-
Role_of_Epigenetic_Memory_in_Human_Induced_Pluripotent_Stem_Cells_Pilot
Study
EGAS00001000742
-
Illumina Human OmniExpress genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000687
-
Unraveling metastatic progression of breast cancer
Study
EGAS00001000760
-
Fetal hemoglobin in sickle cell disease patients from Tanzania
Study
EGAS00001000990
-
Congenital_anosmia_1
Study
EGAS00001001124
-
HipSci___RNAseq___Rare_Monogenic Diabetese
Study
EGAS00001001137
-
Understand_Paratyphoid_Disease___host_responses_to_human_challenge_with_S__Paratyphi_A
Study
EGAS00001001260
-
SNP genotyping data in genes related to trace element homeostasis
Study
EGAS00001001292
-
Breast Cancer - Subtype defined by an amplification of the HER2 gene
Study
EGAS00001001431
-
Premalignant SOX2 overexpression in the fallopian tubes of ovarian cancer patients: Discovery and validation studies
Study
EGAS00001001909
-
FASTQ files of the small RNA-Seq dataset from the POPS cohort
Dataset
EGAD00001004860
-
cfDNA analysis reveals relation of POLR1D amplification to bevacizumab resistance in colorectal cancer patients
Dataset
EGAD00001005761
-
Genetic landscape of SMM
Dataset
EGAD00001005285
-
Single cell sequencing of a post-PD-1 inhibitor metastatic melanoma mass
Dataset
EGAD00001006013
-
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients
Dataset
EGAD00001006888
-
COVID-19 severity correlates with airway epithelium–immune cell interactions identified by single-cell analysis
Dataset
EGAD00001006339
-
Whole exome sequencing of endometriod ovarian cancer tumours
Dataset
EGAD00001006389
-
Genomic characterisation of MGUS
Dataset
EGAD00001006363
-
The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET) - Intratumoural immune heterogeneity
Dataset
EGAD00001006570
-
Hypertension delays viral clearance and exacerbates airway hyperinflammation in patients with COVID-19
Dataset
EGAD00001006828
-
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
-
bulk RNA sequencing, single cell RNA sequencing and nanopore sequencing of T-ALL patients with TCF7-SI1 fusion
Dataset
EGAD00001007010
-
Genetic landscape of inherited retinal dystrophies
Dataset
EGAD00001007022
-
PopCol 16S gut microbiome sequencing
Dataset
EGAD00001007071
-
Single cells of colorectal cancer organoids
Dataset
EGAD00001007305
-
Assessment of epigenetic variation in human iPS cells-Medip
Dataset
EGAD00001000827
-
RNA-seq study of a Princess Margaret Cancer Centre human acute myeloid leukemia patient cohort
Dataset
EGAD00001006576
-
Characterization of mutational signatures in human cancer cell lines reveals episodic APOBEC mutagenesis
Dataset
EGAD00001004202
-
Ovarian Cancer Organoid Biobank - RNASeq data
Dataset
EGAD00001004509
-
The mutational landscape of human somatic and germline cells
Dataset
EGAD00001006641
-
Sequencing component for the whole genome methylation analysis in PBMCs and cell subsets (pilot study)
Dataset
EGAD00001000394
-
Characterization of mutational signatures in human cancer cell lines reveals episodic APOBEC mutagenesis
Dataset
EGAD00001004203
-
RAG mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 Acute Lymphoblastic Leukemia (Whole_Genome_sequencing_data)
Dataset
EGAD00001000634
-
RAG mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 Acute Lymphoblastic Leukemia (Rearrangement_sequencing_data)
Dataset
EGAD00001000635
-
Chromatin accessibility maps of chronic lymphocytic leukemia identify subtype-specific epigenome signatures and transcription regulatory networks
Dataset
EGAD00001002110
-
Tobacco exposure and somatic mutations in normal human bronchial epithelium
Dataset
EGAD00001005193
-
The mutational landscape of normal human endometrial epithelium - Additional Samples
Dataset
EGAD00001005214
-
Analysis of the B cell receptor repertoire in six immune-mediated diseases
Dataset
EGAD00001005431
-
Structural rearrangements generate cell-specific, gene-independent CRISPR-Cas9 loss of fitness effects.
Dataset
EGAD00001004124
-
CBD-RAW-SC-GEX: 10X Single-Cell Gene Expression
Dataset
EGAD00001008007
-
Whole genome sequencing in 1038 index cases reveals novel causative genes in pulmonary arterial hypertension
Dataset
EGAD00001003423
-
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
-
TSCA-LI amplicon sequencing of called variants in WXS data of DSALL.
Dataset
EGAD00001003275
-
BLUEPRINT: Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Dataset
EGAD00001001011
-
SINGLE CELL ANALYSIS OF IN VITRO ERYTHROPOIESIS
Dataset
EGAD00001000979
-
Competitive selection of somatic mutant clones in normal human skin varies with body site
Dataset
EGAD00001006194
-
Multiomic characterization of clonotypic B cells
Dataset
EGAD50000002162
-
Stage-specific gene and transcript dynamics in human male germ cells
Study
EGAS00001006135
-
RNA sequencing data of 142 samples from 142 patients with HER2+ breast cancer treated with letrozole or tamoxifen (SOLTI PAMELA trial)
Study
EGAS00001006410
-
scRNA-seq of patient-derived PDAC organoids and matched CAFs
Study
EGAS00001006661
-
The molecular landscape of glioma in patients with Neurofibromatosis 1.
Study
EGAS00001003186
-
scRNAseq and scATACseq of placebo controlled-trial on MMR non-specific effects
Study
EGAS00001006787
-
Spatial and temporal intra-tumoural heterogeneity in advanced High-Grade Serous Ovarian Cancer: implications for surgical and clinical outcomes
Study
EGAS00001007164
-
AML FLT3 TCR study
Study
EGAS00001007467
-
Non-invasive prenatal diagnosis by genome-wide haplotyping of maternal cell-free plasma DNA
Study
EGAS00001003634
-
Whole genome and whole transcriptome sequencing of patients diagnosed with angiosarcoma.
Study
EGAS00001003895
-
Mutation signatures in melanocytic nevi reveal characteristics of defective DNA repair
Study
EGAS00001004274
-
Human Developmental Biology Resource (HDBR) abnormal fetal samples
Study
EGAS00001006300
-
Whole transcriptome sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Study
EGAS00001004232
-
Molecular profiling of EBV associated diffuse large B-cell lymphoma
Study
EGAS00001006400
-
Multiple Tissue Monitoring in Huntington disease - RNAseq skeletal muscle
Study
EGAS00001006474
-
Alternative lengthening of telomeres in childhood neuroblastoma from genome to proteome
Study
EGAS00001004349
-
502 present-day genotypes included in the '137 ancient human genomes from across the Eurasian steppe' publication
Study
EGAS00001002926
-
503 genotypes from Inner Asia used in 'Close inbreeding and low genetic diversity in Inner Asian human populations despite geographical exogamy' publication
Study
EGAS00001002951
-
The exomic landscape of t(14,18) negative diffuse follicular lymphoma with 1p36 deletion
Study
EGAS00001002594
-
Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population
Study
EGAS00001002641
-
Natural variation of circulating RNAs in human serum
Study
EGAS00001002814
-
Ibrutinib induces a global chromatin reorganisation in chronic lymphocytic leukaemia
Study
EGAS00001002827
-
CCND1-negative MCL
Study
EGAS00001003060
-
Primary breast cancers and paired brain metastases sequencing study
Study
EGAS00001003173
-
Microsatellite unstable colorectal cancers
Study
EGAS00001003366
-
Pancreatic cancer organoids recapitulate disease and allow personalized drug screening
Study
EGAS00001003369
-
COMPARE study: participants typed during UK Biobank version 2 array development phase
Study
EGAS00001003748
-
Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Study
EGAS00001002599
-
T-cell reconstitution after reduced dose ATLG induction in kidney transplant recipients
Study
EGAS00001005941
-
Comprehensive genomic profiling of matched glioblastoma tumours, cell-lines, and xenografts reveals genomic stability and adaptation to disparate growth environments
Study
EGAS00001002709
-
Single cell transcriptomic and genomic profiling of carcinogenesis in patients with familial adenomatous polyposis
Study
EGAS00001003598
-
WXS of 147 lung cancer patients treated with immunotherapy
Study
EGAS00001003781
-
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD37920__Targeted_
Study
EGAS00001003321
-
Molecular profiling of blastic plasmacytoid dendritic cell neoplasm (BPDCN) as compared to acute myeloid leukemia (AML)
Study
EGAS00001003453
-
Single-cell RNA-sequencing reveals that glioblastoma recapitulates a normal neurodevetlopmental hierarchy
Study
EGAS00001004422
-
Characterization of four subtypes in morphologically normal tissue excised proximal and distal to breast cancer
Study
EGAS00001004510
-
Transcriptomic analysis of the Phase 3 COMPARZ clinical trial
Study
EGAS00001004534
-
Whole Genome Sequencing of 317 individuals from the Pacific region
Study
EGAS00001004540
-
Indonesian Genome Diversity Project 2
Study
EGAS00001003654
-
Ultraviolet radiation drives mutations in a subset of mucosal melanomas
Study
EGAS00001004697
-
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
-
Genomics_of_acral_lentiginous_melanoma___RNAseq
Study
EGAS00001003758
-
Single cell T cell Landscape and T Cell Receptor Repertoire Profiling of AML in Context of PD-1 Blockade Therapy
Study
EGAS00001004894
-
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
-
Single cell exome sequencing of lung adenocarcinoma
Study
EGAS00001002972