-
Epigenetic and transcriptional profile of memory B cells in Multiple sclerosis
Study
EGAS50000000872
-
Genetic subtyping by Whole Exome Sequencing across Diffuse Large B Cell Lymphoma and Plasmablastic Lymphoma.
Study
EGAS50000000371
-
Cryptococcosis in Previously Healthy Adults
Study
phs003871
-
Genetic architecture of disease in Greenland is shaped by demographic history, fine-structure, and selection - WGS data
Study
EGAS50000000657
-
Genetic architecture of disease in Greenland is shaped by demographic history, fine-structure, and selection - MEGA chip data
Study
EGAS50000000658
-
bulk ATACseq: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000787
-
scATAC: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000788
-
Circulating, Cell-Free DNA Methylation Patterns Indicate Cellular Sources of Allograft Injury after Liver Transplant
Study
phs003610
-
Next Generation Sequencing to Predict Risk of Events from Coronary Artery Disease
Study
phs003883
-
ATAC-seq in KMS11 vs TKO cells
Study
EGAS50000000076
-
ChIP-seq in KMS11 and TKO cells
Study
EGAS50000000077
-
MicroC in KMS11 and TKO cells
Study
EGAS50000000078
-
Rapid brain tumor classification from sparse epigenomic data
Study
EGAS50000000559
-
Genotypic data of the individuals in HPP project
Dataset
EGAD00010002714
-
Timing and trajectory of BCR-ABL1 driven chronic myeloid leukaemia
Dataset
EGAD00001015473
-
CARE idiopathic subglottic stenosis bulk transcriptomics.
Study
EGAS50000000879
-
Genetically unique biospecimens derived from individuals with or without Type 1 Diabetes
Dataset
EGAD50000001257
-
Whole Genome Sequencing Consortium on Frontotemporal Dementia With Underlying TDP-43 Pathology
Study
phs003309
-
Multiplexed scRNA-Seq Reveals Cellular and Genetic Correlates of SLE
Study
phs002812
-
Kids First: Whole Genome Sequencing Studies of Multiplex Nonsyndromic Cleft Lip/Palate Families
Study
phs002626
-
Single Cell and Spatial Transcriptomics Studies of Fibrosis in Prospective Registry in IBD Study at MGH and GI Disease and Endoscopy Registry
Study
phs003943
-
Sequencing of 3D Organoids Derived From Colorectal Cancer Patients
Study
phs003965
-
Childhood Cancer Data Initiative (CCDI): Comprehensive Genomic Sequencing of Pediatric Cancer Cases (CMRI/KUCC)
Study
phs002529
-
Genomic Changes in Breast Cancer Among Chinese Women in Hong Kong
Study
phs001870
-
A Comprehensive Genetic Study of Classical Hodgkin Lymphoma Using Circulating Tumour DNA
Study
EGAS50000000873
-
Biopsy-Derived Organoids in Personalised Early Breast Cancer Care: Challenges of Tumour Purity and Normal Cell Overgrowth Cap Their Practical Utility
Study
EGAS50000000605
-
The genomic basis of childhood T-lineage acute lymphoblastic leukemia
Study
EGAS50000000016
-
Identification and targeting of extremely high-risk gamma delta T-ALL in children
Study
EGAS50000000018
-
Epigenetic memory of SARS-CoV-2 mRNA vaccination in monocyte-derived macrophages
Study
EGAS50000000341
-
H3K27ac ChIP-seq of lung neuroendocrine tumors
Study
EGAS50000000057
-
The WID-EC test for the detection and risk prediction of endometrial cancer
Study
EGAS00001005033
-
The DNA methylome of cervical cells and risk of ovarian cancer
Study
EGAS00001005045
-
Breast tissue methylation analysis
Study
EGAS00001005070
-
plasma DNA LINE-1 targeted bisulfite sequencing: a new non-invasive multi-cancer detection marker
Study
EGAS50000000446
-
Neurodevelopment_Nantes_hospital
Dac
EGAC50000000542
-
SweGen genetic variation from the Northern Sweden Population Health Study
Dataset
EGAD50000001324
-
SweGen genetic variation from the Swedish Twin Registry
Dataset
EGAD50000001323
-
SweGen whole-genome sequencing from the Northern Sweden Population Health Study
Dataset
EGAD50000001325
-
Heterogeneity in Lysosomal Storage Disorders
Study
phs003459
-
Whole Exome Sequencing of Diffuse Large B-Cell Lymphoma
Study
phs000450
-
UCSF Database for the Advancement of JMML - Integration of Metadata with Omic Data
Study
phs002504
-
National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Pediatric Cardiac Genetics Consortium (PCGC) Study
Study
phs001194
-
Clinical and Genetic Evaluation of Individuals with Undiagnosed Disorders through the Undiagnosed Diseases Network (UDN)
Study
phs001232
-
H3Africa AWIGEN Pilot MetaboChip
Dataset
EGAD00010001258
-
IDH mutant Glioma methylation analysis and prognostic signatures
Study
EGAS00001006961
-
The genetic footprint of the European Roma diaspora: Evidence from the Balkans to the Iberian Peninsula
Study
EGAS50000000746
-
Multi-Omics Study of Lung Cancer in Smokers From EAGLE
Study
phs002992
-
BLUE CORAL: Biology and Longitudinal Epidemiology of PETAL COVID-19 Observational Study
Study
phs003419
-
Platinum Pedigree Consortium Long-Read Sequencing
Study
phs003793
-
Multiple Myeloma Clinical Targeted Sequencing of Patient Samples
Study
phs003908