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186 results for “Hybridisation”

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geo24/100

Strong Correlation of Gene Counts and Differentially Expressed Genes Between a 3′ RNA-Seq and RNA Hybridisation Platform in Transcriptome Analyses from Canine Archival Tissue [3' RNA-Seq]

GEO Series GSE261790. Canis lupus familiaris. 25 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenMar 2024View details →
zenodo24/100

Successful mating and hybridisation in two closely related flatworm species despite significant differences in reproductive morphology and behaviour

<p>Dataset of&nbsp;Article&nbsp; &#39;Successful mating and hybridisation in two closely related flatworm species despite significant differences in reproductive morphology and behaviour&#39; (DOI : 10.1038/s41598-020-69767-5)</p>

opencc-by-4.0Jul 2020View details →
dryad24/100

Data from: Repeated trans-watershed hybridisation among haplochromine cichlids (Cichlidae) was triggered by Neogene landscape evolution

The megadiverse haplochromine cichlid radiations of the East African lakes, famous examples of explosive speciation and adaptive radiation, are according to recent studies, introgressed by different riverine lineages. This study is informed by the first comprehensive mitochondrial and nuclear DNA dataset from extensive sampling of riverine haplochromine cichlids. It includes species from the lower Congo and Angolan (River Kwanza) drainages. Reconstruction of phylogenetic hypotheses revealed the paradox of clearly discordant phylogenetic signals. Closely related mtDNA haplotypes are distributed thousands of kilometers apart and across major African watersheds, whereas some neighbouring species carry drastically divergent mtDNA haplotypes. At shallow and deep phylogenetic layers, strong signals of hybridisation are attributed to the complex late Miocene/early Pliocene palaeo-history of African rivers. Hybridisation of multiple lineages across changing watersheds shaped each of the major haplochromine radiations in lakes Tanganyika, Victoria, Malawi and the Kalahari Palaeolakes, as well as a miniature species flock in the Congo basin (River Fwa). Based on our results, introgression occurred not only on a spatially restricted scale, but massively over almost the whole range of the haplochromine distribution. This provides an alternative view on the origin and exceptional high diversity of this enigmatic vertebrate group.

opencc-zeroDec 2011View details →
zenodo24/100

Hybridisation in Primates: Cryptic Admixture and Adaptive Introgression Appendix C Materials

<p>This dataset includes supporting tables and figures for my PhD thesis at the University of Toronto, entitled "Hybridisation in Primates: Cryptic Admixture and Adaptive Introgression" in partial fulfillment of the degree requires for the Department of Anthropology (Evolutionary Anthropology). The data contains Tables C1-B13 and high resolution images for Figures 4.1-4.5.</p>

opencc-by-4.0Nov 2024View details →
dryad24/100

Data from: Repeated trans-watershed hybridisation among haplochromine cichlids (Cichlidae) was triggered by Neogene landscape evolution

Open the record for dataset details and reuse information.

publicOct 2012View details →
geo24/100

Danio rerio and Pomacentrus moluccensis: comparative genomic hybridisation and early gene response to heat stress

GEO Series GSE4047. Pomacentrus moluccensis; Danio rerio. 8 samples. Type: Expression profiling by array; Genome variation profiling by array.

openGEO-OpenApr 2006View details →
geo20/100

Strong Correlation of Gene Counts and Differentially Expressed Genes Between a 3′ RNA-Seq and RNA Hybridisation Platform in Transcriptome Analyses from Canine Archival Tissue [nCounter®]

GEO Series GSE261791. Canis lupus familiaris. 25 samples. Type: Expression profiling by array.

openGEO-OpenMar 2024View details →
geo20/100

Array-based comparative genomic hybridisation analysis at 1Mb resolution of 44 pilocytic astrocytomas

GEO Series GSE11263. Homo sapiens. 44 samples. Type: Genome variation profiling by genome tiling array.

openGEO-OpenApr 2008View details →
geo20/100

Array based comparative genomic hybridisation analysis of 1 Mb resolution of 21 follicular lymphomas (FL), 31 transformed diffuse large B-cells lymphomas (DLBCL), 29 de novo DLBCL (10 of GC and 19 non

GEO Series GSE56884. Homo sapiens. 81 samples. Type: Genome variation profiling by array.

openGEO-OpenApr 2014View details →
geo20/100

Identification of Candidate Genes for Sporadic Amyotrophic Lateral Sclerosis by Array Comparative Genomic Hybridisation

GEO Series GSE7950. Homo sapiens. 71 samples. Type: Genome variation profiling by genome tiling array.

openGEO-OpenDec 2008View details →
geo20/100

Strong Correlation of Gene Counts and Differentially Expressed Genes Between a 3′ RNA-Seq and RNA Hybridisation Platform in Transcriptome Analyses from Canine Archival Tissue [nCounter]

GEO Series GSE262020. Canis lupus familiaris. 10 samples. Type: Expression profiling by array.

openGEO-OpenMar 2024View details →
geo20/100

Oligoarray comparative genomic hybridisation-mediated mapping of suppressors of an essential receptor tyrosine kinase generated in a deletion-biased mutagenesis screen

GEO Series GSE15224. Caenorhabditis elegans. 6 samples. Type: Genome variation profiling by genome tiling array.

openGEO-OpenJul 2012View details →
zenodo20/100

Fig. 3 in COI-based species delimitation in Indochinese Tetraserica chafers reveal hybridisation despite strong divergence in male copulation organs

Fig. 3 Split network of all examined specimens. Singletons are highlighted in blue, others in orange colours. Tip labels of paraphyletic morphospecies (species names/acronyms shown) are encircled by dashed

opennotspecifiedMar 2019View details →
zenodo20/100

Hybridisation in Primates: Cryptic Admixture and Adaptive Introgression Appendix A Materials

<p>This dataset includes supporting tables and figures for my PhD thesis at the University of Toronto, entitled "Hybridisation in Primates: Cryptic Admixture and Adaptive Introgression" in partial fulfillment of the degree requires for the Department of Anthropology (Evolutionary Anthropology). The data contains Tables A1-A7, high resolution images for Figures 2.1-2.4 and supporting figures A1-A16 that are described in chapter 2 and in Appendix A.&nbsp;</p>

restrictedcc-by-4.0Oct 2024View details →
zenodo20/100

FIGURE 42 in <p class="HeadingRunIn" align="left"><strong>A revision of the <em>Pauropsalta annulata </em>Goding &amp; Froggatt species group (Hemiptera: Cicadidae) based on morphology, calling songs and ecology, with investigations into calling song  structure, molecular phylogenetic relationships and a case of  hybridisation between two subspecies</strong></p>

FIGURE 42. Waveform plots illustrating the lilting component of the male calling song of Pauropsalta kobongoides sp. nov. from four different localities, including: (i) Weengallon (28°22'S 149°03'E), (ii) Barmedman (34°09'S 147°23'E), (iii) Mount Hope (32°50'S 145°53'E), and (iv) Narromine (32°20'S 148°14'E). Mean phrase repetition rates (PRR) for each recording are provided to the right of each plot for reference. Recording (i) was made using RS1, while all other recordings were made using RS5 (see methods).

opennotspecifiedOct 2013View details →
zenodo20/100

FIGURE 39 in <p class="HeadingRunIn" align="left"><strong>A revision of the <em>Pauropsalta annulata </em>Goding &amp; Froggatt species group (Hemiptera: Cicadidae) based on morphology, calling songs and ecology, with investigations into calling song  structure, molecular phylogenetic relationships and a case of  hybridisation between two subspecies</strong></p>

FIGURE 39. Illustrations of male pygofer and internal genitalia, viewed ventrally (left) and laterally from left (right): (A) Pauropsalta kobongoides sp. nov., 65km NNE. of St George (27°32'S 148°50'E); (B) P. corymbiae sp. nov., Bull's Gully via Adavale (25°58'S 144°59'E); (C) P. inversa sp. nov., Eidsvold (25°22'S 151°07'E); (D) P. rubristrigata (Goding and Froggatt), Mt Lofty (34°59'S 138°43'E); (E–F) P. ayrensis Ewart, (E) Eidsvold (25°22'S 151°07'E), (F) Mount Surprise (18°09'S 144°19'E). Scaling is the same for all illustrations except (D), which is scaled differently to the rest.

opennotspecifiedOct 2013View details →
zenodo20/100

FIGURE 37 in <p class="HeadingRunIn" align="left"><strong>A revision of the <em>Pauropsalta annulata </em>Goding &amp; Froggatt species group (Hemiptera: Cicadidae) based on morphology, calling songs and ecology, with investigations into calling song  structure, molecular phylogenetic relationships and a case of  hybridisation between two subspecies</strong></p>

FIGURE 37. Male calling song structure of Pauropsalta decora sp. nov. illustrated in expanded waveform plots (explained in Fig. 8), showing both buzzing and lilting components. The spectrogram at the bottom of the figure displays song frequency, which exhibits no modulation between the song components in this species. This specimen was recorded in the field at Beardmore Dam via St George (27°51'S 148°38'E).

opennotspecifiedOct 2013View details →
zenodo20/100

FIGURE 30 in <p class="HeadingRunIn" align="left"><strong>A revision of the <em>Pauropsalta annulata </em>Goding &amp; Froggatt species group (Hemiptera: Cicadidae) based on morphology, calling songs and ecology, with investigations into calling song  structure, molecular phylogenetic relationships and a case of  hybridisation between two subspecies</strong></p>

FIGURE 30. Waveform plots illustrating the lilting component of the male calling song of Pauropsalta granitica sp. nov. from six different localities, including: (i) Mount Carbine (16°35'S 145°11'E), (ii) 27 km W. of Mount Surprise (18°13'S 144°04'E), (iii) Einasleigh River (18°11'S 144°00'E), (iv) 75 km W. of Georgetown (18°16'S 142°41'E), (v) Savannah Way 2 km E. of Qld/ NT border (17°13'S 138°01'E), and (vi) 8 km W. of Calvert River via Borroloola (16°53'S 137°18'E). Mean phrase repetition rates (PRR) for each recording are provided to the right of each plot for reference. All recordings were made by D. Marshall using RS4, apart from recording (i), which was made using RS1 (see methods).

opennotspecifiedOct 2013View details →
zenodo20/100

FIGURE 26 in <p class="HeadingRunIn" align="left"><strong>A revision of the <em>Pauropsalta annulata </em>Goding &amp; Froggatt species group (Hemiptera: Cicadidae) based on morphology, calling songs and ecology, with investigations into calling song  structure, molecular phylogenetic relationships and a case of  hybridisation between two subspecies</strong></p>

FIGURE 26. Waveform plots illustrating the male calling song of Pauropsalta simplex sp. nov. from four different localities, including: (i) Atherton (17°16'S 145°29'E), (ii) Top of Herberton Range (17°21'S 145°35'E), (iii) 5km W. of Herberton (17°23'S 145°21'E) and (iv) Bluewater Creek Rest Area S. of Townsville (19°11'S 146°33'E). Mean phrase repetition rates (PRR) for each recording are provided to the right of each plot for reference. All recordings were made using RS1, with the exception of recording (iv), which was made by D. Marshall using RS4 (see methods).

opennotspecifiedOct 2013View details →
zenodo20/100

FIGURE 21 in <p class="HeadingRunIn" align="left"><strong>A revision of the <em>Pauropsalta annulata </em>Goding &amp; Froggatt species group (Hemiptera: Cicadidae) based on morphology, calling songs and ecology, with investigations into calling song  structure, molecular phylogenetic relationships and a case of  hybridisation between two subspecies</strong></p>

FIGURE 21. Waveform plots illustrating the male calling song of Pauropsalta tremula sp. nov. from six different localities, including: (i) Lake Broadwater (27°21'S 151°06'E), (ii) Coolmunda Dam (28°26'S 151°14'E), (iii) Miles (27°37'S 150°10'E), (iv) Benarkin (26°53'S 152°08'E), (v) Cooyar (26°59'S 151°50'E), and (vi) Eidsvold (25°22'S 151°07'E). Mean phrase repetition rates (PRR) for each recording are provided to the right of each plot for reference. The Benarkin recording (iv) is a duet that includes the responses of a female, with each female wing-flick indicated by an arrow.

opennotspecifiedOct 2013View details →

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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.

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OpenNeuro

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