-
Genomic analysis of patient-derived xenograft models reveals intratumor-heterogeneity in endometrial cancer and can predict tumor growth inhibition with talazoparib
Study
EGAS00001004666
-
Mapping the epigenomic landscape of human monocytes following innate immune activation reveals context-specific mechanisms driving endotoxin tolerance
Study
EGAS00001007362
-
CLL_Cancer_Whole_Genome_Sequencing
Study
EGAS00001000014
-
TMD_AMLK_Exome_Study
Study
EGAS00001000027
-
High-throughput single-cell DNA sequencing of acute myeloid leukemia tumors with droplet microfluidics
Study
phs001627
-
Childhood Cancer Data Initiative (CCDI): Clonal Evolution During Metastatic Spread in High-Risk Neuroblastoma
Study
phs003111
-
Identification of Genes Involved in Familial Coronary Artery Disease
Study
phs000514
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Ottawa Heart Study
Study
phs000806
-
The Genomic Complexity of Primary Human Prostate Cancer
Study
phs000330
-
Longread sequencing of selected 12q-amplified osteosarcomas
Study
EGAS50000000495
-
RNA-seq of der(1;7)(q10;p10) & control MDS patients
Study
EGAS50000000705
-
Subclonal variation in patients with pediatric T-lymphoblastic leukemia (T-ALL)
Study
EGAS50000000794
-
Integrating Circulating Tumor DNA Analysis and Radiomics for Dynamic Risk Assessment in Localized Lung Cancer
Study
phs003947
-
Whole blood transcriptomics analysis in Antiphospholipid syndrome in patients with Systemic Lupus Erythematosus
Study
EGAS00001007750
-
Variant analysis on FFPE specimen from NSCLC patients (OCAPlus)
Study
EGAS50000001136
-
Shallow whole genome sequencing of ctDNA samples from DETECT study
Study
EGAS50000000911
-
Systematic identification of long non-coding RNAs potentially involved in gastrointestinal carncer
Study
JGAS000011
-
Mutation screening in a large series of Japanese hearing loss patients using massively parallel DNA sequencing analysis.
Study
JGAS000490
-
Mechanisms on relapse after allogeneic hematopoietic cell transplantation in CMML
Study
JGAS000317
-
Mutagenic impact of radiotherapy in B-cell lymphoma and multiple myeloma
Study
EGAS50000000997
-
Fecal microbiome predicts treatment response after the initiation of semaglutide or empagliflozin uptake
Study
EGAS50000000531
-
Whole genome sequencing data of paediatric ETV6::RUNX1 acute lymphoblastic leukemia
Study
EGAS50000001599
-
ER___HER2___PR__breast_Cancer_genome_sequencing
Study
EGAS00001000197
-
Sputum bacterial microbiota in an overall healthy population in Guangdong province, China
Study
EGAS00001006721
-
Whole-genome and transcriptome sequencing of primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma
Study
EGAS00001004332
-
Sputum fungal microbiota in an overall healthy population in Guangdong province, China
Study
EGAS00001006720
-
HipSci HumanHT_12v4 Expression BeadChip analysis-Healthy volunteers
Study
EGAS00001000867
-
Grey_Platelet_Syndrome__GPS_
Study
EGAS00001000091
-
The_International_1q_type_2_diabetes_consortium
Study
EGAS00001000062
-
Cancer_Exome_Resequencing
Study
EGAS00001000206
-
Breast_Cancer_Exome_Sequencing
Study
EGAS00001000211
-
HipSci-Whole Exome sequencing-healthy volunteers
Study
EGAS00001000592
-
Multiple Sclerosis ImmunoChip data
Study
EGAS00001003219
-
Prostate_Cancer_Whole_Genome_Validations
Study
EGAS00001000427
-
SCAT_osteosarcoma_sequencing
Study
EGAS00001000196
-
Whole genome sequencing of adult glioblastoma nuclei
Study
EGAS00001005256
-
Next Generation Children project - WGS study of patients in NICU and PICU and their families
Study
EGAS00001003002
-
FAM50A_Disruption_in_TOV21G_Cells___RNAseq
Study
EGAS00001004156
-
Molecular profiling of an AML case following treatment with a BCL2 inhibitor
Study
EGAS00001004841
-
Amplified EPOR/JAK2 genes define a unique subtype of acute erythroid leukemia
Study
EGAS00001005810
-
Molecular Phenotype of Constitutional TET2 Haploinsufficiency in Humans
Study
EGAS00001003454
-
Somatic Inactivation of Breast Cancer Predisposition Genes in Tumours Associated with Pathogenic Germline Variants
Study
EGAS00001006532
-
Whole genome analysis of pediatric patients with medulloblastoma
Study
EGAS00001006653
-
The molecular landscape of homologous recombination deficient, end-stage, high grade serous ovarian cancer
Study
EGAS00001006789
-
DNA methylation of peripheral blood leukocytes from patients with Li-Fraumeni syndrome
Study
EGAS00001007075
-
Targeted_sequencing_of_blood_DNA_from_Human_twins (2019-05-31)
Dataset
EGAD00001005055
-
Whole exome sequencing of normal CD34+ cells
Dataset
EGAD00001007645
-
Transcriptomic profiling of RIRCD patient skeletal muscle, comparing muscle during affected phase to healthy control, and affected patient with and without additional EARS2 mutations.
Dataset
EGAD00001006381
-
LLDeep DAG2+: scRNA-seq in PBMCs
Dataset
EGAD00001003459
-
ESGI-Identification of novel genes and mechanisms leading to Primary Ciliary Dyskinesia
Dataset
EGAD00001001092