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55 results for “SNP genotype data”
Data from: Genotyping-in-Thousands by sequencing (GT-seq): a cost effective SNP genotyping method based on custom amplicon sequencing
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Data from: Development of SNP genotyping arrays in two shellfish species
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Data from: Fresh Is best: accurate SNP genotyping from koala scats
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Data from: Estimations of linkage disequilibrium, effective population size and ROH-based inbreeding coefficients in Spanish Churra sheep using imputed high-density SNP genotypes
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Data from: Development of highly reliable in silico SNP resource and genotyping assay from exome capture and sequencing: an example from black spruce (Picea mariana)
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SNP data for Syringa vulgaris genotypes
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Illumina SNP Chip and Sequenom MassARRAY genotype data of Swedish Giant Schnauzers with and without hypothyroidism
<p>In this study, we sought to identify the genetic risk factors potentially involved in the susceptibility to hypothyroidism in the high-risk Giant Schnauzer dog breed. The genotype data generated in the study (Illumina 170k CanineHD Bead Chip, Sequenom MassARRAY high-throughput re-genotyping) proved to be essential for the identification and fine-mapping of a locus associated with protection against canine hypothyroidism.</p>
Illumina SNP Chip and Sequenom MassARRAY genotype data of Swedish Giant Schnauzers with and without hypothyroidism
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SNP Genotype and Gene Expression data from induced Pluripotent Stem cells from Parkinson's Disease patients harboring mutations in the GBA1 gene, and from healthy control donors
GEO Series GSE99473. Homo sapiens. 18 samples. Type: Expression profiling by array; SNP genotyping by SNP array; Genome variation profiling by SNP array.
Gene expression and SNP genotype data from induced Pluripotent Stem cells from Parkinson's Disease patients harbouring G2019S mutations in the LRRK2 gene
GEO Series GSE77664. Homo sapiens. 12 samples. Type: SNP genotyping by SNP array; Expression profiling by array.
Gene Expression and SNP genotype data from induced Pluripotent Stem cells from healthy control donors
GEO Series GSE99125. Homo sapiens. 6 samples. Type: Expression profiling by array; SNP genotyping by SNP array.
SNP genotype data from induced Pluripotent Stem cells from healthy control donors
GEO Series GSE99124. Homo sapiens. 3 samples. Type: SNP genotyping by SNP array.
Affymetrix SNP array data for cell line and tumor genotype alignment
GEO Series GSE85838. Homo sapiens. 15 samples. Type: Genome variation profiling by genome tiling array; Third-party reanalysis.
SNP genotyping data from human iPSCs and human fibroblast cells
GEO Series GSE61769. Homo sapiens. 4 samples. Type: Genome variation profiling by SNP array.
SNP genotype data from induced Pluripotent Stem cells from Parkinson's Disease patients harboring mutations in the GBA1 gene, and from healthy control donors
GEO Series GSE99471. Homo sapiens. 13 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
ScienceDex guides
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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.