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Fig. 3. A neighbor-joining phylogenetic tree constructed from a in Isolation and characterization of two unrecorded yeast species in the phylum Basidiomycota
Fig. 3. A neighbor-joining phylogenetic tree constructed from a comparative analysis of 26S rRNA gene sequences showing the relationships of strain DJ1-5-B-10C with closely related species. Bootstrap values (>70%) are shown at the branch nodes. Bar, 0.02 substitutions per nucleotide position.
Fig. 2. A neighbor-joining phylogenetic tree constructed from a in Isolation and characterization of two unrecorded yeast species in the phylum Basidiomycota
Fig. 2. A neighbor-joining phylogenetic tree constructed from a comparative analysis of 26S rRNA gene sequences showing the relationships of strain B2UV-201 with closely related species. Bootstrap values (>70%) are shown at the branch nodes. Bar, 0.01 substitutions per nucleotide position.
Fig. 3. A Neighbor-joining phylogenetic tree reconstructed from a in Isolation and characterization of two unrecorded yeast species in the order Filobasidiales
Fig. 3. A Neighbor-joining phylogenetic tree reconstructed from a comparative analysis of 26S rRNA gene sequences showing the rela- tionships of strain PG1-1-10C with closely related species. Bootstrap values (>70%) based on neighbor-joining methods are shown at the branch nodes. Bar, 0.01 substitutions per nucleotide position.
Fig. 2. A Neighbor-joining phylogenetic tree reconstructed from a in Isolation and characterization of two unrecorded yeast species in the order Filobasidiales
Fig. 2. A Neighbor-joining phylogenetic tree reconstructed from a comparative analysis of 26S rRNA gene sequences showing the relation- ships of strains GW1-3 with closely related species. Bootstrap values (>70%) based on neighbor-joining methods are shown at the branch nodes. Bar, 0.01 substitutions per nucleotide position.
Fig. 3. A neighbor-joining phylogenetic tree reconstructed from a in Description of unrecorded wild yeasts from soil in Republic of Korea under cold conditions
Fig. 3. A neighbor-joining phylogenetic tree reconstructed from a comparative analysis of 26S rRNA gene sequences showing the relationships of strain PG3-4-10C with closely related species. Bootstrap values (>70%) based on neighbor-joining methods are shown at the branch nodes. Bar, 0.01 substitutions per nucleotide position.
Fig. 2. A neighbor-joining phylogenetic tree reconstructed from a in Description of unrecorded wild yeasts from soil in Republic of Korea under cold conditions
Fig. 2. A neighbor-joining phylogenetic tree reconstructed from a comparative analysis of 26S rRNA gene sequences showing the relationships of strain CY-9-10C with closely related species. Bootstrap values (>70%) based on neighbor-joining methods are shown at the branch nodes. Bar, 0.02 substitutions per nucleotide position.
Fig. 58. Neighbor joining tree using Kimura-2 in External morphology of immature stages of Zaretis strigosus (Gmelin) and Siderone galanthis catarina Dottax and Pierre comb. nov., with taxonomic notes on Siderone (Lepidoptera: Nymphalidae: Charaxinae)
Fig. 58. Neighbor joining tree using Kimura-2-Parameter distance model of 37 sequences of species of Siderone Hübner [1823] and Coenophlebia C. Felder and R. Felder, 1862, with 658 base pairs of the mitochondrial gene cytochrome oxidase, Subunit I. Scale bar = 1% of distance.
Figure 3. Neighbor-joining consensus tree for 23 in Morphology and phylogeny of the sea anemone Stichodactyla haddoni (Cnidaria: Anthozoa: Actiniaria) from Chabahar Bay, Iran
Figure 3. Neighbor-joining consensus tree for 23 species, including Iranian sea anemone species (CHIAS1 and CHIAS2), based on 18S rDNA sequences. Cl1: Stichodactylidae; Cl2: Actiniidae; Cl3: Hormathiidae; Cl4: Aiptasiidae; Cl5: Actinostolidae. The numbers beside the branches are bootstrap values with 1000 replications. Bootstrap supports under 50% are not shown in this analysis.
Figure. Interferon alpha-A based phylogenetic tree (neighbor joining method) constructed by MEGA 6.1 for Punjab urial in comparison with other mammalian species sequences available from GenBank (NCBI). in Characterization of interferon alpha of major histocompatibility complex class I in Punjab urial (Ovis vignei punjabiensis)
Figure. Interferon alpha-A based phylogenetic tree (neighbor joining method) constructed by MEGA 6.1 for Punjab urial in comparison with other mammalian species sequences available from GenBank (NCBI).
Figure 3. Median-joining networks for J in Mitochondrial evidence indicates a shallow phylogeographic structure for Jaculus blanfordi (Murray, 1884) populations (Rodentia: Dipodidae)
Figure 3. Median-joining networks for J. blanfordi mitochondrial DNA haplotypes in the different datasets for cyt b (1110 bp), COI (618 bp) and COI + cyt b (313 bp + 284 bp). The numbers of mutations (greater than 1) between the haplotypes are indicated near the branches and circle sizes are proportional to the number of similar haplotypes. See Table 1 for the haplotype designations.
Figure 1. A neighbour-joining tree using 604 cytochrome C oxidase sub-unit I in Phylogenetic relationship among slender loris species (Primates, Lorisidae: Loris) in Sri Lanka based on mtDNA CO1 barcoding
Figure 1. A neighbour-joining tree using 604 cytochrome C oxidase sub-unit I (CO1) sequences from 7 different slender loris (Loris) taxas, rooted using slow loris (Nycticebus) sequences deposited in the GenBank.
Fig. 1. Neighbor-joining tree generated under the Kimura 2 in Cotesia flavipes (Hymenoptera: Braconidae) as a biological control agent of sugarcane stem borers in Colombia's Cauca River Valley
Fig. 1. Neighbor-joining tree generated under the Kimura 2-parameter (K2P) nucleotide substitution model. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1,000 replicates) is shown next to the branches. Abbreviations for sugarcane mills in Colombia's Cauca River Valley are as follows: Manuelita (MN), Mayagüez (MY), Pichichí (PC), Providencia (PV), Riopaila (RP), Risaralda (RS), Sancarlos (SC). GeneBank C. flavipes accessions:Uganda - JQ396735.1, Brazil - DQ232320.1, India - DQ232336.1, Kenya - DQ232317, Thailand - DQ232340.1, USA - DQ232330.1, South Pakistan - JQ396714.1, Jamaica - DQ232321.1, Pakistan - DQ232335.1, Sri Lanka - DQ232327.1, Indonesia - DQ232337.1, Mauritius - DQ232319.1, Reunion - DQ232329.1, Papua New Guinea - DQ232316.1.
Fig. 3. Evolutionary analysis conducted through a neighbor-joining phylogenetic tree between the cox1 in Detection of maize bushy stunt phytoplasma in leafoppers collected in native corn crops grown at high elevations in southeast Mexico
Fig. 3. Evolutionary analysis conducted through a neighbor-joining phylogenetic tree between the cox1 mini-barcode sequences obtained for the red speckled nymphs and Idiodonus wickhami (Hemiptera: Cicadellidae) (both marked with a circle) with reference sequences from GenBank. Bar 5 substitution in 100 positions.
Fig. 4. Evolutionary analysis conducted through a neighbor-joining phylogenetic tree between the 16S in Detection of maize bushy stunt phytoplasma in leafoppers collected in native corn crops grown at high elevations in southeast Mexico
Fig. 4. Evolutionary analysis conducted through a neighbor-joining phylogenetic tree between the 16S rRNA sequences amplified in this study from phytoplasma DNA, bar 1 substitution in 100 positions. Sequences in the grey square belong to the subgroup 16SrI-B. Sequences amplified from leafoppers (Hemiptera: Cicadellidae) Dalbulus elimatus marked with a circle and from Idiodonus wickhami marked with a square.
FIGURE 1 in Science and hobby joining forces for the discovery of three new Corydoras (Siluriformes: Callichthyidae) from the rio Tapajós basin, Brazil, with comments on Corydoras sp. CW111
FIGURE 1 | Corydoras thanatos, holotype, MNRJ 53287, 33.2 mm SL, Novo Progresso Municipality, Pará State, Brazil, stream with unknown name tributary to the rio Jamanxim, rio Tapajós basin.
FIGURE 14 in Science and hobby joining forces for the discovery of three new Corydoras (Siluriformes: Callichthyidae) from the rio Tapajós basin, Brazil, with comments on Corydoras sp. CW111
FIGURE 14 | Uncatalogued aquarium specimen of Corydoras psamathos photographed alive. Photo by Takayuki Shimizu.
FIGURE 5 in Science and hobby joining forces for the discovery of three new Corydoras (Siluriformes: Callichthyidae) from the rio Tapajós basin, Brazil, with comments on Corydoras sp. CW111
FIGURE 5 | Map of the rio Tapajós and adjoining areas, showing the geographical distribution of Corydoras thanatos (black circle), C. hypnos (white star), and C. psamathos (red squares). Each symbol may represent more than one locality.
FIGURE 9 in Science and hobby joining forces for the discovery of three new Corydoras (Siluriformes: Callichthyidae) from the rio Tapajós basin, Brazil, with comments on Corydoras sp. CW111
FIGURE 9 | Paratypes of Corydoras hypnos photographed alive, showing general color pattern and morphology in lateral view in (A) INPA 59775, 26.2 mm SL, (B) INPA 59775, 27.2 mm SL, (C) INPA 59775, 22.2 mm SL, (D) INPA 59774, 28.2 mm SL, and (E) INPA 59774, 22.6 mm SL, all from the rio Jamanxim, rio Tapajós basin, Pará State, Brazil.
FIGURE 13 in Science and hobby joining forces for the discovery of three new Corydoras (Siluriformes: Callichthyidae) from the rio Tapajós basin, Brazil, with comments on Corydoras sp. CW111
FIGURE 13 | Paratypes of Corydoras psamathos photographed alive, showing general color pattern and morphology in lateral view in (A) INPA 59772, 23.7 mm SL, (B) INPA 59773, 30.2 mm SL, and (C) INPA 59773, 29.3 mm SL. Specimen (A) is from the rio Jamanxim, and specimens (B–C) are from the igarapé Santa Júlia, rio Tapajós basin.
FIGURE 4 in Science and hobby joining forces for the discovery of three new Corydoras (Siluriformes: Callichthyidae) from the rio Tapajós basin, Brazil, with comments on Corydoras sp. CW111
FIGURE 4 | Uncatalogued aquarium specimens of Corydoras thanatos photographed alive, showing general color pattern and morphology of (A) a female specimen, and (B) a dimorphic male specimen. Photos by Hans Evers.
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.