-
NHLBI TOPMed: Genomic Activities such as Whole Genome Sequencing and Related Phenotypes in the Framingham Heart Study
Study
phs000974
-
A comprehensive DNA methylation landscape of human and mouse cell lines derived from hematological malignancies
Study
EGAS50000000627
-
Finnish_population_cohort_genotyping_B
Study
EGAS00001001047
-
Double mutant DNMT3A AML: a unique subtype
Study
EGAS00001007966
-
scRNA-seq data of human nuclei collected from the temporal cortex of 17 individuals.
Study
EGAS00001002882
-
Transcriptomic analysis of Acute Myeloid Leukemia stem cells
Study
EGAS00001004402
-
Whole genome sequencing in 1038 index cases reveals novel causative genes in pulmonary arterial hypertension
Dataset
EGAD00001003423
-
TSCA-LI amplicon sequencing of called variants in WXS data of DSALL.
Dataset
EGAD00001003275
-
NINDS Family-Based Whole-Genome Sequencing to Find Modifiers of Age of Onset in Huntington's Disease
Study
phs001071
-
Michigan Polybrominated Biphenyl (PBB) Exposure Registry
Study
phs001862
-
Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Meta-analysis
Study
phs001499
-
Esophageal Squamous Cell Carcinoma Precursor Study
Study
phs002814
-
Whole genome sequencing with linked reads of pediatric glioblastoma samples
Study
EGAS00001003432
-
The Southern African Human Genome Programme
Study
EGAS00001002639
-
Mutational Signature and Transcriptomic Classification Analyses as the Decisive Diagnostic Tools for a Cancer of Unknown Primary with Neuroendocrine Differentiation
Study
EGAS00001003026
-
Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature
Study
EGAS00001006115
-
Whole-genome sequencing of rare disease patients in a national healthcare system
Dataset
EGAD00001006065
-
Investigation of the Causal Etiology in a Patient with T-B+NK+ Immunodeficiency
Study
phs002990
-
Dilgom_Exome
Study
EGAS00001000086
-
Study of the rare and low frequency variants in the Saguenay-Lac-Saint-Jean population
Study
EGAS00001003103
-
C3 SNPs and outcome after lung transplantation
Study
EGAS00001003843
-
Colorectal adenomas, carcinomas and adjacent normal NKI-AvL TGO series NGS-ProToCol
Study
EGAS00001002854
-
EGA FUSE Client
Documentation
access/download/visualisation/fuse-client
-
Genomic Origins and Admixture in Latinos (GOAL)
Study
phs000750
-
NHLBI TOPMed: Genetics of Cardiometabolic Health in the Amish
Study
phs000956