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138
datasets available to search
ShareScore release 0.9.0
Dataset results
138 results for “Exome Sequencing”
Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Congestive Heart Failure Receiving Therapy for Breast Cancer
ClinicalTrials.gov study NCT02610426. IPD Sharing: Not stated. Countries: 1. Publications: 0.
DNA Exome Sequencing TCM for Sjögren's Syndrome
ClinicalTrials.gov study NCT03935373. IPD Sharing: NO. Countries: 1. Publications: 0.
Distinct Mutational Patterns of Infection and Non-Infection-Related Bile Duct Cancers Revealed by Exome Sequencing
GEO Series GSE49656. Homo sapiens. 40 samples. Type: Methylation profiling by array.
Normalization of whole-genome SNP data from acute monocytic leukemia patients for exome sequencing
GEO Series GSE27193. Homo sapiens. 9 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease
GEO Series GSE234607. Homo sapiens. 112 samples. Type: Expression profiling by high throughput sequencing.
Integrated whole-exome and transcriptome sequencing indicated dysregulation of cholesterol metabolism in eyelid sebaceous gland carcinoma
GEO Series GSE219205. Homo sapiens. 20 samples. Type: Genome variation profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Whole exome and transcriptome sequencing of murine tumor models
GEO Series GSE136619. Mus musculus. 55 samples. Type: Expression profiling by high throughput sequencing; Other.
Distinct Mutational Patterns of Infection and Non-Infection-Related Bile Duct Cancers Revealed by Exome Sequencing
GEO Series GSE49666. Homo sapiens. 30 samples. Type: Genome variation profiling by SNP array.
Transcriptional profilling of hESC with and without 17q gain upon induction of replicative stress through HU treatment [targeted exome sequencing]
GEO Series GSE155181. Homo sapiens. 4 samples. Type: Genome variation profiling by high throughput sequencing.
Reproductive history determines ErbB2 locus amplification, WNT signalling and tumor phenotype in a murine breast cancer model [exome sequencing]
GEO Series GSE162347. Mus musculus. 17 samples. Type: Genome variation profiling by high throughput sequencing.
Exome sequencing of a panel of breast cancer cell lines to identify mutations
GEO Series GSE48215. Homo sapiens. 75 samples. Type: Other.
DNA copy number detection from exome sequencing - Exploiting the off-targets (SNP)
GEO Series GSE60168. Homo sapiens. 6 samples. Type: Genome variation profiling by SNP array.
Whole-exome and RNA sequencing of pulmonary carcinoid reveals chromosomal rearrangements associated with recurrence (Affymetrix)
GEO Series GSE141755. Homo sapiens. 25 samples. Type: Expression profiling by array.
Whole exome sequencing of HNSCC PDX with KMT2D-inactivating mutation
GEO Series GSE234824. Homo sapiens. 1 samples. Type: Other.
DNA copy number detection from exome sequencing - Exploiting the off-targets
GEO Series GSE60259. Homo sapiens; Mus musculus. 10 samples. Type: Genome variation profiling by genome tiling array; Genome variation profiling by SNP array.
Exome and whole genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity
GEO Series GSE42363. Homo sapiens. 14 samples. Type: Expression profiling by array.
Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics and 3D genomics
GEO Series GSE83420. Homo sapiens. 2 samples. Type: Other.
Exome Sequencing of Childhood Wilms Tumor
Wilms tumor is the most common kidney cancer of children. To define the mutation spectrum of Wilms tumor, we performed whole-exome sequencing on matched tumor-normal pairs. A further set of tumor samples underwent whole exome sequencing without accompanying normal tissue. Exome data for patients giving consent to have the information available on a public, secure, database is being submitted.
Whole-exome sequencing identifies mutations of BCOR in acute myeloid leukemia with normal karyotype
GEO Series GSE30442. Homo sapiens. 24 samples. Type: Expression profiling by array.
Prenatal Cell-free DNA Screening in Pregnancies With Diverse Genetic Risk Profiles Utilizing Targeted and Whole-exome Sequencing
ClinicalTrials.gov study NCT07106853. IPD Sharing: YES. 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.