-
Novel PARN mutations in Hoyeraal-HReidarsson syndrome patients.
Study
EGAS00001003623
-
Mutations conferring differential treatment response in breast cancer
Study
EGAS00001003626
-
A GWAS for cutaneous leishmaniasis in Brazil
Study
EGAS00001004596
-
Genomic Signatures Reveal DNA Damage Response Deficiency in Brain Metastases of Colorectal Cancer
Study
EGAS00001003659
-
Whole Exome Sequencing of 15 Tumor/Normal pairs of inflammatory hepatocellular adenomas
Study
EGAS00001003686
-
Genetic ancestry contributes to somatic mutations in lung cancers from admixed Latin American populations
Study
EGAS00001004752
-
Targeted panel data for newly diagnosed myeloma patients.
Study
EGAS00001002859
-
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
-
High-grade serous ovarian cancer refined with single-cell RNA-sequencing
Study
EGAS00001004987
-
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
-
The T cell receptor repertoire of tumor infiltrating T cells is predictive and prognostic for cancer survival
Study
EGAS00001005201
-
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
-
LCM-ATACseq on human lung macrophages
Study
EGAS00001006167
-
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
-
Molecular analysis of FIT interval colorectal cancers
Study
EGAS00001004683
-
Human pan-cancer plasma cfRNA study - raw data
Study
EGAS00001006755
-
scRNAseq of human primary nasal epithelium differentiated at air-liquid interface exposed to SARS-CoV2
Study
EGAS00001005633
-
USARC 10X Genomics Single Cell DNA Sequencing Data
Study
EGAS00001006144
-
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
-
Induced pluripotent stem cell lines (iPSC lines) produced from skin and blood cells.
Study
EGAS00001006262
-
Single cell multi-omic data of glioblastoma evolution under therapy
Study
EGAS00001004909
-
Deep whole genome sequencing identifies recurrent genomic alterations in breast cancer cell lines and patient derived xenograft models
Study
EGAS00001006285
-
Combined targeting of BRD4-associated Promoter Activation and NFKB Immunomodulation in ARID1A-mutated Gastric Adenocarcinoma
Study
EGAS00001006397
-
Illumina RNA sequencing for HLA expression qauntification
Study
EGAS00001004931