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Whole-genome sequencing in 14 cases and whole-exome sequencing in 90 cases of Chinese ESCC
Dataset
EGAD00001001691
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The mutational landscape of human somatic and germline cells
Dataset
EGAD00001006643
-
The evolving mutational landscape of normal human esophagus
Dataset
EGAD00001004158
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A compendium of mutational signatures due to environmental exposures
Dataset
EGAD00001004583
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Next Generation Sequencing in an IBD Pedigree Whole Genome Data
Dataset
EGAD00001000399
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The landscape of somatic mutation in normal colorectal epithelial cells
Dataset
EGAD00001004193
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WGBS data of solid liver tumor DNA, and WGBS data of cell-free DNA derived from human blood, for CancerDetector study
Dataset
EGAD00001004317
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Neuroblastoma relapse trio series from the AMC
Dataset
EGAD00001001360
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Targeted Sequencing of 173 genes
Dataset
EGAD00001002115
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Massive parallel RNA sequencing of highly purified mesenchymal cells derived from bone marrow specimens of 45 low-risk myelodysplastic syndrome cases
Dataset
EGAD00001002658
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Comparison of transcriptional response of induced pluripotent stem (iPS) cell-derived and monocyte-derived macrophages to bacterial lipopolysaccharide stimulation
Dataset
EGAD00001001106
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The evolving mutational landscape of normal human esophagus
Dataset
EGAD00001004159
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Reconstruction of human phylogenetic trees using single-cell genome sequencing
Study
EGAS00001004824
-
RNA sequencing of CD8 T cells from melanoma patients prior to and during checkpoint immunotherapy and untreated healthy controls
Study
EGAS00001004081
-
Characterization of MCSP+ melanoma DCC and MelDCC lines
Study
EGAS00001006702
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Clonal dynamics of normal hepatocyte expansions in homeostatic human livers and their association with the biliary epithelium
Study
EGAS00001006962
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cfDNAme allows early prediction of PE
Study
EGAS00001007071
-
iNeuron_RNAseq
Study
EGAS00001004238
-
PEACE melanoma 14
Study
EGAS00001007081
-
Single-cell and bulk RNA-sequencing of nivolumab-treated glioblastoma
Study
EGAS00001007110
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Molecular analysis of cancer genomes in children with Lynch syndrome: exploring causal associations
Study
EGAS00001007146
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Regions of common inter-individual DNA methylation differences in human monocytes.
Study
EGAS00001002265
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This study aims to evaluate the relationship between cardiometabolic risk factors and the most common genetic variation (SNPs)
Study
EGAS00001007818
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Cold Ischemia Study
Study
EGAS00001008233
-
Colorectal adenomas and carcinomas NKI-AvL TGO series Gut2009
Study
EGAS00001002758
-
Mutational spectrum of highly differentiated, fusion-negative rhabdomyosarcoma (set 2).
Study
EGAS00001002771
-
Aneurysmal Subarachnoid Hemorrhage patients with or without vasospasm
Study
EGAS00001003092
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Cancer_Mastectomy__Exome_
Study
EGAS00001003319
-
Comprehensive investigation of genome architecture of gastric adenocarcinoma with whole-genome sequencing in the Chinese population.
Study
EGAS00001002404
-
Hip OA Functional Genomics
Study
EGAS00001002483
-
Mutational spectrum of highly differentiated, fusion-negative rhabdomyosarcoma (set 1).
Study
EGAS00001002630
-
WGS of breast cancer diagnosed during pregnancy and matched control
Study
EGAS00001002685
-
Transcriptomic analysis of human hematopoietic populations sorted from umbilical cord blood.
Study
EGAS00001004968
-
Boson HCV infected liver bulk RNASeq study
Study
EGAS00001004996
-
Dissecting the Spatial Heterogeneity of Single Circulating Tumor Cells in Hepatocellular Carcinoma
Study
EGAS00001005204
-
PELICAN33 longitudinal clinical and autopsy phenomic assessment in lethal metastatic prostate cancer
Study
EGAS00001005399
-
PCR-free HiSeqX whole genome sequence data on 120 samples with triplet repeat expansions (premutation and full expansions)
Study
EGAS00001002462
-
Genomic profiling of matched well differentiated and de-differentiated liposarcoma.
Study
EGAS00001002807
-
Celiac disease-specific intestinal T cells analyzed with HLA-class II tetramers, RNA-seq and mass cytometry have a narrow, autoimmune-associated phenotype
Study
EGAS00001003017
-
Oral mucosa organoids as a potential model for personalized therapies
Study
EGAS00001003628
-
Single cell sequencing of endoscopic biopsies from Barrett's oesophagus and proximal tissue from the normal GI tract
Study
EGAS00001003144
-
Genomic profiling of paediatric glioma cell lines
Study
EGAS00001003006
-
Genomic, transcriptomic and epigenomic profiling of GCTB
Study
EGAS00001003730
-
SNP arrays for chemotherapy response project
Study
EGAS00001004519
-
The Jerusalem Perinatal Study (JPS) aimed to examine the developmental origins of cardiometabolic risk.
Study
EGAS00001004075
-
Genomic_landscape_of_liver_cirrhosis
Study
EGAS00001004329
-
Whole genome sequencing of glioblastoma reveals enrichment of non-coding constraint mutations in known and novel genes
Study
EGAS00001004379
-
Bulk RNAseq gene expression of baseline tumors from metastatic urothelial bladder cancer patients (IMvigor210) and metastatic renal cell carcinoma (IMmotion150)
Study
EGAS00001004386
-
WES sequencing of malignant peripheral nerve sheath tumours
Study
EGAS00001004527
-
Gut microbiota analysis after 3months probiotic-like bacteria or placebo treatment in subjects with metabolic syndrome
Study
EGAS00001003585
-
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