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Exome sequencing to identify predisposition to Wilms tumour
Study
EGAS00001000904
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Identifying causative mutations for Thrombocytopenia with Absent Radii
Study
EGAS00001000054
-
Exome_sequencing_of_a_Novel_Primary_T_Cell_Immunodeficiency_Kindred
Study
EGAS00001000099
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Samples from the Greek island of Crete, MANOLIS cohort
Study
EGAS00001000067
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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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BRAF_and_MEK_resistant_cell_line_clones
Study
EGAS00001000172
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Genomic profiling of ovarian adult type granulosa cell tumors
Study
EGAS00001002833
-
Gastric_Mutational_Signatures__GMS_
Study
EGAS00001002938
-
Gastric_Mutational_Signatures__GMS_
Study
EGAS00001002939
-
WES analysis in identifying additive genetic factors that may contribute to the occurrence of moyamoya in neurofibromatosis type 1
Study
EGAS00001003053
-
Somatic point mutation data from microsatellite unstable colorectal cancers
Study
EGAS00001003101
-
Neoadjuvant chemotherapy alters the genomic landscape and immune microenvironment of breast cancers
Study
EGAS00001003354
-
TRACERx 100: RRBS data from a subset of the first 100 TRACERx tumours
Study
EGAS00001003484
-
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Study
EGAS00001000874
-
Whole genome sequencing of 25 South African individuals with myasthenia gravis
Study
EGAS00001003462
-
Autoimmunity_and_immunodeficiency_COVID19
Study
EGAS00001004489
-
Alveolar Rhabdomyosarcoma case report
Study
EGAS00001004828
-
ABIS_1_MeDIP-seq
Study
EGAS00001001099
-
Whole_exome_sequencing_for_clarification_of_rare_causes_of_axonal_Charcot_Marie_Tooth_disease_
Study
EGAS00001002067
-
MYOSEQ project
Study
EGAS00001002069
-
Lebanon_LowCov_seq
Study
EGAS00001002084
-
HDAC inhibitors in synovial sarcoma cells
Study
EGAS00001002637
-
Illumina Omni5 SNP chip genotyping of MacTel cases and unaffected controls for a genome-wide association study
Study
EGAS00001002249
-
A whole genome analysis of single fetal human stem cells from the liver and the intestine
Study
EGAS00001002886
-
Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia - Acute myeloid leukemia
Study
EGAS00001005464
-
EPIC arrays data for chemotherapy response project
Study
EGAS00001004515
-
PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysm in humans
Study
EGAS00001005518
-
Deregulation of DUX4 and ERG in acute lymphoblastic leukemia
Study
EGAS00001001923
-
Single-cell RNA-seq data of the tumor microenvironment of lymphocyte-rich Hodgkin lymphoma and other Hodgkin lymphoma subtypes
Study
EGAS00001005541
-
Origins and timing of emerging lesions in advanced renal cell carcinoma
Study
EGAS00001005897
-
Using human induced pluripotent stem cell-derived oligodendrocytes to explore cellular phenotypes associated with t(1;11) translocation.
Study
EGAS00001004595
-
RNA sequencing of undifferentiated sarcomas
Study
EGAS00001003291
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___visium
Study
EGAS00001006045
-
Mutational landscape of eccrine porocarcinoma (sweat gland tumour)
Study
EGAS00001004632
-
Case Report: Precision medicine target revealed by in-vitro modelling of relapsed, refractory ALL from a child with neurofibromatosis
Study
EGAS00001006187
-
Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data
Study
EGAS00001003504
-
Tumor microenvironment study of ovarian granulosa cell tumors
Study
EGAS00001006478
-
Reliable assessment of telomere maintenance mechanisms in neuroblastoma
Study
EGAS00001006510
-
Detection and genomic analysis of BRAF fusions in Juvenile Pilocytic Astrocytoma through the combination and integration of multi-omic data
Study
EGAS00001006388
-
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
-
Chip_seq_oesophageal_adenocarcinoma_
Study
EGAS00001007180
-
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
-
Single-cell RNA-seq of peripheral blood mononuclear cells in classic Hodgkin lymphoma
Study
EGAS00001007569
-
A standardised framework for robust fragmentomic feature extraction from cell-free DNA sequencing data
Study
EGAS00001008051
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell renal cell carcinoma -- CA209-010
Dataset
EGAD00001006026