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15,277 results for “GENETICS”
Fig. 6 in Update of genetic information for the white-clawed crayfish in Spain, with new insights into its population genetics and origin
Fig. 6 Mismatch distributions, observed and expected, in the Spanish populations as a whole and in the 'Northern' and 'Central' genetic clusters detected. The neutrality test Fs, D and R2 values are also shown
Fig. 1 in Update of genetic information for the white-clawed crayfish in Spain, with new insights into its population genetics and origin
Fig. 1 Location of the white-clawed crayfish populations analysed. Table 1 provides details for each population
Fig. 2 Mitochondrial haplotype network using the 590 in Differentiation of North African foxes and population genetic dynamics in the desert-insights into the evolutionary history of two sister taxa, Vulpes rueppellii and Vulpes vulpes
Fig. 2 Mitochondrial haplotype network using the 590-bp concatenated sequences from Cyt-b and D-loop and a total of 46 sequences (same as in Fig. 1, except for C. lupus not being used as an outgroup in the TCS network). a Neighbour-Net network based on uncorrected patristic distances as implemented in SPLITSTREE. Canis lupus (DQ480504) was used as an outgroup. Numbers indicate bootstrap values. Scale bar represents 0.01 sequence divergence. Highlighoed are the four species, the three V. vulpes clades and the location within the network of the V. vulpes sample from Egypt. Colour patterns are concordant with Fig. 1 and b. b Statistical parsimony network assuming a 95 % parsimony threshold, as constructed by TCS. Symbol size and branch lengths are proportional to the number of shared individuals per haplotype and the number of mutational steps amongst haplotypes, respectively. Numbers in black background also refer to the number of mutation steps between species and V. vulpes clades. Symbols and colours are concordant with Fig. 1 and a. Haplotype codes, sample origin and corresponding accession numbers are available in Online Resource Table S1
Fig. 3 in Differentiation of North African foxes and population genetic dynamics in the desert-insights into the evolutionary history of two sister taxa, Vulpes rueppellii and Vulpes vulpes
Fig. 3 Population structure analyses of V. vulpes using 32 microsatellite loci analysed with STRUCTURE software. a STRUCTURE HARVESTER output. Mean values of likelihood [L(K)] on ohe lefo, and Delta K values using the Evanno method (Evanno et al. 2005) on ohe righo. b Structure bar plot of Bayesian assignment of 35 individuals to two (K =2, lefo graphic) and three clusters (K =3, righo graphic). Horizonoal bars represent individuals, while colours wiohin a bar represent probability of assignment of each individual to a cluster. Country of origin for each individual is indicated between each structure bar plots
Fig. 2 a in Does size matter? Comparative population genetics of two butterflies with different wingspans
Fig. 2 a Map showing the groups formed when individuals were divided into populations based on sampling proximity (AGA Agastyamalais, ANA Anamalais, WAC Wayanad and Coorg, and NKAR North Karnataka). b and c Spatial multivariate analysis in sPCA. Squares represent first axis sPCA scores for b ML and c YB. In this figure, the color of the squares denotes positive (black) or negative (white) spatial autocorrelation, and the size of the squares denotes the magnitude of genetic variance. Thus, squares of different sizes are used to represent different absolute values: large black squares are well differentiated from large white squares, but small squares are less differentiated
Fig. 1 Sampling locations. A in Does size matter? Comparative population genetics of two butterflies with different wingspans
Fig. 1 Sampling locations. A map of the Western Ghats showing sampling locations for both species. Inset: map of India showing the location of the Western Ghats in blue
Fig. 2 Minimum-spanning network among 44 in Mitochondrial evidence for genetic diversity and low phylogeographic differentiation in the Marsh Warbler Acrocephalus palustris (Aves: Acrocephalidae)
Fig. 2 Minimum-spanning network among 44 COI haplotypes of Marsh Warbler (see Table S2). Size of circles represents the relative frequency of given haplotypes and each line between black nodes indicates a single mutational step
Fig. 3 in Mitochondrial evidence for genetic diversity and low phylogeographic differentiation in the Marsh Warbler Acrocephalus palustris (Aves: Acrocephalidae)
Fig. 3 Left: Mismatch distribution. Expected (solid line) and observed (broken line) mismatch distribution under population expansion model. Right: Bayesian skyline plot representing the historical demographic
Fig. 3 a in Phylogeographic patterns of genetic diversity in the common spadefoot toad, Pelobates fuscus (Anura: Pelobatidae), reveals evolutionary history, postglacial range expansion and secondary contact
Fig. 3 a Bayesian phylogenetic analysis based on a 571-bp fragment of the mitochondrial cyt b gene. Only haplotype sequences have been used. Spea bombifrons was used as outgroup. Asterisks denote Bayesian posterior probabilities values: *95–98 %; **99–100 %. b Haplotype network reconstruction of 29 haplotypes of Pelobates fuscus fuscus (W) and of 13 haplotypes of P. f. vespertinus (E), based on the analysis of a 571-bp fragment of the mitochondrial cytochrome b gene. Size of circles is proportional to the number of individuals sharing a given haplotype. The frequency of each haplotype has been computed based on published data (Crottini et al. 2007) and on new sequences
Fig. 1 in Phylogeographic patterns of genetic diversity in the common spadefoot toad, Pelobates fuscus (Anura: Pelobatidae), reveals evolutionary history, postglacial range expansion and secondary contact
Fig. 1 Geographic locations of the 59 analyzed populations of Pelobates. The limit of the geographic distribution of Pelobates fuscus is indicated with the solid line. The dashed line indicates the presumptive position of the contact zone between P. f. fuscus
Fig. 7 in Phylogeographic patterns of genetic diversity in the common spadefoot toad, Pelobates fuscus (Anura: Pelobatidae), reveals evolutionary history, postglacial range expansion and secondary contact
Fig. 7 Predictive potential niche models (black areas) of Pelobates f. fuscus (a and c) and P. f. vespertinus (b and d) for Last Glacial Maximum based on the MIROC (a and b) and CCSM (c and d) models. Models are above the average 10-percentile training threshold.
Fig. 5 A in Phylogeographic patterns of genetic diversity in the common spadefoot toad, Pelobates fuscus (Anura: Pelobatidae), reveals evolutionary history, postglacial range expansion and secondary contact
Fig. 5 A multilocus cline at four diagnostic allozyme loci along transect in the contact zone of Pelobates fuscus fuscus and P. f. vespertinus. The vertical axis shows the frequency of genetic variants diagnostic for P. f. fuscus (variation diagnostic for P. f. vespertinus is the inverse)
Fig. 2 in Phylogeographic patterns of genetic diversity in the common spadefoot toad, Pelobates fuscus (Anura: Pelobatidae), reveals evolutionary history, postglacial range expansion and secondary contact
Fig. 2 Unweighted pair group method with arithmetic mean phenogram (a) and neighbor-joining tree (b) showing genetic (allozyme) relationship among the Pelobates species populations sampled based on Nei's (1978) unbiased genetic distance (DNei); bootstrap values ≥ 70 %. Correspondence analysis of allele frequencies among the studied samples of P. fuscus (c), where dark circles represent P. f. vespertinus samples, gray circles are samples from the contact zone from Kursk Province of Russia, open circles are P. f. fuscus samples from Eastern
Fig. 4 Phylogenetic tree 1 in Evidence from morphological and genetic data confirms that Colossendeis tenera Hilton, 1943 (Arthropoda: Pycnogonida), does not belong to the Colossendeis megalonyx Hoek, 1881 complex
Fig. 4 Phylogenetic tree 1: Large tree: Phylogenetic tree based on maximum likelihood analysis of 545 bases of the CO1 gene of 44 specimens of Colossendeidae. ML bootstrap and Bayesian posterior probability support (if>50/0.5) are drawn on branches. Small tree:
Fig. 3 in Morphological and genetic analyses of xeniid soft coral diversity (Octocorallia; Alcyonacea)
Fig. 3 Bayesian phylogenetic tree of Ovabunda, Xenia, Bayerxenia and Heteroxenia. Node labels indicate Bayesian posterior probabilities and maximum likelihood bootstrap support values (in italics) based on
Fig. 1 in Evidence from morphological and genetic data confirms that Colossendeis tenera Hilton, 1943 (Arthropoda: Pycnogonida), does not belong to the Colossendeis megalonyx Hoek, 1881 complex
Fig. 1 Reported distribution ranges of C. megalonyx (black) from the ScarMARbin database (access data 25.4.2012), C. tenera (white), and the locations of the C. angusta specimens analyzed in this study (gray). Map: Ocean Data View version 4
Fig. 1 in Morphological and genetic analyses of xeniid soft coral diversity (Octocorallia; Alcyonacea)
Fig. 1 Colony morphology of Xeniidae: a Heteroxenia and Bayerxenia (here Bayerxenia sp.1). Siphonozooids are seen as white rings between the polyps. b Ovabunda and Xenia (here Xenia sp. 5). These genera lack siphonozooids
Fig. 1 in Genetic differentiation of the African dwarf crocodile Osteolaemus tetraspis Cope, 1861 (Crocodylia: Crocodylidae) and consequences for European zoos
Fig. 1 Distribution map of African dwarf crocodiles according to the results of Eaton et al. (2009a) and this study. The three divergent evolutionary lineages are shaded (Western Africa, Ogooué Basin,
Fig. 2 in Genetic variation within the cosmopolitan aquatic fungus Lignincola laevis (Microascales, Ascomycota)
Fig. 2 The phylogenetic tree based on the Bayesian analysis of the ITS/28S ribosomal RNA and the MCM7 genes. Posterior probabilities and maximum parsimony bootstrap support values are shown on the branches. '–' Not supported or bootstrap value <50
Fig. 1 a–c Lignincola laevis. a Ascoma inside mangrove wood. b Ascus. c Ascospore. Bars a 50 in Genetic variation within the cosmopolitan aquatic fungus Lignincola laevis (Microascales, Ascomycota)
Fig. 1 a–c Lignincola laevis. a Ascoma inside mangrove wood. b Ascus. c Ascospore. Bars a 50 μm; b, c 10 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.