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Multi-layered molecular characterization defines prognostic subtypes of lung adenocarcinoma in Asian never-smokers
Study
EGAS00001003705
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Genomic Analysis of Primary Plasma Cell Leukemia reveals Complex Structural Alterations and High Risk Mutational Patterns
Study
EGAS00001003834
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PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysm in humans
Study
EGAS00001005518
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Macrophage response in preterm infants compared to term infants
Study
EGAS00001004974
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hereditary BrEAst Case CONtrol study
Study
EGAS00001005043
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Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia - Acute myeloid leukemia
Study
EGAS00001005464
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Origins and timing of emerging lesions in advanced renal cell carcinoma
Study
EGAS00001005897
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Illumina HiSeqX and HiSeq 2000 whole genome sequence data on 3,001 ALS samples including 212 with known C9orf72 repeat expansions
Study
EGAS00001002598
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The European Bank for Induced Pluripotent stem cells (EBiSC) is designed to address the increasing demand by iPSC researchers for quality-controlled, disease-relevant research grade iPSC lines, data and cell services.In this study Whole Genome Sequencing was performed on a selection of lines from the project.
Study
EGAS00001002755
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Gastric_Mutational_Signatures__GMS_
Study
EGAS00001002939
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Whole genome sequencing of 25 South African individuals with myasthenia gravis
Study
EGAS00001003462
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HDAC inhibitors in synovial sarcoma cells
Study
EGAS00001002637
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Alveolar Rhabdomyosarcoma case report
Study
EGAS00001004828
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Illumina Omni5 SNP chip genotyping of MacTel cases and unaffected controls for a genome-wide association study
Study
EGAS00001002249
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A whole genome analysis of single fetal human stem cells from the liver and the intestine
Study
EGAS00001002886
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EPIC arrays data for chemotherapy response project
Study
EGAS00001004515
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Single-cell RNA-seq data of the tumor microenvironment of lymphocyte-rich Hodgkin lymphoma and other Hodgkin lymphoma subtypes
Study
EGAS00001005541
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RNA sequencing of undifferentiated sarcomas
Study
EGAS00001003291
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Mutational landscape of eccrine porocarcinoma (sweat gland tumour)
Study
EGAS00001004632
-
Using human induced pluripotent stem cell-derived oligodendrocytes to explore cellular phenotypes associated with t(1;11) translocation.
Study
EGAS00001004595
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Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___visium
Study
EGAS00001006045
-
Case Report: Precision medicine target revealed by in-vitro modelling of relapsed, refractory ALL from a child with neurofibromatosis
Study
EGAS00001006187
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Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data
Study
EGAS00001003504
-
South Asia Rheumatic Heart Disease Genetics Network
Study
EGAS00001003565
-
Detection and genomic analysis of BRAF fusions in Juvenile Pilocytic Astrocytoma through the combination and integration of multi-omic data
Study
EGAS00001006388
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Time-dependent characterization of CNS response in COVID-19
Study
EGAS00001006442
-
T cell reactivity of MHC epitopes
Study
EGAS00001006445
-
Multiple Sclerosis risk variants regulate gene expression in innate and adaptive immune cells
Study
EGAS00001004087
-
Subtype-associated epigenomic landscape and 3D genome structure in bladder cancer
Study
EGAS00001005071
-
Identification and functional characterisation of a rare MTTP variant underlying familial non-alcoholic fatty liver disease
Study
EGAS00001005254
-
Transcriptomic analysis of cell-of-origin CNS neuroblastoma, FOXR2 activated
Study
EGAS00001007247
-
Human data for chromatin accessibility (ATAC-Seq and scATAC-Seq) and transcriptome (RNA-Seq and scRNA-Seq) in eight B-cell precursors, from HSC to Naive B cells
Study
EGAS00001007296
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Genomic profiling of IBC
Study
EGAS00001007520
-
Single-cell RNA-seq of peripheral blood mononuclear cells in classic Hodgkin lymphoma
Study
EGAS00001007569