-
Dopaminergic neuron differentiation of human embryonic stem cells
Study
EGAS50000001099
-
Germline Mutations and Developmental Mosaicism Underlying EGFR-Mutant Lung Cancer
Study
phs003379
-
Single cell RNAseq of stenotic, inflamed and non-inflamed transmural lesions from patients with Crohn's disease
Dataset
EGAD50000000559
-
Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations
Study
EGAS00001003027
-
Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison
Study
EGAS00001001191
-
Bisulfite-converted duplexes for the strand-specific detection and quantification of rare mutations
Study
EGAS00001002406
-
Comparison of Custom Capture for Targeted Next Generation DNA Sequencing
Study
phs000811
-
Circulating Tumor Cell Heterogeneity in Neuroendocrine Prostate Cancer by Single Cell Copy Number Analysis
Study
phs002462
-
The Northern Manhattan Family Study - a Sub-Study of the Epidemiologic Study of Stroke Outcome in 3 Ethnic Groups: The Northern Manhattan Study
Study
phs002406
-
Tumor Fraction Guided Cell-Free DNA Profiling in Metastatic Cancer Patients
Study
phs002290
-
NHLBI TOPMed: Whole Genome Sequencing of Venous Thromboembolism (WGS of VTE)
Study
phs001402
-
Retinoblastoma Aqueous Humor Liquid Biopsy Repository
Study
phs003077
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Northern Manhattan Study (NOMAS)
Study
phs003028
-
Genomic Alterations in Normal Breast Tissues Preceding Breast Cancer Diagnosis (GANPBC)
Study
phs003822
-
Acute Respiratory Distress Network (ARDSNet) Study 02 Late Steroid Rescue Study (LaSRS) (ARDSNet-LaSRS-BioLINCC)
Study
phs003769
-
Single cell RNA seq of breast cancer stem cells
Study
JGAS000305
-
Shallow Whole Genome Sequencing of Patient Derived Xenografts
Study
EGAS50000000191
-
DCIS fresh frozen fragmentomics dataset
Study
EGAS50000001475
-
Mutational signature in colorectal cancer induced by genotoxic pks+ E. coli
Study
EGAS00001003934
-
Lineage-specific genome architecture links disease variants to target genes
Study
EGAS00001001911
-
TGF-β attenuates tumour response to PD-L1 blockade by contributing to exclusion of T cells.
Study
EGAS00001002556
-
Uveal melanoma patient with germline MBD4 nonsense mutation
Study
EGAS00001003362
-
This study explored and validated the clinical application of targeted NGS of circulating tumor DNA in identifying tumor-specific mutations and uncovering clinical actionable targets in a variety of solid tumors in large patient cohorts.
Study
EGAS00001002251
-
Identification_of_the_underlying_causal_variant_in_a_multi_generational_family_with_autosomal_dominant_common_variable_immunodeficiency
Study
EGAS00001000269
-
The ICGC-TCGA DREAM Somatic Mutation Calling - Tumour Heterogeneity Challenge
Study
EGAS00001002092
-
Mutations in SPINK2 induce azoospermia
Study
EGAS00001002450
-
Exome Sequecning of MDS xenografted samples
Study
EGAS00001005329
-
Cancer immune control needs senescence induction by Stat1 dependent cell cycle regulator pathways in tumours
Study
EGAS00001004151
-
Spatio-temporal analysis of prostate tumors in situ suggests pre-existence of treatment-resistant clones
Study
EGAS00001006113
-
An Isogenic Cell Line Panel for Sequence-based Screening of Targeted Anti-cancer Drugs
Study
EGAS00001005974
-
Human NXPE1 mediates variation in sialic acid O-acetylation in Colon Tissue
Study
EGAS00001007704
-
Genomic Advances in Sepsis (GAinS): RNA-seq
Dataset
EGAD00001008730
-
MutWP5: CRUK Mutographs of Cancer: Cancer Mastectomy (WG)(Novaseq)
Dataset
EGAD00001010114
-
Whole exome sequencing data from non-small-cell lung cancer patients receiving immunotherapy prognosis
Dataset
EGAD00001006096
-
How to encrypt files with Crypt4gh
Documentation
submission/data/file-preparation/crypt4gh
-
DAC Portal documentation
Documentation
access/data-access-committee/dac-portal
-
Data Access Commitee for schizophrenia and control cases sequencing data
Dac
EGAC00001002810
-
Walter and Eliza Hall Institute Research Data Access Committee
Dac
EGAC00001003372
-
Data access committee for the head and neck project
Dac
EGAC00001000374
-
DAC for WGS data Romanians and Roma/Rroma (Romania)
Dac
EGAC00001001184
-
Latency and interval therapy affect the evolution in metastatic colorectal cancer.
Dac
EGAC00001001198
-
DNA mate pair and RNAseq data of conventional osteosarcomas DAC
Dac
EGAC00001001306
-
MTLE small RNA-sequencing and RNA-sequencing Data Access Committee
Dac
EGAC00001001427
-
SEGA RNA-sequencing and small RNA-sequencing Data Access Commitee
Dac
EGAC00001001467
-
Tytgat Institute for Liver and Intestinal Research Data Access Committee
Dac
EGAC00001001483
-
Tytgat Institute for Liver and Intestinal Research Data Access Committee
Dac
EGAC00001001485
-
Tytgat Institute for Liver and Intestinal Research Data Access Committee
Dac
EGAC00001001615
-
Phase Ib of olaparib and capivasertib data access committee
Dac
EGAC00001001887
-
Patient-derived gene and protein expression signatures of NGLY1 deficiency
Dac
EGAC00001002287
-
Tytgat Institute for Liver and Intestinal Research Data Access Committee
Dac
EGAC00001002437
-
Garvan/St Vincent’s Prostate Cancer Tissue and Data Access Committee
Dac
EGAC00001002769
-
Lymphoma Biology and Survival / Applied Tumor Genomics / University of Helsinki
Dac
EGAC00001002849
-
EGAD00000000121
Dataset
EGAD00000000121
-
USA-BSTN
Dataset
EGAD00010002024
-
EGAD00010000371
Dataset
EGAD00010000371
-
Greece
Dataset
EGAD00010002021
-
Human Throid Cancer and CDK4/6 inhibition Data Access Commitee
Dac
EGAC00001003446
-
Data access committee for neural retina and retinal organoid data
Dac
EGAC50000000019
-
Centre for Drug Repurposing and Medicines Research Data Access Committee
Dac
EGAC00001002764
-
Developmental and Stem Cell Biology department - Hospital for Sick Children
Dac
EGAC00001002951
-
WGBS and oxBS-seq for APL
Study
EGAS00001005610
-
RNA sequencing of AD, MCI and control ONS cells
Study
EGAS00001006594
-
Evolutionary histories of breast cancer and related clones
Study
EGAS00001006282
-
Whole exome and genome sequencing investigations of perinatal death
Study
EGAS00001006295
-
microRNA and isomiR profiling of Stage 1 epithelial ovarian carcinoma
Study
EGAS00001006617
-
LUMC Department Pathology, Bone and Soft Tissue Tumor Group
Dac
EGAC50000000763
-
Phenotype data
Dataset
EGAD00001009966
-
LUMC Department Cell and Chemistry Biology, Ten Dijke group
Dac
EGAC50000000585
-
Nature and Contribution of Noncoding, Regulatory Mutations in Neurodevelopmental Disorders
Study
phs001874
-
Genomic analysis of primary plasma cell leukemia reveals complex structural alterations and high risk mutational patterns
Study
phs002022
-
Methylation-Based Immune Deconvolution in Prostate Cancer Patients Before and After Radical Prostatectomy
Study
phs003660
-
Detection and localization of surgically resectable cancers with a multi-analyte blood test
Study
EGAS00001002764
-
Single cell eQTL map of T cell activation
Dataset
EGAD00001008197
-
META-PRISM
Dataset
EGAD00001009684
-
cfDNA and CDX/PDX methylation profiling in Small Cell Lung Cancer
Dataset
EGAD00001008673
-
AVENIO Expanded ctDNA panel sequence alignments (BAMs) from plasma DNA of lung cancer patients from the OSCILLATE trial
Study
EGAS50000000103
-
Gene Expression Signatures in CATHGEN
Study
phs000551
-
Breast Cancer Risk Pathways
Study
phs001044
-
Copy Number Variation in Congenital Kidney Malformations
Study
phs000565
-
Genomic Resistance Patterns to Second Generation Androgen Blockade in Paired Tumor Biopsies of Metastatic Castrate-Resistant Prostate Cancer
Study
phs001447
-
NHLBI TOPMed: Childhood Asthma Management Program (CAMP)
Study
phs001726
-
Single-cell characterization of human GBM reveals regional differences in tumor-infiltrating leukocyte activation
Study
EGAS50000000302
-
Peripheral blood RNA sequencing of samples for a healthy cohort and a cohort with cancer patients
Dataset
EGAD50000000414
-
Mitochondrial DNA mosaicism in human somatic cells
Study
EGAS50000000254
-
The landscape of Usher syndrome-associated transcript isoforms in the human neural retina
Study
EGAS50000000504
-
Resolving complex duplication variants using long read genome sequencing in autism spectrum disorder
Study
EGAS50000000390
-
Vitamin-D-Kids Asthma
Study
phs004051
-
Circulating cell-free DNA methylation profiles as noninvasive multiple sclerosis biomarkers: A proof-of-concept study
Study
EGAS50000001277
-
CLUSTER RNAseq Study of Juvenile Idiopathic Arthritis patients in methotrexate cohort
Study
EGAS50000000995
-
Whole-genome bisulfite sequencing for high-grade glioma
Study
JGAS000197
-
CLUSTER Read-counts matrix of RNAseq Datasets of JIA in methotrexate cohort
Study
EGAS50000001501
-
A Study to Evaluate Denosumab in Young Patients With Primary Breast Cancer (D-Beyond)
Study
EGAS00001003252
-
Multi-omics analysis of cocaine use disorder in postmortem brain tissue of the ventral striatum [Proteomics data to study EGAS50000000623]
Study
EGAS00001007945
-
Targeted sequencing of follicular lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001005238
-
Deciphering Intratumoral Molecular Heterogeneity in Clear Cell Renal Cell Carcinoma with a Radiogenomics Platform
Study
EGAS00001003846
-
Mapping_regulatory_variation_in_sensory_neurons_using_IPS_lines_from_the_HIPSCI_project
Study
EGAS00001001149
-
Genome Wide Association Study:GR@ACE Stage I
Study
EGAS00001003424
-
ENU_CCK_81_cetuximab_pilot_project
Study
EGAS00001001743
-
ENU_NCI_H508_cetuximab_fixed_concentration_project
Study
EGAS00001001744
-
ENU_NCI_H508_Cetuximab_SecondRound
Study
EGAS00001001745