-
Genomics_of_acral_lentiginous_melanoma
Study
EGAS00001003740
-
HCA_Female_Reproductive_Adult_WSSS_RNA
Study
EGAS00001004727
-
NRG1 Fusions in KRAS Wild-type Pancreatic Cancer (H021)
Study
EGAS00001002759
-
Premalignant SOX2 overexpression in the fallopian tubes of ovarian cancer patients: Discovery and validation studies
Study
EGAS00001001909
-
Genomics_of_acral_lentiginous_melanoma___RNAseq
Study
EGAS00001003758
-
Transcriptome sequencing of intravenous leiomyomatosis and uterine myoma
Study
EGAS00001002504
-
The aim of this study was to identify underlying hub genes and dysregulated pathways associated with the development of HCC using bioinformatics analysis.
Study
EGAS00001002526
-
Progression to AML is predictable and distinct from age related clonal hematopoiesis
Study
EGAS00001002570
-
NanoSring of PBMC from bladder cancer and RCC patients
Study
EGAS00001004229
-
Transcriptome profiling of human plucked frontal and occipital hair follicles
Study
EGAS00001002832
-
Exploring_the_heterogeneity_of_sarcoma_using_single_cell_sequencing_
Study
EGAS00001002866
-
Identification of hypermutation and defective mismatch repair in ctDNA from metastatic prostate cancer
Study
EGAS00001003899
-
Long cell-free DNA molecules in maternal plasma
Study
EGAS00001005515
-
Single cell exome sequencing of lung adenocarcinoma
Study
EGAS00001002972
-
Patterns of transcription factor programs and immune pathway activation define four major subtypes of SCLC with distinct therapeutic vulnerabilities
Study
EGAS00001004888
-
Whole exome sequencing on Pediatric MDS patients
Study
EGAS00001005432
-
Single-cell DNA sequencing on Pediatric MDS
Study
EGAS00001005433
-
Benchmarking of ProSolo, a new probabilistic single nucleotide variant caller for single cell DNA sequencing data. This study provides the whole exome sequencing dataset used in this assessment.
Study
EGAS00001004123
-
Panbody_nanoseq
Study
EGAS00001005521
-
COVID_19_UK_CIC_Spatial
Study
EGAS00001005817
-
Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Surname.
Study
EGAS00001002535
-
T-cell reconstitution after reduced dose ATLG induction in kidney transplant recipients
Study
EGAS00001005941
-
Paediatric_and_adult_nasal_RNAseq___COVID19
Study
EGAS00001004391
-
Pathogenic Neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq
Study
EGAS00001005530
-
Understanding_hematopoietic_stem_cell_mobilization_and_engraftment_
Study
EGAS00001004620
-
Human Developmental Biology Resource (HDBR) abnormal fetal samples
Study
EGAS00001006300
-
Integrative analysis of non-small cell lung cancer patient-derived xenografts identifies unique proteotypes associated with patient outcomes
Study
EGAS00001006068
-
molecular profiles of serum-derived extracellular vesicles in high-grade serous ovarian cancer
Study
EGAS00001006350
-
Juntendo Muscle Study (JMS)
Study
EGAS00001006362
-
Multiple Tissue Monitoring in Huntington disease - RNAseq skeletal muscle
Study
EGAS00001006474
-
Muscle SATellite cell study (MSAT)
Study
EGAS00001006363
-
SARS-CoV-2 host genetics and COVID-19 outcomes in admixed Brazilians with extreme phenotypes
Study
EGAS00001006376
-
NOTCH-mutations drive immune-escape mechanisms in B cell malignancies
Study
EGAS00001005793
-
Discovery and capture of novel dynamic DNA methylation in human sperm with preferential links to altered folate metabolism
Study
EGAS00001003617
-
Multiple Tissue Monitoring in Huntington disease - RNAseq fibroblasts
Study
EGAS00001006472
-
Multiple Tissue Monitoring in Huntington disease - RNAseq adipose tissue
Study
EGAS00001006473
-
scRNA-seq of patient-derived PDAC organoids and matched CAFs
Study
EGAS00001006661
-
Measurement of SARS-CoV-2 variants fraction in infected alveolar cells
Study
EGAS00001006730
-
scRNAseq and scATACseq of placebo controlled-trial on MMR non-specific effects
Study
EGAS00001006787
-
Characterization of chromatin accessibility in metastatic prostate cancer
Study
EGAS00001006698
-
Clinical utility of combined low-pass whole genome and targeted sequencing in liquid biopsies for diagnosis and monitoring of pediatric solid tumors
Study
EGAS00001006913
-
Personalized Onco-Genomic Project for pediatric and adolescent patients in British Columbia
Study
EGAS00001006967
-
Spatial and temporal intra-tumoural heterogeneity in advanced High-Grade Serous Ovarian Cancer: implications for surgical and clinical outcomes
Study
EGAS00001007164
-
Selective advantage of mutant stem cells in human clonal hematopoiesis is associated with attenuated response to inflammation and aging
Study
EGAS00001007358
-
Single-cell proteogenomics of MDS upon AZA
Study
EGAS00001007427
-
AML FLT3 TCR study
Study
EGAS00001007467
-
Subclonal somatic copy number alterations emerge and dominate in recurrent osteosarcoma
Study
EGAS00001007486
-
Organ_maturation_in_preparation_for_birth__Peds_RFA__to_develop_a_tissue__resource_and_a_single_cell_atlas_of_organ_development_and_maturation_for__dissemination_among_the_scientific_and_clinical_community__RNA
Study
EGAS00001008256
-
Single cell sequencing of a post-PD-1 inhibitor metastatic melanoma mass
Dataset
EGAD00001006013
-
WES and RNA-seq of triple-negative breast cancers from the MyBrCa cohort
Dataset
EGAD00001009311
-
Oesophageal adenocarcinoma WGS from LUD2015-005 study (NCT02735239, EudraCT 2015-005298-19)
Dataset
EGAD00001009400
-
Somatic mutant selection is altered by prior NOTCH1 mutation in ageing esophageal epithelium
Dataset
EGAD00001015259
-
Somatic mutant selection is altered by prior NOTCH1 mutation in ageing esophageal epithelium
Dataset
EGAD00001015260
-
Single cell transcriptional evolution of myeloid leukaemia of Down syndrome – scRNA
Dataset
EGAD00001015452
-
Alloreactive T-cell receptor (TCR) repertoire in kidney transplantation
Dataset
EGAD00001007695
-
Whole blood RNA-sequencing of covid-19 patients and healthy controls
Dataset
EGAD00001007776
-
bulk RNA sequencing, single cell RNA sequencing and nanopore sequencing of T-ALL patients with TCF7-SI1 fusion
Dataset
EGAD00001007010
-
COVID-19 severity correlates with airway epithelium–immune cell interactions identified by single-cell analysis
Dataset
EGAD00001006339
-
Genomic characterisation of MGUS
Dataset
EGAD00001006363
-
Targeted myeloid panel DNA-Sequencing Mutations Matrix Validation Cohort
Dataset
EGAD00001008506
-
Whole exome sequencing of endometriod ovarian cancer tumours
Dataset
EGAD00001006389
-
The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET) - Intratumoural immune heterogeneity
Dataset
EGAD00001006570
-
Paired-WGS Sequencing of Primary lymphomas of the central nervous system (PCNSL)
Dataset
EGAD00001007806
-
Neuroblastoma patient Total RNA Seq data
Dataset
EGAD00001008124
-
An Integrated Approach to Patient Stratification and Therapy Selection in Acute Myeloid Leukemia
Dataset
EGAD00001006701
-
Glioblastoma stem cell lines RNA-seq (Guilhamon et al.)
Dataset
EGAD00001006813
-
Hypertension delays viral clearance and exacerbates airway hyperinflammation in patients with COVID-19
Dataset
EGAD00001006828
-
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients
Dataset
EGAD00001006888
-
Single-cell gene expression data from CD8+ T cells from two Austrian COVID19 patients stimulated with wildtype and mutant SARS-Cov-2 peptides
Dataset
EGAD00001006995
-
Genetic landscape of inherited retinal dystrophies
Dataset
EGAD00001007022
-
PopCol 16S gut microbiome sequencing
Dataset
EGAD00001007071
-
An atlas of the developing human fetal spine
Dataset
EGAD00001009801
-
Pulmonary atypical carcinoid multi-omic dataset on up to 42 tumours from same patient
Dataset
EGAD00001009296
-
Bulk RNA sequencing of Singapore colorectal cancer patients (SG-BULK)
Dataset
EGAD00001008512
-
Transcriptome analysis for intrahepatic cholangiocarcinoma
Dataset
EGAD00001008544
-
Adult-type Granulosa Cell Tumour of the Ovary RNA Sequencing
Dataset
EGAD00001007812
-
Single-Cell Atlas of Common Variable Immunodeficiency shows germinal center-associated epigenetic dysregulation in B cell responses
Dataset
EGAD00001008575
-
Single cells of colorectal cancer organoids
Dataset
EGAD00001007305
-
Dataset for the Pearl study
Dataset
EGAD00001007979
-
RNA-seq data
Dataset
EGAD00001008553
-
DNA methylation changes upon growth hormone treatment in children with idiopathic short stature
Dataset
EGAD00001008641
-
Organoid Derivation Project: WGS (2023-06-22)
Dataset
EGAD00001011090
-
Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing
Dataset
EGAD00001007794
-
Dataset for other_cancer-RNA
Dataset
EGAD00001008847
-
T-cell reconstitution after reduced dose ATLG induction in kidney transplant patients
Dataset
EGAD00001008478
-
Tobacco exposure and somatic mutations in normal human bronchial epithelium
Dataset
EGAD00001005193
-
Next Generation Children project
Dataset
EGAD00001007780
-
Multiregional single cell RNA sequencing of human renal cell carcinoma
Dataset
EGAD00001008030
-
Upper cortical layer-driven network impairment in schizophrenia - 10x genomics v3 snRNA-seq and Visium spatial transcriptomics datasets
Dataset
EGAD00001009173
-
WGS data for manuscript titled: Multi-omic features of oesophageal adenocarcinoma in patients treated with preoperative neoadjuvant therapy
Dataset
EGAD00001008646
-
Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis
Dataset
EGAD00001009280
-
Southern African Prostate Cancer Study (SAPCS) Ethnic Disparity
Dataset
EGAD00001009067
-
cfDNA analysis reveals relation of POLR1D amplification to bevacizumab resistance in colorectal cancer patients
Dataset
EGAD00001005761
-
RNA-seq study of a Princess Margaret Cancer Centre human acute myeloid leukemia patient cohort
Dataset
EGAD00001006576
-
The mutational landscape of human somatic and germline cells
Dataset
EGAD00001006641
-
Somatic mutations in facial skin from countries of contrasting skin cancer risk
Dataset
EGAD00001009666
-
Whole genome sequencing
Dataset
EGAD00001009746
-
POETIC clinical Trial Ki67 Bookend Breast Cancer Targeted Exome and RNAseq Project
Dataset
EGAD00001010919
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - DNA
Dataset
EGAD00001009812
-
Somatic mutation and clonal evolution normal breast tissue WGS
Dataset
EGAD00001010123