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15,277 results for “GENETICS”
Figure 6 in Effects of nanoparticles treatments and salinity stress on the genetic structure and physiological characteristics of Lavandula angustifolia Mill.
Figure 6. Results of the AMOVA test revealed a significant genetic diversity between the treated samples
Figure 5 in Effects of nanoparticles treatments and salinity stress on the genetic structure and physiological characteristics of Lavandula angustifolia Mill.
Figure 5. UPGMA tree of the studied samples according to essential oil compositions (treatment's code as in Table 1).
Figure 3 in Effects of nanoparticles treatments and salinity stress on the genetic structure and physiological characteristics of Lavandula angustifolia Mill.
Figure 3. Effects of Fe O and ZnO nanoparticles on concentration of the leaves Fe2+ amounts. Whiskers indicate the standard deviation, 2 3 and dissimilar letters showed the significant variation based on Duncan test (P≤ 0.05).
Figure 4 in Effects of nanoparticles treatments and salinity stress on the genetic structure and physiological characteristics of Lavandula angustifolia Mill.
Figure 4. Effects of ZnO and Fe O nanoparticles on intracellular Zn 2+ concentration. Whiskers reveal the standard deviation, and 2 3 dissimilar letters showed the significant variation according to Duncan test (P≤ 0.05).
Genetic analysis of mycobacteria isolated from suspect bovine tuberculosis lesions in Wolaita, Ethiopia - code and datasets.
<p>Bovine tuberculosis (bTB), caused by Mycobacterium bovis and other members of the Mycobacterium tuberculosis complex (MTBC), is a significant concern for livestock and public health in Ethiopia. This study aimed to assess the prevalence and causative agents of bTB in cattle from four abattoirs in the Wolaita region of Ethiopia. </p>
Figure 2 in A genetic method to differentiate Petromyzon marinus ammocoetes from those of the paired species Lampetra fluviatilis and L. planeri
Figure 2. - PCR-RFLP results of the 560 bp Cytb fragment using HinfI restriction enzyme. Pistes 1-2: L. fluviatilis; 3: Ladder 100 bp; 4 to 6: L. planeri; 7 to 11: P. marinus; 12: Ladder Bacteriophage lambda digested by EcoR1- HindIII.
Figure 1. - Study stream locations where lamprey were collected. 1 in A genetic method to differentiate Petromyzon marinus ammocoetes from those of the paired species Lampetra fluviatilis and L. planeri
Figure 1. - Study stream locations where lamprey were collected. 1: Gironde basin; 1a: Livenne River; 1b: Dronne River; 1c: Dordogne River; 1d: Cere River; 2: Loire basin; 3: Meuse basin.
Supporting data and code for: Demographic and genetic impacts of powdery mildew in a young oak cohort
<p>This is a new release following the submission of the related PCI recommended manuscript to the <em>Annals of Forest Science</em> journal. It contains the necessary scripts to produce most of the analyses and figures of the manuscript. Apart from minor modifications following the recommendation in '<em>PCI Forest and Wood Sciences</em>', the main change is the addition of an extra dataset "Data_S2.txt" to the additional datasets. This dataset was previously included as a table in the 'supplementary material' file.</p>
Figure 1 in Morphological and genetic variations of Diplodus vulgaris along the Tunisian coasts
Figure 1. - Locations of sampling sites along the Tunisian coasts. Ì: marine samples. ●: lagoon samples. STS: Siculo-Tunisian Strait. West-Med: Western Mediterranean basin. East-Med: Eastern Mediterranean basin.
Figure 2. - A in Morphological and genetic variations of Diplodus vulgaris along the Tunisian coasts
Figure 2. - A: Location of the 11 landmarks (1-11) used for constructing the truss network on D. vulgaris and the six additional points (12-17) used to draw the conventional linear measurements. Landmarks and additional points illustrated as black dots. Truss network illustrated as continuous lines. Conventional linear measurements illustrated as discontinuous lines. B: Discriminated head region and discrimination related variables.
Figure 3 in Morphological and genetic variations of Diplodus vulgaris along the Tunisian coasts
Figure 3. - DFA scores of morphometric characters using conventional linear measurements and truss elements on the plan DF1-DF2.
Figure 2 in Genetic differentiation in Scriptaphyosemion geryi (Lambert, 1958) suggests the existence of a species complex
Figure 2. - Consensus tree based on Maximum Likelihood (PHYML), Parsimony (TNT), and Bayesian phylogenetic analysis (number of generation = 6 108, burn-in = 25%). Numbers above or below the branches are percentages of bootstrap values based on 1000 replicates for respectively each method (except for Bayesian inferences where the numbers represent the percentage of trees with best likelihood scores in which the particular node was found). Numbers on the right side of the tree represent genetically-defined clades.
Figure 3 in Genetic differentiation in Scriptaphyosemion geryi (Lambert, 1958) suggests the existence of a species complex
Figure 3. - Histogram representing the distribution of the Kimura 2 distances (D) observed between the 13 different Chromaphyosemion species, in white (ranged from 0.024 to 0.120), between S. geryi populations of the same clade, in grey (from 0.001 to 0.026), and between S. geryi populations from different clades, in black (from 0.030 to 0.083).
Fig. 4 in Coloration patterns of the tegmina of Mahanarva spectabilis (Hemiptera: Cercopidae): biological, morphological and genetic bases
Fig. 4. Genetic distances between different species of spittlebugs and different wing color patterns of M. spectabilis, where YB = straw-yellowish hue with black spots; RB = reddish hue with black spots; R = total reddish hue; B = total black hue.
Fig. 3 in Coloration patterns of the tegmina of Mahanarva spectabilis (Hemiptera: Cercopidae): biological, morphological and genetic bases
Fig. 3. Comparative biometrics of M. spectabilis by sex and wing color patterns. Distributions observed for head length (A) and width (B), pronotum length (C) and width (D), scutellum length (E) and width (F), and tegmen length (G) and width (H). In cases (A) to (D) and (H), sex × wing color pattern interaction was not significant; thus p-values and letters refer to mean comparison between sexes or among wing color patterns, where means followed by different letters were found to be significantly different. In the other cases, (E) to (G), sex × wing color pattern interaction was found to be significant, and its analysis was conducted: p-values and letters refer to mean comparison among wing color patterns within sex, where different letters indicate significant differences, whereas distributions marked with a same symbol (* or +) indicate a significant difference between the sexes for a given wing color pattern. ANOVA followed by Tukey's test at 5% significance probability level was used in all cases.
Fig. 2 in Coloration patterns of the tegmina of Mahanarva spectabilis (Hemiptera: Cercopidae): biological, morphological and genetic bases
Fig. 2. Box plot representation of the distribution of the offspring's tegminal coloration pattern proportions obtained for each type of mating cross, according to parents' wing color pattern, regardless of sex. Each box spans from the first to the third quartile (interquartile range). The segment inside the box and the filled circle indicate median's and mean's locations, respectively. Whiskers above and below the box extend either to the maximum/minimum data value or to the most extreme value falling within the extent equivalent to 1.5 × interquartile range, starting from the box; points exceeding these limits are considered suspected outliers and are marked with unfilled circles. Different letters within each quadrant indicate significantly different mean proportions (Tukey's test, α = 5%). Value in parentheses are, in the order they appear, the number of replicates (i.e., the number of couples from which at least 8 offspring were obtained, that grew to adulthood), the total number of offspring generated from these replicates that grew to adulthood, the ANOVA residual degrees of freedom, and the ANOVA F-test p-value. *Insufficient n for analysis.
Fig. 1 in Coloration patterns of the tegmina of Mahanarva spectabilis (Hemiptera: Cercopidae): biological, morphological and genetic bases
Fig. 1. Relative frequency of 484 adults collected at the Embrapa Dairy Cattle experimental field in the town of Coronel Pacheco, Minas Gerais, Brazil, from which 242 couples were formed, with their 1,484 offspring, with regard to wing color patterns, regardless of sex.
Fig. 1 in Genetic identification and biological characterization of Baculovirus isolated from Helicoverpa armigera (Lepidoptera: Noctuidae) in Brazil
Fig. 1. Phylogenetic relationships among HearNPV isolates (BR1, BR2, BR3, Br4, and GEM) based on analysis of concatenated nucleotide sequences of the lef-8 and lef-9. The evolutionary history was inferred by using the Maximum Likelihood method. The tree with the highest log likelihood (−799.3699) is shown. The percentage of trees in which the associated taxa clustered together is shown next to the branches. Initial tree(s) for the heuristic search were obtained by applying the Neighbor-Joining method to a matrix of pairwise dis- tances estimated using the Maximum Composite Likelihood (MCL) approach. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. The analysis involved 14 nucleotide sequences. All posi- tions containing gaps and missing data were eliminated.
Fig. 2 in Genetic identification and biological characterization of Baculovirus isolated from Helicoverpa armigera (Lepidoptera: Noctuidae) in Brazil
Fig. 2. Survival curves of Helicoverpa armigera (Lepidoptera: Noctuidae) afer feeding on corn leaves inoculated with 1 × 106 polyhedra per mL of baculovirus isolated. Gemstar®LC, BR1, BR2, BR3, BR4, and in control obtained with KaplanMeier estimator.
Figure 1. A in The giant salamanders (Cryptobranchidae): Part A. palaeontology, phylogeny, genetics, and morphology
Figure 1. A North American giant salamander (Cryptobranchus alleganiensis) shows the characteristic morphology of the cryptobranchids; large robust dorso-ventrally flattened head and body, small eyes, thick legs with stubby digits, lateral folds of skin for respiration, and sensory papillae for detecting water movement and prey (laterally flattened tail not shown). Image and copyright by Ray Miebaum.
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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.