-
Transcriptomic and chromatin accessibility profiling in T cells for the MTOR genetics paper.
Dataset
EGAD50000001307
-
Whole Exome Sequencing of paired gDNAs and PPGL tumor DNA from patients with cyanotic congenital heart disease
Dataset
EGAD50000001201
-
Single-cell RNA-sequencing of CSF cells and PBMCs from individuals with neurological disorders
Dataset
EGAD50000001173
-
Anti-MPO BCR sequences described in 'Anti-myeloperoxidase IgM B cells in anti-neutrophil cytoplasmic antibody-associated vasculitis'
Dataset
EGAD50000001112
-
WES of head and neck cancer patients refractory to anti-PD-1 therapy
Dataset
EGAD50000001011
-
Targeted RNA-Seq
Dataset
EGAD50000000980
-
Clinical and demographics data from IMvigor210, IMvigor211, IMvigor130 and IMvigor010
Dataset
EGAD50000001101
-
Dataset for WGS and RNA samples of acute myeloid leukemia with MNX1 expression (non-hipo)
Dataset
EGAD50000001097
-
IMPRESS_all
Dataset
EGAD50000000882
-
Targeted capture sequencing to identify MYC, BCL2, and BCL6 rearrangements in non-Hodgkin lymphoma
Dataset
EGAD50000000489
-
CITE-seq AdaptNK
Dataset
EGAD50000000329
-
Endoresist panel sequencing
Dataset
EGAD50000000350
-
InterPregGen-GWAS-UZB-1
Dataset
EGAD00010001918
-
Large deletion predisposes to familial melanoma
Study
EGAS50000001496
-
Whole genome sequencing of HSPCs and pAML
Dataset
EGAD00001006338
-
FIT interval CRCs versus Screen-detected CRCs
Dataset
EGAD00001006409
-
Somatic whole exome sequencing of a hypermutated gliosarcoma case
Dataset
EGAD00001006816
-
Summary statistics of meta-analysis using two genome-wide association study of inflammatory bowel disease in Koreans.
Dataset
EGAD00001006983
-
Mutational_burden_in_skin_following_UV_treatment_Nanoseq
Study
EGAS00001007681
-
Genetic landscape of pediatric ependymoma
Study
EGAS00001000254
-
BGISEQ-500 Cancer Dataset - WGS tumour/normal pairs
Study
EGAS00001002298
-
Matched_Pair_Cell_Line_Tumour_RNAseq
Study
EGAS00001000434
-
Mutational_burden_in_skin_following_UV_treatment_WGS
Study
EGAS00001007682
-
Evaluation_of_size_selection_on_cancer_specific_sequencing_libraries
Study
EGAS00001000293
-
Paroxysmal_Neurological_Disorders___rare_epilepsies
Study
EGAS00001000421
-
Genetic landscape of pediatric Rhabdomyosarcoma
Study
EGAS00001000256
-
Genetic landscape of pediatric Osteosarcoma
Study
EGAS00001000263
-
Deep sequencing of the gut microbiome from 946 healthy donors of the Milieu Intérieur cohort
Study
EGAS00001004437
-
All available datasets of DEEP
Study
EGAS00001001608
-
SPECTA__NGS_Screening_Program_for_Efficient_Clinical_Trial_Access
Study
EGAS00001000728
-
Chromatin accessibility analysis of TFEB overexpression in LT-HSC
Study
EGAS00001004971
-
SJCRH Patient-derived orthotopic xenografts of pediatric brain tumors
Study
EGAS00001005533
-
Transcriptome_analysis_of_LCM_samples_
Study
EGAS00001003862
-
StemNet - in vitro differentiation of human hepatocytes
Study
EGAS00001004201
-
Potent neutralizing antibodies against SARS-CoV-2
Study
EGAS00001004412
-
Comprehensive genetic analysis of Epstein-Barr virus-associated hematological malignancy
Study
EGAS00001003159
-
RNA-seq bam
Study
EGAS00001005161
-
Molecular profiling of DLBCL patients treated in the PETAL trial
Study
EGAS00001005828
-
COIN CRC GWAS data
Study
EGAS00001005421
-
Study of Korean Parkinson's disease
Study
EGAS00001006811
-
Transcriptomic analysis of MYC overexpression in LT-HSC.
Study
EGAS00001004970
-
Targeted sequencing of healthy blood and bone marrow
Dataset
EGAD00001008189
-
Single-cell RNA-seq of patient-derived organoids across three generations
Dataset
EGAD00001008431
-
SOX11+ and SOX11- mantle cell lymphoma cell lines RNAseq data
Dataset
EGAD00001009421
-
Characterization of OCIAML-22 Fractions via ATAC-Seq, RNA-Seq and WGS
Dataset
EGAD00001009271
-
Paired ONT and downsampled Illumina cfDNA dataset
Dataset
EGAD00001009392
-
iPSC and iNeuron RNAseq, chip-seq and single cell CRISPR activation
Dataset
EGAD00001010050
-
RNAseq Atlas in HCC tumors
Dataset
EGAD00001015341
-
oncogenic gene fusions in primary colon cancers
Dataset
EGAD00001003291
-
560 whole-genome sequenced breast cancers
Study
EGAS00001001178
-
Whole exome sequencing and target gene sequencing of ESCC cases and healthy controls from Henan high-risk region
Dataset
EGAD00001004556
-
GoNL release 5 raw SNV calls
Dataset
EGAD00001000743
-
Raw sequencing data for donor and patient fecal samples
Dataset
EGAD00001004371
-
DDD DATAFREEZE 2017-12-15: 13,462 trios and probands only - phenotypic and family descriptions
Dataset
EGAD00001004388
-
This dataset contains fastq and BAM data from female adipose tissue.
Dataset
EGAD00001002202
-
Chromatin 3D interactions mediate genetic effects on gene expression (ChIP-seq)
Dataset
EGAD00001004871
-
Single-cell RNA sequencing of cytokine-induced T cell responses
Dataset
EGAD00001005290
-
RNA sequencing of cytokine-induced T cell responses
Dataset
EGAD00001005291
-
Single cell RNA sequencing of colorectal cancer
Dataset
EGAD00001005198
-
Risk Assessment of Cerebrovascular Events (RACE) Study
Study
phs000456
-
Epigenomics Studies in Acute Myeloid Leukemia (AML)
Study
phs001027
-
Enhancer Mapping in Chronic Lymphocytic Leukemia
Study
phs001704
-
The Genomic Analysis of Medulloblastoma
Study
phs000409
-
The Genomics of Pilocytic Astrocytoma Formation in Neurofibromatosis Type 1
Study
phs000563
-
Children's Hospital of Philadelphia: GWAS of Left-Sided Cardiac Defects
Study
phs000781
-
Single-Cell Profiling of Premature Neonate Airways Reveals a Continuum of Myeloid Differentiation
Study
phs003427
-
Genomic Characterization of Pediatric Low-Grade Gliomas
Study
phs001054
-
STAMPEED: Cardiovascular Health Study (CHS) GWAS to identify genetic variants associated with aging and CVD risk factors and events
Study
phs000226
-
Genomic landscape of Neutrophilic Leukemias of Ambiguous Diagnosis
Study
phs001799
-
Center for Common Disease Genomics (CCDG) - Cardiovascular: Harvard Gene-Diet Interaction in a Costa Rican Cohort
Study
phs002282
-
Genetic Analysis of Substance Use Disorder Using the Indiana Biobank Data
Study
phs003025
-
Grady Trauma Project (GTP)
Study
phs002046
-
The Diabetes Heart Study (DHS)
Study
phs001012
-
Genome-Wide Association Study of Lung Cancer Susceptibility in Never-Smoking Women in Asia
Study
phs000716
-
Phylogenetic Analyses of Melanoma Reveal Complex Patterns of Metastatic Dissemination
Study
phs000941
-
Transcriptomic Profiling of Peripheral Immune Cells in a Trial of Ruxolitinib with Nivolumab for Anti-PD1 Non-Responsive cHL
Study
phs003601
-
Genomics of Acute Myeloid Leukemia
Study
phs000159
-
Pathologically Expanded Peripheral B Cell-Helper T Cells in Rheumatoid Arthritis
Study
phs001262
-
CAGE analysis for non-small cell lung carcinoma
Study
JGAS000070
-
Human periportal liver assembloids recapitulate periportal liver tissue in vitro
Study
EGAS50000000994
-
Sequencing data of tumor tissue obtained from GANNET53 study patients
Study
EGAS50000000935
-
RNA-Sequencing of cervical cancers
Study
EGAS50000000087
-
ROBUST (NCT02285062)
Study
EGAS50000000333
-
Single-cell RNA sequencing of pediatric Hodgkin Lymphoma to study the inhibition of T cell subtypes
Study
EGAS50000000432
-
Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
Study
EGAS00001000287
-
Genetic landscape of non-Down syndrome acute megkaryoblastic leukemia
Study
EGAS00001000379
-
A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Dataset
EGAD50000001156
-
RNA-seq of longitudinal human blood and nose swab samples from a controlled human infection experiment with SARS-CoV-2 virus
Dataset
EGAD50000000942
-
RNA-sequencing from duodenal bipsies of Celiac disease patients
Dataset
EGAD50000000491
-
Multi-layered molecular characterization defines prognostic subtypes of lung adenocarcinoma in Asian never-smokers
Study
EGAS00001003705
-
Genetic landscape of pediatric Medulloblastoma
Study
EGAS00001000347
-
ESGI_Identification_of_novel_genes_and_mechanisms_leading_to_Primary_Ciliary_Dyskinesia
Study
EGAS00001000523
-
ICGC Oesophageal adenocarcinoma - pilot samples
Study
EGAS00001000559
-
ICGC Oesophageal adenocarcinoma - Barrett's samples
Study
EGAS00001000726
-
BRAF_and_MEK_resistant_cell_line_clones
Study
EGAS00001000172
-
South Asia Rheumatic Heart Disease Genetics Network
Study
EGAS00001003565
-
Whole genome sequencing of 25 South African individuals with myasthenia gravis
Study
EGAS00001003462
-
Autoimmunity_and_immunodeficiency_COVID19
Study
EGAS00001004489
-
Macrophage response in preterm infants compared to term infants
Study
EGAS00001004974
-
MYOSEQ project
Study
EGAS00001002069