-
Integrated genomic characterization of adrenocortical carcinoma
Study
EGAS00001000665
-
Transcriptomic hallmarks and RNA isoform diversity in human neurodegenerative disease
Study
EGAS50000000132
-
HCA_Thymus_Disease
Study
EGAS00001004310
-
Whole Genome Sequencing of Neuroblastoma
Study
EGAS00001000222
-
Biased allelic expression in human primary fibroblast single cells.
Study
EGAS00001001009
-
An_evaluation_of_different_strategies_for_large_scale_pooled_sequencing_study_design_
Study
EGAS00001000134
-
UAMS Smoldering Myeloma Myeloma Sequencing
Study
EGAS00001003629
-
Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis
Study
EGAS00001001788
-
The proliferative history shapes the DNA methylome of B-cell tumor and predicts clinical outcome
Study
EGAS00001004640
-
Risk and modifying factors in Frontotemporal Dementia
Study
EGAS00001004895
-
Comparative transcriptome of CD34+ hematopoietic progenitors from myeloproliferative patients and control donors
Study
EGAS00001005106
-
Single cell RNA sequencing of synovial B cells in early Rheumatoid Arthritis
Study
EGAS00001005144
-
Whole genome sequence and RNA-seq data from paired tumour and germline samples from mesothelioma patients.
Study
EGAS00001005196
-
Linking the epigenetic landscape in chronic lymphocytic leukemia to deregulated chromatin networks
Study
EGAS00001002518
-
Monitoring of leukemia clones in B-cell acute lymphoblastic leukemia at diagnosis and during treatment by single-cell DNA amplicon sequencing
Study
EGAS00001005029
-
TRACERx Renal 100
Study
EGAS00001002793
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Gastric_Organoids
Study
EGAS00001003151
-
Circulating tumor cells Exome sequencing from breast cancer
Study
EGAS00001005228
-
Khoe-San genomes reveal unique variation and confirm deepest population divergence in Homo sapiens
Study
EGAS00001004459
-
Patient-derived neuroblastoma model system OHC-NB1
Study
EGAS00001003031
-
Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity
Study
EGAS00001005675
-
BARIA baseline first 100 individuals transcriptomes
Study
EGAS00001005704
-
De novo assembly of 150 Danish genomes reveals rich structural complexity
Study
EGAS00001002108
-
Resequencing (MIPS) of candidate genes for Keratoconus (2020)
Study
EGAS00001004267
-
Full blood mRNA sequencing of myotonic dystrophy type 1 patients after cognitive behavioural therapy
Study
EGAS00001005830
-
Identification of Germline Monoallelic Mutations in IKZF2 in Patients with Immune Dysregulation.
Study
EGAS00001005874
-
Targeted sequencing of diffuse large B-cell lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001005953
-
Changes in alternative splicing and associated neo-antigens due to therapy
Study
EGAS00001004524
-
Accurate detection of tumor-specific fusion genes reveals strongly immunogenic personal neo-antigens
Study
EGAS00001004877
-
Clonal somatic copy number altered driver events inform drug sensitivity in high-grade serous ovarian cancer
Study
EGAS00001006200
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Pancreatic_Organoids
Study
EGAS00001003520
-
An Atlas of Cells in the Human Tonsil
Study
EGAS00001006375
-
Targeted therapy of advanced parathyroid carcinoma guided by genomic and transcriptomic profiling (hipo_021)
Study
EGAS00001006747
-
The impact of BNT162b2 mRNA vaccine against SARS-CoV-2 on adaptive and innate immune responses
Study
EGAS00001006818
-
Immune and clinicopathological features predict HER2-positive breast cancer prognosis in the neoadjuvant NeoALTTO and CALGB 40601 trials
Study
EGAS00001007563
-
Discovery of immunotherapy targets for pediatric solid and brain tumors by exon-level expression
Study
EGAS00001007766
-
Genomic_Advances_in_Sepsis__GAinS__genotyping
Study
EGAS00001007786
-
Submitters and requesters Statistics
Documentation
about/statistics/community
-
MutWP1: CRUK Grand Challenge Mutographs of Cancer: Oesophageal adenocarcinoma
Dataset
EGAD00001006083
-
H3Africa - Identification and characterization of novel hereditary neurological disease genes in Mali.
Study
EGAS00001003016
-
H3Africa - Kidney Disease Research Network
Study
EGAS00001006558
-
Surgical Treatment for Ischemic Heart Failure (STICH-BioLINCC)
Study
phs003493
-
After the completion of CINECA, EUCANCan, and euCanSHare. What's next?
Blog
cineca-eucancan-and-eucanshare-were-concluded-in-june
-
Metadata Public API
Documentation
discovery/metadata/public-metadata-api
-
Low T cell diversity is associated with poor outcome in bladder cancer - Bulk TCRseq data
Study
EGAS50000000940
-
Catalogue Statistics
Documentation
about/statistics/catalogue
-
Microbiome
Dataset
EGAD50000002027
-
Variant calling dataset from the whole-exome study of familial pulmonary fibrosis in the Canary Islands-VCF files
Dataset
EGAD50000001152
-
DIAMOND PCR : plasma DNA LINE-1 targeted bisulfite sequencing, a new non-invasive multi-cancer detection marker
Dataset
EGAD50000000646
-
EOSC4Cancer Longitudinal Synthetic Colorectal Cancer Genomic data developed at BSC
Dataset
EGAD50000000276
-
Acral Melanoma PDXs from the admixed Brazilian Population- Human RNA expression data from Patient Derived Xenograft samples - htseq count files
Dataset
EGAD00001015747
-
scDNA-seq for 'Early evolutionary branching across spatial domains predisposes to clonal replacement under chemotherapy in neuroblastoma'
Dataset
EGAD00001015414
-
WES data for Early evolutionary branching across spatial domains predisposes to clonal replacement under chemotherapy in neuroblastoma
Dataset
EGAD00001015413
-
SNF_OLINK_20
Dataset
EGAD00001011147
-
Somatic L1 retrotransposition in normal colorectal epthelium
Dataset
EGAD00001010183
-
Ither2 RNA-Seq dataset - Implementation of pediatric precision oncology into clinical practice: The individualized Therapies for Children with cancer program “iTHER”
Dataset
EGAD00001010179
-
Ither2 WXS dataset - Implementation of pediatric precision oncology into clinical practice: The individualized Therapies for Children with cancer program “iTHER”
Dataset
EGAD00001010178
-
Rare Disease Synthetic Dataset
Dataset
EGAD00001008392
-
PELICAN33 Phenomic Dataset
Dataset
EGAD00001007800
-
Prediction of HLA genotypes using NGS data
Dataset
EGAD00001007733
-
Transcriptome Analysis of Malignant Peripheral Nerve Sheath Tumor-like Melanoma
Dataset
EGAD00001007000
-
Profiling molecular heterogeneity in human primary microglia
Dataset
EGAD00001005736
-
RNA-seq FASTQ files from newborn screening dried blood spot samples
Dataset
EGAD00001004991
-
Targeted bisulfite sequencing
Dataset
EGAD00001004785
-
A compendium of mutational signatures due to environmental exposures
Dataset
EGAD00001004583
-
Neuroblastoma relapse trio series from the AMC
Dataset
EGAD00001001360
-
Genetics of gene expression in human macrophage response to Salmonella
Dataset
EGAD00001003204
-
Comparison of transcriptional response of induced pluripotent stem (iPS) cell-derived and monocyte-derived macrophages to bacterial lipopolysaccharide stimulation
Dataset
EGAD00001001106
-
Multi-omics analysis defines core genomic alterationsin pheochromocytomas and paragangliomas
Dataset
EGAD00001000986
-
Exome sequencing of Congenital Heart Disease families Toronto
Dataset
EGAD00001000799
-
Exome sequencing of patients with Ewings sarcoma
Dataset
EGAD00001000333
-
Uncovering the Genetic Architecture of Colorectal Cancer with Focus of Rare and Less Frequent Variants
Study
phs001415
-
Hepatitis C Antiviral Long-term Treatment Against Cirrhosis (HALT-C)
Study
phs000430
-
Broccoli Sprouts Extracts Trial (BEST-COPD-BioLINCC)
Study
phs004022
-
Prader-Willi Syndrome and Early-onset Morbid Obesity Natural History Protocol
Study
phs000575
-
Using Genomics to Reduce Breast Cancer Disparities in the African Diaspora
Study
phs001687
-
Efficacy of a Therapeutic Treatment Trial in Angelman Syndrome
Study
phs000701
-
The Role of CDX2 in Controlling ABCB1 Expression and Chemosensitivity in Human Colon Cancer
Study
phs002903
-
Kids First: Genomic Etiologies of CHARGE Syndrome, Related Conditions and Structural Anomalies
Study
phs002592
-
Action to Control Cardiovascular Risk in Diabetes (ACCORD) Clinical Trial
Study
phs001411
-
Patient Registry for Primary Pulmonary Hypertension (PPH Registry-BioLINCC)
Study
phs004275
-
Exploratory novel biomarker and resistance mechanism of milademetan, an MDM2 inhibitor, in MDM2 amplified intimal sarcoma from an open-label phase 1b/2 trial ���NCCH1806/MK004���
Study
JGAS000619
-
The Role of CTCF in the Organization of the Centromeric 11p15 Imprinted Domain Interactome
Study
phs002408
-
Treatment Options for Type 2 Diabetes in Adolescents and Youth (TODAY)
Study
phs002447
-
Genetic Predictors of Adverse Radiotherapy Effects (Gene-PARE)
Study
phs000772
-
Analysis of the Whole Transcriptomes of Human Testis with Complete Spermatogenesis and of Human Testes with Sertoli Cell-Only Syndrome
Study
phs001777
-
The National Heart, Lung, and Blood Institute (NHLBI)-funded Next Generation Genetic Association Studies (NextGen) Consortium: Phenotyping Lipid traits in iPS derived hepatocytes Study (PhLiPS Study)
Study
phs001341
-
Center for Common Disease Genomics (CCDG) - Cardiovascular: Emory Cohort
Study
phs001880
-
CPTAC: Proteogenomic Studies of Ovarian Tumor Responses to Agents Targeting the DNA Damage Response
Study
phs003152
-
Whole Genome Profiling to Detect Schizophrenia Methylation Markers
Study
phs000608
-
CIP: Obesity-Diabetes Familial Risk, Viva La Familia Study
Study
phs000616
-
GATA2 Deficiency
Study
phs002311
-
Single Cell and Tissue Level Functional Genomics Analysis of Astrocyte-Related Mechanisms in Taupathy
Study
phs002197
-
Transcriptomic Profiling of Oropharyngeal Squamous Cell Carcinoma
Study
phs002935
-
Whole genome sequencing of core-binding factor leukemia
Study
phs000414
-
Autism Post-Mortem Brain RNA-Sequencing: SRRM4 Splicing Study
Study
phs000872
-
Search for Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (GoKinD study participants and parents), NIDDK
Study
phs000088
-
Cross-Species Single-Cell Analysis of Pancreatic Ductal Adenocarcinoma Reveals Antigen-Presenting Cancer-Associated Fibroblasts
Study
phs001840
-
NextGen Consortium: GENESiPS Study: Identifying the Gene Networks of Insulin Resistance
Study
phs001139
-
CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD)
Study
phs000126