-
DERMATLAS__Porocarcinoma_WES
Study
EGAS00001005720
-
DERMATLAS__Porocarcinoma_RNAseq
Study
EGAS00001005721
-
DERMATLAS__Poroma_RNAseq
Study
EGAS00001005759
-
DERMATLAS__Poroma_WES
Study
EGAS00001007705
-
Exome sequencing of UK Birth Cohorts - Born in Bradford
Dataset
EGAD00001015370
-
Exome sequencing of UK Birth Cohorts - Avon Longitudinal Study of Parents and Children
Dataset
EGAD00001015371
-
Exome sequencing of UK Birth Cohorts - Millennium Cohort Study
Dataset
EGAD00001015372
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015376
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015377
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015378
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015379
-
Chromatin 3D interactions mediate genetic effects on gene expression
Study
EGAS00001003485
-
Pediatric Low-Grade Glioma RNA and Targeted Sequencing
Study
EGAS00001004242
-
A living biobank of breast cancer organoids captures disease heterogeneity
Study
EGAS00001002158
-
Molecular landscape of blastic plasmacytoid dendritic cell neoplasm
Study
EGAS00001006166
-
Host pathogen interaction long read transcriptome
Study
EGAS00001006779
-
Egypt_Genome_Project___high_coverage_whole_genome_sequencing
Study
EGAS00001000482
-
Primary prostate Hi-C
Study
EGAS00001005014
-
This study aims to evaluate the relationship between cardiometabolic risk factors and the most common genetic variation (SNPs)
Study
EGAS00001007818
-
ISA Nutrition 2015
Dataset
EGAD00010002678
-
Genetic and immune landscape evolution defines subtypes of MMR deficient colorectal cancer
Study
EGAS00001005769
-
Genetic and immune landscape evolution defines subtypes of MMR deficient colorectal cancer
Dataset
EGAD00001008334
-
Pancreatic islets PISA RNA-seq samples
Study
EGAS00001005535
-
Genetics and therapeutic responses to TIL therapy of pancreatic cancer PDX models
Study
EGAS00001005596
-
Reconstruction of human phylogenetic trees using single-cell genome sequencing
Study
EGAS00001004824
-
Dataset that contains runs of submission 16
Dataset
EGAD50000000295
-
Longitudinal peripheral blood DNA methylation profiling of endoscopic response to tofacitinib in moderate-to-severe ulcerative colitis patients
Study
EGAS00001006968
-
Genomics analysis of mucinous tumours of the ovary and related neoplasms
Study
EGAS00001003545
-
Genome-wide SNP genotyping of Central African rainforest hunter-gatherers and neighbouring agriculturalists
Study
EGAS00001000605
-
Whole-Genome Sequencing of a Healthy Aging Cohort.
Study
EGAS00001002306
-
Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis
Dataset
EGAD00001009280
-
Whole exome and transcriptome sequencing of biliary tract cancer
Study
EGAS00001000950
-
Northern Ireland COhort for the Longitudinal study of Ageing
Study
EGAS00001007915
-
Nasal DNA methylation at three CpG sites predicts childhood allergic disease
Study
EGAS00001005189
-
RNA-Sequencing and Somatic Mutation Status of Adrenocortical Tumors: Novel Pathogenetic Insights
Study
EGAS00001004533
-
Genetic and epigenetic variation at regulatory regions contribute to cancer evolution under endocrine treatment
Study
EGAS00001006340
-
Methylation-based deconvolution of cell-free DNA
Study
EGAS00001007493
-
Data Access Committee Clinical Genetics at Karolinska Institutet (DAC-CG-KI)
Dac
EGAC00001002960
-
Dataset that contains runs of submission 71
Dataset
EGAD50000000101
-
A GWAS study with the AlpeDPD study cohort
Study
EGAS00001007855
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - DNA
Dataset
EGAD00001009812
-
Raw data for "Spatial and temporal transcriptomics of medulloblastoma with chromothripsis identifies multiple genetic clones that resist to treatment and lead to relapse"
Dataset
EGAD00001010260
-
Mapping the epigenomic landscape of human monocytes following innate immune activation reveals context-specific mechanisms driving endotoxin tolerance
Study
EGAS00001007362
-
Whole genome sequencing of individuals from Latvia: the first step towards the population-specific reference of genetic variation
Study
EGAS00001007406
-
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH1
Study
EGAS00001001854
-
Single-cell proteogenomics of MDS upon AZA
Study
EGAS00001007427
-
H3Africa - Stroke Investigative Research and Education Networks
Study
EGAS00001007331
-
Genome-wide data from Agta hunter-gatherers in Philippines
Study
EGAS00001005315
-
Whole genome sequencing of 108 epileptic patients from CENet cohort
Study
EGAS00001007507
-
DNA methylation and the adverse metabolic outcomes of adiposity
Study
EGAS00001001922
-
Genetic and methylation profiles distinguish benign, malignant and spitzoid melanocytic tumors
Study
EGAS00001006205
-
Linking the epigenetic landscape in chronic lymphocytic leukemia to deregulated chromatin networks
Study
EGAS00001002518
-
Unraveling the genetics of transformed splenic marginal zone lymphoma
Study
EGAS00001006389
-
DNA methylation and somatic mutations converge on cell cycle and define similar evolutionary histories in brain tumors
Study
EGAS00001001255
-
Integrated genomic characterization of IDH1 mutant Glioma malignant progression
Study
EGAS00001001588
-
Genetics of non-syndromic idiopathic autism spectrum disorders in India
Study
EGAS00001006060
-
Genome wide variation in the Angolan Namib desert reveals unique Pre-Bantu ancestry
Study
EGAS00001007011
-
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Study
EGAS00001007045
-
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
-
Single cell multi-omic data of glioblastoma evolution under therapy
Study
EGAS00001004909
-
Detection of rare mutations, copy number variation, and DNA methylation in the same template DNA molecules
Study
EGAS00001006839
-
Transcriptome profiling of human plucked frontal and occipital hair follicles
Study
EGAS00001002832
-
Mutator phenotype and specific mutational signature explain an increased risk of hematological malignancies in patients with Xeroderma Pigmentosum
Study
EGAS00001004511
-
COVID19 Host Genetic Initiative
Study
EGAS00001005304
-
Spatial concordance of DNA methylation classification in diffuse glioma
Study
EGAS00001005434
-
Combination therapies to inhibit LCK tyrosine kinase and mTOR signaling in T-cell Acute Lymphoblastic Leukemia
Study
EGAS00001005945
-
Molecular programs of melanoma brain metastases (MBM)
Study
EGAS00001005976
-
Loss of Epigenetic Barrier is Required for Enhancer Hijacking-Mediated Oncogenic Transcription
Study
EGAS00001006140
-
Bulk-tissue RNA-sequencing paired nuclear and cytoplasmic fractions of anterior prefrontal cortex, cerebellar cortex and putamen tissues from post-mortem neuropathologically-confirmed control individuals.
Study
EGAS00001006380
-
HSP90 inhibitor resistant cell line
Study
EGAS00001006381
-
Genetic variants of the COL4A3, COL4A4, and COL4A5 genes contribute to thinned glomerular basement membrane lesions in sporadic IgA nephropathy patients
Study
EGAS00001006519
-
Gene copy number variation in pediatric mental illness in a general population
Study
EGAS00001006659
-
Erythroid/megakaryocytic differentiation confers BCL-XL dependency and venetoclax resistance in acute myeloid leukemia
Study
EGAS00001006819
-
BLUEPRINT Epigenetic characterization of megakaryocytes and erythroblasts
Study
EGAS00001001641
-
Identification of gene mutations and fusion genes in patients with Sézary Syndrome
Study
EGAS00001001706
-
Pre-neoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma
Study
EGAS00001006692
-
AfricanNeo aDNA Study
Study
EGAS00001007519
-
SMARCB1 loss activates patient-specific distal oncogenic enhancers in malignant rhabdoid tumors
Study
EGAS00001007590
-
Genetic Landscape of Esophageal Squamous Cell Carcinoma Defined by Exome Sequencing on Chinese Patient Cohort and Cell Lines
Study
EGAS00001000932
-
Multimodal Epigenetic Sequencing Analysis (MESA) of Cell-free DNA for Non-invasive Cancer Detection
Study
EGAS00001006462
-
The European MAPPYACTS trial: Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies
Study
EGAS00001005935
-
Nala GSI GSAv3 PGx Study
Study
EGAS00001007710
-
RNA-seq of Liver Cancer
Study
EGAS00001002879
-
Genomic_profiling_of_B_other_Adult_ALL_RNA
Study
EGAS00001003428
-
Genomic_profiling_of_B_other_Adult_ALL_WGS
Study
EGAS00001002474
-
Disease and phenotype relevant genetic variants identified from histone acetylomes in human hearts
Study
EGAS00001003586
-
Transcriptome Analysis Offers a Comprehensive Illustration of the Genetic Background of Pediatric Acute Myeloid Leukemia
Study
EGAS00001003701
-
Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria
Study
EGAS00001007036
-
RNAseq
Study
EGAS00001007165
-
Whole genome and whole exome sequencing of epilaptic patients
Study
EGAS00001002825
-
Chip_seq_oesophageal_adenocarcinoma_
Study
EGAS00001007180
-
Understanding_hematopoietic_stem_cell_mobilization_and_engraftment_
Study
EGAS00001004620
-
The genetic history of the southern Andes from present-day Mapuche ancestry
Study
EGAS00001007200
-
H3Africa AWIGEN Pilot MetaboChip
Dataset
EGAD00010001258
-
GLASS-NL DNA-Methylation
Study
EGAS00001007546
-
IMPRESS: Improved Methylation Profiling using Restriction Enzymes and smMIP Sequencing, Combined with New Biomarker Panel, Creating Multi-Cancer Detection Assay
Study
EGAS00001007559
-
Genetic Effects on the Skin Methylome in Healthy Older Twins
Study
EGAS00001007816
-
Identification of the cause of juvenile parkinsonism in a case_SYNJ1
Study
EGAS00001007686
-
Submission 208 - study_title 1
Study
EGAS50000000321
-
Pediatric Non-Down Syndrome Acute Megakaryoblastic Leukemia is Characterized by Distinct Genomic Subsets with Varying Outcomes
Study
EGAS00001002183