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.
6,335
datasets available to search
ShareScore release 0.9.0
Dataset results
6,335 results for “direct”
Figure 2 in Cryptic but direct costs of an epidemic caused by Batrachochytrium dendrobatidis in the endangered Sardinian newt Euproctus platycephalus (Amphibia, Caudata)
Figure 2. Estimated difference between the values of the smoothed curves for infected and uninfected individuals obtained by GAMs fitted to investigate the age-dependent variation in SVL, in Euproctus platycephalus. Male estimates are shown on the left, females on the right. The shaded area corresponds to the 95% confidence interval of the difference between mean predicted values. When the shaded area excludes zero, the predicted values for the two populations are considered significantly different from each other.
Figure 3 in Cryptic but direct costs of an epidemic caused by Batrachochytrium dendrobatidis in the endangered Sardinian newt Euproctus platycephalus (Amphibia, Caudata)
Figure 3. Smooth functional relationships (left) and estimated difference between the values of the curves (right) for infected and uninfected populations obtained by GAMs fitted to investigate the age-dependent variation in the proportion of individuals of Euproctus platycephalus. On the left, shaded areas represent 95% confidence interval, and data points have been jittered to improve visualization. On the right, the 95% confidence interval of the difference between mean predicted values: when the shaded area excludes zero, the predicted values for the two populations are considered significantly different from each other.
Figure 1 in Cryptic but direct costs of an epidemic caused by Batrachochytrium dendrobatidis in the endangered Sardinian newt Euproctus platycephalus (Amphibia, Caudata)
Figure 1. Smooth functional relationships estimated by GAMs fitted to investigate the age-dependent variation in Svl, in Euproctus platycephalus. Male estimates are shown on the left, females on the right. Shaded areas represent 95% confidence interval. Data points have been jittered to improve visualization.
Data for "Direct, Indirect, and Self-Trapped Excitons in Cs2AgBiBr6"
<p>Structures of the unit cell and polymorphous supercell of Cs2AgBiBr6 and the self-trapped exciton in the material.</p>
Fig. 3 in Direct Growth Measurements of Two Deep-sea Scalpellid Barnacles, Scalpellum stearnsii and Graviscalpellum pedunculatum
Fig. 3. in situ shell increment after 350-d deployment of Scalpellum stearnsii (narrow strip below the light calceinstained band). Pictures under fluorescent and normal light were overlaid.
Fig. 2 in Direct Growth Measurements of Two Deep-sea Scalpellid Barnacles, Scalpellum stearnsii and Graviscalpellum pedunculatum
Fig. 2. Changes in capitulum lengths of Scalpellum stearnsii (solid lines) and Graviscalpellum pedunculatum (broken lines between 35 - 55 mm) over 8-month rearing at Nara (a) and 2-year rearing at Okinawa (b). Different colors indicate different individuals.
Fig. 1 in Direct Growth Measurements of Two Deep-sea Scalpellid Barnacles, Scalpellum stearnsii and Graviscalpellum pedunculatum
Fig. 1. Scalpellid barnacles Scalpellum stearnsii (a) and Graviscalpellum pedunculatum (b). The S. stearnsii individual showed maximum absolute increments at Okinawa, with small shell plates. Capitulum length measured is shown as a black line.
Fluorescence-activated droplet sequencing (FAD-seq) directly provides sequences of screening hits in antibody discovery
<p>Contains source datas (e.g. uncropped gels, FASTQ nanopore sequences, numeric data) and the python scripts for Fluorescence-activated droplet sequencing (FAD-seq) publication</p>
Tables of direct, indirect and networks estimates and Forests plots of pairwise comparisons for all secondary outcomes
<p>Supplementary File #12 for Cochrane review entitled: "Non-invasive respiratory support in preterm infants as primary mode: a network meta-analysis"</p>
vanBeest iScience 2024: The direct and indirect pathways of the basal ganglia antagonistically influence cortical activity and perceptual decisions.
<p>Data for the paper 'The direct and indirect pathways of the basal ganglia antagonistically influence cortical activity and perceptual decisions.' by van Beest et al. 2024, iScience: https://doi.org/10.1016/j.isci.2024.110753</p> <p>Code to analyze data is available via https://github.com/EnnyvanBeest/vanBeest_iScience2024.</p> <p> </p> <p> </p>
Supplemental Video for "Direct Two-Dimensional Goniometric Steering of Vacuum Electrospray Ion Beams for Angular Time-of-Flight Studies"
<p>Supplemental video for the paper submitted to RSI titled "Direct Two-Dimensional Goniometric Aiming of Vacuum Electrospray Ion Beams for Angular Time-of-Flight Studies". </p> <p>A dual-axis goniometer is used to directly aim a vacuum electrospray ionization source (vESI). This device enables the ion beam to be aimed onto a target to dramatically increase the SNR of downstream diagnostics while also enable angular time-of-flight studies of the vESI plumes.</p>
Structure Databases: Predicted Influence of Organic Structure Directing Agents on Al Distributions in CHA Zeolites
<p>Structures and energies associated with the paper: Predicted Influence of Organic Structure Directing Agents on Al Distributions in CHA Zeolites</p>
ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep1 (run3)
<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 1 (run 3)</p>
ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep2 (run1)
<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 2 (run 1).</p>
ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) Mettl3 Knockout
<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). </p>
ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep2 (run3-1)
<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 2 (run 3-1; the files are splited two two parts because of limitations of file size).</p>
ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep2 (run2)
<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 2 (run 2)</p>
ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep1 (run2)
<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 1 (run 2). </p>
ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep1 (run1 and 4)
<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 1 (run 1 and 4). </p>
ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep2 (run3-2)
<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 2 (run 3-2; the files are splited two two parts because of limitations of file size).</p>
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.