-
The genomic landscape of cutaneous squamous cell carcinoma from immunosuppressed and immunocompetent patients reveals common drivers and a novel mutational signature associated with chronic azathioprine exposure
Study
EGAS00001002612
-
A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Study
EGAS00000000052
-
Exome sequencing of early and late passage Patient Derived Xenogratf Tumoroids with matched Patient Derived Xenogratfs and matched normal liver
Study
EGAS50000000185
-
SU2C-MARK Lung Cancer Consortium - Checkpoint Blockade Response Project
Study
phs002822
-
Transcriptome of 2-Hydroxypropyl-Beta-Cyclodextrin Treatment in Niemann-Pick Disease Type C1
Study
phs002392
-
Validation of Gene Array to Predict Bacterial Co-infection In Adults Hospitalized with Viral Lower Respiratory Tract Infections (LRTI)
Study
phs001248
-
The Nurses' Health Study (NHS) GWAS of Mammographic Density
Study
phs000975
-
Methylation Profiles of Cell-Free DNA Using Nanopore Sequencing
Study
phs002950
-
Whole Genome and Exon Capture Sequencing of Bladder Cancers
Study
phs000535
-
Efficacy of Ustekinumab Followed by Abatacept for the Treatment of Psoriasis Vulgaris (PAUSE)
Study
phs003395
-
The Prostate, Lung, Colon, Ovary Screening Trial (PLCO)
Study
phs001286
-
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
-
Identification of four new susceptibility loci for testicular germ cell tumour, including variants near GAB2, GSPT1 and ZFPM1
Study
EGAS00001001302
-
CD49f single-cell methylomes
Study
EGAS00001002789
-
Molecular and Clonal Evolution in Recurrent Metastatic Gliosarcoma
Study
EGAS00001004076
-
Revealing active mutational processes in tumours using DigiPico/MutLX at unprecedented accuracy
Study
EGAS00001003555
-
Germline MBD4 Mutations and Predisposition to Uveal Melanoma
Study
EGAS00001003941
-
Ongoing_mutagenesis_RNAseq
Study
EGAS00001002364
-
Spatial heterogeneity in medulloblastoma
Study
EGAS00001001014
-
Integrative genomic analyses reveal androgen-driven somatic alteration landscape in early-onset prostate cancer
Study
EGAS00001000400
-
From matrimonial practices to genetic diversity in Southeast Asian populations: the signature of the matrilineal puzzle
Study
EGAS00001003727
-
Glioblastoma initiating cells are sensitive to histone demethylase inhibition due to epigenetic deregulation
Study
EGAS00001003750
-
Novel mutations in TOP2A in gliomas
Study
EGAS00001004556
-
A Phase I/II Trial of T Cell Receptor Gene Therapy Targeting HPV-16 E7 for HPV-Associated Cancers
Study
phs002286
-
Effect of 28-day administration of Urolithin A to sedentary elderly on muscle gene expression
Study
EGAS00001003638
-
Expressed Pseudogenes in the Transcriptional Landscape of Human Cancers
Study
phs000525
-
STAMPEED: Myocardial Infarction Genetics Consortium (MIGen)
Study
phs000294
-
Systematic immune cell dysregulation and molecular subtypes revealed by single cell RNA-seq of subjects with type 1 diabetes
Study
EGAS50000000231
-
Sensitive urothelial cancer detection via high volume urine DNA analysis
Study
EGAS50000000630
-
Single-cell/single-nucleus RNA-seq of Embryonal Tumor with Multilayered Rosettes (ETMR)
Study
EGAS50000000937
-
Development of Novel Histiocytic Sarcoma Organoid Model for Drug Discovery
Study
JGAS000807
-
Spatial and temporal genomic evolution in glioblastoma
Study
EGAS00001001033
-
Targeted_sequencing_of_blood_DNA_from_Human_twins_
Study
EGAS00001002210
-
Tissue-specific cell-free DNA degradation quantifies circulating tumor DNA burden
Study
EGAS00001004657
-
Somatic_mutation_and_clonal_evolution_in_premalignant_lung_disease___WGS
Study
EGAS00001002747
-
ICGC Oesophageal adenocarcinoma - 100 tumour samples
Study
EGAS00001000724
-
Single-cell transcriptomics identifies pathogenic T-helper 17.1 cells and pro-inflammatory monocytes in ICI-related pneumonitis
Study
EGAS00001006762
-
Whole-genome sequencing of rare disease patients in a national healthcare system
Dataset
EGAD00001006065
-
A spatial human thymus cell atlas mapped to a continuous tissue axis
Dataset
EGAD00001015384
-
A genome-wide meta analysis on stroke and ischemic stroke within four populations
Study
EGAS00000000060
-
A Somatic Reference Standard for Cancer Genome Sequencing
Study
phs000932
-
In Vivo Cytokine eQTL Interactions from a Lupus Clinical Trial
Study
phs001702
-
A Prospective Study of Lifestyle, the Gut Microbiome, and Diverticulitis
Study
phs003531
-
Whole Exome Sequencing of a Lung Adenocarcinoma Patient Across Three Time Points
Study
EGAS50000000812
-
Independent development of lymphoid and histiocytic malignancies from a shared early precursor
Study
EGAS00001001353
-
Pediatric tumor in a single child of three large nuclear families
Study
EGAS00001005321
-
SIGi001-A-13 / SAMEA104386250 WGS data
Dataset
EGAD50000001031
-
SIGi001-A-3 / SAMEA4448571 WGS data
Dataset
EGAD50000001041
-
EDi014-A / SAMEA4459369 WGS data
Dataset
EGAD50000001051
-
SIGi001-A-7 / SAMEA4448730 WGS data
Dataset
EGAD50000001060
-
SIGi001-A-1 / SAMEA4451096 WGS data
Dataset
EGAD50000001073
-
SIGi001-A-10 / SAMEA4451117 WGS data
Dataset
EGAD50000001074
-
SIGi001-A-11 / SAMEA4451118 WGS data
Dataset
EGAD50000001075
-
SIGi001-A-12 / SAMEA104237570 WGS data
Dataset
EGAD50000001076
-
SIGi001-A-2 / SAMEA4451116 WGS data
Dataset
EGAD50000001077
-
SIGi001-A-6 / SAMEA4447426 WGS data
Dataset
EGAD50000001078
-
SIGi001-A-4 / SAMEA4448632 WGS data
Dataset
EGAD50000001088
-
SIGi001-A-5 / SAMEA4448708 WGS data
Dataset
EGAD50000001092
-
SIGi001-A-8 / SAMEA4448777 WGS data
Dataset
EGAD50000001093
-
SIGi001-A-9 / SAMEA4447499 WGS data
Dataset
EGAD50000001095
-
Harnessing_transposons_for_drug_resistance_gene_discovery_in_cancer
Study
EGAS00001000468
-
GWAS and Meta-analysis on Frontal Fibrosing Alopecia in two European Populations
Study
EGAS00001003460
-
eccDNA in maternal plasma
Study
EGAS00001003827
-
Ovarian cancer sample size analysis
Dataset
EGAD00001005947
-
Autosomal recessive
Study
phs000848
-
Genetics of Schizophrenia in an Ashkenazi Jewish Case-Control Cohort
Study
phs000448
-
The Genomic Landscape of Juvenile Myelomonocytic Leukemia
Study
phs000973
-
Identification of Structural Variants Relevant to Autism by Pacific Biosciences HiFi Whole-Genome Sequencing
Study
phs002698
-
Reference Profiles of ExRNAs in Normal Human Pregnancy
Study
phs003182
-
Very Low Tumor Mutation Burden Identifies Inflamed Recurrent Glioblastomas Responsive to Cancer Immunotherapy
Study
phs002270
-
Neoadjuvant Pazopanib in Renal Cell Carcinoma
Study
phs002053
-
Airway Epithelial Cell Culture RNA Expression
Study
phs002472
-
Whole genome sequencing of PDAC tissues an PDOs
Study
EGAS50000000193
-
Comparison Across Multiple Types of Sleep Deprivation
Study
phs003924
-
Genomic Signatures of Intestinal Metaplasia in Six Countries with Varying Incidence of Stomach Cancer
Study
EGAS50000001056
-
Broad utility of ultrasensitive analysis of ctDNA dynamics across solid tumors treated with immunotherapy
Study
EGAS50000001271
-
Single cell RNA and ATAC sequencing data from GBM patients
Study
EGAS50000000547
-
Bulk RNA-seq paired fastq files from i3Ns harbouring a SNCA A53T mutation, with or without RSL3 treatment
Dataset
EGAD50000002209
-
EstMB cohort participants sequenced with MGISEQ-2000 platform
Dataset
EGAD50000002213
-
Tenk10k Phase 1: Whole Genome Sequencing
Study
EGAS50000001654
-
Exome_sequencing_of_a_cohort_of_Rett_syndromelike_patients
Study
EGAS00001002059
-
Sequencing of liver cancer cell lines
Study
EGAS00001002237
-
Inference_of_B_cell_clonality_and_function_from_single_cell_RNA_seq_data
Study
EGAS00001002963
-
WGS/RNA-seq pair of an inflammatory hepatocellular adenoma (IHCA)
Study
EGAS00001003025
-
Prime editing for functional repair in patient-derived disease models
Study
EGAS00001004611
-
Molecular characterization of endothelial cells under conditions associated with hematopoietic niche formation in humans
Study
EGAS00001002736
-
BCR_repertoire_sequencing
Study
EGAS00001003185
-
Drop-BS: High-Throughput Single-Cell Bisulfite Sequencing on a Microfluidic Droplet Platform
Study
phs002123
-
CALGB 80303:Genome-Wide Association Study of Advanced Pancreatic Cancer Patients - A Randomized Phase III trial of Gemcitabine Plus Bevacizumab versus Gemcitabine Plus Placebo in Patients with Advanced Pancreatic Cancer
Study
phs000250
-
Emirati Phased Diploid T2T Trio-Assembly of a Female Individual
Dataset
EGAD50000001754
-
GenomeDenmark Phase 2 - MHC haplotypes
Dataset
EGAD00001003455
-
Whole Genome Sequencing of a Triple Negative Breast Cancer Patient: Matched Primary Tumor, Normal, Metastasis and Xenograft samples
Study
phs000245
-
WGS_skin_punches
Study
EGAS00001004465
-
A new beta-globin mutation responsible of a beta-thalassemia (HbVar database ID 2928) was observed in 8 unrelated French families. The mutation carriers originated from Nord-Pas-de-Calais, a Northern French region where the chief town is Lille.5 unrelated mutation carriers were genotyped for a set of 12 microsatellites from chromosome 11, around the beta-globin gene. Among the 5 mutation carriers, 4 were genotyped for 97 European Ancestry Informative SNPs (EAIMs). 32 controls from Nord-Pas-de-Calais were genotyped for the microsatellites and SNPs.
Dac
EGAC00001000245
-
nanoCUSA
Study
EGAS50000000187
-
RNA sequencing of BCP-LBL patients samples
Dataset
EGAD50000000419
-
The Normal Human Tissue Sequencing Project: Non-Diseased, Non-Malignant Tissues
Study
phs000819
-
Transcriptional profiles of Kleefstra syndrome (EHMT1 and EHMT2) and healthy fibroblasts
Dataset
EGAD50000002343
-
Evaluation_of_size_selection_on_cancer_specific_sequencing_libraries
Study
EGAS00001000293
-
Genetics of Microcephalic Osteodysplatics Primordial Dwarfism
Study
EGAS00001000064