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.
5,946
datasets available to search
ShareScore release 0.9.0
Dataset results
5,946 results for “diabetes type 2”
Multi-Omic Integrated networks connect DNA methylation and miRNA with skeletal muscle plasticity to chronic exercise in type 2 diabetic obesity
GEO Series GSE58250. synthetic construct; Homo sapiens. 102 samples. Type: Non-coding RNA profiling by array; Expression profiling by array; Methylation profiling by array.
Differential promoter methylation of macrophage genes correlates with impaired vascular growth in ischemic muscles of hyperlipidemic and type 2 diabetic mice
GEO Series GSE65803. Mus musculus. 21 samples. Type: Methylation profiling by high throughput sequencing.
Circulating Exosomal miR-20b-5p is Elevated in Type 2 Diabetes and Could Impair Insulin Action in Human Skeletal Muscle.
GEO Series GSE102295. Homo sapiens. 6 samples. Type: Expression profiling by array.
Sodium ferrous citrate and 5-aminolevulinic acid improve type 2 diabetes by maintaining muscle and mitochondrial health
GEO Series GSE201092. Mus musculus. 6 samples. Type: Expression profiling by array.
Expression data from peripheral blood mononuclear cells(PBMCs) in newly diagnosed type 2 diabetes
GEO Series GSE168437. Homo sapiens. 4 samples. Type: Expression profiling by array; Non-coding RNA profiling by array.
Gene expression profiles of beta-cell enriched tissue obtained by Laser Capture Microdissection from subjects with type 2 diabetes
GEO Series GSE20966. Homo sapiens. 20 samples. Type: Expression profiling by array.
Disrupted Circadian Oscillations in Type 2 Diabetes are Linked to Altered Rhythmic Mitochondrial Metabolism in Skeletal Muscle [Affymetrix]
GEO Series GSE182120. Homo sapiens. 49 samples. Type: Expression profiling by high throughput sequencing.
Single-cell Transcriptomic Atlas of Gingival Mucosa in Type 2 Diabetes
GEO Series GSE188217. Mus musculus. 2 samples. Type: Expression profiling by high throughput sequencing.
DNA methylation data throughout human muscle cell differentiation in individuals with type 2 diabetes and controls
GEO Series GSE166787. Homo sapiens. 56 samples. Type: Methylation profiling by genome tiling array.
Disrupted Circadian Oscillations in Type 2 Diabetes are Linked to Altered Rhythmic Mitochondrial Metabolism in Skeletal Muscle
GEO Series GSE182121. Homo sapiens. 235 samples. Type: Expression profiling by high throughput sequencing; Expression profiling by array.
Adipocyte Precursor Cells from First Degree Relatives of type 2 diabetic patients feature changes of hsa-mir-23a-5p, -193a-5p, and -193b-5p and Insulin-Like Growth Factor 2 expression [smallRNA-seq]
GEO Series GSE162133. Homo sapiens. 4 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Summary level-data accompanying "A functional locus at 8q21.13 associated to FABP4 levels and causally links coronary artery disease and type 2 diabetes"
<p><strong>Introduction</strong></p> <p>These are the <em>Summary Level-data</em> as presented in:</p> <p>"A functional locus at 8q21.13 associated to FABP4 levels and causally links coronary artery disease and type 2 diabetes". <em>Unpublished</em>. (tentative title)</p> <p>If you use these data please cite this DOI or the (pre)print when available. When you have any questions or comments regarding this study or these files, please contact me via:</p> <p><strong>Sander W. van der Laan, PhD</strong> | <em>Central Diagnostics Laboratory, Division Laboratory, Pharmacy and Biomedical genetics, Circulatory Health Program, University Medical Center Utrecht, Utrecht University</em> | s.w.vanderlaan-2 [at] umcutrecht [dot] nl or s.w.vanderlaan [at] gmail [dot] com | @swvanderlaan</p> <p> </p> <p><strong>Files and description</strong></p> <p>There are three files available:</p> <ol> <li>meta.GWAS.FABP4.1Gp1.EUR.MODEL1.* - Gzipped file containing all the (unfiltered) meta-analysis results for model 1 (FABP4 ~ SNP + age + sex + PC1-10 + study specific covariates). <ul> <li>Discovery dataset ends with: "summaryQC.ELISAonly.txt.gz"</li> <li>Replication dataset ends with: "summaryQC.OLINKonly.txt.gz"</li> <li>Combined dataset ends with: "summaryQC.txt.gz"</li> </ul> </li> <li>meta.GWAS.FABP4.1Gp1.EUR.MODEL2.* - Gzipped file containing all the (unfiltered) meta-analysis results for model 2 (FABP4 ~ SNP + age + sex + PC1-10 + study specific covariates + BMI). <ul> <li>Discovery dataset ends with: "summaryQC.ELISAonly.txt.gz"</li> <li>Replication dataset ends with: "summaryQC.OLINKonly.txt.gz"</li> <li>Combined dataset ends with: "summaryQC.txt.gz"</li> </ul> </li> <li>meta.GWAS.FABP4.1Gp1.EUR.MODEL3.* - Gzipped file containing all the (unfiltered) meta-analysis results for model 3 (FABP4 ~ SNP + age + sex + PC1-10 + study specific covariates + BMI + eGFR). <ul> <li>Discovery dataset ends with: "summaryQC.ELISAonly.txt.gz"</li> <li>Replication dataset ends with: "summaryQC.OLINKonly.txt.gz"</li> <li>Combined dataset ends with: "summaryQC.txt.gz"</li> </ul> </li> </ol> <p>All these files have the same lay-out and are gzipped. The reference used for meta-analysis of GWAS was 1000G phase 1, version 3 (so called 'ALL.wgs.integrated_phase1_v3.20101123.snps_indels_sv.sites'-panel) using data from the EUR populations. For a more detailed explanation of these columns and the reason to include them, please refer to <a href="https://doi.org/10.1093/hmg/ddn288">De Bakker <em>et al.</em> Hum Mol Genet 2008</a>. </p> <ul> <li><em>VARIANTID</em> - variantID as represented in 1000G phase 1, version 3.</li> <li><em>CHR</em> - chromosome numbers [1-22 and X, Y, MT].</li> <li><em>POS</em> - base pair position.</li> <li><em>MINOR</em> - minor allele as present in 1000G.</li> <li><em>MAJOR</em> - major allele as present in 1000G.</li> <li><em>MAF</em> - minor allele frequency as present in 1000G.</li> <li><em>CODEDALLELE</em> - coded allele, <em>i.e.</em> the effect allele, as represented (and harmonized) across cohorts. Note that this is not necessarily the minor allele!</li> <li><em>OTHERALLELE</em> - the other allele, <em>i.e.</em> the non-effect allele.</li> <li><em>CAF</em> - coded allele frequency, <em>i.e.</em> the effect allele frequency. Note that this is not necessarily the minor allele frequency!</li> <li><em>N_EFF</em> - the effective sample size corrected for the imputation quality.</li> <li><em>Z_SQRTN</em> - Z-score of the effective sample-size-weighted meta-analysis.</li> <li><em>P_SQRTN</em> - P-value of the effective sample-size-weighted meta-analysis.</li> <li><em>BETA_FIXED</em> - beta from the fixed-effects model.</li> <li><em>SE_FIXED</em> - standard error from the fixed-effects model.</li> <li><em>Z_FIXED</em> - z-score from the fixed-effects model.</li> <li><em>P_FIXED</em> - P-value from the fixed-effects model.</li> <li><em>BETA_LOWER_FIXED</em> - 95% lower confidence interval of the beta from the fixed-effects model.</li> <li><em>BETA_UPPER_FIXED</em> - 95% upper confidence interval of the beta from the fixed-effects model.</li> <li><em>BETA_GC</em> - beta after correcting the fixed-effects beta for genomic inflation.</li> <li><em>SE_GC</em> - standard error after correcting the fixed-effects SE for genomic inflation.</li> <li><em>Z_GC</em> - Z-score after correcting the fixed-effects Z-score for genomic inflation.</li> <li><em>P_GC</em> - P-value after correcting the fixed-effects p-value for genomic inflation.</li> <li><em>BETA_RANDOM</em> - beta from the random-effects model.</li> <li><em>SE_RANDOM</em> - standard error from the random-effects model.</li> <li><em>Z_RANDOM</em> - Z-score from the random-effects model.</li> <li><em>P_RANDOM</em> - P-value from the random-effects model.</li> <li><em>BETA_LOWER_RANDOM</em> - 95% lower confidence interval of the beta from the random-effects model.</li> <li><em>BETA_UPPER_RANDOM</em> - 95% upper confidence interval of the beta from the random-effects model.</li> <li><em>COCHRANS_Q</em> - Cochran's Q as a measure of heterogeneity between studies (<a href="https://wiki.joannabriggs.org/pages/viewpage.action?pageId=9273407">see this wiki</a>).</li> <li><em>DF</em> - degrees of freedom, equals the number of studies included for the respective variant (<em>N</em>) minus 1, <em>i.e.</em> <em>DF = N-1</em>.</li> <li><em>P_COCHRANS_Q</em> - P-value of Cochran's heterogeneity test.</li> <li><em>I_SQUARED</em> - <em>I<sup>2</sup></em> as a measure of heterogeneity between studies (<a href="https://wiki.joannabriggs.org/display/MANUAL/3.3.10.2+Quantification+of+the+statistical+heterogeneity%3A+I+squared">see this wiki</a>).</li> <li><em>TAU_SQUARED</em> - <em>Tau<sup>2</sup></em> as a measure of true heterogeneity between studies (<a href="https://wiki.joannabriggs.org/display/MANUAL/3.3.10.3+Tau-squared+for+random+effects+model+meta-analysis">see this wiki</a>).</li> <li><em>DIRECTIONS</em> - the sign of beta in each contributing cohort, annotated as “.” if the variant is missing from a particular cohort.</li> <li><em>GENES_250KB</em> - list of all genes as mapped using GENCODE v19 (GRCh37, hg19, Feb2009) with 250kb.</li> <li><em>NEAREST_GENE</em> - the gene closest to the respective variant.</li> <li><em>NEAREST_GENE_ENSEMBLID</em> - the ENSEMBLID of the nearest gene.</li> <li><em>NEAREST_GENE_STRAND</em> - strand on which the nearest gene is present.</li> <li><em>VARIANT_FUNCTION</em> - variant function as taken from dbSNP v150.</li> <li><em>CAVEAT</em> - potential issue as reported by <a href="https://github.com/swvanderlaan/MetaGWASToolKit">MetaGWASToolKit</a>, <em>e.g.</em> if the variant is an A/T or C/G SNP with allele frequency between 0.35 and 0.65 (indicating strandedness ambiguity).</li> <li><em>QC</em> - utility column, can be used to filter out all the variants with <em>e.g.</em> 'CAF' < 0.001, 'DF' <= 2, 'N_EFF' < 5000 and 'CAVEAT' having an issue depending on the dataset used (discovery, replication, or combined).</li> </ul> <p> </p>
Patient journeys in type 2 diabetes treatments as part of the findings from Co-design Activity 1
<p>This is an enlargeable figure to elaborate on Figure 47 of Chininthorn's Ph.D. thesis.</p>
FIGURE 1. a–e in A genome-wide association search for type 2 diabetes genes in African Americans.
FIGURE 1. a–e. Hemielimaea adeviara sp. nov., Liu, Song and Yuan. a. Stridulatory area of male left tegmen; b. Stridulatory area of male right tegmen; c. Male stridulaotry file on underside of left tegmen, whole view; d. Central quarter part of stridulatory file on underside of left tegmen; e. Apical area of male subgenital plate; f. Male abdominal apex in dorsal view; g. Male abdominal apex in lateral view; h. Male phallic sclerite in dorsal view.
Neuroendocrine Brake for Type 2 Diabetes Mellitus
ClinicalTrials.gov study NCT00450710. IPD Sharing: Not stated. Countries: 1. Publications: 0.
BMS-646256 in Obese and Overweight Type 2 Diabetics
ClinicalTrials.gov study NCT00541567. IPD Sharing: Not stated. Countries: 0. Publications: 0.
The Effect of Continuous Glucose Monitoring in Individuals With Newly Diagnosed Type 2 Diabetes
ClinicalTrials.gov study NCT06471699. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Effects of First-Line Oral Hypoglycemics in Bone Markers of Treatment Naïve Saudi Adults With Type 2 Diabetes
ClinicalTrials.gov study NCT06439758. IPD Sharing: NO. Countries: 0. Publications: 0.
Evaluation of Efficacy and Safety of Combination Therapy of Henagliflozin Proline, Retagliptin and Metformin in New Diagnosed Type 2 Diabetes Patients
ClinicalTrials.gov study NCT06417489. IPD Sharing: UNDECIDED. Countries: 0. Publications: 0.
Exercise and Diet in Type 2 Diabetic Women
ClinicalTrials.gov study NCT00763074. IPD Sharing: Not stated. Countries: 0. Publications: 0.
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.