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Figure 1 in Data from: Genetic isolation between two recently diverged populations of a symbiotic fungus
Figure 1 Map cf tSe sampling site in SSiSlang (Ludac) witS indicaticn cf tSe quadrats. SC, unvegetated quadrat; SEA, SEB, and SEC, seagrass quadrats.
Supplementary material 1 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Supplementary material 1 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Supplementary material 2 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Supplementary material 2 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
FIGURE 2 in Genista anglica s.l. (Fabaceae): genetic similarities between Iberian and Italian populations
FIGURE 2. Maximum clade credibility (MCC) tree resulting from BEAST phylogenetic analysis (20,000,000 generations) based on plastid (trnL-F) sequences data of Genista anglica group from Fernández Prieto et al. (2016) and new sequences. Support values are displayed on tree branches as posterior probability. Only the new samples codes are shown in the tree rapresentation. A TCS haplotype network, constructed with the same samples of ingroup of the phylogenetic tree is represented. Samples of each clade of the tree are represented with the same color in the haplotype network and the G. silana and G. brutia samples are indicated in the tree by circles and triangles with different lines patrons respectively, as in the corresponding circles of the haplotype network.
FIGURE 1 in Genista anglica s.l. (Fabaceae): genetic similarities between Iberian and Italian populations
FIGURE 1. Distribution map of populations of Genista anglica, G. silana and G. brutia analysed in this study. Black triangles correspond to populations studied in Fernández Prieto et al. (2016). White circles represent the new populations analysed in this study.
FIGURE 3 in Genista anglica s.l. (Fabaceae): genetic similarities between Iberian and Italian populations
FIGURE 3. Distribution of trnL-F haplotypes found in the Genista anglica, G. brutia and G. silana samples of phylogenetic group E. Black triangles correspond with populations studied in Fernández Prieto et al. (2016). Small white circles correspond to the new populations analysed in this study. Haplotype network is represented (below), the diameter of circles represents the number of samples that is shown by each haplotype. The colours of circles are the same represented in the maps for each haplotype.
The genetic diversity, phylogeography, and population structure of Pacific harbor seals reveal isolation at the southern end of their distribution
<p>The Pacific harbor seal (<em>Phoca vitulina richardii</em>) occurs in the Mexican Pacific region at the southernmost edge of the subspecies' distribution, along 700 km of coastline and on nine islands west of the Baja California peninsula. Its abundance corresponds to 3% of its total abundance in the north Pacific Ocean. The species is considered relatively sedentary and highly philopatric, which make it vulnerable to stochastic processes; thus, reproductive and genetic isolation of the Mexican Pacific colonies is expected. This study aimed to genetically characterize the harbor seal in the Mexican Pacific to inform conservation efforts. We estimated the levels of genetic diversity for five colonies, using a 572-base pair mitochondrial DNA control region fragment and nine microsatellite loci. We examined the population genetic structure and its phylogeographic patterns. We found 15 variable sites that defined 18 mitochondrial DNA haplotypes. Results show one of the lowest levels of diversity reported for the species (overall haplotype diversity <em>h</em> = 0.626 ± SD 0.041; overall nucleotide diversity π = 0.0018 ± SD 0.0013; mean expected heterozygosity H<sub>E</sub> = 0.537). We found a stronger genetic structure with both markers than in the larger regions of the north Pacific, from Alaska to California. The Pacific harbor seal colonies found in Mexico may have their origins in northern colonies, via a founder event. We found only four haplotypes in common with those observed (451) along the rest of the Pacific colonies, while nine of the 14 haplotypes exclusive to the Mexican Pacific are private.</p>
Fig. 8 in Taxonomic revision of the southern hemisphere pygmy forget-me-not group (Myosotis; Boraginaceae) based on morphological, population genetic and climate-edaphic niche modelling data
Fig. 8. Myosotis antarctica subsp. traillii photographs and distribution map. (a) Habit. (b, d) Rosette leaf tips: (b) adaxial and (d) abaxial sides. (c) Flower. (e) Nutlets. (f) Map of georeferenced herbarium specimens observed by J. M. Prebble (35). Whie scale bars: 2 mm; black scale bars: 1 mm. Photo credits: a, e by J. M. Prebble (a: WELT SP100487, Tiwai Point, Southland, South Island; e: WELT SP104518, cultivated ex Mason Bay, Stewart Island). b, c © Te Papa by H. M. Meudt (b: WELT SP090544, Manihi Rd, Taranaki, North Island; c: WELT SP090629, Hukanui, Gisborne, North Island; d: WELT SP090631, Waipuna, Gisborne, North Island).
Fig. 2 in Taxonomic revision of the southern hemisphere pygmy forget-me-not group (Myosotis; Boraginaceae) based on morphological, population genetic and climate-edaphic niche modelling data
Fig. 2. Maps of MaxEnt niche models for pygmy Myosotis in New Zealand and southern South America. (a) Myosotis glauca (light blue circles). (b) M. pygmaea (green circles). (c, h) M. "Volcanic Plateau" (grey triangles). (d) M. brevis (yellow cir-cles). (e) M. drucei (dark blue circles; excluding individuals identified as M. "Volcanic Plateau"). (f) M. drucei (dark blue circles) + M. pygmaea (green circles) + M. "Volcanic Plateau" (grey triangles) (g) M. antarctica (pink circles; Chilean locations), note scale is the same as for maps of New Zealand. a–f use models based on the nine-layer model (see Table 1), whereas g and h are based on the sevenlayer model.
Fig. 5 in Taxonomic revision of the southern hemisphere pygmy forget-me-not group (Myosotis; Boraginaceae) based on morphological, population genetic and climate-edaphic niche modelling data
Fig. 5. Myosotis glauca photographs and distribution map. (a) Habit. (b) Rosette leaves, adaxial and abaxial sides. (c) Calyces, left to right most to least mature. (d) Nutlets. (e) Map of georeferenced herbarium specimens observed by J. M. Prebble (16). White scale bars: 2 mm; black scale bar: 1 mm. Photo credits: all by J. M. Prebble (WELT SP093285, Nevis Valley, Otago).
Fig. 4 in Taxonomic revision of the southern hemisphere pygmy forget-me-not group (Myosotis; Boraginaceae) based on morphological, population genetic and climate-edaphic niche modelling data
Fig. 4. Myosotis brevis photographs and distribution map. (a) Habit. (b) Inflorescence showing cauline leaf abaxial side. (c) Inflorescence showing cauline leaf adaxial side, calyces, and flower. (d) Rosette leaf adaxial side showing colour morphs. (e) Flower. (f) Nutlet. (g) Map of georeferenced herbarium specimens observed by J. M. Prebble (25). White scale bars: 2 mm; black scale bar: 1 mm. Photo credits: a–e © Te Papa by H. M. Meudt (a: WELT SP090549, Te Ikaamaru Bay, Wellington; b, c: WELT SP090545, Ngawi, Wairarapa; d: WELT SP090543, Stent Road, Taranaki; e: WELT SP090550, Ohau Bay, Wellington); f by J. M. Prebble (WELT SP090543, cultivated ex Stent Road, Taranaki).
Fig. 7. Myosotis antarctica subsp. antarctica. Illustration reproduced from Bot. Antarct. Voy. I in Taxonomic revision of the southern hemisphere pygmy forget-me-not group (Myosotis; Boraginaceae) based on morphological, population genetic and climate-edaphic niche modelling data
Fig. 7. Myosotis antarctica subsp. antarctica. Illustration reproduced from Bot. Antarct. Voy. I. (Fl. Antarct.) Part I, plate 38 (Hooker 1844). Illustration by W. H. Fitch. This image is in the public domain, downloaded from the Biodiversity Heritage Library (https:// www.biodiversitylibrary.org/page/13448452#page/81/ mode/1up, accessed 8 June 2021). Draft pencil drawings for this figure are attached to the type specimen of M. antarctica (K0007878799; visible online at http:// apps.kew.org/herbcat/getImage.do?imageBarcode= K000787899, accessed 8 June 2021), which was collected by J. D. Hooker from Campbell Island.
Fig. 6 in Taxonomic revision of the southern hemisphere pygmy forget-me-not group (Myosotis; Boraginaceae) based on morphological, population genetic and climate-edaphic niche modelling data
Fig. 6. Myosotis antarctica subsp. antarctica photographs and distribution maps. (a, b) Habit. (c) Rosette leaves abaxial and adaxial sides. (d) Flower. (e) Nutlets. (f) Map of mainland New Zealand distribution based on georeferenced herbarium specimens observed by J. M. Prebble (163). (g) Map of Campbell Island distribution based on georeferenced herbarium specimens observed by J. M. Prebble (14). (h) Map of Chilean distribution based on georeferenced herbarium specimens observed by J. M. Prebble (2). White scale bars: 2 mm; black scale bars: 1 mm. Photo credits: a, c, e by J. M. Prebble (a: WELT SP102777, Mt Azimuth, Campbell Island; c: WELT SP093293, Port Hills, Canterbury, South Island E: WELT SP100466, cultivated ex Mt Peel, Western Nelson. South Island). b, d © Te Papa by H. M. Meudt (b: WELT SP106592, Matiri Range, Western Nelson, South Island; d: WELT SP107322, Mt Starveall, Western Nelson, South Island).
Fig. 3 in Taxonomic revision of the southern hemisphere pygmy forget-me-not group (Myosotis; Boraginaceae) based on morphological, population genetic and climate-edaphic niche modelling data
Fig. 3. Plots displaying (a, c) omission and commission values and (b, d) area under the receiving operating characteristic curve (AUC) for two pygmy forget-me-not taxa: (a, b) M. "Volcanic Plateau" and (c, d) M. drucei, modelled using MaxEnt and all nine environmental layers for the New Zealand extent.
Fig. 1. Maps displaying all 290 in Taxonomic revision of the southern hemisphere pygmy forget-me-not group (Myosotis; Boraginaceae) based on morphological, population genetic and climate-edaphic niche modelling data
Fig. 1. Maps displaying all 290 occurrence points used for Myosotis pygmy species group niche modelling (Supplementary Table S1). Maps, clockwise from top: World, New Zealand, Campbell Island, and southern South America. Colour represents a priori species: M. antarctica (pink circles); M. drucei (dark blue circles); M. pygmaea (green circles); M. brevis (yellow circles); M. glauca (light blue circles); M. "Volcanic Plateau" (grey triangles).
Soil requirements, genetic diversity and population history of the Juniperus sabina L. varieties in Europe and Asia
<p>Dataset comprises genotypes of 335 individuals of J. sabina. </p>
Figure 4 in Genetic diversity of Undaria pinnatifida populations from China and their genetic relationship with those from Įapan and Korea as revealed by mitochondrial and nuclear DNA sequences
Figure 4: Maximum likelihood phylogenetic tree inferred from the alignment of ITS1 sequences. Support values are shown as in Figure 3. The ribotypes detected in the Chinese samples in the present study are indicated with bold italicized fonts. Alaria esculenta was used as an outgroup to root the tree. The branch length is proportional to the sequence divergence indicated by the scale bar (substitutions per site).
Figure 3 in Genetic diversity of Undaria pinnatifida populations from China and their genetic relationship with those from Įapan and Korea as revealed by mitochondrial and nuclear DNA sequences
Figure 3: Maximum likelihood phylogenetic tree inferred from the alignment of the combined cox3 and tatC–tLeu sequences. Bootstrap values and Bayesian posterior probabilities>50% are shown, and "-" indicates a value <50%. The branch length is proportional to the sequence divergence indicated by the scale bar (substitutions per site). Refer to Uwai et al. (2006a) for explanation of the haplotype names and classification of the clades I to IV. The haplotypes detected in the Chinese samples in the present study are indicated with bold italicized fonts. Lessoniopsis littoralis was used as an outgroup to root the tree.
Figure 2 in Genetic diversity of Undaria pinnatifida populations from China and their genetic relationship with those from Įapan and Korea as revealed by mitochondrial and nuclear DNA sequences
Figure 2: Geographic distribution of haplotypes in natural and farmed populations of Undaria pinnatifida from China (A) and statistical parsimony network (B) of ITS1 sequences. The color areas in the pie charts are proportional to the ribotype frequency in the map. Small circles indicate undetected ribotypes. Each line connecting ribotypes represents one base mutation. The ribotypes detected in the Chinese samples in the present study are indicated in the ribotype network by the same colors as those in the map.
Figure 1 in Genetic diversity of Undaria pinnatifida populations from China and their genetic relationship with those from Įapan and Korea as revealed by mitochondrial and nuclear DNA sequences
Figure 1: Geographic distribution of haplotypes in natural and farmed populations of Undaria pinnatifida from China (A) and statistical parsimony network (B) of the combined cox3 and tatC–tLeu sequences. The color areas in the pie charts are proportional to the haplotype frequency in the map. Refer to Uwai et al. (2006a) and Table 3 for explanation of the haplotype names and classification of the clades I to IV, which are enclosed by boxes with lines of different patterns. Small circles indicate undetected haplotypes. Each line connecting haplotypes represents one base mutation. The haplotypes detected in the Chinese samples in the present study are indicated in the haplotype network with the same colors as those in the map.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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