life |
| Q46826992 | Dissecting the ancient rapid radiation of microgastrine wasp genera using additional nuclear genes. |
| Q104693653 | Diverse Phylogenomic Datasets Uncover a Concordant Scenario of Laurasiatherian Interordinal Relationships |
| Q30847878 | Effectiveness of phylogenomic data and coalescent species-tree methods for resolving difficult nodes in the phylogeny of advanced snakes (Serpentes: Caenophidia). |
| Q33199482 | Efficiently resolving the basal clades of a phylogenetic tree using Bayesian and parsimony approaches: a case study using mitogenomic data from 100 higher teleost fishes |
| Q89599719 | Eleven grand challenges in single-cell data science |
| Q46091758 | Embracing Uncertainty in Reconstructing Early Animal Evolution |
| Q61796024 | Embracing heterogeneity: coalescing the Tree of Life and the future of phylogenomics |
| Q29616065 | Eukaryotic evolution, changes and challenges |
| Q22337190 | Evaluating multiple alternative hypotheses for the origin of Bilateria: An analysis of 18S rRNA molecular evidence |
| Q46470901 | Evaluating nuclear protein-coding genes for phylogenetic utility in beetles |
| Q30656825 | Evaluating phylogenetic informativeness as a predictor of phylogenetic signal for metazoan, fungal, and mammalian phylogenomic data sets |
| Q30351880 | Evolution of protein indels in plants, animals and fungi. |
| Q21147035 | Evolution of river dolphins |
| Q33549045 | Evolution of the nocturnal Nearctic Sphaeropthalminae velvet ants (Hymenoptera: Mutillidae) driven by Neogene orogeny and Pleistocene glaciation. |
| Q41023638 | Evolution of viruses and cells: do we need a fourth domain of life to explain the origin of eukaryotes? |
| Q36631996 | Evolutionary medicine: A meaningful connection between omics, disease, and treatment |
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| Q33639207 | Evolutionary relationships among marine cercozoans as inferred from combined SSU and LSU rDNA sequences and polyubiquitin insertions |
| Q35737897 | Expanding character sampling for ciliate phylogenetic inference using mitochondrial SSU-rDNA as a molecular marker |
| Q90105325 | Extracting phylogenetic signal from phylogenomic data: Higher-level relationships of the nightbirds (Strisores) |
| Q34222621 | First large-scale DNA barcoding assessment of reptiles in the biodiversity hotspot of Madagascar, based on newly designed COI primers |
| Q54556318 | First molecular evidence for reassessing phylogenetic affinities between genets (Genetta) and the enigmatic genet-like taxa Osbornictis, Poiana and Prionodon (Carnivora, Viverridae) |
| Q28250109 | Fossils impact as hard as living taxa in parsimony analyses of morphology |
| Q28658690 | From algae to angiosperms-inferring the phylogeny of green plants (Viridiplantae) from 360 plastid genomes |
| Q29547249 | Genome-scale approaches to resolving incongruence in molecular phylogenies |
| Q30341468 | Genomic biodiversity, phylogenetics and coevolution in proteins |
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| Q34590251 | Genomic outposts serve the phylogenomic pioneers: designing novel nuclear markers for genomic DNA extractions of lepidoptera |
| Q34520696 | Genus-level phylogeny of snakes reveals the origins of species richness in Sri Lanka. |
| Q28600987 | Geological Changes of the Americas and their Influence on the Diversification of the Neotropical Kissing Bugs (Hemiptera: Reduviidae: Triatominae) |
| Q28279444 | Global eukaryote phylogeny: Combined small- and large-subunit ribosomal DNA trees support monophyly of Rhizaria, Retaria and Excavata |
| Q24643849 | Higher-order phylogeny of modern birds (Theropoda, Aves: Neornithes) based on comparative anatomy. II. Analysis and discussion |
| Q28728486 | Highly incomplete taxa can rescue phylogenetic analyses from the negative impacts of limited taxon sampling |
| Q30991088 | How Should Genes and Taxa be Sampled for Phylogenomic Analyses with Missing Data? An Empirical Study in Iguanian Lizards |
| Q77892032 | How good are deep phylogenetic trees? |
| Q56637950 | How our view of animal phylogeny was reshaped by molecular approaches: lessons learned |
| Q28710489 | How to handle speciose clades? Mass taxon-sampling as a strategy towards illuminating the natural history of Campanula (Campanuloideae) |
| Q22066022 | Identifying the Basal Angiosperm Node in Chloroplast Genome Phylogenies: Sampling One's Way Out of the Felsenstein Zone |
| Q64267643 | Inadvertent Paralog Inclusion Drives Artifactual Topologies and Timetree Estimates in Phylogenomics |
| Q33650399 | Including RNA secondary structures improves accuracy and robustness in reconstruction of phylogenetic trees |
| Q24555203 | Incomplete taxon sampling is not a problem for phylogenetic inference |
| Q34147941 | Increased taxon sampling is advantageous for phylogenetic inference |
| Q51623511 | Increasing taxon sampling using both unidentified environmental sequences and identified cultures improves phylogenetic inference in the Prorodontida (Ciliophora, Prostomatea). |
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| Q21093401 | Inferring phylogenies with incomplete data sets: a 5-gene, 567-taxon analysis of angiosperms |
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| Q40172520 | Integration of complete chloroplast genome sequences with small amplicon datasets improves phylogenetic resolution in Acacia. |
| Q33790927 | Integrative modeling of gene and genome evolution roots the archaeal tree of life |
| Q55892705 | Interrelationships of basal synapsids: cranial and postcranial morphological partitions suggest different topologies |
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| Q34764053 | Large multi-gene phylogenetic trees of the grasses (Poaceae): progress towards complete tribal and generic level sampling |
| Q33551811 | Large multi-locus plastid phylogeny of the tribe Arundinarieae (Poaceae: Bambusoideae) reveals ten major lineages and low rate of molecular divergence |
| Q58482881 | Large-Scale Parsimony Analysis of Metazoan Indels in Protein-Coding Genes |
| Q27490945 | Leveraging skewed transcript abundance by RNA-Seq to increase the genomic depth of the tree of life |
| Q24798589 | Long branch attraction, taxon sampling, and the earliest angiosperms: Amborella or monocots? |
| Q28143615 | Long-branch attraction phenomenon and the impact of among-site rate variation on rodent phylogeny |
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| Q28657692 | Mitogenomic sequences effectively recover relationships within brush-footed butterflies (Lepidoptera: Nymphalidae) |
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| Q31080515 | Molecular phylogenetic analysis of Fringillidae, "New World nine-primaried oscines" (Aves: Passeriformes). |
| Q57196959 | Molecular phylogenetics for conservation biology |
| Q30665919 | Molecular phylogenetics: state-of-the-art methods for looking into the past |
| Q28681907 | Molecular phylogenies support homoplasy of multiple morphological characters used in the taxonomy of Heteroscleromorpha (Porifera: Demospongiae) |
| Q54802188 | Molecular phylogeny based on increased number of species and genes revealed more robust family-level systematics of the order Euryalida (Echinodermata: Ophiuroidea) |
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| Q54597443 | Molecular phylogeny of major lineages of Trichadenotecnum and a review of diagnostic morphological characters (Psocoptera: Psocidae) |
| Q28757488 | Molecular phylogeny of the Drosophila obscura species group, with emphasis on the Old World species |
| Q54508877 | Molecular phylogeny of the Platyhelminthes |
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| Q59284530 | Molecular phylogeny of the hyperdiverse genusSarcophaga(Diptera: Sarcophagidae), and comparison between algorithms for identification of rogue taxa |
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| Q43419492 | Molecular systematics of the barklouse family Psocidae (Insecta: Psocodea: 'Psocoptera') and implications for morphological and behavioral evolution |
| Q33520143 | Molecular systematics of the bubblegum coral genera (Paragorgiidae, Octocorallia) and description of a new deep-sea species |
| Q28731533 | Molecular systematics of the deep-sea hydrothermal vent endemic Brachyuran family Bythograeidae: a comparison of three Bayesian species tree methods |
| Q54663964 | Molecular systematics of the gonorynchiform fishes (Teleostei) based on whole mitogenome sequences: implications for higher-level relationships within the Otocephala. |
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| Q47283296 | Morphology's role in phylogeny reconstruction: perspectives from paleontology |
| Q29300654 | Multilocus phylogeny and rapid radiations in Neotropical cichlid fishes (Perciformes: Cichlidae: Cichlinae) |
| Q24814022 | Multiple sequence alignment accuracy and evolutionary distance estimation |
| Q54540968 | Myzostomida Are Not Annelids: Molecular and Morphological Support for a Clade of Animals with Anterior Sperm Flagella |
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| Q30425374 | New approaches for unravelling reassortment pathways |
| Q57042726 | New insights on systematics and phylogenetics of Mediterranean Blaps species (Coleoptera: Tenebrionidae: Blaptini), assessed through morphology and dense taxon sampling |
| Q31041545 | New perspective on uncultured bacterial phylogenetic division OP11. |
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| Q30854088 | On the distribution of interspecies correlation for Markov models of character evolution on Yule trees |
| Q101633736 | On the phylogenetic relationships of the Cretaceous snakes with legs, with special reference toPachyrhachis problematicus(Squamata, Serpentes) |
| Q44279794 | Optimal selection of gene and ingroup taxon sampling for resolving phylogenetic relationships |
| Q28740451 | Overcoming the effects of rogue taxa: Evolutionary relationships of the bee flies |
| Q52078101 | Parsimony, likelihood, and the role of models in molecular phylogenetics. |
| Q30000689 | Performance of single and concatenated sets of mitochondrial genes at inferring metazoan relationships relative to full mitogenome data |
| Q33937414 | PhyloMap: an algorithm for visualizing relationships of large sequence data sets and its application to the influenza A virus genome |
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| Q33282873 | Phylogenetic analyses under secondary structure-specific substitution models outperform traditional approaches: case studies with diploblast LSU. |
| Q24671012 | Phylogenetic analysis of arthropods using two nuclear protein-encoding genes supports a crustacean + hexapod clade |
| Q21283977 | Phylogenetic inference in Rafflesiales: the influence of rate heterogeneity and horizontal gene transfer |
| Q36727846 | Phylogenetic inference of calyptrates, with the first mitogenomes for Gasterophilinae (Diptera: Oestridae) and Paramacronychiinae (Diptera: Sarcophagidae) |
| Q33495765 | Phylogenetic inference under varying proportions of indel-induced alignment gaps |
| Q55435443 | Phylogenetic information and experimental design in molecular systematics. |
| Q31171461 | Phylogenetic modeling of heterogeneous gene-expression microarray data from cancerous specimens |
| Q57707014 | Phylogenetic relationships among Heliconiinae genera based on morphology (Lepidoptera: Nymphalidae) |
| Q42667656 | Phylogenetic resolution and habitat specificity of members of the Photobacterium phosphoreum species group |
| Q46557478 | Phylogenetic signal and its decay in mitochondrial SSU and LSU rRNA gene fragments of Anisoptera |
| Q34184295 | Phylogenetic signal and noise: predicting the power of a data set to resolve phylogeny |
| Q57141402 | Phylogenetic utility of indels within ribosomal DNA and β-tubulin sequences from fungi in the Rhizoctonia solani species complex |
| Q111622596 | Phylogenetics of the Pezizaceae, with an emphasis on Peziza |
| Q35174263 | Phylogenetics, ancestral state reconstruction, and a new infrafamilial classification of the pantropical Ochnaceae (Medusagynaceae, Ochnaceae s.str., Quiinaceae) based on five DNA regions |
| Q49277100 | Phylogenomic Perspective on the Relationships and Evolutionary History of the Major Otocephalan Lineages |
| Q56865120 | Phylogenomic evidence overturns current conceptions of social evolution in wasps (Vespidae) |
| Q30572538 | Phylogenomics and a posteriori data partitioning resolve the Cretaceous angiosperm radiation Malpighiales |
| Q28247594 | Phylogenomics and the reconstruction of the tree of life |
| Q91826581 | Phylogenomics provides robust support for a two-domains tree of life |
| Q31058110 | Phylogeny and biogeography of the most diverse clade of South American gymnophthalmid lizards (Squamata, Gymnophthalmidae, Cercosaurinae). |
| Q52566724 | Phylogeny and evolutionary radiation of the marine mussels (Bivalvia: Mytilidae) based on mitochondrial and nuclear genes. |
| Q55877577 | Phylogeny of Drepanosauridae (Reptilia: Diapsida) |
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| Q56784952 | Phylogeny of the Lemuridae: Effects of Character and Taxon Sampling on Resolution of Species Relationships within Eulemur |
| Q54553085 | Phylogeny of the riodinid butterfly subtribe Theopeina (Lepidoptera: Riodinidae: Nymphidiini) |
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| Q28743242 | Potential pitfalls of modelling ribosomal RNA data in phylogenetic tree reconstruction: evidence from case studies in the Metazoa |
| Q30672936 | Potential pitfalls of reconstructing deep time evolutionary history with only extant data, a case study using the canidae (mammalia, carnivora). |
| Q56270132 | Preliminary morphological analysis of relationships between the spider wasp subfamilies (Hymenoptera: Pompilidae): revisiting an old problem |
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| Q45252022 | Profiling phylogenetic informativeness |
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| Q33978889 | Recent progress in reconstructing angiosperm phylogeny. |
| Q40010537 | Reconstructing the phylogenetic relationships of the earth's most diverse clade of freshwater fishes--order Cypriniformes (Actinopterygii: Ostariophysi): a case study using multiple nuclear loci and the mitochondrial genome |
| Q54802079 | Redescription of the skull of ‘Trionyx’ kyrgyzensis and improved phylogenetic taxon sampling of Cretaceous and Palaeogene soft-shelled turtles (Trionychidae) of Asia, including the oldest crown trionychids |
| Q44026398 | Relative character-state space, amount of potential phylogenetic information, and heterogeneity of nucleotide and amino acid characters |
| Q40924828 | Resolving the phylogeny of a speciose spider group, the family Linyphiidae (Araneae). |
| Q111622602 | Ribosomal DNA systematics of Ceratobasidium and Thanatephorus with Rhizoctonia anamorphs |
| Q53920478 | Rooting phylogenetic trees with distant outgroups: a case study from the commelinoid monocots. |
| Q31014818 | Rooting phylogenies using gene duplications: an empirical example from the bees (Apoidea). |
| Q31056205 | Sequence Data, Phylogenetic Inference, and Implications of Downward Causation |
| Q111629152 | Sequences of 72 plastid genes support the early divergence of Cornales in the asterids |
| Q56521766 | Sheathbill-like birds (Charadriiformes: Chionoidea) from the Oligocene and Miocene of Australasia |
| Q30955136 | Should we be worried about long-branch attraction in real data sets? Investigations using metazoan 18S rDNA. |
| Q28960287 | Simple Phylogenetic Tree Searches Easily "Succeed" with Large Matrices of Single Genes |
| Q57405556 | Skull anatomy ofDakosaurus andiniensis(Thalattosuchia: Crocodylomorpha) and the phylogenetic position of Thalattosuchia |
| Q44951084 | Sorting wheat from chaff in multi-gene analyses of chlorophyll c-containing plastids. |
| Q28140460 | Subtribal and generic relationships of Maxillarieae (Orchidaceae) with emphasis on Stanhopeinae: combined molecular evidence |
| Q51704905 | Summarizing a posterior distribution of trees using agreement subtrees. |
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| Q51962600 | Systematics of the cyclostome subfamilies of braconid parasitic wasps (Hymenoptera: Ichneumonoidea): a simultaneous molecular and morphological Bayesian approach. |
| Q35609555 | Targeted amplicon sequencing (TAS): a scalable next-gen approach to multilocus, multitaxa phylogenetics. |
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| Q39041838 | The Evolutionary Origin of Diversity in Chagas Disease Vectors. |
| Q39593552 | The Identification of the Closest Living Relative(s) of Tetrapods: Phylogenomic Lessons for Resolving Short Ancient Internodes |
| Q21284016 | The bee tree of life: a supermatrix approach to apoid phylogeny and biogeography |
| Q35202971 | The challenge of constructing large phylogenetic trees |
| Q35172421 | The chloroplast genome of Hyoscyamus niger and a phylogenetic study of the tribe Hyoscyameae (Solanaceae) |
| Q47110852 | The complete mitochondrial genome of parasitic nematode Camallanus cotti: extreme discontinuity in the rate of mitogenomic architecture evolution within the Chromadorea class |
| Q89072888 | The complete mitochondrial genomes of Tarsiger cyanurus and Phoenicurus auroreus: a phylogenetic analysis of Passeriformes |
| Q24679379 | The deepest divergences in land plants inferred from phylogenomic evidence |
| Q29618181 | The earliest angiosperms: evidence from mitochondrial, plastid and nuclear genomes |
| Q46664336 | The effects of increasing genetic distance on alignment of, and tree construction from, rDNA internal transcribed spacer sequences |
| Q29028229 | The higher-level phylogeny of Archosauria (Tetrapoda: Diapsida) |
| Q21089760 | The hymenopteran tree of life: evidence from protein-coding genes and objectively aligned ribosomal data |
| Q35653694 | The impact of taxon sampling on phylogenetic inference: a review of two decades of controversy |
| Q47860790 | The origin of red algae and the evolution of chloroplasts |
| Q41356201 | The origin of turtles: a paleontological perspective |
| Q34527319 | The phylogenetic placement of chondrichthyes: inferences from analysis of multiple genes and implications for comparative studies |
| Q55871807 | The phylogenetic position of the comb jellies (Ctenophora) and the importance of taxonomic sampling |
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| Q28285586 | The phylogeny of Cetartiodactyla: the importance of dense taxon sampling, missing data, and the remarkable promise of cytochrome b to provide reliable species-level phylogenies |
| Q57816408 | The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae) |
| Q43909626 | The position of gnetales among seed plants: overcoming pitfalls of chloroplast phylogenomics |
| Q51422695 | The probability of correctly resolving a split as an experimental design criterion in phylogenetics. |
| Q34067661 | The root of the angiosperms revisited |
| Q28274433 | The value of sampling anomalous taxa in phylogenetic studies: major clades of the Asteraceae revealed |
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| Q44194282 | Towards building the tree of life: a simulation study for all angiosperm genera |
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| Q28708935 | Understanding phylogenetic incongruence: lessons from phyllostomid bats |
| Q47780379 | Unexpected phylogenetic positions of the genera Rupirana and Crossodactylodes reveal insights into the biogeography and reproductive evolution of leptodactylid frogs |
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| Q30867401 | Using multi-locus allelic sequence data to estimate genetic divergence among four Lilium (Liliaceae) cultivars |
| Q22066318 | Using plastid genome-scale data to resolve enigmatic relationships among basal angiosperms |
| Q35629307 | Utility of characters evolving at diverse rates of evolution to resolve quartet trees with unequal branch lengths: analytical predictions of long-branch effects |
| Q24791276 | Visualization of the phylogenetic content of five genomes using dekapentagonal maps |
| Q46825299 | When do species-tree and concatenated estimates disagree? An empirical analysis with higher-level scincid lizard phylogeny |
| Q24804391 | Where does fission yeast sit on the tree of life? |
| Q35866752 | Why should we investigate the morphological disparity of plant clades? |
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