-
Whole genome bisufite sequencing of smoking and non-smoking mother-child pairsBisufite sequencing, RNA-seq and ChIP-Seq data of whole blood samples from smoking and non-smoking mothers and their children at gestation/birth and follow-up years.
Study
EGAS00001000455
-
502 present-day genotypes included in the '137 ancient human genomes from across the Eurasian steppe' publication
Study
EGAS00001002926
-
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD37920__Targeted_
Study
EGAS00001003321
-
Microsatellite unstable colorectal cancers
Study
EGAS00001003366
-
Alternative lengthening of telomeres in childhood neuroblastoma from genome to proteome
Study
EGAS00001004349
-
HipSci___RNAseq___Rare_Monogenic Diabetese
Study
EGAS00001001137
-
Characterization of four subtypes in morphologically normal tissue excised proximal and distal to breast cancer
Study
EGAS00001004510
-
Whole Genome Sequencing of 317 individuals from the Pacific region
Study
EGAS00001004540
-
Premalignant SOX2 overexpression in the fallopian tubes of ovarian cancer patients: Discovery and validation studies
Study
EGAS00001001909
-
Transcriptome sequencing of intravenous leiomyomatosis and uterine myoma
Study
EGAS00001002504
-
Transcriptome profiling of human plucked frontal and occipital hair follicles
Study
EGAS00001002832
-
Single cell exome sequencing of lung adenocarcinoma
Study
EGAS00001002972
-
Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Surname.
Study
EGAS00001002535
-
Understanding_hematopoietic_stem_cell_mobilization_and_engraftment_
Study
EGAS00001004620
-
Discovery and capture of novel dynamic DNA methylation in human sperm with preferential links to altered folate metabolism
Study
EGAS00001003617
-
Stage-specific gene and transcript dynamics in human male germ cells
Study
EGAS00001006135
-
molecular profiles of serum-derived extracellular vesicles in high-grade serous ovarian cancer
Study
EGAS00001006350
-
SARS-CoV-2 host genetics and COVID-19 outcomes in admixed Brazilians with extreme phenotypes
Study
EGAS00001006376
-
Selective advantage of mutant stem cells in human clonal hematopoiesis is associated with attenuated response to inflammation and aging
Study
EGAS00001007358
-
RNA sequencing data of 142 samples from 142 patients with HER2+ breast cancer treated with letrozole or tamoxifen (SOLTI PAMELA trial)
Study
EGAS00001006410
-
Panbody_nanoseq
Study
EGAS00001005521
-
T-cell reconstitution after reduced dose ATLG induction in kidney transplant recipients
Study
EGAS00001005941
-
Multiple Tissue Monitoring in Huntington disease - RNAseq skeletal muscle
Study
EGAS00001006474
-
NOTCH-mutations drive immune-escape mechanisms in B cell malignancies
Study
EGAS00001005793
-
Multiple Tissue Monitoring in Huntington disease - RNAseq adipose tissue
Study
EGAS00001006473
-
Multiple Tissue Monitoring in Huntington disease - RNAseq fibroblasts
Study
EGAS00001006472
-
Characterization of chromatin accessibility in metastatic prostate cancer
Study
EGAS00001006698
-
Single-cell proteogenomics of MDS upon AZA
Study
EGAS00001007427
-
Organ_maturation_in_preparation_for_birth__Peds_RFA__to_develop_a_tissue__resource_and_a_single_cell_atlas_of_organ_development_and_maturation_for__dissemination_among_the_scientific_and_clinical_community__RNA
Study
EGAS00001008256
-
Oesophageal adenocarcinoma WGS from LUD2015-005 study (NCT02735239, EudraCT 2015-005298-19)
Dataset
EGAD00001009400
-
Whole blood RNA sequencing of individuals from Nepal
Dataset
EGAD00001011131
-
Data Access Committee for the DNA sequencing data included in the study "A generalizable machine learning framework for classifying DNA repair defects using ctDNA exomes”
Dac
EGAC00001003111
-
DAC for the Study EGAS00001006374:
Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies.
snRNAseq of 79 (61 CM patients + 18 controls).
Dac
EGAC00001002804
-
Tumor Profiler DAC
Dac
EGAC50000000199
-
ITER-FIISC Data Access Committee (FPF)
Dac
EGAC50000000473
-
KIR imputation panel
Study
JGAS000314
-
Reproducibility of 10x Genomics single cell RNA sequencing method in the immune cell environment
Study
EGAS00001005905
-
Transcriptome analysis of soft tissue sarcoma
Study
EGAS50000001672
-
Colorectal cancer functional annotation - ATAC
Study
EGAS50000000205
-
Metabolic requirements of the metastasis-initiating tumour cell population using oral squamous cell carcinoma (OSCC) as a model system
Study
EGAS00001004765
-
PBMC
Study
EGAS50000000654
-
Integrated Genomic and Transcriptomic Analysis Reveals Unique Characteristics of Hepatic Metastases and Pro-metastatic Role of Complement C1q in Pancreatic Ductal Adenocarcinoma
Study
EGAS00001004821
-
Single cell sequencing reveals expanded cytotoxic CD4+ T cells and two clusters of peripheral helper T cells in synovial fluid of ACPA+ RA patients
Study
EGAS00001005241
-
Melanoma post mortem analysis
Dataset
EGAD00010001717
-
Circulating tumor DNA, pathological and immunologic responses to neoadjuvant nivolumab or nivolumab plus relatlimab and chemoradiotherapy in resectable esophageal/gastroesophageal junction cancer
Study
EGAS00001007299
-
SNP array datas of 'Matched' cancer/PNE
Study
EGAS00001003331
-
High-resolution analysis for urinary DNA jagged ends
Study
EGAS00001005603
-
Stage-1 meta-analysis with GC correction
Dataset
EGAD00001004800
-
IPF Core Biopsy Study Gene Expression Data
Dataset
EGAD00001007566
-
PTA__thyroid_
Study
EGAS00001007833
-
PTA_thyroid__RNA_
Study
EGAS00001007946
-
Molecular Biomarkers in Glioma (Mechanisms and Therapeutic Implications of Hypermutation in Gliomas)
Study
phs001967
-
Method to Assess Lung Water Accumulation During Exercise
Study
phs003346
-
Evaluation of Nuclear DNA from Rootless Hairs for Forensic Purposes
Study
phs002979
-
Genome Sequencing of Circulating Tumor Cells for Minimally Invasive Molecular Characterization of Multiple Myeloma Pathology
Study
phs003084
-
Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE)
Study
phs001252
-
Human Pilocytic Astrocytoma Single Cell RNA Sequencing
Study
phs001854
-
Whole Exome and Targeted Sequencing in Tourette Syndrome Multiplex Families
Study
phs000415
-
Somatic Mutations in Single Human Neurons from Patients with Congenital Neurodegenerative Diseases
Study
phs003005
-
Systems Analysis of Single-Cell Heterogeneity Underlying Glioma Drug Resistance
Study
phs003501
-
Genetic Underpinnings of Ethnic Disparities in Bone Toxicities Between Hispanic and Non-Hispanic Children Treated for Acute Lymphoblastic Leukemia
Study
phs002317
-
Mapping Disease Pathways for Biliary Atresia
Study
phs003458
-
The Somatic Mutational Landscape of Thyroid Cancer in Patients with Germline PTEN Mutations
Study
phs003640
-
HudsonAlpha Long Read Sequencing Data of Individuals with Rare Suspected Genetic Conditions
Study
phs003537
-
Programs, Origins, and Immunomodulatory Functions of Myeloid Cells in Gliomas
Study
phs003756
-
Genomic Landscape of Colorectal Cancer in a Multi-Ancestry Cohort
Study
phs003464
-
Defining Cutaneous Gene Expression Signatures in Juvenile Dermatomyositis
Study
phs003884
-
Kids First: Pediatric Research Project on the Genomic Analysis of Congenital Diaphragmatic Hernia
Study
phs001110
-
Whole Genome Sequencing for Metastatic Mutational Burden in Extraskeletal Myxoid Chondrosarcoma
Study
phs003305
-
CSER: Exome Sequencing in Diverse Populations in Colorado and Oregon/CHARM Cancer Health Assessments Reaching Many
Study
phs002111
-
Development of cell lines and mouse models of bone and soft tissue sarcoma to establish novel treatment
Study
JGAS000618
-
Single-cell multidimensional profiling of tumor cell heterogeneity in supratentorial ependymomas
Study
EGAS50000001513
-
Response to tumor-infiltrating lymphocyte adoptive therapy is associated with preexisting CD8+ T-myeloid cell networks in melanoma
Study
EGAS50000001217
-
Pipeline Olympics: Continuous benchmarking of computational workflows for DNA methylation sequencing data
Study
EGAS50000000541
-
An_exome_sequencing_study_of_the_HIV_elite_long_term_non_progressors_and_rapid_progressors__CASCADE_cohorts_
Study
EGAS00001000522
-
Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region mutation and known pathogenic mutation in SPG11
Study
EGAS00001001849
-
Clonal evolution in myeloma: the impact of maintenance lenalidomide and depth of response on the genetics and sub-clonal structure of relapsed disease in uniformly treated newly diagnosed patients
Study
EGAS00001003539
-
HCA_Thymus_Disease
Study
EGAS00001004310
-
An_evaluation_of_different_strategies_for_large_scale_pooled_sequencing_study_design_
Study
EGAS00001000134
-
H3Africa - Deciphering Developmental Disorders in Africa
Study
EGAS00001008319
-
noninvasive lung cancer subtyping
Study
EGAS00001007717
-
Monitoring of leukemia clones in B-cell acute lymphoblastic leukemia at diagnosis and during treatment by single-cell DNA amplicon sequencing
Study
EGAS00001005029
-
Transgenerational transmission of reproductive and metabolic dysfunction in the male progeny of polycystic ovary syndrome
Study
EGAS00001007079
-
H3Africa - Identification and characterization of novel hereditary neurological disease genes in Mali.
Study
EGAS00001003016
-
International Parkinson's Disease Genomics Consortium (IPDGC), NeuroX Dataset
Study
phs000918
-
ITER-FIISC Data Access Committee (Sepsis)
Dac
EGAC50000000641
-
Single-cell RNA-seq of murine splenocytes from Bcl6tg/+ and Cd70-/-; Bcl6tg/+ diffuse large B-cell lymphoma mouse models and Cd70-/- and wild-type controls.
Study
EGAS00001007570
-
Immunopeptidomics of colorectal cancer organoids reveals a sparse HLA class I neoantigen landscape and no increase in neoantigens with interferon or MEK-inhibitor treatment
Study
EGAS00001003886
-
Preeclampsia InterPregGen Consortium: GWAS meta-analysis summary statistics for European fetal preeclampsia cases versus controls and GWAS genotype data for European fetal preeclampsia cases
Study
EGAS00001001048
-
LOGGIC Core BioClinical Data Bank: Added clinical value of RNA-Seq in an international molecular diagnostic registry for pediatric low-grade glioma patients
Study
EGAS00001007072
-
MPNST study - LCM WGS data
Dataset
EGAD50000002568
-
Methylation data
Dataset
EGAD50000002295
-
Southern African Prostate Cancer Study (SAPCS) 70 whole bloods
Dataset
EGAD50000001626
-
Oncoscan CNV FFPE SNP-arrays (Affymetrix, Thermo Fisher Scientific) for the study "Molecular profiling of EBV associated diffuse large B-cell lymphoma"
Dataset
EGAD00010002363
-
Liv_PTB_Transcriptomics
Dataset
EGAD00010002065
-
Complete sequencing dataset of study EGAS00001002795
Dataset
EGAD00001004572
-
Pseudogene_RNAseq
Study
EGAS00001000606
-
BAP1_sequence_of_uveal_melanoma_cell_lines
Study
EGAS00001001520
-
Low_input_LC__ISC_
Study
EGAS00001001856
-
Gene expression from human iPSC derived motor neurons.
Study
EGAS00001003785