-
HLA-DR is absent in primitive macrophages through epigenetic silencing of master regulator CIITA
Study
EGAS00001006981
-
Exome-seq, RNA-Seq, SNP array profiling of gastric tumor samples and cell lines.
Study
EGAS00001000736
-
Recursive splicing in long vertebrate genes
Study
EGAS00001001170
-
1000 Genomes Used for Cloud Testing
Study
phs000710
-
Rna-Seq Leiomyosarcoma subtypes
Study
EGAS00001004783
-
CIDR: The Role of Rare Coding Variation in Prostate Cancer in Men of African Ancestry - RESPOND Project 2
Study
phs002637
-
Melanoma multi site metastases
Dataset
EGAD00001005487
-
Patient Microbiome and Surgical Site Infection in Spine Surgery
Study
phs003358
-
Whole Exome Sequencing in Alopecia Areata Identifies Rare Mutations in KRT82
Study
phs002632
-
HGSOC genome-wide SNP (project ITH)
Dataset
EGAD00010002482
-
Melanoma multi site metastases
Dataset
EGAD00001005483
-
The mutational landscape of human somatic and germline cells
Dataset
EGAD00001006643
-
The mutational landscape of human somatic and germline cells
Dataset
EGAD00001006642
-
The Gene Partnership (TGP) - eMERGE Data
Study
phs000495
-
Nasal MicroRNA during Bronchiolitis and Age 6y Asthma: MARC-35 Cohort
Study
phs003564
-
Genetic Discovery and Application in a Clinical Setting: Continuing a Partnership (eMERGE Phase II)
Study
phs000948
-
Center for Common Disease Genomics [CCDG] - Cardiovascular ATVB: Atherosclerosis Thrombosis and Vascular Biology
Study
phs001592
-
Childhood Cancer Data Initiative (CCDI): Pediatric In Vivo Testing Program - Neuroblastoma
Study
phs003163
-
Childhood Cancer Model Atlas
Study
EGAS00001006320
-
Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma
Study
EGAS00001005328
-
Virginia PrIMeD Study
Study
phs003609
-
GEnomics and Transcriptomics of Human INsulinoma (GETHIN)
Study
phs001422
-
Genetic Studies of Chronic Kidney Disease (CKD)
Study
phs001828
-
Longitudinal Studies of Patients with Familial Platelet Disorder with Associated Myeloid Malignancy (FPDMM)
Study
phs003075
-
Investigation of mutational signatures associated with DNMT3A deficiency (2019-04-03)
Dataset
EGAD00001004889