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23,351 results for “Comparative”
Fig. 5 in Comparative morphology study of the male genitalia in the tribe Astathini from China (Coleoptera: Cerambycidae)
Fig. 5. Tegmen of Bacchisa, dorsal view. A–F. R2> 1/20. A. B. atritarsis. B. B. basalis. C. B. comate. D. B. dioica. E. B. fortunei. F. B. rigida. G. R2 <1/20, B. guerryi. Scale bar = 0.5 mm.
Fig. 2 in Comparative morphology study of the male genitalia in the tribe Astathini from China (Coleoptera: Cerambycidae)
Fig. 2. Tegmen in dorsal view. A. Anastathes parvus hainana. B. A. robustus. C. Bacchisa fortunei. D. Plaxomicrus ellipticus. E. Tetraophthalmus episcopalism. F. T. janthinipennis cyanopterus. G. T. janthinipennis janthinipennis. Scale bar = 0.5 mm.
Figs 1 in Comparative morphology study of the male genitalia in the tribe Astathini from China (Coleoptera: Cerambycidae)
Figs 1. Male genitalia of Astathini (Anastathes robustus Gressitt, 1940). A. Male genitalia, lateral view. B. Base of tegmen, dorsal view. C. Base of tegmen, lateral view. D. Median lobe plus median struts, dorsal view. E. 8th abdominal sternum. F. Rod at apex of internal sac. Abbreviation: ed. ejaculatory duct; is. internal sac; ll. lateral lobes; ml. median lobe; ms. median struts; ri. ringed part; ro. roof; rod. rod; sg. spiculum gastrale; st. sternum; te. tergaum. Scale bars = 0.5 mm.
Fig. 4 in Comparative morphology study of the male genitalia in the tribe Astathini from China (Coleoptera: Cerambycidae)
Fig. 4. Median lobe plus median struts and rod at apex of internal sac, dorsal view. A–B. Anastathes parvus hainana. C–D. A. robustus. E–F. Bacchisa dioica. G–H. Plaxomicrus ellipticus. I–J. Tetraophthalmus episcopalism. K–L. T. janthinipennis cyanopterus. M–N. T. janthinipennis janthinipennis. Scale bars = 0.5 mm.
Figure 1 in Comparative biology and growth rate of the two predatory mites, Cydnoseius negevi and Neoseiulus californicus (Acari: Phytoseiidae), reared on two pea cultivars
Figure 1. Age-specific fecundity (mx) and survivorship (lx) of Cydnoseius negevi and Neoseiulus californicus reared on two pea cultivars fed on nymphal stages of Tetranychus urticae at 27 ± 1°C.
Figs 4–15 in Comparative morphological study on the genus Leptura Linnaeus of China (Coleoptera: Cerambycidae: Lepturinae)
Figs 4–15. Adults of Leptura, dorsal view. 4. L. alticola Gressitt, holotype. 5. L. aethiops Poda. 6. L. ambulatrix (Gressitt), holotype. 7. L. ambulatrix (Gressitt). 8–9. L. arcuata Panzer. 10–11. L. arcifera (Blanchard). 12–15. L. auratopilosa (Matsushita). 11. L. semilunata Gressitt, holotype, synonym of L. arcifera. 12. Strangalia quadranglithoracica Tamanuki, holotype, synonym of L. auratopilosa. 13. S. auratopilosa Matsushita, holotype, synonym of L. auratopilosa. 4, 7–11, 13–15. Female. 5–6, 12. Male. Scale bars= 5 mm.
Figs 28–39 in Comparative morphological study on the genus Leptura Linnaeus of China (Coleoptera: Cerambycidae: Lepturinae)
Figs 28–39. Adults of Leptura, dorsal view. 28. L. formosomontana Kano, holotype. 29–30. L. tattakana (Kano, 1933). 31. L. ochraceofasciata ochrotela Bates. 32. L. quadrifasciata Linnaeus. 33–34. L. subtilis Bates. 35. L. zonifera (Blanchard). 36–38. L. taranan (Kano) 39. L. tatsienlua Gressitt, holotype. 29. S. horishana Matsushita, holotype, synonym of L. tattakana. 30. S. mushana Tamanuki, holotype, synonym of L. tattakana. 36. L. taranan (Kano), holotype. 28–29, 31–33, 35, 37, 39. Female. 30, 34, 36, 38. Male. Scale bars= 5 mm.
Figs 1–3 in Comparative morphological study on the genus Leptura Linnaeus of China (Coleoptera: Cerambycidae: Lepturinae)
Figs 1–3. Structures of Leptura (L. aurosericans Fairmaire, 1895, female). 1. Dorsal view. 2. Ventral view. 3. Head, frontal view.
Figs 55–58. Female genitalia. 55–56. L in Comparative morphological study on the genus Leptura Linnaeus of China (Coleoptera: Cerambycidae: Lepturinae)
Figs 55–58. Female genitalia. 55–56. L. auratopilosa (Matsushita). 57–58. L. aurosericans Fairmaire. 55, 57. Dorsal view. 56, 58. Ventral view, with ovipositor. Scale bars= 1 mm.
Figs 16–27 in Comparative morphological study on the genus Leptura Linnaeus of China (Coleoptera: Cerambycidae: Lepturinae)
Figs 16–27. Adults of Leptura, dorsal view. 16–18. L. aurosericans Fairmaire. 19. L. fisheriana Gressitt, holotype. 20–21. L. duodecimguttata Fabricius. 22. L. gradatula Holzschuh, paratype. 23. L. grahamiana Gressitt, holotype. 24–25. L. linwenhsini Ohbayshi & Chou. 26–27. L. lavinia Gahan. 18. L. aurosericans Fairmaire, holotype. 24. L. linwenhsini Ohbayshi & Chou, paratype. 25. L. linwenhsini Ohbayshi & Chou, holotype. 27. L. lavinia Gahan, holotype. 16, 19–20, 23–24, 26–27. Female. 17–18, 21–22, 25. Male. Scale bars= 5 mm.
Webis Comparative Questions 2022
<p>Webis Comparative Questions 2022 dataset contains about 31,000 questions labeled as comparative or not.</p> <p>3,500 comparative questions are labeled on the token level with comparison objects, aspects, predicates, or none.</p> <p>For 950 questions, text passages that potentially answer the questions are labeled with the stance: pro first comparison object, pro second, neutral, or no stance.</p>
Comparative genomics of human distal lung Streptococci
<p><strong>Comparative genomics of human lung streptococcal isolates</strong></p> <p>1. All analysis pipelines and scripts are on the GitHub page of Slipa Kanungo: <a href="https://github.com/slipa17/Whole-genome-sequencing-and-comparative-genomics-of-human-lung-streptococcal-isolates">https://github.com/slipa17/Whole-genome-sequencing-and-comparative-genomics-of-human-lung-streptococcal-isolates</a></p> <p>2. Additional analysis pipelines (especially Dataset S12) are on the GitHub page of Garance Sarton-Lohéac: <a href="https://github.com/gsartonl/Publication_Sarton-Loheac_2022">https://github.com/gsartonl/Publication_Sarton-Loheac_2022</a></p> <p>3. All raw data were uploaded to NCBI SRA BioProject <a href="https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1001255">PRJNA1001255</a></p> <p><strong>Supplementary Table bundle: for peer review purposes</strong></p> <p><strong>Supplementary Datasets</strong></p> <ul> <li><strong>Dataset S1_Lung_Streptococcus_genomes_metaQUAST: </strong>MetaQUAST (Quality Assessment Tool for Metagenome Assemblies) output including HTML and PDF reports, summary statistics including total contigs, assembly size, and N50. Coverage analysis assesses how well reference genomes are represented, contig length distribution plots visualize contig length ranges, mis-assembly analysis detects potential errors and graphical representations to visualize assemblies.</li> <li><strong>Dataset S2_Lung_streptococcus_isolate_genomes: </strong>Nucleotide FASTA files of six lung streptococcal isolates obtained that were obtained via whole genome sequencing.</li> <li><strong>Dataset S3_Lung_isolates_genome_annotation_prokka: </strong>Output folders after annotation of six lung streptococcal isolates with PROKKA. This includes protein FASTA, GenBank files and GFF annotations.</li> <li> <p><strong>Dataset S4_TYGS_dDDH_analysis: </strong>Contains results of TYGS analysis from DSMZ including downloadable reports. Outputs including taxonomic identification with genus, species, and strain details, a TYGS index for tracking genomes, genome quality assessment metrics, GBDP whole genome and 16S rRNA phylogenetic tree files, comparisons with reference type strains in the TYGS database with table.</p> </li> <li> <p><strong>Dataset S5_Reference_type_strains_TYGS_genomes: </strong>Nucleotide FASTA files of 47 closely related reference <em>Streptococcus</em> genomes listed by TYGS and downloaded from NCBI.</p> </li> <li> <p><strong>Dataset S6_Reference_type_strains_TYGS_proteins: </strong>Protein FASTA files of 47 closely related reference <em>Streptococcus</em> genomes listed by TYGS and downloaded from NCBI. </p> </li> <li> <p><strong>Dataset S7_Lung_streptococcus_isolate_proteins: </strong>Protein FASTA files of 6 six lung streptococcal isolates. </p> </li> <li> <p><strong>Dataset S8_OrthoFinder_core_genome: </strong>OrthoFinder is a bioinformatics tool that offers comprehensive outputs for orthology inference across multiple genomes. The output includes overall statistics, gene duplication information, orthologous genes, orthologous gene tree, single copy orthologous genes and STAG evolutionary trees.</p> </li> <li> <p><strong>Dataset S9_Pan-Strep_BLAST_db: </strong>BLAST database using the <code>makeblastdb</code> command of NCBI datasets command line tool. This is constructed using protein FASTA files of 47 closely related reference <em>Streptococcus</em> genomes listed by TYGS and downloaded from NCBI.</p> </li> <li><strong>Dataset S10_OrthoVenn_cluster_files: </strong>OrthoVenn is a web-based tool for orthologous gene comparison. Downloadable results include Venn diagrams depicting shared and unique orthologous clusters amongst species, tabular results detailing genes within each cluster and their annotations. Functional enrichment analysis for Gene Ontology terms and KEGG pathways are also provided. enhances biological insights.</li> <li> <p><strong>Dataset S11_COG_analysis: </strong>Results of COG analysis of six lung streptococcal isolates individually using eggNOG (evolutionary genealogy of genes: Non-supervised Orthologous Groups) webtool. The output includes information on Clusters of Orthologous Groups (COGs) categorizing them into functional groups such as metabolism, information storage and processing, and cellular processes and signalling.</p> </li> <li> <p><strong>Dataset S12_CAZymes_lung_streptococci: </strong>Results of CAZyme analysis using a custom rule-based pipeline mostly based on dbCAN (Database for Carbohydrate-Active enZymes) provides information on the carbohydrate-active enzymes present in genomic datasets. The output includes the annotation of enzymes involved in the degradation, modification, or biosynthesis of carbohydrates: glycoside hydrolases (GH), glycosyltransferases (GT), carbohydrate-binding modules (CBM), Auxillary Activities (AA), Carbohydrates Esterases (CE) and Polysaccharide lyases (PL).</p> </li> <li> <p><strong>Dataset S13_pneumolysin_analysis: </strong>Results alignment and phylogeny of Pnuemolysin protein in <em>Streptococcus pneumoniae</em>, <em>Streptococcus pseudopneumoniae</em> and Streptococcus isolate P2E5 found by ABRIcate analysis. Visual plots by pyGenomeViz.</p> </li> <li> <p><strong>Dataset S14_capsule_analysis:</strong> Results from BLAST analysis of <em>Streptococcus pneumoniae </em>D39 capsular biosynthesis operon genes against the Pan-Strep (Dataset S10). Extracted of matching genes followed alignment and phylogeny. Visual plots by pyGenomeViz.</p> </li> <li> <p><strong>Dataset S15_Lung_isolate_HOMD_TYGS_comparison: </strong>Protein FASTA files of 47 closely related reference <em>Streptococcus</em> genomes listed by TYGS and downloaded from NCBI, 6 six lung streptococcal isolates and 47 streptococcal genomes from downloaded from human oral microbiome database (eHOMD).</p> </li> </ul>
Supplementary material 2 from: Steinberg E, Nieves M, Mudry M (2014) Multiple sex chromosome systems in howler monkeys (Platyrrhini, Alouatta). Comparative Cytogenetics 8(1): 43-69. https://doi.org/10.3897/compcytogen.v8i1.6716
Supplementary Figure S. (doi: 10.3897/CompCytogen.v8i1.6716.app2) File format: Microsoft Word file (doc).:
Supplementary material 1 from: Gruber S, Haddad C, Kasahara S (2012) Karyotype analysis of seven species of the tribe Lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques. Comparative Cytogenetics 6(4): 409-423. https://doi.org/10.3897/compcytogen.v6i4.3945
Giemsa-stained metaphases I. a. Aparasphenodon bokermanni, 2n = 24; b. Itapotihyla langsdorffii, 2n = 24; c. Trachycephalus sp., 2n = 24; d. T. mesophaeus, 2n = 24; e. T. typhonius, 2n = 24; f. Phyllodytes edelmoi, 2n = 22. g. P. luteolus, 2n = 22. Bar = 10 m.
Figure 3: The microscopy images fo neuronal cells generated by SWCNT (a) and MWCNT (b)-COMPARATIVE STUDY OF SINGLE- AND MULTI-WALL CARBON NANOTUBES WITH APPLICATION IN CEREBRAL ANEURYSM
<p>Carbon nanotubes (CNTs) are nanometer-scale cylindrical graphitic struc-<br> tures that exhibit extraordinary physical properties as determined by their<br> structure [6]. Developing neural implants and the process of neuron regener-<br> ation are extremely di±cult. Nerve cells require the right environment and<br> the right growth factors at the right time to grow and proliferate. The elec-<br> trical conductive properties of these nanotubes o®er the possibility of using<br> it as a replacement to transmit and receive signals. The resulting 'hair like'<br> conductive wires that incorporate the properties of electrodes, permeable mi-<br> cro°uidic conduits and the porosity of the CNTs was found to promote cell<br> growth, migration and proliferation. The bridging consists either of an axon<br> or bundles of axons and dendrites. In some cases the bridge is covered with<br> clusters of cells [7]. These bridges form very e±ciently over quartz surfaces<br> which are apparently very poor surfaces for cell attachment. Fig. 2 shows the<br> evolution of a network generated by SWCNT and MWCNT. The data show<br> that cells ¯rst aggregate at the NT islands. As they complete this step axons<br> and dendrites begin to form and to build connections.<br> Also, has been observed for MWCNT higher connections than for SWCNT,<br> Figure 3.</p>
Figure 2: The microscopy images fo neuronal cells control (a) generated by MWCNT (b) and SWCNT (c)-COMPARATIVE STUDY OF SINGLE- AND MULTI-WALL CARBON NANOTUBES WITH APPLICATION IN CEREBRAL ANEURYSM
<p>Fig. 2 shows the evolution of a network generated by SWCNT and MWCNT. The data show<br> that cells ¯rst aggregate at the NT islands. As they complete this step axons and dendrites begin to form and to build connections.</p>
Figure 1: The structure of CNT-COMPARATIVE STUDY OF SINGLE- AND MULTI-WALL CARBON NANOTUBES WITH APPLICATION IN CEREBRAL ANEURYSM
<p>Carbon nanotubes (CNTs) are nanometer-scale cylindrical graphitic struc-<br> tures that exhibit extraordinary physical properties as determined by their<br> structure [6]. Developing neural implants and the process of neuron regener-<br> ation are extremely difcult. Nerve cells require the right environment and<br> the right growth factors at the right time to grow and proliferate. The elec-<br> trical conductive properties of these nanotubes o®er the possibility of using<br> it as a replacement to transmit and receive signals. The resulting 'hair like'<br> conductive wires that incorporate the properties of electrodes, permeable mi-<br> cro°uidic conduits and the porosity of the CNTs was found to promote cell<br> growth, migration and proliferation. The bridging consists either of an axon<br> or bundles of axons and dendrites. In some cases the bridge is covered with<br> clusters of cells [7]. These bridges form very e±ciently over quartz surfaces<br> which are apparently very poor surfaces for cell attachment.</p>
Unveiling Variations: A Comparative Study of VR Headsets Regarding Eye Tracking Volume, Gaze Accuracy, and Precision
<p>This repository contains the supplementary material to the paper "Unveiling Variations: A Comparative Study of VR Headsets Regarding Eye Tracking Volume, Gaze Accuracy, and Precision".</p> <p>Functions for converting between Fick angles, 3D vectors, and visual angles are authored by Per Baekgaard, available at <em><a href="https://github.com/baekgaard/fickpy">https://github.com/baekgaard/fickpy</a> </em></p> <p> </p> <p>In detail:</p> <p>- Dataset</p> <ul> <li>Analysis scripts</li> </ul> <p>- The Unity application:</p> <ul> <li>testHTCTobiiPro - TobiiPro licence is not included in the upload</li> <li>testViveProEye_sranipal</li> <li>testAndroid <ul> <li>scene: eval_viveFocus3, when building apk, use only Wave as xr provider</li> <li>scene: eval_metaQuestPro, Meta Quest Pro standalone</li> <li>scene: eval_metaQuestPro_pcVr, Meta Quest Pro tethered</li> </ul> </li> </ul>
FIGURE 4 in Comparative cytogenetic survey of the giant bonytongue Arapaima fish (Osteoglossiformes: Arapaimidae), across different Amazonian and Tocantins/Araguaia River basins
FIGURE 4 | Metaphase plates of Arapaima gigas from Mamirauá (MAM) population (Amazon River basin) hybridized with repetitive DNA sequences, including mono-, di- and trinucleotide microsatellites and the multigene families U2 snDNA. Bar=5 µm.
FIGURE 2 in Comparative cytogenetic survey of the giant bonytongue Arapaima fish (Osteoglossiformes: Arapaimidae), across different Amazonian and Tocantins/Araguaia River basins
FIGURE 2 | Karyotypes of Arapaima gigas male (A–C) and female (D–F) from Javaé (JAV) population (Araguaia-Tocantins River basin), sequentially arranged from Giemsa-stained (A and D), C-banded (B and E), and double-FISH (C and F) with 5S rDNA (green) and 18S rDNA (red) labeled chromosomes. Bar=5 µm.
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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.