-
Reference epigenome Islet-derived-iPSC01 h3k4me3 ChIP-Seq data generated from KEP study
Dataset
EGAD00001007440
-
Reference epigenome Islet-derived-iPSC01 h3k9me3 ChIP-Seq data generated from KEP study
Dataset
EGAD00001007441
-
Reference epigenome Islet-derived-iPSC01 input ChIP-Seq data generated from KEP study
Dataset
EGAD00001007442
-
Reference epigenome Islet-derived-iPSC02 h3k27ac ChIP-Seq data generated from KEP study
Dataset
EGAD00001007443
-
Reference epigenome Islet-derived-iPSC02 h3k27me3 ChIP-Seq data generated from KEP study
Dataset
EGAD00001007444
-
Reference epigenome Islet-derived-iPSC02 h3k36me3 ChIP-Seq data generated from KEP study
Dataset
EGAD00001007445
-
Reference epigenome Islet-derived-iPSC02 h3k4me1 ChIP-Seq data generated from KEP study
Dataset
EGAD00001007446
-
Reference epigenome Islet-derived-iPSC02 h3k9me3 ChIP-Seq data generated from KEP study
Dataset
EGAD00001007448
-
Reference epigenome Islet-derived-iPSC02 input ChIP-Seq data generated from KEP study
Dataset
EGAD00001007449
-
danMAC5
Dataset
EGAD00001009756
-
van Hijfte snRNA glioblastoma dataset
Dataset
EGAD00001009871
-
Pre-neoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma
Dataset
EGAD00001011097
-
Characterising the evolutionary dynamics of cancer proliferation in single-cell clones with SPRINTER
Dataset
EGAD00001015411
-
GEnetics of Nephropathy - an International Effort (GENIE) GWAS of Diabetic Nephropathy in the UK GoKinD and All-Ireland Cohorts
Study
phs000389
-
Gene Expression and Regulatory Networks in Human Leukocytes - Immunological Variation Consortium
Study
phs000815
-
Genome-Wide Association Study of Genetic Susceptibility for Graft-vs-Host Disease Cohort 1
Study
phs002185
-
Palindromic Amplification of The ERBB2 Oncogene in HER2-Positive Breast Cancer
Study
phs001261
-
CCDG CVD: VIRGO - Variation in Recover-Role of Gender on Outcomes of Young Acute Myocardial Infarction (AMI) Patients
Study
phs001259
-
P647 Targeted resequencing project
Dataset
EGAD00001000383
-
Renal habitat WXS
Dataset
EGAD00001010125
-
Res1_PC9_exp2_MC_01.04.22
Dataset
EGAD00001012233
-
Res1_HT29_exp2_MC_03.03.22
Dataset
EGAD00001012231
-
Res1_H23_exp2_MC_13.07.22
Dataset
EGAD00001012234
-
The ALT pathway generates telomere fusions that can be detected in the blood of cancer patients
Dataset
EGAD00001012101
-
Altered Interactions between Circulating and Tissue-Resident CD8 T Cells with the Colonic Mucosa Define Checkpoint Inhibitor Colitis
Study
phs003418
-
Intratumoral plasma cells predict outcomes to PD-L1 blockade in non-small cell lung cancer
Study
EGAS00001005013
-
Identification Of Pathogenic Mutations And Application Of Polygenic Risk Scores In Early-Onset Diabetes Patients
Study
EGAS50000000991
-
ScRNA sequencing and snp-array genotyping of peripheral immune cells in Type 1 diabetes mellitus (T1DM)
Dataset
EGAD50000000345
-
Population_based_analysis_of_POT1_variants_in_a_cutaneous_melanoma_case_control_cohort
Study
EGAS00001006870
-
Vitamin C boosts DNA demethylation in TET2 germline mutation carriers
Study
EGAS00001006916
-
Spatial whole exome sequencing of metastatic melanoma
Dataset
EGAD00001005819
-
Whole exome sequencing of sequential samples from a CLL patient over the course of venetoclax treatment, BCR inhibitor treatment, and venetoclax re-treatment
Dataset
EGAD00001008685
-
Whole exome and RNA sequencing data from urothelial bladder cancer patients treated with anti-PD-(L)1
Dataset
EGAD00001010324
-
WGS sequencing of an ES tumor sample
Dataset
EGAD00001015607
-
bulkRNAseq of ovarian cancer cell lines
Dataset
EGAD50000002059
-
CNV dataset
Dataset
EGAD00010001074
-
McGill EMC Release 4 in tissue "Brodmann (1909) area 8;Brodmann (1909) area 9"
Dataset
EGAD00001001286
-
Illumina_WXS_T-CELL-XEN
Dataset
EGAD00001002101
-
Bulk exome sequencing of primary GBM - SF 10360
Dataset
EGAD00001002274
-
Whole genome sequencing of a breast cancer cohort with known functional homologous recombination status
Dataset
EGAD00001008027
-
Proteomics of 7-member healthy family (father, mother, their three biological daughters and monozygotic twin sons)
Dataset
EGAD00001009985
-
WGS and ONT Bams Accompanying Loose Ends Dataset
Dataset
EGAD00001011047
-
ATAC-seq of cohesin-mutated and -wildtype adult AMLs
Dataset
EGAD00001011267
-
Whole Genome Scan for Pancreatic Cancer Risk in the Pancreatic Cancer Cohort Consortium and Pancreatic Cancer Case-Control Consortium (PanScan)
Study
phs000206
-
Temporal Lobe Epilepsy and Retrotransposons
Study
phs002067
-
Clinical and Genetic Evaluation of Individuals with Undiagnosed Disorders through the Undiagnosed Diseases Network (UDN)
Study
phs001232
-
Maternally-Inherited SPTBN1 Mutation
Dataset
EGAD50000001726
-
Identifying the role of ID3 in DNA repair and maintenance of genome integrity (RNA-seq)
Dataset
EGAD00001008198
-
Colorectal organoids and tumoroids - pulldown
Dataset
EGAD00001001208
-
Illumina_RNA_T-CELL-XEN
Dataset
EGAD00001002079
-
Illumina_WGS_MET-CELL-XEN
Dataset
EGAD00001002086
-
Illumina_WGS_T-CELL-XEN
Dataset
EGAD00001002090
-
Illumina_WXS_MET-CELL-XEN
Dataset
EGAD00001002097
-
Case Report of a Leukemic Patient with Invasive Mucormycosis
Dataset
EGAD00001001692
-
Bulk exome sequencing of primary GBM - SF 10282
Dataset
EGAD00001002275
-
Bulk exome sequencing of primary GBM - SF 10345
Dataset
EGAD00001002273
-
Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencing
Dataset
EGAD00001006079
-
GCAT| WGS VCF QC Genotype V1
Dataset
EGAD00001007774
-
Germline WES data of pediatric cancer patients
Dataset
EGAD00001008763
-
RNA sequencing of AD, MCI and control OM cells
Dataset
EGAD00001008707
-
WGS Study From Pediatrics
Dataset
EGAD00001008011
-
Patient WGS
Dataset
EGAD00001009660
-
RNA-seq of AD, MCI and control ONS cells
Dataset
EGAD00001009395
-
TDB-mediated activation of NK cells
Dataset
EGAD00001010895
-
RAD21-ChIP-Seq of cohesin-mutated and wildtpye adult AMLs
Dataset
EGAD00001011199
-
Patient Registry for Primary Pulmonary Hypertension (PPH Registry-BioLINCC)
Study
phs004275
-
Mapping Disease Pathways for Biliary Atresia
Study
phs003458
-
The earliest stages of neoplastic transformation in Familial Adenomatous Polyposis
Dataset
EGAD00001015477
-
Somatic mutant selection is altered by prior NOTCH1 mutation in ageing esophageal epithelium
Dataset
EGAD00001015257
-
Somatic mutant selection is altered by prior NOTCH1 mutation in ageing esophageal epithelium
Dataset
EGAD00001015258
-
Somatic mutant selection is altered by prior NOTCH1 mutation in ageing esophageal epithelium
Dataset
EGAD00001015259
-
Genome-wide association study for Bladder Cancer Risk
Study
phs000346
-
Cellular indexing of transcriptomes and epitopes sequencing of peritoneal fluid from patients with achalasia
Dataset
EGAD50000000252
-
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Study
phs003047
-
Exome_sequence_of_probands_in_Barrett_s_oesophagus_families
Study
EGAS00001000531
-
UROMOL 2020 - RNA-seq data
Study
EGAS00001004693
-
UROMOL 2020 - SNP data
Study
EGAS00001004862
-
GINS3 fibroblast RNAseq
Study
EGAS00001006038
-
Follicular lymphoma at diagnosis, treated in first line with immunochemotherapy
Study
EGAS00001006674
-
Pre-diagnostic saliva microbiota of Finnish children with autoimmune diseases
Study
EGAS00001006949
-
NEC
Study
EGAS00001007013
-
Combination Immune Checkpoint Inhibition in Australian Rare Cancers_WES
Dataset
EGAD00001015465
-
Whole genome sequencing data of relapsed paediatric KMT2A-rearranged acute lymphoblastic leukemia
Dataset
EGAD50000001593
-
Ion Proton WES raw and processed data from and novel immunodeficiency proband.
Dataset
EGAD50000000524
-
Detection of MEIS2 inversion using ONT adaptive sequencing
Dataset
EGAD50000000893
-
Structural variants
Dataset
EGAD50000000741
-
Average_hypermethylation_TF_sites
Dataset
EGAD00010002411
-
Identifying the role of ID3 in DNA repair and maintenance of genome integrity (ATAC-seq)
Dataset
EGAD00001008199
-
RNAseq of LC2AD with AD80 or DMSO
Dataset
EGAD00001003316
-
Exome reads
Dataset
EGAD00001003841
-
Illumina_RNA_MET-CELL-XEN
Dataset
EGAD00001002075
-
LBC1936 gvcfs
Dataset
EGAD00001006414
-
GCAT| WGS VCF Raw Genotypes V1
Dataset
EGAD00001008210
-
The University of Hong Kong Intestinal Metaplasia Organoids Study scCNV Data
Dataset
EGAD00001015423
-
GBM-Space: Joint Transcriptome and Chromatin Accessibility Profiling of Glioblastoma (10x Genomics - Multiome)
Dataset
EGAD00001015526
-
PacBio WGS based analysis of complex chromosomal rearrangements
Dataset
EGAD00001015593
-
A pan-infection single-cell atlas of human T cells unlocks systematic antigen-specificity inference
Dataset
EGAD00001016118
-
Age related Macular Degeneration (AMD)-- Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: A Joint Genome Wide Association Study
Study
phs000182
-
Breast Cancer Family Registry
Study
phs002835
-
Comprehensive genomic analysis of colorectal cancer with microsatellite instability
Study
JGAS000113