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1,344 results for “: phylogenomics”
Data from: Phylogenomic analyses reveal convergent patterns of adaptive evolution in elephant and human ancestries
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Data from: Post K-Pg diversification of the mammalian order Eulipotyphla as suggested by phylogenomic analyses of ultra-conserved elements
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Data from: Model choice, missing data and taxon sampling impact phylogenomic inference of deep Basidiomycota relationships
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Data from: Using phylogenomics to resolve mega-families: an example from Compositae
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Data from: Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
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Data from: Exploiting gene families for phylogenomic analysis of myzostomid transcriptome data
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Data from: Chloroplast phylogenomic analysis of chlorophyte green algae identifies a novel lineage sister to the Sphaeropleales (Chlorophyceae)
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Data from: Phylogenomics supports incongruence between ecological specialization and taxonomy in a charismatic clade of buck moths
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Data from: Using phylogenomics to understand the link between biogeographic origins and regional diversification in ratsnakes
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Data from: Phylogenomics of a rapid radiation: the Australian rainbow skinks
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Figures 19–24 in Taxonomy in the phylogenomic era: species boundaries and phylogenetic relationships among North American ants of the Crematogaster scutellaris group (Formicidae: Hymenoptera)
Figures 19–24. Crematogaster workers, showing lateral view of body (A), full-face view of head (B) and dorsal view of body (C). 19, C. mutans worker (CASENT0922736); 20, C. colei (CASENT0922726); 21, C. detecta holotype (CASENT0863461); 22, C. larreae paratype (CASENT0005943); 23, C. depilis (CASENT0005668); 24, C. californica lectotype (CASENT0923319). Images courtesy of AntWeb (www.antweb.org); photographers Wade Lee (19, 20), Zachary Griebenow (21), April Nobile (22, 23), Michele Esposito (24).
Fig. 1 in UCE Phylogenomics of New World Cryptopone (Hymenoptera: Formicidae) Elucidates Genus Boundaries, Species Boundaries, and the Vicariant History of a
Fig. 1. Relationships among Cryptopone lineages based on analysis of 2,232 UCE loci and the SWSC-EN partitioning scheme. Among lineages, the South American clade is separate from the North/Central American clade of Cryptopone and they are not closely related.The constituent species of the South American clade are transferred to the resurrected genus Wadeura. All node support values are at maximum (UFB/SH-aLRT values of 100/100).The photo insets are of Wadeura holmgreni (CASENT0373370, Credit: Michelle Esposito) and C. gilva (CASENT0003325, Credit: April Nobile). The same tree with support values is available in Supp Fig. 1 (online only).
Fig. 9 in Phylogenomics of Ichneumoninae (Hymenoptera, Ichneumonidae) reveals pervasive morphological convergence and the shortcomings of previous classifications
Fig. 9. Abzaria latipetiolaris. (A) lateral habitus; (B) Head and pronotum in laterofrontal view; (C) propodeum and petiole in dorsolateral view. [Colour figure can be viewed at wileyonlinelibrary.com].
Fig. 3 in Phylogenomics of Ichneumoninae (Hymenoptera, Ichneumonidae) reveals pervasive morphological convergence and the shortcomings of previous classifications
Fig. 3. Summary of relationships among outgroup taxa as recovered with the matrix with 50% completeness partitioned by PartitionFinder. Detail on bottom left shows a strict consensus of the relationships obtained with the four different matrices under different completeness levels and partition schemes. Numbers correspond to bootstrap support; nodes with no numbers indicate 100% clade support. [Colour figure can be viewed at wileyonlinelibrary.com].
Fig. 3 in Museomics: Phylogenomics of the Moth Family Epicopeiidae (Lepidoptera) Using Target Enrichment
Fig. 3. Phylogenetic tree from maximum likelihood analysis of 36 taxa based on 378 loci. If the support values are not displayed on the branch, it means it is equal to 100/100.When displayed, numbers are the SH-aLRT support (%)/ultrafast bootstrap support (%).The images are representative species (indicated with numbers; not to scale).The three families are represented by an arrow and a letter. S, Sematuridae; P, Pseudobistonidae; and E, Epicopeiidae.
Fig. 5. A in Deep Instability in the Phylogenetic Backbone of Heteroptera is Only Partly Overcome by Transcriptome-Based Phylogenomics
Fig. 5. A scatter plot of QF scores obtained for each individual analyzed based on nucleotide (x-axis) or amino acid (y-axis) data.
Fig. 13–15 in Species Paraphyly and Social Parasitism: Phylogenomics, Morphology, and Geography Clarify the Evolution of the Pseudomyrmex elongatulus Group (Hymenoptera:
Fig. 13–15. Pseudomyrmex elongatulus group, workers, full-face dorsal view of head (a), and lateral profile of body (b). 13, P. capillatus, holotype, Mexico (CASENT0863535); 14, P. exoratus, holotype worker, Mexico (CASENT0863539); 15, P. fasciatus, holotype, Costa Rica (CASENT0863540). Images from AntWeb (www.antweb.org); photographer Phil Ward.
Fig. 15 in UCE Phylogenomics of New World Cryptopone (Hymenoptera: Formicidae) Elucidates Genus Boundaries, Species Boundaries, and the Vicariant History of a
Fig. 15. Holotype of Wadeura holmgrenita (CASENT0637779), lateral and dorsal views. Scale is the same for both images.
Fig. 3 in Phylogenomic analysis and morphological data suggest left-right swimming behavior evolved prior to the origin of the pelagic Phylliroidae (Gastropoda: Nudibranchia)
Fig. 3 Anatomical details of Phylliroe bucephala. a Cross section of one of the 4 gonad lobules. Note the male part in the middle of the lobule, and the female part at the periphery (arrows). b Cross section of dorsal hind part with dorsal digestive gland branch. Note the lack of mucus glands in the epidermis. Arrows indicate cnidocysts, arrowhead points towards dorsal fin-like mantle. c Cross section of stomach, with remnants of food. d Digestive gland epithelium with 3 cnidocysts (arrows). e Cross section
Fig. 1 in The phylogenomic revolution and its conceptual innovations: a text mining approach
Fig. 1 Selected trending concepts in phylogenomic research. Frequency represents the number of word instances divided by the total number of words published in a given year. Error bars represent ± 1 standard error,
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.