-
GWAS study on arsenic-exposed population
Study
EGAS00001001168
-
Exome sequencing of Fibromyalgia patients
Study
EGAS00001003826
-
Genetic regulation of gene expression in human brain cell types
Study
EGAS00001006345
-
GWAS in a dengue Thai cohort
Study
EGAS00001002756
-
Identification of improved IL28B SNPs and haplotypes for prediction of drug response in treatment of hepatitis C using massively parallel sequencing in a cross-sectional European cohort
Study
EGAS00001000096
-
Mutational dynamics of triple negative breast cancer over neoadjuvant chemotherapy treatment reveal frequent whole genome duplication events
Study
EGAS00001008261
-
Genome-wide mutational consequences of nucleotide excision repair-deficiency through XPC deletion in a human adult stem cell culture
Study
EGAS00001002681
-
NSCCG CRC GWAS data
Study
EGAS00001005412
-
H3Africa Chip Design - Aim of designing a cost-effective GWAS chip with content appropriate for use in genomics studies of individuals from the African continent.
Study
EGAS00001002976
-
Genome‐wide postnatal changes in immunity following fetal inflammatory response
Study
EGAS00001003635
-
GWAS of SJS/TEN in Thai population
Study
EGAS00001008316
-
PAS Pedigrees: Identification of novel genetic variants contributing to cardiovascular disease in pedigrees with premature atherosclerosis.
Study
EGAS00001000052
-
Fetal hemoglobin in sickle cell disease patients from Tanzania
Study
EGAS00001000990
-
The Haplotype Reference Consortium
Study
EGAS00001001710
-
COIN CRC GWAS data
Study
EGAS00001005421
-
GWAS data (Illumina 2.5 M SNPs) in Cuban cohorts of dengue disease
Study
EGAS00001002276
-
RNA sequencing in primary inflammatory (TPP) macrophages following deletion of a disease-associated gene desert at chr21q22, disruption of ETS2, or treatment of ETS2-edited macrophages with a HIF1α stabiliser.
Study
EGAS00001007553
-
Exome sequencing reveals pathogenic variants in known and novel candidate genes for severe sperm motility disorders
Study
EGAS00001005018
-
Cell-type eQTLs for single-cell Mendelian Randomisation
Study
EGAS50000000687
-
Whole genome sequencing of six ethnic groups from Burkina Faso, Cameroon, and Tanzania
Study
EGAS00001003648
-
Searching for variants associated with endometriosis
Study
EGAS00001001741
-
Pancreatic islets PISA RNA-seq samples
Study
EGAS00001005535
-
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Uzbeks (DNA samples from the Institute of Immunology, Uzbek Academy of Sciences, Tashkent, Uzbekistan; Republic Specialized Scientific Practical Medical Centre of Obstetrics and Gynecology, Tashkent, Uzbekistan)
Study
EGAS00001000416
-
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Kazakhs (DNA samples from the Scientific Center of Obstetrics, Gynecology and Perinatology, Almaty, Kazakhstan; Gulnara Svyatova, Principal Investigator
Study
EGAS00001000417
-
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001002602
-
MRCA and MRCE SNP genotypes
Study
EGAS00000000137
-
Mapping the epigenomic landscape of human monocytes following innate immune activation reveals context-specific mechanisms driving endotoxin tolerance
Study
EGAS00001007362
-
Procardis study on novel susceptibility genes for coronary artery disease (CAD)
Study
EGAS00000000055
-
HSC_population_dynamics___KX003_samples
Study
EGAS00001003550
-
Transrenal DNA Analysis
Study
EGAS50000000766
-
Methylation-based deconvolution of cell-free DNA
Study
EGAS00001007493
-
The Sys4MS cohort: a prospective cohort of patients with Multiple Sclerosis and omics
Study
EGAS00001007145
-
PBMC gene expression profiles in diet treated celiac disease upon oral gluten challenge
Study
EGAS00001004860
-
Association of DNA-methylation profiles with immune responses in breast cancer patients
Study
EGAS00001004211
-
Genotype data from 'Evidence of the interplay of genetics and culture in Ethiopia'
Study
EGAS00001005171
-
Male-biased migration from East Africa introduced pastoralism into southern Africa
Study
EGAS00001005232
-
Cell of Origin and Early Evolution of Leukemia in Down Syndrome
Study
EGAS00001004780
-
The Genetic Basis of Preeclampsia in an Andean Population Adapted to High Altitude
Study
EGAS00001004625
-
Paired healthy & tumor organoid Biobank _B15PON
Study
EGAS00001005865
-
Patient-derived organoids_Vumc
Study
EGAS00001005947
-
Genomic insights into the population history of the Resande or Swedish Travellers
Study
EGAS00001006176
-
Fragmentomic features of individuals with different cfDNA concentrations
Study
EGAS50000000692
-
Population Genomics of Native Americans from Andes and Amazon
Study
EGAS00001004639
-
HSC_population_dynamics_KSP_samples
Study
EGAS00001002762
-
Repertoire and clinical hierarchy of AR locus alterations in castration-resistant prostate cancer
Study
EGAS50000001101
-
Single-Gene vs. Panel Sequencing in Advanced HR+/HER2− Breast Cancer
Study
EGAS00001008200
-
Genomic Signatures of Intestinal Metaplasia in Six Countries with Varying Incidence of Stomach Cancer
Study
EGAS50000001056
-
ImmunAID
Study
EGAS50000001393
-
Smoking-dependent expression alterations in nasal epithelium reveal immune impairment linked to germline variation and lung cancer risk
Study
EGAS00001006137
-
Circulating Tumor DNA analysis in Relapsed/Refractory Germ Cell Tumors Treated with Salvage High-Dose Chemotherapy - IGG-04 Study
Study
EGAS50000001510