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Transcriptomic analysis of human hematopoietic populations sorted from umbilical cord blood.
Study
EGAS00001004968
-
We performed an integrative analysis to determine genomic aberrations common to sporadic schwannomas.
Study
EGAS00001001886
-
Boson HCV infected liver bulk RNASeq study
Study
EGAS00001004996
-
Knee_OA_Functional_Genomics
Study
EGAS00001001899
-
Targeted panel data for newly diagnosed myeloma patients.
Study
EGAS00001002859
-
RNA sequencing in blood samples of cluster headache patients
Study
EGAS00001001918
-
A_compendium_of_mutational_signatures_due_to_environmental_exposures
Study
EGAS00001002060
-
Mutational Landscape of Plasmablastic Lymphoma
Study
EGAS00001004906
-
Blood RNA-seq from Mexican DMD patients and healthy controls
Study
EGAS00001004907
-
Discovering genetic causes of optic atrophy syndromes through whole exome sequencing
Study
EGAS00001003850
-
The T cell receptor repertoire of tumor infiltrating T cells is predictive and prognostic for cancer survival
Study
EGAS00001005201
-
High-grade serous ovarian cancer refined with single-cell RNA-sequencing
Study
EGAS00001004987
-
Dissecting the Spatial Heterogeneity of Single Circulating Tumor Cells in Hepatocellular Carcinoma
Study
EGAS00001005204
-
Single-cell RNA sequencing reveals cell-type specific eQTLs in peripheral blood mononuclear cells
Study
EGAS00001002560
-
Relapse series of two Pediatric ALL patients
Study
EGAS00001005001
-
RNA sequencing data of 66 matched primary and recurrent high grade serous ovarian cancer
Study
EGAS00001002660
-
The_British_Autozygosity_Populations_BioResource
Study
EGAS00001002742
-
Comprehensive molecular profiling of high-grade serous ovarian cancer
Study
EGAS00001003804
-
Solve-RD Solving the Unsolved Rare Dieseases
Study
EGAS00001003851
-
Platelet response in aspirin adherent pregnant women
Study
EGAS00001005188
-
Whole genome analysis of mutation hotspots in gastric cancer
Study
EGAS00001002872
-
PELICAN33 longitudinal clinical and autopsy phenomic assessment in lethal metastatic prostate cancer
Study
EGAS00001005399
-
Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples
Study
EGAS00001005323
-
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___BD___WGS
Study
EGAS00001003014
-
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___TPS___WGS
Study
EGAS00001003089
-
The WID-CIN test identifies women with, and at risk of, cervical intraepithelial neoplasia grade 3 and invasive cervical cancer (CIN3+)
Study
EGAS00001005078
-
COVID_19_Challenge_Project_Single_Cell_Profiling
Study
EGAS00001005696
-
Whole genome sequencing of multiple myeloma identifies novel structural and non-coding mutations.
Study
EGAS00001003164
-
The distinct DNA methylome of acute lymphoblastic leukemia
Study
EGAS00001005203
-
Sequencing of an adolescent patient with germline RET mutant alveolar rhabdomyosarcoma
Study
EGAS00001004359
-
Genomic characterization of co-existing biliary tract intraepithelial neoplasia and carcinoma lesions reveals distinct evolutionary paths of gallbladder cancer
Study
EGAS00001005402
-
Genotyping by OncoArray and Global Screening Array for colorectal cancer risk prediction
Study
EGAS00001005411
-
46 CLL Whole Genome Sequencing Study
Study
EGAS00001003254
-
Mutational_burden_in_human_hair_follicles
Study
EGAS00001004462
-
Single cell RNA sequencing of normal endometrial derived organoids uncovers novel cell type markers for prognostication
Study
EGAS00001004466
-
Identifying the role of ID3 in DNA repair and maintenance of genome integrity
Study
EGAS00001004478
-
Acquiring and sequencing of all 24 single human chromosomes
Study
EGAS00001003300
-
Genomewide copy number alteration screening of circulating plasma DNA
Study
EGAS00001006031
-
USARC 10X Genomics Single Cell DNA Sequencing Data
Study
EGAS00001006144
-
Molecular analysis of FIT interval colorectal cancers
Study
EGAS00001004683
-
scRNAseq of human primary nasal epithelium differentiated at air-liquid interface exposed to SARS-CoV2
Study
EGAS00001005633
-
DGCR8 and the six hit, three-step model of schwannomatosis
Study
EGAS00001005665
-
LCM-RNAseq on human lung macrophages
Study
EGAS00001006168
-
Defining structural variation associated with breast cancer susceptibility by long-read genome sequencing
Study
EGAS00001005872
-
Cell-free DNA and bone marrow samples from myelodysplastic syndromes
Study
EGAS00001005992