-
Homopolymer switches DAC
Dac
EGAC50000000159
-
Data Access Committee for data from EGAS00001007708
Dac
EGAC00001003486
-
DAC_ICARUS_BREAST01
Dac
EGAC50000000344
-
AG_Kramann
Dac
EGAC50000000422
-
Institute for Translational Epigenetics
Dac
EGAC50000000057
-
Data Access Committee for data from EGAS00001007484
Dac
EGAC00001003459
-
DAC related to monozygotic twins discordant for ALS
Dac
EGAC00001003524
-
LUMC Department Anatomy, human iPSCs for cardiovascular diseases
Dac
EGAC50000000772
-
Germline Sequencing for Aggressive Prostate Carcinoma
Study
phs000661
-
Extracellular microRNA Biomarkers for Diagnostic and Prognostic Assessment of Preeclampsia at Triage
Study
phs003169
-
The MALT1 Locus and Peanut Avoidance in the Risk for Peanut Allergy
Study
phs001851
-
NHLBI TOPMed: Trans-Omics for Precision Medicine (TOPMed) Whole Genome Sequencing Project: Cardiovascular Health Study
Study
phs001368
-
Identification of Novel Therapeutic Targets for Calcific Aortic Valve Stenosis Using Integrative Genomics
Study
phs003541
-
Transcriptome-Wide Association Study (TWAS) to Identify Susceptibility Genes for Colorectal Cancer
Study
phs002813
-
NCI's Collection of Studies for General Cancer Research
Study
phs003967
-
An atlas of transcribed enhancers across helper T cell diversity for decoding human diseases
Study
JGAS000689
-
Identification of responsible genes and development of standardized medicine for familial breast cancer by genetic analysis with NGS technology
Study
JGAS000224
-
An efficient procedure for the recovery of DNA from formalin-fixed paraffin-embedded tissue sections
Study
JGAS000520
-
Development of blood-based biomarkers for precision medicine in castration-resistant prostate cancer
Study
JGAS000330
-
Sequencing of an organoid biobank for childhood soft tissue sarcoma.
Study
EGAS00001005912
-
Cell-free DNA methylome and fragmentome analysis for disease relapse monitoring in patients with Ewing Sarcoma
Study
EGAS50000001415
-
DNA methylation database for gynecological cancer detection, classification and assay development
Study
EGAS50000000417
-
A prospective trial comparing adaptive long-read sequencing and short-read genome sequencing for genetic diagnosis of cerebellar ataxia
Study
EGAS50000000573
-
Genetic scoring guide for personalized risk assessment in pediatric B-cell precursor Acute Lymphoblastic Leukemia
Study
EGAS00001007239
-
Benchmark Dataset for Somatic Mutation Calling in Cell-Free DNA
Dataset
EGAD50000001870