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3,878 results for “Molecular data”
Fig. 10 in Six new species of Zaischnopsis Ashmead (Hymenoptera: Chalcidoidea: Eupelmidae) from China based on morphological and molecular data
Fig. 10. SEM photos of dorsellum and propodeum. A. Zaischnopsis covid Jiang & Peng sp. nov. B. Z. fuscolivida Tang & Peng sp. nov. C. Z. lii Jiang & Peng sp. nov. D. Z. pacis Jiang & Peng sp. nov. E. Z. campaniformis Tang & Peng sp. nov. F. Z. zhongi Jiang & Peng sp. nov.
Fig. 7. SEM photos. A‒F. Head. A in Six new species of Zaischnopsis Ashmead (Hymenoptera: Chalcidoidea: Eupelmidae) from China based on morphological and molecular data
Fig. 7. SEM photos. A‒F. Head. A. Zaischnopsis covid Jiang & Peng sp. nov. B. Z. fuscolivida Tang & Peng sp. nov. C. Z. lii Jiang & Peng sp. nov. D. Z. pacis Jiang & Peng sp. nov. E. Z. campaniformis Tang & Peng sp. nov. F. Z. zhongi Jiang & Peng sp. nov. G. Z. covid, front part of frons, show sculpture and setae. H. Z. campaniformis, sculpture and setae around anterior ocellus. I. Z. lii, front part of frons, show sculpture and setae.
Fig. 6 in Six new species of Zaischnopsis Ashmead (Hymenoptera: Chalcidoidea: Eupelmidae) from China based on morphological and molecular data
Fig. 6. Zaischnopsis zhongi Jiang & Peng sp. nov. A. Body, lateral view. B. Mesosoma, dorsal view. C. Head, front view. D. Head, dorsal view. E. Fore wing. F. Head, lateral view. G. Antenna. H. Mesosoma, lateral view. I. Propodeum.
Fig. 5 in Six new species of Zaischnopsis Ashmead (Hymenoptera: Chalcidoidea: Eupelmidae) from China based on morphological and molecular data
Fig. 5. Zaischnopsis campaniformisTang & Peng sp. nov. A. Body, lateral view.B. Mesosoma, dorsal view. C. Head, front view. D. Head, dorsal view. E. Fore wing. F. Antenna. G. Mesosoma, lateral view. H. Head, lateral view. I. Propodeum.
Fig. 9 in Six new species of Zaischnopsis Ashmead (Hymenoptera: Chalcidoidea: Eupelmidae) from China based on morphological and molecular data
Fig. 9. SEM photos of antennae. A‒B. Zaischnopsis covid Jiang & Peng sp. nov. C‒D. Z. fuscolivida Tang & Peng sp. nov. E‒F. Z. lii Jiang & Peng sp. nov. G‒H. Z. campaniformis Tang & Peng sp. nov. I. Z. pacis Jiang & Peng sp. nov.
Fig. 2 in Six new species of Zaischnopsis Ashmead (Hymenoptera: Chalcidoidea: Eupelmidae) from China based on morphological and molecular data
Fig. 2. Zaischnopsis fuscolivida Tang & Peng sp. nov. A. Body, lateral view. B. Mesosoma, dorsal view. C. Head, front view. D. Head, dorsal view. E. Fore wing. F. Head, lateral view. G. Antenna. H. Mesosoma, lateral view. I. Propodeum.
Fig. 1 in Six new species of Zaischnopsis Ashmead (Hymenoptera: Chalcidoidea: Eupelmidae) from China based on morphological and molecular data
Fig. 1. Zaischnopsis covid Jiang & Peng sp. nov. A. Body, lateral view. B. Mesosoma, dorsal view. C. Head, front view. D. Head, dorsal view. E. Fore wing. F. Head, lateral view. G. Antenna. H. Mesosoma, lateral view. I. Propodeum.
Functional and molecular characterization of suicidality factors using phenotypic and genome-wide data
<p>GWAS summary statistics for Functional and molecular characterization of suicidality factors using phenotypic and genome-wide data published in Molecular Psychiatry by Quintero Reis A, Newton BA, Kessler R, Polimanti R, and Wendt FR.</p>
Fig. 7 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 7. Area cladogram for Paralamyctes based on relationships under most congruent parameters for combined morphological and molecular data (Fig. 3, left cladogram). Stable clades are indicated (present in at least six parameter sets for the combined data).
Fig. 5 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 5. Details of the pretarsus of Henicopidae, showing characters 57 and 58 in Appendix 1. A. Paralamyctes (Thingathinga) grayi, dorsal view. B. Paralamyctes (Thingathinga) validus, anterior view. C. Paralamyctes (Haasiella) trailli, anterior view. D. Cermatobius japonicus, posterior view. E. Lamyctes emarginatus, anterior view. F. Anopsobius neozelanicus, dorsal view. All scales 10 m.
Fig. 3 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 3. Cladograms based on the combined analysis of all data (morphological + molecular). Cladogram at left is the single shortest tree of 7343 steps obtained for the most congruent parameter set (111); cladogram at right is strict consensus for all 12 parameters. Numbers on branches indicate jackknife frequencies.
Fig. 4 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 4. Graphic plots of sensitivity analyses. Black square = monophyly of indicated clade under gap cost and transversion:transition ratio shown along the axes; grey square = monophyly in some minimal length cladograms; white square = non-monophyly.
Fig. 2 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 2. Cladograms based on the combined analysis of all molecular data. Cladogram at left is the single tree at 7174 steps obtained for the most congruent parameter set (111); cladogram at right is strict consensus for all 12 parameter sets. Numbers on branches indicate jackknife frequencies.
Fig. 1 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 1. Strict consensus of 10 000 shortest cladograms based on morphological data (134 steps; CI = 0.56; RI = 0.86). Branches for the ingroup (Henicopidae) appear darker than those for the outgroup (Lithobiidae). Numbers above branches indicate jackknife frequencies; numbers below branches indicate absolute Bremer support and relative fit difference, RFD, shown as a percentage (see text for a description of these support measures). Labels on branches indicate groups recovered in all morphological analyses (Anopsobiinae, Lamyctes-Henicops Group within Henicopini, Zygethobiini) and traditional membership of Henicopinae. Paralamyctes (unresolved) is traditionally assigned to Henicopini.
Tissue microarray data and processing scripts for The molecular consequences of androgen activity in the human breast
<p>This repository contains raw and processed data from the CODEX imaging dataset in this publication.</p> <p>The RAW data tables provide the resulting nuclei and membrane staining signals obtained from the nuclei segmentation described in the Methods.</p> <p>The processed data file provides the clustered and annotated version described in Methods.</p> <p>The repository also contains two scripts describing the processing of snRNA-seq and snATAC-seq data.</p>
Data underlying OpenPBTA Manuscript Figures and Molecular Alterations
<p>This upload contains CSV files that represent data contained in plots shown in the OpenPBTA manuscript. It is intended to facilitate inspection of the underlying data shown in each figure and to explicitly capture which samples are included in figures (where applicable). Please see the README included in the upload for more information about individual files.</p> <p>To <strong>reproduce the figures</strong>, we recommend using the code in the analysis repository: <a href="https://github.com/AlexsLemonade/OpenPBTA-analysis">https://github.com/AlexsLemonade/OpenPBTA-analysis</a>. Please see the <code>figures/</code> directory documentation in the repository and the documentation for figure generation scripts (<code>figures/scripts/README.md</code>).</p> <p>The version of the upload corresponds to the version of the release in the analysis repository.</p>
Simulation data and code used for the publication in Magn. Reson. "Time-domain proton-detected local-field NMR for molecular structure determination in complex lipid membranes"
<p>Simulation data used in the publication Magn. Reson. "Time-domain proton-detected local-field NMR for molecular structure determination in complex lipid membranes". The simulation data set, and the code developed to generate such data, are included. Details in the published paper </p>
Research data supporting: "TimeSOAP: Tracking high-dimensional fluctuations in complex molecular systems via time variations of SOAP spectra"
<p>This repository contains the set of data shown in the paper <strong>"<em>Time</em>SOAP: Tracking high-dimensional fluctuations in complex molecular systems via time variations of SOAP spectra"</strong>, published on The Journal of Chemical Physics (DOI: 10.1063/5.0147025).</p>
Figure 5. BEAST chronogram from a data set corresponding with Table 1 in Verifying Australian Nilotanypus Kieffer (Chironomidae) In A Global Perspective: Molecular Phylogenetic And Temporal Analyses, New Species And Emended Generic Diagnoses
Figure 5. BEAST chronogram from a data set corresponding with Table 1. Values at nodes are time to most recent common ancestor (tmrca) with HPD (95% Highest Posterior Density) intervals in parentheses. The time scale is in millions of years before present.
FIG. 33 in A new subfamily classification of the highly diversified Dorippidae H. Milne Edwards, 1837 (Crustacea, Decapoda, Brachyura, Dorippoidea), using morphological, molecular and palaeotonlogical data, with special emphasis on its unique female reproductive system
FIG. 33. — Callosities in Dorippoidinae n. subfam. (Dorippoides) and Dorippinae n. stat. (Dorippe): A, callosity reduced to a thin calcified band: Dorippoides facchino (Herbst, 1785), ♂ 25.3 × 32.0 mm, Malaysia, Johore, Pontian, ZRC 1991.6672. B, no apparent callosity in male Dorippoides nudipes Manning & Holthuis, 1986, ♂ 16.2 × 19.4 mm, Iran, ZRC 2017.1227. C, callosity as a thick, elongated bulge: Dorippe quadridens (Fabricius, 1793), ♂ 39.0 × 41.4 mm, Thailand, Pattani Province, ZRC 2003.0126. D-F, callosity as a hemicircular structure: close-up views from different angles: D, E. Dorippe sinica Chen, 1980. D, ♀ 36.2 × 39.5 mm, China, Guangdong, Nanao Island, ZRC 1999.0470; E, ♂ 36.6 × 38.6 mm, Japan, Kochi, Shikoku, SMF 57855. F, D. frascone (Herbst, 1785), ♂ 29.7 × 31.0 mm, Philippines, Exp. Panglao 2004, ZRC 2008.0076. G, H, callosity as an arched double cup: D. tenuipes Chen, 1980, South China Sea, ZRC 1999.0009: G, ovigerous ♀ 17.3 × 19.6 mm; H, ♂ 13.2 × 14.2 mm. Abbreviations: b, branchiostegite; c, callosity; cx2-cx5, P2-P5 coxae; f, sulcated part of coxa; l, onepiece lateroventral part of coxa; m, membrane; p, pleon; pr, process of retention of female pleonal somite 2; pl6, exposed pleurite 6; P2-P5, pereiopods 2-5; r, rim of carapace posterior margin; s, strip along posterior rim; 1, 2, pleonal somites 1, 2; t, bottom of callosity with special texture; 7, 8, thoracic sternites 7, 8.
ScienceDex guides
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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.