-
Clinical and demographics data from IMvigor210, IMvigor211, IMvigor130 and IMvigor010
Dataset
EGAD50000001101
-
Single-cell RNA-sequencing of CSF cells and PBMCs from individuals with neurological disorders
Dataset
EGAD50000001173
-
Genomic and Transcriptomic Data in GBM Patients Undergoing anti-PDL1 Therapy
Dataset
EGAD50000001154
-
Whole Exome Sequencing of paired gDNAs and PPGL tumor DNA from patients with cyanotic congenital heart disease
Dataset
EGAD50000001201
-
Brazilian Genomes
Study
EGAS50000000730
-
Head and Neck Organoid Biobank cohort, Issing et. al., 2025, RNA + WES data
Dataset
EGAD50000001733
-
Transcriptome profiling of slice cultures of human embryonic forebrain
Dataset
EGAD50000001690
-
Comprehensive analyses of genetic aberrations in cholangiolocarcinoma
Study
JGAS000597
-
Bisulfite sequencing of cell-free DNA in NMOSD patients
Study
JGAS000515
-
TB-DAR Genotyping Study
Study
EGAS00001007216
-
The Druze analysis group
Study
EGAS00001000963
-
(h)MeDIP-Seq of high-risk prostate cancer
Study
EGAS00001001019
-
WGS bam
Study
EGAS00001005159
-
arrayCGH for copy number profiling on tumor DNA from pediatric cancer tissue samples
Study
EGAS00001005197
-
COIN CRC GWAS data
Study
EGAS00001005421
-
WES bam
Study
EGAS00001005160
-
Dedifferentiated_Melanoma
Study
EGAS00001003471
-
GWAS in bullous pemphigoid in Germans
Study
EGAS00001004627
-
NLG-LBC-05 ctDNA
Study
EGAS00001005835
-
Comprehensive de novo variant discovery with HiFi long-read sequencing
Study
EGAS00001006479
-
Illumina short-reads and 10X Genomics linked-reads sequencing data for MCF7 and a primary breast tumor sample
Dataset
EGAD00001005724
-
CRUK Accelerator: oesophageal adenocarcinoma whole exome and RNA-seq raw sequencing data
Dataset
EGAD00001008489
-
Whole genome sequencing of HSPCs and pAML
Dataset
EGAD00001006338
-
Paired-WGS-two-families-with-GBA-variants-and-Parkinsons-disease
Dataset
EGAD00001006561
-
Bulk RNAseq data of scrambled and siRNA-mediated knock-down of the minor spliceosome snRNA U6atac
Dataset
EGAD00001008034
-
Combined DNA Methylation and Genotyping via scTAMARA-seq (DNA)
Dataset
EGAD00001015496
-
SOX11+ and SOX11- mantle cell lymphoma cell lines RNAseq data
Dataset
EGAD00001009421
-
RNAseq Atlas in HCC tumors
Dataset
EGAD00001015341
-
Human and rat skeletal muscle multiomic profiling sequencing data
Dataset
EGAD00001008323
-
Targeted DNA sequencing on bulk bone marrow and peripheral blood
Dataset
EGAD00001011083
-
Sequencing of Cervical Cancer
Study
phs000723
-
Autosomal recessive
Study
phs000848
-
Gene Expression of Small Cell Carcinoma of the Ovary-Hypercalcemic Type (SCCOHT)
Study
phs001528
-
The Immunogenetics of Measles Immunity - Measles (MMR) vaccination (NIAID/NIH)
Study
phs001630
-
Myocardial Infarction Genetics Exome Sequencing Consortium: U. of Leicester
Study
phs001000
-
Ataxia Gene Identification by Integrated Genomic Analysis
Study
phs000757
-
Neoadjuvant Pazopanib in Renal Cell Carcinoma
Study
phs002053
-
FusionSeq: a modular framework for finding gene fusions by analyzing Paired-End RNA-Sequencing data
Study
phs000311
-
NHLBI TOPMed: Trans-Omics for Precision Medicine (TOPMed) Whole Genome Sequencing Project: Cardiovascular Health Study
Study
phs001368
-
HGG panel sequencing
Study
EGAS50000000221
-
Single-nuclei RNA sequencing of pheochromocytoma and paraganglioma arising from germline SDHB mutations
Dataset
EGAD50000000505
-
Cergentis FFPE-TLC sequencing of colorectal carcinoma
Dataset
EGAD50000000618
-
Bulk RNA sequencing of human T and B cells before and after interleukin-2 immunotherapy
Dataset
EGAD50000000661
-
Characterisation of Cyr61-enriched myeloid angiogenic cells
Study
EGAS50000000533
-
Reconstitution of Human Brain Cell Diversity in Organoids via Four Protocols [scRNAseq]
Study
EGAS50000000662
-
Raw sequencing data from chromosome conformation capture, RNA sequencing and chromatin assays in human primary monocytes
Dataset
EGAD50000001116
-
Single-cell RNA sequencing of human IL-18R supported CAR T cells targeting oncofetal Tenascin C
Study
EGAS50000000772
-
Whole Exome Sequencing of controls performed at the Broad Institute on a cohort from Bristol, UK
Dataset
EGAD50000000716
-
Matched_breast_cancer_fusion_gene_study
Study
EGAS00001000031
-
Measurement of the Male Germline Mutation Rate Using Sequential Sperm Samples
Study
phs003716