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75 results for “cytochrome c oxidase”
Figure 3. Phylogenetic relationships inferred from cytochrome c oxidase subunit I in Pseudocryptic speciation of Chrysochroa fulgidissima (Coleoptera: Buprestidae) with two new species from Korea, China and Vietnam
Figure 3. Phylogenetic relationships inferred from cytochrome c oxidase subunit I (664 bp). Colours represented within each terminal taxa denote biogeographical populations of Chrysochroa fulgidissima as given in Table 1. Numbers above branches are indicated by the neighbour-joining bootstrap value, Bayesian posterior probabilities, and the maximum likelihood bootstrap proportions. Numbers cited under branches are parsimony bootstrap symmetric resampling and jackknife support, respectively. The topology was constructed by Bayesian phylogenetic analysis.
Figure 2. Cytochrome oxidase c subunit I in An integrative approach to characterize cryptic species in the Thoracostoma trachygaster Hope, 1967 complex (Nematoda: Leptosomatidae)
Figure 2. Cytochrome oxidase c subunit I. Neighbourjoining tree based on P-distances with haplotypes from 2007 and the new haplotypes found in 2009 and 2010 (represented by numbers followed by clade – I, II, or III). The haplotypes from clade I and II that were recovered from 2007 appear underlined in the tree. The corresponding taxon names of the other clades can be found in Derycke et al. (2010a).
Figure 1. Best selected tree from a maximum likelihood reconstruction for the cytochrome c oxidase subunit I in Integrating DNA and morphological taxonomy to describe diversity in poorly studied microscopic animals: new species of the genus Abrochtha Bryce, 1910 (Rotifera: Bdelloidea: Philodinavidae)
Figure 1. Best selected tree from a maximum likelihood reconstruction for the cytochrome c oxidase subunit I data set under the general time reversible model with gamma distribution, displaying all compatible groupings and with average branch lengths proportional to numbers of substitutions per site, indicated by the scale bar. Bootstrap support values above 80% are shown below each branch; posterior probabilities above 0.8 from 36 000 sampled trees from the Bayesian analysis are shown above each branch. Support values for within-species relationships are not shown. Filled circles indicate clades (and singlets) identified by the 4¥ rule; open diamonds indicate clades (and singlets) identified by the generalized mixed yule coalescent model. Names refer to the species and the clonal populations.
FIGURE 3. Neighbor-joining tree for Cytochrome C Oxidase Subunit I in Two new species and three new provincial records of Neoperla (Plecoptera: Perlidae) from Nanling Mountains, China
FIGURE 3. Neighbor-joining tree for Cytochrome C Oxidase Subunit I (COI) sequences (659 bp) from Neoperla annulatispina Mo, Li & Wang, sp. nov. and N. nigromarginata Li & Zhang, 2014, modeled by Kimura-2-parameter (K2P).
Figure 2. The cytochrome c oxidase 1 in Evidence Of A Putative Novel Species Of Avian Schistosome Infecting Planorbella Trivolvis
Figure 2. The cytochrome c oxidase 1 (COI) phylogenetic tree including members of the avian Schistosomatidae. Nodal support indicated by Bayesian posterior probabilities. GenBank accession numbers precede taxon names. The representative sample from this study is in bold.
FIGURE 8—Phylogenetic tree inferred using Bayesian Inference derived from cytochrome c oxidase subunit I in How many species of genus Lernaeopoda Blainville, 1822 (Siphonostomatoida: Lernaeopodidae) are there in the southwestern Atlantic?
FIGURE 8—Phylogenetic tree inferred using Bayesian Inference derived from cytochrome c oxidase subunit I (COI) gene dataset. Numbers in the nodes represent posterior probability (<0.95 are not shown).
Supplementary material 2 from: Hrabina P, Pernerová L, Suchomel J, Robovský J (2023) Utility of cytochrome c oxidase I for the deciphering of unstable phylogeny and taxonomy of gorals, genus Nemorhaedus Hamilton Smith, 1827 (Bovidae, Ovibovina). ZooKeys 1181: 81-110. https://doi.org/10.3897/zookeys.1181.108019
List of taxa and GenBank accession numbers used for the original gene analysis with 134 COI sequences
Supplementary material 1 from: Hrabina P, Pernerová L, Suchomel J, Robovský J (2023) Utility of cytochrome c oxidase I for the deciphering of unstable phylogeny and taxonomy of gorals, genus Nemorhaedus Hamilton Smith, 1827 (Bovidae, Ovibovina). ZooKeys 1181: 81-110. https://doi.org/10.3897/zookeys.1181.108019
Goral species recognized in the 20th and 21st centuries across several basic sources, which seemed to assess gorals independently and/or using different data
Cytochrome C Oxidase Activity in Newly Diagnosed Glioblastoma Multiforme (GBM)
ClinicalTrials.gov study NCT02997423. IPD Sharing: YES. Countries: 1. Publications: 3.
Data from: Site specific distribution of oak rhizosphere associated oomycetes revealed by cytochrome c oxidase subunit II metabarcoding
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Data from: Cytochrome c oxidase subunit 1 barcode data of fish of the Nayband National Park in the Persian Gulf and analysis using meta-data flag several cryptic species
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Data from: Rapid and accurate taxonomic classification of insect (Class Insecta) cytochrome c oxidase subunit 1 (COI) DNA barcode sequences using a naïve Bayesian classifier
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Figure 2 from: Grzywacz B, Tatsuta H (2017) Phylogenetic relationship of Japanese Podismini species (Orthoptera: Acrididae: Melanoplinae) inferred from a partial sequence of cytochrome c oxidase subunit I gene. Journal of Orthoptera Research 26: 11-19. https://doi.org/10.3897/jor.26.14547
Figure 2 - Phylogenetic tree of Podismini based on the Bayesian analysis (BI) of concatenated COI sequences. BI posterior probability (PP) and maximum likelihood bootstrap values (BV) are shown near resolved branches (only support values above 50% are shown) as PP/BV. The respective clades are marked with a square and Roman numeral. We examined Ognevia longipennis from China because of the availability and thus did not treat this specimen as Japanese Podismini (see also text). Light green frames denote the Japanese Podismini analyzed in the present study.
Figure 2 from: Grzywacz B, Tatsuta H (2017) Phylogenetic relationship of Japanese Podismini species (Orthoptera: Acrididae: Melanoplinae) inferred from a partial sequence of cytochrome c oxidase subunit I gene. Journal of Orthoptera Research 26: 11-19. https://doi.org/10.3897/jor.26.14547
Figure 2 - Phylogenetic tree of Podismini based on the Bayesian analysis (BI) of concatenated COI sequences. BI posterior probability (PP) and maximum likelihood bootstrap values (BV) are shown near resolved branches (only support values above 50% are shown) as PP/BV. The respective clades are marked with a square and Roman numeral. We examined Ognevia longipennis from China because of the availability and thus did not treat this specimen as Japanese Podismini (see also text). Light green frames denote the Japanese Podismini analyzed in the present study.
Figures 2–3. Mitochondrial cytochrome c oxidase subunit 1 in Molecular confirmation of the occurrence of Anguilla interioris (Actinopterygii: Anguilliformes) in North Maluku of Indonesia and mitochondrial DNA haplotype diversity among existing specimens
Figures 2–3. Mitochondrial cytochrome c oxidase subunit 1 (CO1) 551 bp sequence analyses. (2) Phylogenetic analysis based on maximum likelihood algorithm with the sample codes, GenBank or BOLD accession numbers and sample sites shown. Bootstrap percentages are shown at the tree nodes. (3) Haplotype network with the haplotypes labelled as H1 to H9. The circle size is proportional to the number of samples, and different sample sites are represented by different colours. Small white circle represents median vector which is the hypothesized or missing haplotype. Each dash on the line symbolizes one mutational step.
Figure 2. A neighbour-joining tree using 604 cytochrome c oxidase subunit I in Phylogenetic relationship among slender loris species (Primates, Lorisidae: Loris) in Sri Lanka based on mtDNA CO1 barcoding
Figure 2. A neighbour-joining tree using 604 cytochrome c oxidase subunit I (CO1) sequences from 7 different slender loris (Loris) taxas found in Sri Lanka with their external appearance.
Figure 3. A neighbor joining tree using cytochrome c oxidase subunit 1 in DNA barcoding of black cherry aphid Myzus cerasi (Fabricus, 1775) (Hemiptera: Aphididae) populations collected from Prunus avium and Prunus cerasus
Figure 3. A neighbor joining tree using cytochrome c oxidase subunit 1 sequences from Myzus cerasi populations.
Figure 2c from: Cocuzza GEM, Di Silvestro S, Giordano R, Rapisarda C (2015) Congruence between cytochrome oxidase I (COI) and morphological data in Anuraphis spp. (Hemiptera, Aphididae) with a comparison between the utility of the 5' barcode and 3' COI regions. ZooKeys 529: 123-144. https://doi.org/10.3897/zookeys.529.6081
Figure 2c - MrBayes tree estimated using 648 bp at the 3' end of COI for selected Anuraphis species.
Figure 2d from: Cocuzza GEM, Di Silvestro S, Giordano R, Rapisarda C (2015) Congruence between cytochrome oxidase I (COI) and morphological data in Anuraphis spp. (Hemiptera, Aphididae) with a comparison between the utility of the 5' barcode and 3' COI regions. ZooKeys 529: 123-144. https://doi.org/10.3897/zookeys.529.6081
Figure 2d - MrBayes tree estimated using 658 bp at the 5' end of COI for selected Anuraphis species.
Figure 1a from: Cocuzza GEM, Di Silvestro S, Giordano R, Rapisarda C (2015) Congruence between cytochrome oxidase I (COI) and morphological data in Anuraphis spp. (Hemiptera, Aphididae) with a comparison between the utility of the 5' barcode and 3' COI regions. ZooKeys 529: 123-144. https://doi.org/10.3897/zookeys.529.6081
Figure 1a - Neighbor-Joining tree showing relationships among selected Anuraphis species estimated using 648 bp at the 3' end of the COI mitochondrial gene. Distance were estimated using the p-distance model of sequence evolution.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.