Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
3
datasets available to search
ShareScore release 0.7.1
Dataset results
3 results for “Illumina MiSeq”
Silene uralensis aggregate, circumpolar species : dataset, Miseq Illumina RAW READS
<p>This dataset includes 43 samples of circumpolar species included in the <em>Silene uralensis</em> aggregate, sensu http://panarcticflora.org/. Forty-eight low copy nuclear genes were enriched with <em>Silene-</em>specific probes. The samples were sequenced with the Miseq technology from the short read Illumina platform. An excel sheet with samples information is included.</p> <p>Two other datasets are associated to this one, called "Silene uralensis aggregate, circumpolar species : dataset, Novaseq Illumina RAW READS SET 1" on Zenodo 10.5281/zenodo.12699639 and "Silene uralensis aggregate, circumpolar species : dataset, Novaseq Illumina RAW READS SET 2" on Zenodo 10.5281/zenodo.12700012. These three datasets belong to a study about phylogenetics in the circumpolar <em>Silene uralensis</em> aggregate. </p> <div> <div> <div> </div> <div> <div> <div> </div> <div> <p> </p> <p> </p> </div> </div> </div> </div> </div>
Data from: Massively parallel multiplex DNA sequencing for specimen identification using an Illumina MiSeq platform
Genetic information is a valuable component of biosystematics, especially specimen identification through the use of species-specific DNA barcodes. Although many genomics applications have shifted to High-Throughput Sequencing (HTS) or Next-Generation Sequencing (NGS) technologies, sample identification (e.g., via DNA barcoding) is still most often done with Sanger sequencing. Here, we present a scalable double dual-indexing approach using an Illumina Miseq platform to sequence DNA barcode markers. We achieved 97.3% success by using half of an Illumina Miseq flowcell to obtain 658 base pairs of the cytochrome c oxidase I DNA barcode in 1,010 specimens from eleven orders of arthropods. Our approach recovers a greater proportion of DNA barcode sequences from individuals than does conventional Sanger sequencing, while at the same time reducing both per specimen costs and labor time by nearly 80%. In addition, the use of HTS allows the recovery of multiple sequences per specimen, for deeper analysis of genetic variation in target gene regions.
Data from: Massively parallel multiplex DNA sequencing for specimen identification using an Illumina MiSeq platform
Open the record for dataset details and reuse information.
ScienceDex guides
Understand access before you commit
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.