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562 results for “genetic divergences”
Type I Interferon induces binding of STAT1 to Bcl6: Divergent Roles of STAT-family transcription factors in the T follicular helper cell genetic program
GEO Series GSE51531. Mus musculus. 1 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Clonal Selection Drives Genetic Divergence of Metastatic Medulloblastoma
GEO Series GSE34356. Homo sapiens. 36 samples. Type: Methylation profiling by array; Genome variation profiling by SNP array.
Clonal Selection Drives Genetic Divergence of Metastatic Medulloblastoma [Affymetrix SNP6 Arrays]
GEO Series GSE34280. Homo sapiens. 17 samples. Type: Genome variation profiling by SNP array.
FIGURE 24 in Disentangling vines: a study of morphological crypsis and genetic divergence in vine snakes (Squamata: Colubridae: Ahaetulla) with the description of five new species from Peninsular India
FIGURE 24. Images of live uncollected individuals of Ahaetulla perroteti from the Nilgiris showing sexual dimorphism, (a) Head lateral of male, (b) Head lateral of female, (c) Head dorsal of female, (d) Threat display, (e) Whole animal.
Figure 20. Lectotype Pseudoanthidium eversmanni. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 20. Lectotype Pseudoanthidium eversmanni. A, dorsal view; B, ventral metasoma; C, labels; D, S5 showing sternal combs; E, S7.
Figure 9. Dorsal habitus, females. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 9. Dorsal habitus, females. A, vertex Pseudoanthidium nanum (Kalpetran, Switzerland); B, vertex P. scapulare (Rich, Morocco); C, mesonotum P. nanum (Kalpetran, Switzerland); D, mesonotum P. scapulare (Rich, Morocco); E, metasoma P. nanum (Kalpetran, Switzerland); F, metasoma P. scapulare (Rich, Morocco).
Figure 4. Lectotype, Pseudoanthidium reptans. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 4. Lectotype, Pseudoanthidium reptans. A, face; B, dorsal view; C, labels; D, ventral view; E, apex of metasoma, showing tips of gonostyli.
Figure 3 in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 3. Best-scoring maximum likelihood tree based on analyses of the (A) 75% UCE matrix and (B) 100% UCE matrix. Numbers shown at nodes are maximum likelihood bootstrap values based on 1000 bootstrap replicates in RAxML. Only bootstrap values greater than 50% are shown. Terminals are labelled with a DNA extraction code corresponding to the whole-body extraction performed for UCE sequencing, the DNA extraction code for the same specimen based on single leg extractions performed for barcode sequencing, the species name, collection locality and either as male (m) or female (f). Three specimens (1800, 1802 and 1805) were only sequenced following the UCE protocol and thus have only a UCE extraction code.
Figure 1. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 1. A, nest of Pseudoanthidium stigmaticorne, in a capsule of Tulipa biflora Pall. (Lisya Bay, Crimea). Insert in lower right shows close-up of the same nest. Three males eventually emerged (photo Alexander V. Fateryga); B, Pseudoanthidium stigmaticorne nesting in a stem of Crambe maritima L. (Arabatskaya Strelka sand spit, Crimea). A pin is inserted to mark the nest (photo Sergey P. Ivanov).
Figure 17. Dorsal habitus, females. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)
Figure 17. Dorsal habitus, females. A, vertex Pseudoanthidium stigmaticorne (Arzens, France); B, vertex P. cribratum (Bukhara, Uzbekistan); C, mesonotum P. stigmaticorne (Arzens, France); D, mesonotum P. cribratum (Bukhara, Uzbekistan); E, metasoma P. stigmaticorne (Arzens, France); F, metasoma P. cribratum (Bukhara, Uzbekistan).
FIGURE 11. Caparinia ictonyctis Lawrence, 1955, female. A in Validation of the status of a species with high CO1 and low nuclear genetic divergences: the scab mite Caparinia ictonyctis stat. res. (Acariformes: Psoroptidae) parasitizing the African hedgehog Atelerix albiventris
FIGURE 11. Caparinia ictonyctis Lawrence, 1955, female. A—dorsal view; B—ventral view; C—tarsus and tibia III in ventral view, D—leg IV in ventral view. Scale bars: 100 µm = A, B; 50 µm = C, D.
FIGURE 10. Caparinia ictonyctis Lawrence, 1955, male. A—tarsus I in Validation of the status of a species with high CO1 and low nuclear genetic divergences: the scab mite Caparinia ictonyctis stat. res. (Acariformes: Psoroptidae) parasitizing the African hedgehog Atelerix albiventris
FIGURE 10. Caparinia ictonyctis Lawrence, 1955, male. A—tarsus I in dorsal view; B—same in ventral view; C—tarsus II in dorsal view, D—same in ventral view; E—tarsus III in ventral view; F—tarsus IV in ventral view.
FIGURE 8. Caparinia ictonyctis Lawrence, 1955, tritonymph. A—leg I in Validation of the status of a species with high CO1 and low nuclear genetic divergences: the scab mite Caparinia ictonyctis stat. res. (Acariformes: Psoroptidae) parasitizing the African hedgehog Atelerix albiventris
FIGURE 8. Caparinia ictonyctis Lawrence, 1955, tritonymph. A—leg I in ventral view; B—tarss, tibia, and genu I in dorsal view; C—leg II in ventral view, D—tarsus, tibia, and genu II in dorsal view; E—leg III in ventral view; F—leg IV in ventral view.
FIGURE 1 in Validation of the status of a species with high CO1 and low nuclear genetic divergences: the scab mite Caparinia ictonyctis stat. res. (Acariformes: Psoroptidae) parasitizing the African hedgehog Atelerix albiventris
FIGURE 1. SEM images of male of Caparinia ictonyctis stat. res. A—Dorsal view; B—Gnathosoma, dorsal view; C— Supracoxal organ; D—Tarsus I, dorsal view; E—Posterior opisthosoma, dorsal view; F—Same, ventral view.
FIGURE 4 in A new species of Uroplatus (Gekkonidae) from Ankarana National Park Madagascar, of remarkably high genetic divergence
FIGURE 4. Specimens of Uroplatus fetsy sp. nov. (a–b), female holotype ZSM 288/2004 (FGZC 552), collected in 2004; (c–d) female ZCMV 12147, caught in 2011 (tissue sample only; specimen not collected); (e) female paratype UADBA-R 70849 (MSZC 577), collected in 2018. Inset pictures show coloration of oral mucosa of the respective specimens. (f–g) specimens probably assignable to U. fetsy photographed by J. Ganzhorn at Ankarana; the smaller specimen shown in g and on the right in f is most likely a male specimen, recognizable by the enlarged tail base and indentations in the tail.
Fig. 2 in Genetic and morphological divergence among Gravel Bank Grasshoppers, Chorthippus pullus (Acrididae), from contrasting environments
Fig. 2 Morphometric distances measured on each individual of C. pullus sampled for the study. For descriptions of numbered traits, see Table 1
Fig. 1 in Genetic and morphological divergence among Gravel Bank Grasshoppers, Chorthippus pullus (Acrididae), from contrasting environments
Fig. 1 Geographic locations and genetic composition of the seven populations of the Gravel Bank Grasshopper included in the study. ISA, LOI and LIN (Bavaria, Germany) are gravel bank populations (solid circles); OPP, GRU (both Brandenburg, Germany), UHY (Saxony, Germany) and MIS (Ukraine) are heath populations (open circles). Population composition shown in pie-diagrams, with slice size proportional to frequency of corresponding allele (coded as in Table 2); the two most frequent alleles (A and C) represented in grey and black, respectively; all others in white. Shaded area is the species' range (Maas et al. 2002; I. Landeck unpublished data)
Fig. 3 Haplotype network derived from the Cpunl-1 in Genetic and morphological divergence among Gravel Bank Grasshoppers, Chorthippus pullus (Acrididae), from contrasting environments
Fig. 3 Haplotype network derived from the Cpunl-1 data set; alleles coded as in Table 2. Pie diameters proportional to number of individuals carrying that particular haplotype (see inlet at bottom right); numbers next to pies or pie slices indicate how many individuals carried that particular haplotype. Shading of pies and slices (see inlet at top right) reflects frac- tions of haplotypes contributed by the different populations; Bavarian and eastern German (Brandenburg + Saxony) populations presented as two pools based on pairwise FST values (no significant differentiation detected within either region). Solid dots represent missing haplotypes; dashed lines indicate that multiple connections among haplotypes are possible but not favored
FIGURE 1 in Genetic and shell-shape analyses of Orlitia borneensis (Testudines: Geoemydidae) reveal limited divergence among founders of the European zoo population
FIGURE 1. Ventral and dorsal view of a shell of Orlitia borneensis showing the landmarks used in this study.
FIGURE 3. A in Genetic variation among populations of, and evidence of deep divergence within, the Rio Grande Chirping Frog, Eleutherodactylus campi (Anura Eleutherodactylidae)
FIGURE 3. A: Sampling localities of four haplotypes (42 samples) of Eleutherodactylus campi and three haplotypes (six samples) of E. cystignathoides with some points offset for clarity. The geographic positions of sampling localities were approximated for sequences obtained from GenBank. B: Unrooted TCS network generated using PopART. Lines intersecting node lines correspond to the number of mutational steps between haplotypes and clades. The geographic origins of haplotypes are color-coded, circle sizes roughly reflect the frequency of each haplotype, and the number in parenthesis indicates the number of individuals sharing a haplotype.
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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.