-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB58_C
Dataset
EGAD00001001772
-
WXS files for paper titled 'Genomic Landscape of Pediatric Myelodysplastic Syndromes'
Dataset
EGAD00001003781
-
BLUEPRINT release August 2016, RNA-Seq for monocyte - T=0days, on genome GRCh38
Dataset
EGAD00001002360
-
BLUEPRINT release August 2015, DNase-Hypersensitivity for inflammatory macrophage, on genome GRCh38
Dataset
EGAD00001001573
-
BLUEPRINT release August 2015, RNA-Seq for plasma cell, on genome GRCh38
Dataset
EGAD00001001523
-
BLUEPRINT release August 2015, RNA-Seq for monocyte - None, on genome GRCh38
Dataset
EGAD00001001532
-
SPECTA: NGS Screening Program for Efficient Clinical Trial Access
Dataset
EGAD00001000894
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB33_F
Dataset
EGAD00001001731
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB51_F
Dataset
EGAD00001001761
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB57_F
Dataset
EGAD00001001770
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW18_M
Dataset
EGAD00001001795
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW12_C
Dataset
EGAD00001001784
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW12_M
Dataset
EGAD00001001786
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW2_C
Dataset
EGAD00001001811
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW22_F
Dataset
EGAD00001001800
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW24_M
Dataset
EGAD00001001804
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW29_F
Dataset
EGAD00001001809
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW38_M
Dataset
EGAD00001001819
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW32_M
Dataset
EGAD00001001816
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW38_C
Dataset
EGAD00001001817
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW3_M
Dataset
EGAD00001001822
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB62_F
Dataset
EGAD00001001779
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB28_C
Dataset
EGAD00001001721
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB22_M
Dataset
EGAD00001001708
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB24_F
Dataset
EGAD00001001713
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB52_M
Dataset
EGAD00001001765
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB57_M
Dataset
EGAD00001001771
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB60_C
Dataset
EGAD00001001775
-
Dataset for Direct Detection of Early-Stage Cancers using Circulating Tumor DNA
Dataset
EGAD00001003601
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW14_M
Dataset
EGAD00001001789
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW15_C
Dataset
EGAD00001001790
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW18_C
Dataset
EGAD00001001793
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW47_C
Dataset
EGAD00001001826
-
Exome sequencing of patients with rare neurological disorders
Dataset
EGAD00001000346
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW4_M
Dataset
EGAD00001001834
-
BLUEPRINT release August 2015, DNase-Hypersensitivity for macrophage, on genome GRCh38
Dataset
EGAD00001001581
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW20_M
Dataset
EGAD00001001798
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW24_C
Dataset
EGAD00001001802
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW47_F
Dataset
EGAD00001001827
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW46_C
Dataset
EGAD00001001823
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW27_C
Dataset
EGAD00001001805
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW2_F
Dataset
EGAD00001001812
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB55_F
Dataset
EGAD00001001767
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB62_C
Dataset
EGAD00001001778
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW18_F
Dataset
EGAD00001001794
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW29_C
Dataset
EGAD00001001808
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW3_F
Dataset
EGAD00001001821
-
BLUEPRINT release August 2016, ChIP-Seq for macrophage - T=6days B-glucan, on genome GRCh38
Dataset
EGAD00001002314
-
BLUEPRINT release August 2016, RNA-Seq for monocyte - None, on genome GRCh38
Dataset
EGAD00001002338
-
BLUEPRINT release August 2016, DNase-Hypersensitivity for erythroblast, on genome GRCh38
Dataset
EGAD00001002350
-
Whole exome sequencing data from CD4 T cells, NK cells, monocytes and granulocytes from Alzheimer's disease patients and control individuals
Dataset
EGAD00001015757
-
BLUEPRINT release August 2016, DNase-Hypersensitivity for Acute Lymphocytic Leukemia - CTR, on genome GRCh38
Dataset
EGAD00001002499
-
UROMOL 2020 - RNA-seq data validation
Dataset
EGAD00001006967
-
HPS1 patient monocyte-derived macrophage and control macrophage RNAseq with and without infection
Dataset
EGAD00001006978
-
Evaluation of Nuclear DNA from Rootless Hairs for Forensic Purposes
Study
phs002979
-
A Microwell Platform for High-Throughput Longitudinal Phenotyping and Selective Retrieval of Organoids
Study
phs003315
-
Genetic Underpinnings of Ethnic Disparities in Bone Toxicities Between Hispanic and Non-Hispanic Children Treated for Acute Lymphoblastic Leukemia
Study
phs002317
-
CONNECTS Master Protocol for Clinical Trials targeting Macro- and Micro-Immuno-Thrombosis, Vascular Hyperinflammation, and Hypercoagulability and Renin-Angiotensin-Aldosterone System (RAAS) in Hospitalized Patients with COVID-19 (ACTIV-4 Host Tissue)
Study
phs003708
-
Final results and ctDNA analyses from the randomized phase 3 IMpassion031 trial evaluating peri-operative atezolizumab for early-stage triple-negative breast cancer
Study
EGAS50000000974
-
DynaTag for efficient profiling of transcription factors in small samples and single cells
Study
EGAS50000001074
-
The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments.
Study
EGAS00001002682
-
Angelman, Rett, Prader-Willi Syndrome Consortium (ARP) Rett Syndrome Natural History Protocol
Study
phs000574
-
Detection of rare mutations, copy number variation, and DNA methylation in the same template DNA molecules
Study
EGAS00001006839
-
Genetics of Chemotherapy Induced Peripheral Neuropathy in N08C1 and N08CB
Study
phs001480
-
High Density SNP Association Analysis of Lung Cancer
Study
phs000753
-
Ischemic Stroke Genetics Study (ISGS)
Study
phs000102
-
Natural History, Pathogenesis and Outcome of Melorheostosis
Study
phs001976
-
Longitudinal Study of Genetic Causes of Intrahepatic Cholestasis
Study
phs001288
-
Genomic Analyses in Neoadjuvant Immunotherapy-Treated Head and Neck Cancers
Study
phs002864
-
The Gene Partnership (TGP) - eMERGE Data
Study
phs000495
-
PGRN-RIKEN: Genetic Determinants of Clinical Cardiovascular Events in Patients Receiving Statins
Study
phs000963
-
Large Scale Genotyping of Psychiatric Disorders
Study
phs001413
-
Identification of Cancer Predisposition Genes in Breast Cancer Families
Study
phs000480
-
Genome-Wide Association Study of Heparin-Induced Thrombocytopenia
Study
phs002863
-
Developing Allelic Imbalance Analysis from Single-Nucleus RNA-Seq Data
Study
phs003749
-
Heterogeneity in Lysosomal Storage Disorders
Study
phs003459
-
In vitro reconstitution of epigenetic reprogramming in the human germ line
Study
JGAS000690
-
MRCA and MRCE SNP genotypes
Study
EGAS00000000137
-
Organoid BulkRNAseq
Study
EGAS50000000659
-
The Federated EGA network
Blog
the-federated-ega-network
-
Ultrasensitive detection of minor allele fractions in maternal samples based on microhaplotype analysis
Study
EGAS00001007057
-
GENETIC HISTORY OF ITALY
Study
EGAS00001001458
-
Automated system for scoring hematoxylin and eosin-stained ovarian cancer sections by identifying single cells uncovered that stromal cell ratio is a significant predictor for overall survival and progression-free survival.
Study
EGAS00001001694
-
UK10K NEURO ASD TAMPERE
Study
EGAS00001000115
-
Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping
Study
EGAS00001002622
-
Homozygous loss-of-function variants in European cosmopolitan and isolate populations
Study
EGAS00001001606
-
Transcriptional and DNA binding profiling of CEBPE in REH acute lymphoblastic leukaemia cells using shRNA RNA-Seq and ChIP-Seq
Study
EGAS00001002877
-
scRNA-seq data of human nuclei collected from the temporal cortex of 17 individuals.
Study
EGAS00001002882
-
Uncovering tumor intrinsic and extrinsic factors that regulate hepatocellular carcinoma growth using patient derived xenograft assays
Study
EGAS00001004020
-
Patient-derived tumoroids from CIC::DUX4 rearranged sarcoma identify MCL1 as a therapeutic target
Study
EGAS00001008039
-
ATAC-seq of a selected group of AML cases
Dataset
EGAD00001007583
-
Whole Genome Sequencing of clonal expansions of single healthy somatic cells (human, female)
Dataset
EGAD00001000666
-
ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer
Study
phs001221
-
The Collaborative Study on the Genetics of Alcoholism (COGA)
Study
phs000763
-
DAC for achalasia risk consortium (arc)
Dac
EGAC00001000394
-
DAC for aflatoxin project Qidong patient samples
Dac
EGAC00001000679
-
DAC for the cfSort study (tissue deconvolution)
Dac
EGAC00001003222
-
DAC for seminoma genomic data
Dac
EGAC00001000231
-
DAC for study WES of pituitary tumors
Dac
EGAC00001000443
-
Data Access Committee for Hui Lab
Dac
EGAC00001000454