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ShareScore release 0.9.0
Dataset results
11 results for “Statistical Identifiability”
GWAS Summary Statistics for Publication: Identifying novel genetic and phenotypic associations to genomic features by leveraging off-target reads in exome sequencing data
<p>This dataset contains summary statistics for genome-wide association studies (GWAS) conducted on genomic features derived from off-target reads in whole-exome sequencing (WES) data. The study utilized tools like Seeing Beyond the Target (SBT) and ImReP to construct novel phenotypic features from unmapped reads in ~50,000 participants in the UK Biobank. Features include mitochondrial DNA (mtDNA) copy number, ribosomal DNA (rDNA) copy number (5S, 18S, 28S), immune repertoire metrics (e.g., T-cell receptor alpha diversity), and microvial genome load (viral and fungal).</p> <p>Summary statistics can be used for replication studies, meta-analyses, or further exploration of these phenotypes.</p>
Summary statistics for "Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's Disease"
<p>These are the burden test results (summary statistics) for the publication:</p> <p>"Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s Disease",</p> <p>Nature Genetics, 2022.</p> <p> </p> <p><em>Format: tab-separated-value.</em></p> <p><em>Fields:</em></p> <ul> <li><em>gene_stable_id: Ensembl gene id</em></li> <li><em>gene_name: standard gene name</em></li> <li><em>pvalue: burden test significance (likelihood ratio test, population structure correction based on 6 PCA components)</em></li> <li><em>cmac_all: sum of minor allele dosages across all contributing samples and variants</em></li> <li><em>group: variant group (LOF, LOF+REVEL>=75, LOF+REVEL>=50, LOF+REVEL>=25, see publication methods for further selection criteria).</em></li> <li><em>beta/se: beta/se of logistic ordinal regression (see publication methods). Positive = risk-increasing. Negative = risk-decreasing.</em></li> </ul> <p> </p>
Summary statistics - Imputed gene associations identify replicable trans-acting genes enriched in transcription pathways and complex traits
<p>Summary statistics for all trans-acting/target gene pairs tested in our manuscript.</p> <p>Preprint available: <a href="https://doi.org/10.1101/471748">https://doi.org/10.1101/471748</a></p>
Statistical Methods for Identifying Sequence Motifs Affecting Point Mutations
<p>Scripts and derived data for the indicated paper. Links to the <a href="https://zenodo.org/record/1204695">original data</a> and <a href="https://zenodo.org/record/3497585">library source code</a> used to generate this material. Inflate the ENU_mutation_classification.tar.gz archive, remove the ENU_mutation_classification/classifier directory (this will be replaced). Move all others archives into the ENU_mutation_classification directory and inflate them.</p>
Summary statistics for: Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans
<p>Summary statistics of single POE-CpG based and POE-CpG co-methylation module based phenome-wide association analyses for the manuscript "Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans"</p>
Identifying cell states in single-cell RNA-seq data at statistically maximal resolution
<p>In this repository we provide the datasets for the results of the Cellstates method as shown in the article: “Identifying cell states in single-cell RNA-seq data at statistically maximal resolution” by Pascal Grobecker, Thomas Sakoparnig, and Erik van Nimwegen.</p> <p>A preprint is available under the following DOI: https://doi.org/10.1101/2023.10.31.564980</p> <p>There is a README file that describes the contents and formats of each of the tab-separated values files. There is one subdirectory containing files with Cellstates' results on the dataset of Zeisel et al. (DOI: 10.1016/j.cell.2018.06.021) which is accompanied by another README file describing the formats and contents of these files. </p>
Supplementary tables for "Theme Enrichment Analysis: A Statistical Test for Identifying Significantly Enriched Themes in a List of Stories with an Application to the Star Trek Television Franchise"
<p>Supplementary tables for the manuscript "Theme Enrichment Analysis: A Statistical Test for Identifying Significantly Enriched Themes in a List of Stories with an Application to the Star Trek Television Franchise".</p> <p>Supplementary Information File 1 contains a table of Star Trek TOS/TAS/TNG television series episodes featuring the Klingon alien race. The criterion for inclusion is that the Klingons were deemed by the authors to have been featured throughout the episode in a way that is central to the story plot.</p> <p>Supplementary Information File 2 contains tables of over-represented Literary Theme Ontology version 0.1.1 literary themes in Star Trek TOS/TAS/TNG television series storysets as identified by the hypergeometric test.</p> <p>Supplementary Information File 3 contains tables of over-represented Literary Theme Ontology version 0.1.1 literary themes in Star Trek TOS/TAS/TNG television series storysets as identified by the TF-IDF statistic.</p>
Application of GIS and Spatial Statistics in identifying the rental value of shop lot in a shopping mall based on location factor
<p>GIS Property Data</p>
TPP statistics data for: Plurifaceted proteomics method identifies a key regulator of translation during stem cells maintenance and differentiation
<p>Statistics data from TPP package.</p>
Single cell RNA-seq data of human hESCs to evaluate Oscope - a statistical pipeline for identifying oscillatory genes in unsynchronized single cell RNA-Seq
GEO Series GSE64016. Homo sapiens. 460 samples. Type: Expression profiling by high throughput sequencing.
Summary statistics for "Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke"
<p>Summary statistics of the GWA studies presented in <a href="https://doi.org/10.1101/718221">https://doi.org/10.1101/718221</a></p> <p>These are the summary statistics of all imputed SNPs, minus those that showed big differences in allele frequency between different populations (see manuscript for details).</p> <p>Header description:</p> <p>"rs_id" = the rs-id for the variant</p> <p>"chromosome" = the chromosome of the variant</p> <p>"base_pair_location" = the location in bases, according to human reference genome hg19</p> <p>"effect_allele" = the allele that is tested for association with the phenotype</p> <p>"other_allele" = the other allele</p> <p>"effect_allele_frequency" = the allele frequency of the effect allele (not necessarily the minor allele frequency)</p> <p>"IMPUTE2_info" = the imputation quality score as computed by IMPUTE2</p> <p>"beta" = the beta-coefficient from BOLT-LMM</p> <p>"standard_error" = the standard error of beta</p> <p>"p-value" = the p-value for association from BOLT-LMM</p> <p>To convert beta and standard error to odds ratios, you need to know the fraction of cases of the respective GWAS. These can be found in the supplementary material of the manuscript. Use the following formula with the case fraction μ: log OR = β / (μ * (1 - μ)). See the manuscript for more explanation.</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.