-
Genetic analyses in patients with T or NK cells-associated disorders
Study
JGAS000658
-
An epidemiological study examining the relationship among food, health, and genome
Study
JGAS000678
-
Whole-genome-sequencing and Whole-exome-sequencing in Myopathy
Study
JGAS000365
-
Exome analysis of cardiomyopathy patients with PKP2 variants
Study
JGAS000566
-
Exome analysis of cardiomyopathy patients with DSG2 variants
Study
JGAS000565
-
Application of organoid culture system of human gastrointestinal and thoracic cancer in genome medicine
Study
JGAS000749
-
Whole-genome-sequencing, Whole-exome-sequencing and RNA-sequencing in Sporadic ALS
Study
JGAS000393
-
Deciphering molecular mechanisms underlying hematological malignancies and development of novel therapeutic approaches
Study
JGAS000603
-
Comprehensive survey for the construction of an integrated database of food, gut microbiome, and health information (the "Sukoyaka Health Survey")
Study
JGAS000681
-
Amplicon sequencing of duodenal adenoma
Study
JGAS000352
-
Transcriptome of human trophoblast stem cells derived from normal and HDP placentas
Study
JGAS000660
-
Whole-exome-sequencing and Whole-genome-sequencing and RNA-sequencing in Familial amyotrophic lateral sclerosis (ALS)
Study
JGAS000358
-
Whole-exome-sequencing in Frontotemporal dementia (FTD)
Study
JGAS000374
-
Singel-cell RNA sequencing and CUT&RUN sequencing of human RUNX2-deficient osteoblasts
Study
JGAS000663
-
Reference Panel for Imputation Analysis Based on Whole Genome Sequencing Data of 3,256 Japanese Individuals(BioBank Japan genotype data)
Study
JGAS000746
-
Exome analysis of cardiomyopathy patients with TNNT2 variant
Study
JGAS000567
-
CINECA_synthetic_cohort_ita_ingestion_test
Dataset
EGAD50000000369
-
Submission 6 - study_title 1
Study
EGAS50000000420
-
CLL Genome
Study
EGAS00000000092
-
Cerebrospinal fluid methylome-based liquid biopsies
Study
EGAS00001006029
-
Reconstructing the dispersals and adaptive history of Bantu-speaking populations in Africa and North America
Study
EGAS00001002078
-
Genomic Epidemiology of Complex Diseases in Population-based Brazilian Cohorts
Study
EGAS00001001245
-
IDH mutant Glioma methylation analysis and prognostic signatures
Study
EGAS00001006961
-
Breast tissue methylation analysis
Study
EGAS00001005070
-
Genome Asia 100K Project
Study
EGAS00001002921
-
Indonesian RNA-seq data
Study
EGAS00001003671
-
Immunogenomic landscape of hematological malignancies
Study
EGAS00001004444
-
Uterine leiomyoma: DNA methylation, chromatin activity and gene expression
Study
EGAS00001004499
-
A reference map of potential determinants for the human serum metabolome
Study
EGAS00001004512
-
The Molecular Landscape of Asian Breast Cancers Reveals Clinically Relevant Population-Specific Differences
Study
EGAS00001004518
-
Patient-tailored design for selective co-inhibition of leukemic cell subpopulations
Study
EGAS00001004614
-
Submission 18 - study_title 2
Study
EGAS50000000366
-
Accurate detection and classification of pediatric sarcomas based on cell-free DNA fragmentation patterns
Study
EGAS00001005127
-
Transcriptomic and epigentic analysis of human peripheral blood NK cell subsets revealing role of Bcl11b in differentiation
Study
EGAS00001005025
-
The WID-EC test for the detection and risk prediction of endometrial cancer
Study
EGAS00001005033
-
The DNA methylome of cervical cells and risk of ovarian cancer
Study
EGAS00001005045
-
Bulk-tissue RNA-sequencing of anterior cingulate cortex samples derived from Lewy body disease patients
Study
EGAS00001005305
-
Genetics causes of male infertility in 185 patient-parent trios from Netherlands and UK
Study
EGAS00001005417
-
Multi-omics integration reveals only minor long-term molecular and functional sequelae in immune cells of individuals recovered from COVID-19
Study
EGAS00001005529
-
Enhancer profiling to identify identifies epigenetic markers of endocrine resistance in metastatic castration resistant prostate cancer patients
Study
EGAS00001006161
-
Single-cell RNA-seq analysis for COVID19 patients
Study
EGAS00001006560
-
Genomic map of Poland in open access - digitization of biomolecular resources of the Biobank University of Lodz laboratory
Study
EGAS50000000154
-
UK10K OBESITY TWINSUK
Study
EGAS00001000306
-
UK10K_OBESITY_GS
Study
EGAS00001000242
-
UK10K_OBESITY_SCOOP
Study
EGAS00001000124
-
UK10K COHORT ALSPAC
Study
EGAS00001000090
-
UK10K COHORT TWINSUK
Study
EGAS00001000108
-
McGill Epigenomics Mapping Centre
Study
EGAS00001000995
-
Analysis of DNA methylation in normal B cells and chronic lymphocytic leukemia
Study
EGAS00001000534
-
The Southern African Human Genome Programme
Study
EGAS00001002639
-
Reference epigenomes generated as part of the International Human Epigenomics Consortium (IHEC)
Study
EGAS00001000552
-
Indonesian Genome Diversity Project
Study
EGAS00001003054
-
The NIHR BioResource Rare Diseases BRIDGE consortium sequencing projects
Study
EGAS00001001012
-
Analysis of IDHwt-glioblastoma samples from paired primary and recurrent tumor samples
Study
EGAS00001003184
-
Exome-sequencing identifies new oncogenes and tumor suppressor genes recurrently altered in hepatocellular carcinoma
Study
EGAS00001000217
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal
Study
EGAS00001003774
-
Integrated Genomic Analysis of Chronic Lymphocytic Leukaemia
Study
EGAS00001001306
-
Genomic and transcriptomic landscape of T-cell lymphoblastic lymphoma compared to T-cell acute lymphoblastic leukemia: similar subtypes and different fusions
Study
EGAS00001007767
-
Neuroblastoma tumor heterogeneity and cell plasticity (from PDX and cell lines)
Study
EGAS00001004781
-
NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Study
EGAS00001007703
-
Comprehensive Genomic and Transcriptomic Analysis of Rare Cancers for Guiding of Therapy (H021)
Study
EGAS00001004813
-
Combined genetic and transcriptome analysis of patients with Systemic Lupus Erythematosus (SLE)
Study
EGAS00001003662
-
Gene expression-based prediction of pazopanib efficacy in sarcoma (HIPO, H021)
Study
EGAS00001005836
-
Genetic Legacy of Punan Hunter-Gatherer Groups in Indonesian Borneo
Study
EGAS00001004471
-
Therapeutic Targeting of Ependymoma as Informed by Oncogenic Enhancer Profiling
Study
EGAS00001002696
-
The_Little_Princess_Knowledge_Bank_RNAseq
Study
EGAS00001005244
-
Spatiotemporal Genomic Profiling of Intestinal Metaplasia Reveals Clonal Dynamics of Gastric Cancer Progression
Study
EGAS00001007067
-
BLUEPRINT Hematopoietic Stem/Progenitor Cell Methylomes
Study
EGAS00001002070
-
The_British_Autozygosity_Populations_BioResource
Study
EGAS00001001565
-
Transcriptomic response of miRNAs of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans
Study
EGAS00001004192
-
DIPG RNA and exome sequencing
Study
EGAS00001004749
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_squamous_cell_carcinoma
Study
EGAS00001002725
-
Host genetic determinants of HIV infection
Study
EGAS00001005245
-
GCAT | Genomes for life: cohort study of the genomes of Catalonia
Study
EGAS00001003018
-
BLUEPRINT Bisulfite-seq (CNAG)
Study
EGAS00001000418
-
Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia - Acute myeloid leukemia
Study
EGAS00001005464
-
Pediatric HGG WES and RNA-Seq
Study
EGAS00001005687
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___visium
Study
EGAS00001006045
-
Single-cell ATAC-seq analysis for COVID19 patients
Study
EGAS00001006559
-
DNA methylation landscape of prostate cancer
Study
EGAS00001006670
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___single_cell_RNA_sequencing
Study
EGAS00001003519
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_WES
Study
EGAS00001007745
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_RNAseq
Study
EGAS00001007746
-
Submission 10 - study_title 1
Study
EGAS50000000072
-
Dataset that contains runs of submission 74
Dataset
EGAD50000000456
-
Genetic Determinants of Transcriptional Variation in Primary Human Monocytes Across Multiple Contexts
Study
EGAS00001007111
-
Somatic L1 retrotranspositions in normal human cells
Study
EGAS00001006213
-
Epigenetic Modifications and Their Role in Human Disease: A Genomic Perspective on Inherited and Environmental Factors
Study
EGAS50000000374
-
The Genetic Analysis of multiple sclerosis
Study
EGAS00000000101
-
Passive and active DNA methylation and the interplay with genetic variation in gene regulation
Study
EGAS00001000446
-
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs
Study
EGAS00001001632
-
Histological Transformation and Progression in Follicular Lymphoma: a Clonal Evolution Study
Study
EGAS00001001709
-
Canadian prostate cancer samples (CPC-GENE) for PanProstate study
Study
EGAS00001003037
-
Whole transcriptome and exome sequencing of childhood ALL
Study
EGAS00001001858
-
German early-onset prostate cancer cohort of the Pan-Prostate Cancer Genome (PPCG) project
Study
EGAS00001003373
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006233
-
MRCA and MRCE SNP genotypes
Study
EGAS00000000137
-
The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals.
Study
EGAS00001003511
-
Whole genome and whole exome sequencing of serial biopsies of relapsed/refractory diffuse large B-cell lymphoma.
Study
EGAS00001007053
-
DERMATLAS__Leiomyosarcoma_WES
Study
EGAS00001007628