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scRNA-seq raw data
Dataset
EGAD00001006436
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47 urothelial cancer patients WES and 38 RNAseq
Dataset
EGAD00001011063
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WXS Normal Samples Javelin head and neck 100
Dataset
EGAD00001011321
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Spatially resolved cellular and molecular drivers of cardiac remodelling in healthy and failing human hearts: Adult RNA (2025-07-31)
Dataset
EGAD00001015668
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Clonal dynamics of normal haematopoiesis across the human lifespan
Dataset
EGAD00001007851
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ALCHEMIST Study
Study
phs001140
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Genomewide Association Study of Alcohol Use and Alcohol Use Disorder in Australian Twin-Families (OZ-ALC GWAS)
Study
phs000181
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National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study: Whole Exome Resequencing in Glaucoma
Study
phs000558
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Genome-Wide Association Study of Sporadic and Familial Testicular Germ Cell Tumors
Study
phs001303
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Age related Macular Degeneration (AMD)-- Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: A Joint Genome Wide Association Study
Study
phs000182
-
VCRC - Giant Cell Arteritis Longitudinal Study
Study
phs000588
-
eMERGE: Genetics of Complex Pediatric Disorders from the Center for Applied Genomics
Study
phs001165
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TARGET Trial Study Cohort
Study
phs003720
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Gene expression of human Th17 cells before and after activation
Study
JGAS000005
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Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Study
EGAS00001002390
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Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis
Study
EGAS00001001258
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Chronic lymphocytic leukemia IGHV somatic hypermutation detection by targeted capture next-generation sequencing
Study
EGAS00001006887
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Evaluation of EBUS-TBNA Aspirates from Advanced NSCLC for Comprehensive Sequencing Platforms Including Whole Genome Sequencing
Study
EGAS00001007708
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The University of Hong Kong Intestinal Metaplasia Organoids Study
Study
EGAS00001007899
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A new beta-globin mutation responsible of a beta-thalassemia (HbVar database ID 2928) was observed in 8 unrelated French families. The mutation carriers originated from Nord-Pas-de-Calais, a Northern French region where the chief town is Lille.5 unrelated mutation carriers were genotyped for a set of 12 microsatellites from chromosome 11, around the beta-globin gene. Among the 5 mutation carriers, 4 were genotyped for 97 European Ancestry Informative SNPs (EAIMs). 32 controls from Nord-Pas-de-Calais were genotyped for the microsatellites and SNPs.
Dac
EGAC00001000245
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ChIP-sequencing fragment coverage
Dataset
EGAD00010001671
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HIPO016 - glioblastoma tumour methylation microarray profiling
Dataset
EGAD00010001797
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InterPregGen-GWAS-UZB-1
Dataset
EGAD00010001918
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imputed_bacterial_meningitis
Dataset
EGAD00010002327
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SNP array
Dataset
EGAD00010002597
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The chemotherapeutic CX-5461 is extremely mutagenic and may increase cancer risk
Dataset
EGAD50000000036
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Idiopathic Collapsing Glomerulopathy in Brazilian patients
Study
EGAS50000000064
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Single-cell transcriptomic analyses of peripheral blood mononuclear cells from patients with colorectal cancer metastasized to the peritoneum
Dataset
EGAD50000000247
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CITE-seq AdaptNK
Dataset
EGAD50000000329
-
Endoresist panel sequencing
Dataset
EGAD50000000350
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Cityscape Serum peptide Mass Spec data
Dataset
EGAD50000000369
-
PBMC scRNA-seq data using 10X Genomics platform
Dataset
EGAD50000000370
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Characterization of Clonal Evolution in Microsatellite Unstable Metastatic Cancers through Multi-Regional Tumor Sequencing
Study
phs001925
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WGS data of patient derived organoids (PDO) generated from dMMR colorectal tumor subclones
Dataset
EGAD50000000427
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paired-end FASTQ files from the study: Identification of the cause of juvenile parkinsonism in a case_SYNJ1
Dataset
EGAD50000000413
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BCR sequences and metadata for cultured single B-cell clones from blood
Dataset
EGAD50000000343
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Clinical panel sequencing of cancer of unknown primary using Comprehensive cancer panel (CCP)
Dataset
EGAD50000000655
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RNAseq profiles from the CheckMate-142 clinical trial
Dataset
EGAD50000000609
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WES and RNAseq dataset
Dataset
EGAD50000000337
-
ISA Nutrition 2015
Dataset
EGAD00010002678
-
Ischemia Reperfusion Responses in Human Lung Transplants at the Single Cell Resolution
Dataset
EGAD50000000704
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DNA methylation changes associated with hyperglycemia in type 1 diabetes
Dataset
EGAD50000000545
-
ST dataset from subcortical white matter MS lesions (CA & CI) and controls
Dataset
EGAD50000000520
-
RNA-seq of STIC lesions and adjacent normal samples
Dataset
EGAD50000000289
-
TIRE-seq_PDN
Dataset
EGAD50000001261
-
Transcriptome profiling of head and neck squamous cell carcinomas with paired patient-derived xenografts
Dataset
EGAD50000000995
-
Whole-exome sequencing of tumor samples
Dataset
EGAD50000001150
-
Whole-transcriptome sequencing of tumor samples
Dataset
EGAD50000001151
-
WES of head and neck cancer patients refractory to anti-PD-1 therapy
Dataset
EGAD50000001011
-
Shallow whole genome sequencing DETECT samples
Dataset
EGAD50000001333