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23,351 results for “Comparative”
FIGURE 3 in Tracking the evolutionary pathways among Brazilian Lebiasina species (Teleostei: Lebiasinidae): a chromosomal and genomic comparative investigation
FIGURE 3 | Metaphase chromosomes of Lebiasina minuta hybridized with microsatellite probes (A, B and C) and telomeric probes (D), using red signals. Scale bar = 5 µm.
FIGURE 2 in Tracking the evolutionary pathways among Brazilian Lebiasina species (Teleostei: Lebiasinidae): a chromosomal and genomic comparative investigation
FIGURE 2 | Male and female karyotypes of Lebiasina minuta after A. Giemsa staining, B. C-banding, and C. "double-FISH" with 5S (red) and 18S (green) rDNA probes. Scale bar = 5 µm.
FIGURE 1 in Tracking the evolutionary pathways among Brazilian Lebiasina species (Teleostei: Lebiasinidae): a chromosomal and genomic comparative investigation
FIGURE 1 | Distribution of Lebiasina species with available cytogenetic data, highlighting the Brazilian state of Pará (orange) and Ecuadorian (purple) territories A. 1. L. bimaculata, 2. L. melanoguttata (Sassi et al., 2019), and 3. L. minuta (this study). B. Highlights the position of A in South America, and C. indicates that, although close, species 2 and 3 does not share an overlapped distribution.
FIGURE 1 in Comparative cytogenetic analyses in Ancistrus species (Siluriformes: Loricariidae)
FIGURE 1 | Karyotypes of Ancistrus aguaboensis (A–B) and Ancistrus cf. multispinis (C–D) submitted do Giemsa staining (A–C) and C-banding (B–D). The chromosomes pairs with NORs sites are evidenced in the figure details (boxes). Bar = 10 µm.
FIGURE 2 in Comparative cytogenetic analyses in Ancistrus species (Siluriformes: Loricariidae)
FIGURE 2 | Karyotypes of Ancistrus aguaboensis (A–B) and Ancistrus cf. multispinis (C–D) submitted to FISH using 5S rDNA, 18S rDNA and (TTAGGG)n probes. In (A–C), 5S rDNA (in red) and 18S rDNA (in green) sites; in (B–D), terminal red markers evidenced (TTAGGG)n sites. Bar = 10 µm.
Figure 11 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 11. The efficacy of RM of orange peels against human pathogenic bacteria. ****Extremely significant among compared groups at p <0.05 level. Test 1: RM of Valen-cia orange; Test 2: RM of Mandarin orange; Test 3: RM of African navel orange.
Figure 6 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 6. The structure of bioactive compounds of RM of African Navel orange peel (1) Limonene; (2) Hexadecanoic acid, 2-hydroxy-1- (hydroxymethyl) ethyl; (3) 9,12-Octadecadienoic acid (Z,Z)-, methyl ester; (4) Terephthalic acid, di(2-ethylhexyl) ester; (5) α-Sitosterol; (6) α-D-Glucopyranose, 4-O-α-D-galactopyranosyl-; (7) 2-Methoxy-4-vinylphenol; (8) Eugenol; (9) cis-Vaccenic acid; (10) De-canal; (11) Vitamin E; (12) Dichloroxylenol.
Figure 3 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 3. GC-MS chromatogram of the RMs of orange peels. (A) RM of Valencia orange; (B) RM of Mandarin orange; (C) RM of African Navel orange.
Figure 2 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 2. The morphology of orange fruits. (A) Valenica orange; (B) Madarin orange; (C) African Navel orange.
Figure 5 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 5. The structure of bioactive compounds of RM of Mandarin orange peel (1) Lim-onene; (2) Octadecanoic acid, 2-hydroxy-1- (hydroxymethyl) ethyl; (3) Hexadecanoic acid, 2-hydroxy-1-(hydroxymethyl) ethyl; (4) Tetradecanamide; (5) n-Hexadecanoic acid; (6) α-D-Mannofuranoside, 1-O-(10-undecenyl)-; (7) 3-Deoxy-d-mannoic lactone; (8) Desulpho-sinigrin; (9) 2-Methoxy-4-vinylphenol; (10) Decanal; (11) Vitamin E; (12) 1-Monolinoleoylglycerol trimethylsilyl ether.
Figure 4 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 4. The structure of bioactive compounds of RM of Valencia orange peel (1) Limonene; (2) 9-Octadecenamide, (Z)-; (3) Hexadecanoic acid, 2- hy-droxy-1-(hydroxymethyl)ethyl; (4) Octadecanoic acid, 2-hydroxy-1-(hydroxymethyl)ethyl; (5) Tetradecanamide; (6) Hexadecanamide; (7) Ethyl iso-allocholate; (8) Ethyl α-d-glucopyranoside; (9) d-Glycero-d-galacto-heptose; (10) α-Sitosterol; (11) Vitamin E; (12) 4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5,6,7-trimethoxy-.
Figure 1 in Molecular classification and comparative phylogeographic study of insectivorous bat species (Pipisitrellus coromandra) from Punjab, Pakistan
Figure 1. Mutation analysis of representative sequence of specimen collected from (Kahna/District Lahore KA-III) with first top BLAST search result of species Pipistrellus coromandra from India (Accession No: MG821188).
Figure 3 in Molecular classification and comparative phylogeographic study of insectivorous bat species (Pipisitrellus coromandra) from Punjab, Pakistan
Figure 3. Neighbour-joining tree of genetic similarity based on COI gene. Data consisted of sequences from this study (n=20) and sequence data of closely related and similar species from other countries (n=59). Numbers at nodes are bootstrap support percentages of 70 or greater. The evolutionary distances were computed using the Kimura 2-parameter method (Kimura, 1980) in MEGA7.
Figure 2 in Molecular classification and comparative phylogeographic study of insectivorous bat species (Pipisitrellus coromandra) from Punjab, Pakistan
Figure 2. Mutation analysis of representative sequence of specimen collected from (Kahna/District Lahore KA-III) with top second BLAST search result of species Pipistrellus tenuis from Vietnam (Accession No: HM541298).
Fig. 1 in Comparative analysis of morphospace of Neotropical Sericini (Coleoptera: Scarabaeidae): disparity in the light of species diversity and activity patterns
Fig. 1 Measured traits and specimen habitus (examples). Schematic drawings of a Sericini beetle (from Ahrens, 2004): A dorsal view; D partial lateral aspect; B head, dorsal view, C head lateral view; E leg, ventrolateral view; F Maladera cardoni; G Neoserica sp.; H Anomioserica sp.; I Oxyserica sp.; J Symmela mutabilis; K Astanea producta. EL maximal elytra length, EW maximal body width, MEL maximal length of metepisternum, ED maximal eye diameter, IOD minimal interocular distance, MCL maximal length of metacoxa, MTL maximal length of metatibia, MTW maximal width of metatibia
Fig. 5 in Comparative analysis of morphospace of Neotropical Sericini (Coleoptera: Scarabaeidae): disparity in the light of species diversity and activity patterns
Fig. 5 Patterns of disparity derived from discrete morphological data: plots of axis 1 and 2 from principal coordinate analysis. Color coding of Neotropical genera corresponds to that of Fig. 4
Fig. 3 in Comparative analysis of morphospace of Neotropical Sericini (Coleoptera: Scarabaeidae): disparity in the light of species diversity and activity patterns
Fig. 3 Boxplots for selected genera of the total body length (in mm), of the ratio maximal body width/ maximal elytra length (EL), of the ratio metatibial length/maximal metatibial width, of the ratio maxi-
Fig. 4 in Comparative analysis of morphospace of Neotropical Sericini (Coleoptera: Scarabaeidae): disparity in the light of species diversity and activity patterns
Fig. 4 Patterns of disparity derived from morphospace: plots of PC 1 and 2 A raw data (all); B raw data (BL excluded), C log-normalized data (all); D log-normalized data (BL excluded)
Fig. 2 in Comparative analysis of morphospace of Neotropical Sericini (Coleoptera: Scarabaeidae): disparity in the light of species diversity and activity patterns
Fig. 2 Illustration of potential trait correlation: A elytral length vs total body length, B maximum body width vs. vs total body length, C maximum body width vs. elytral length, D size of eyes (i.e., maximum ratio ocular diameter/minimum interocular distance) vs maxi-
Cowl comparative performance evaluation
<p>Results of a comparative performance evaluation between: <a href="https://swot.sisinflab.poliba.it/cowl">Cowl</a> (version 0.7.2), <a href="https://owl-cpp.sourceforge.net">owlcpp</a> (version 0.3.3), <a href="http://owlcs.github.io/owlapi">OWL API</a> (version 5.5.0), and <a href="https://owlready2.readthedocs.io">Owlready2</a> (version 0.46).</p> <p>Generated using the <a href="http://swot.sisinflab.poliba.it/evowluator">evOWLuator</a> framework on a subset of the <a href="../record/10791">ORE 2014 Reasoner Competition</a> dataset.</p> <p>Publication: <a title="Persistent link using digital object identifier" href="https://doi.org/10.1016/j.iot.2024.101439" target="_blank" rel="noreferrer noopener"><span><span>https://doi.org/10.1016/j.iot.2024.101439</span></span></a></p>
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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.