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34 results for “ploidy level”

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dryad32/100

Data from: Varying levels of clonality and ploidy create barriers to gene flow and challenges for conservation of an Australian arid-zone ecosystem engineer, Acacia loderi

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publicDec 2015View details →
dryad32/100

Data from: Detection of individual ploidy levels with genotyping-by-sequencing (GBS) analysis

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publicJan 2017View details →
dryad32/100

Data from: Population structure, relatedness and ploidy levels in an apple gene bank revealed through genotyping-by-sequencing

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publicJul 2019View details →
dryad32/100

Data from: Wide variation in ploidy level and genome size in a New Zealand freshwater snail with coexisting sexual and asexual lineages

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publicMay 2011View details →
dryad32/100

Valenzuela phylogenomic dataset from: Illumina whole genome sequencing indicates ploidy level differences within the Valenzuela flavidus (Psocodea: Psocomorpha: Caeciliusidae) species complex

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publicNov 2021View details →
zenodo28/100

Figure 3 from: Shiotani Y, Fukuda T, Marchuk EA, Petrunenko EA, Krestov PV, Bondarchuk SN, Nishikawa Y, Shimamura T, Fujimura Y, Nakamura K (2020) Merger of Betula tatewakiana (Betulaceae) from northern Japan with northeast Asian B. ovalifolia based on ploidy level. PhytoKeys 170: 83-91. https://doi.org/10.3897/phytokeys.170.58585

Figure 3 Leaf traits of B. tatewakiana and B. ovalifolia. White hairs on adaxial leaf surface (A, C, E) and densely resinous glands on abaxial leaf surface (B, D, F) are shown for the holotype of B. tatewakiana (H. Suzuki and M. Ohki, s.n., A, B), B. tatewakiana of our collection (Yuki Shiotani 38, C, D), and B. ovalifolia in Russia (Koh Nakamura 14188, E, F). Scale bar: 1 mm.

opencc-by-4.0Dec 2020View details →
zenodo28/100

Figure 2 from: Shiotani Y, Fukuda T, Marchuk EA, Petrunenko EA, Krestov PV, Bondarchuk SN, Nishikawa Y, Shimamura T, Fujimura Y, Nakamura K (2020) Merger of Betula tatewakiana (Betulaceae) from northern Japan with northeast Asian B. ovalifolia based on ploidy level. PhytoKeys 170: 83-91. https://doi.org/10.3897/phytokeys.170.58585

Figure 2 Somatic chromosomes at metaphase of B. tatewakiana and B. ovalifolia. Photomicrographs of B. tatewakiana from Sarabetsu mire (A, 2n = 56: HUBG 14746 A) and Nishibetsu mire (C, 2n = 56: Yuki Shiotani 29), and B. ovalifolia from Primorsky Krai (E, 2n = 56: Koh Nakamura 14198) are shown. B, D, F are drawings of A, C, E, respectively. Scale bar: 5 µm.

opencc-by-4.0Dec 2020View details →
zenodo28/100

Figure 1 from: Shiotani Y, Fukuda T, Marchuk EA, Petrunenko EA, Krestov PV, Bondarchuk SN, Nishikawa Y, Shimamura T, Fujimura Y, Nakamura K (2020) Merger of Betula tatewakiana (Betulaceae) from northern Japan with northeast Asian B. ovalifolia based on ploidy level. PhytoKeys 170: 83-91. https://doi.org/10.3897/phytokeys.170.58585

Figure 1 Species distribution ranges of Betula ovalifolia (A) and B. tatewakiana (B). Map data 2020 (C) Google.

opencc-by-4.0Dec 2020View details →
dryad28/100

Data from: Hybridization between two cryptic filamentous brown seaweeds along the shore: analysing pre- and post-zygotic barriers in populations of individuals with varying ploidy levels

We aimed to study the importance of hybridization between two cryptic species of the genus Ectocarpus, a group of filamentous algae with haploid-diploid life cycles that include the principal genetic model organism for the brown algae. In haploid-diploid species, the genetic structure of the two phases of the life cycle can be analysed separately in natural populations. Such life cycles provide a unique opportunity to estimate the frequency of hybrid genotypes in diploid sporophytes and meiotic recombinant genotypes in haploid gametophytes allowing the effects of reproductive barriers preventing fertilization or preventing meiosis to be untangle. The level of hybridization between E. siliculosus and E. crouaniorum was quantified along the European coast. Clonal cultures (568 diploid, 336 haploid) isolated from field samples were genotyped using cytoplasmic and nuclear markers to estimate the frequency of hybrid genotypes in diploids and recombinant haploids. We identified admixed individuals using microsatellite loci, classical assignment methods and a newly developed Bayesian method (XPloidAssignment), which allows the analysis of populations that exhibit variations in ploidy level. Over all populations, the level of hybridization was estimated at 8.7%. Hybrids were exclusively observed in sympatric populations. More than 98% of hybrids were diploids (40% of which showed signs of aneuploidy) with a high frequency of rare alleles. The near absence of haploid recombinant hybrids demonstrates that the reproductive barriers are mostly post-zygotic and suggests that abnormal chromosome segregation during meiosis following hybridisation of species with different genome sizes could be a major cause of interspecific incompatibility in this system.

opencc-zeroDec 2016View details →
dryad28/100

Data from: Hybridization between two cryptic filamentous brown seaweeds along the shore: analysing pre- and post-zygotic barriers in populations of individuals with varying ploidy levels

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publicFeb 2017View details →
dryad28/100

Data from: Sensitivity to phosphorus limitation increases with ploidy level in a New Zealand snail

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publicNov 2012View details →
dryad28/100

Data from: Mutational effects depend on ploidy level: all else is not equal

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publicApr 2013View details →
geo24/100

Increased levels of aneuploidy and deregulation of ploidy controlling genes are associated with maintained cultures of hMSC

GEO Series GSE39250. Homo sapiens. 8 samples. Type: Expression profiling by array.

openGEO-OpenOct 2012View details →
geo12/100

Transcriptome response to change in ploidy level in Arabidopsis

GEO Series GSE6828. Arabidopsis thaliana. 11 samples. Type: Expression profiling by array.

openGEO-OpenJan 2007View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record