-
Genetics of gene expression in human macrophage response to Salmonella
Dataset
EGAD00001003204
-
Whole exome and targeted DNA sequencing data for formalin-fixed paraffin embedded tissue from de novo small cell prostatic carcinoma cases
Dataset
EGAD00001004139
-
Transcriptome Analysis of Malignant Peripheral Nerve Sheath Tumor-like Melanoma
Dataset
EGAD00001007000
-
Assessment of genetic and epigenetic variation in human IPS cells-RNA
Dataset
EGAD00001000604
-
WGBS data of solid liver tumor DNA, and WGBS data of cell-free DNA derived from human blood, for CancerDetector study
Dataset
EGAD00001004317
-
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
-
Clonal dynamics of normal hepatocyte expansions in homeostatic human livers and their association with the biliary epithelium
Study
EGAS00001006962
-
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
-
Molecular analysis of cancer genomes in children with Lynch syndrome: exploring causal associations
Study
EGAS00001007146
-
Regions of common inter-individual DNA methylation differences in human monocytes.
Study
EGAS00001002265
-
Transcriptomic analysis of human hematopoietic populations sorted from umbilical cord blood.
Study
EGAS00001004968
-
Dissecting the Spatial Heterogeneity of Single Circulating Tumor Cells in Hepatocellular Carcinoma
Study
EGAS00001005204
-
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_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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
Endothelium-derived stromal cells contribute to bone marrow niche formation
Study
EGAS00001004946
-
Tumorigenic role of Musashi-2 in aggressive mantle cell lymphoma
Study
EGAS00001006613
-
Single cell RNAseq of lung adenocarcinoma
Study
EGAS00001005021
-
Cachexia - Non-Cachexia Metagenome Analysis
Study
EGAS00001007156
-
Multiomic profiling of pleomorphic rhabdomyosarcoma
Study
EGAS00001007230
-
Comprehensive single-cell genome analysis at nucleotide resolution using the PTA Analysis Toolbox
Study
EGAS00001007288
-
H3K27ac ChIP-seq in primary inflammatory (TPP) macrophages
Study
EGAS00001007562
-
Idiosyncratic and generic single nuclei and spatial transcriptional patterns in papillary and anaplastic thyroid cancers
Study
EGAS00001007574
-
Transcriptomic predictors of survival for palbociclib + endocrine therapy vs. capecitabine in aromatase inhibitor-resistant breast cancer from GEICAM/2013-02 PEARL
Study
EGAS00001008177
-
Lung_Cell_Atlas__Paediatric_RNA
Study
EGAS00001008299
-
Lung_Cell_Atlas__Paediatric_Spatial
Study
EGAS00001008300
-
Blood neutrophils in COPD derive from activated progenitors in the bone marrow
Dataset
EGAD00001008788
-
Blood neutrophils in COPD derive from activated progenitors in the bone marrow sc Rhapsody
Dataset
EGAD00001009704
-
Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (tumour data)
Dataset
EGAD00001010274
-
Blood neutrophils in COPD derive from activated progenitors in the bone marrow sc Seqwell
Dataset
EGAD00001008908
-
Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (normal data)
Dataset
EGAD00001010295
-
CcRCC_metabolic_heterogeneity
Dataset
EGAD00001015780
-
RNA-seq dataset: Single-cell spatial analysis of pediatric high-grade glioma reveals a novel population of immunosuppressive and tumor-promoting SPP1+/GPNMB+ myeloid cells
Dataset
EGAD00001015450
-
scEC&T-seq manuscript data
Dataset
EGAD00001010071
-
Genomic and transcriptomic landscape of T-cell lymphoblastic lymphoma compared to T-cell acute lymphoblastic leukemia: similar subtypes and different fusions
Dataset
EGAD00001015357
-
Personalized analysis of ctDNA for detection of molecular residual disease and recurrence in a cohort of surgically treated patients with head and neck squamous cell carcinoma
Study
EGAS50000001018
-
H3Africa - Consortium WGS
Study
EGAS00001005972
-
Adipose Tissue Omics In Obesity
Study
phs003390
-
Ongoing Replication Stress Tolerance and Clonal T Cell Responses Distinguish Liver and Lung Recurrence and Patient Outcomes in Pancreatic Ductal Adenocarcinoma
Study
phs003597
-
Prediction of Resistance and Sensitivity to HER2 Targeted Therapy in the Neoadjuvant Setting
Study
phs003275
-
Recurrent DNMT3B gene rearrangements are associated with unfavorable outcome in dicentric (9;20)-positive pediatric BCP-ALL
Study
EGAS00001007383
-
Disorders/Differences of Sex Development (DSD) Study Performed at UCLA in Collaboration with the DSD-Translational Research Network (DSD-TRN), with the Support of the Gabriella Miller Kids First Pediatric Research Program
Study
phs001178
-
Relationship between low LDL cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: a US-based cross-sectional observational study using electronic medical records
Study
phs001588
-
Sporadic Amyotrophic Lateral Sclerosis (ALS): Parent-Offspring and Twin Sequencing Study
Study
phs000831
-
NIPT samples for systematic evaluation of NIPT aneuploidy detection software tools
Dataset
EGAD00001007712
-
FASTQ files of total RNA-Seq data from the POPS PET (pre-eclamptic) samples
Dataset
EGAD00001003508
-
FASTQ files of total RNA-Seq data from the POPS SGA (Small for Gestational Age) samples
Dataset
EGAD00001003507
-
The PEMDAC phase 2 study of pembrolizumab and entinostat in patients with metastatic uveal melanoma
Study
EGAS00001005478
-
Summary statistics from genome-wide association study in glioma of 12,488 cases and 18,169 controls.
Study
EGAS00001003372
-
RNA-seq study of human long-term and short-term hematopoietic stem cells from umblical cord blood with lentiviral overexpression of S1PR3
Study
EGAS00001004798
-
Clinical outcomes and immune correlates of response to nivolumab plus chemoradiotherapy in women with locally-advanced cervical cancer – NiCOL study
Study
EGAS00001007297
-
ARID1A Mutations in Endometriosis-Associated Ovarian Carcinomas
Study
EGAS00000000075
-
DO NOT USE - Whole genome sequencing of SI-NETs from six patients
Study
EGAS00001005009
-
ICGC Prostate Cancer Whole Genome Sequencing
Dataset
EGAD00001000891
-
Shallow Whole Genome Sequencing of Patient Derived Xenografts
Dataset
EGAD50000000277