-
Genetic and methylation profiles distinguish benign, malignant and spitzoid melanocytic tumors
Study
EGAS00001006205
-
Linking the epigenetic landscape in chronic lymphocytic leukemia to deregulated chromatin networks
Study
EGAS00001002518
-
Unraveling the genetics of transformed splenic marginal zone lymphoma
Study
EGAS00001006389
-
DNA methylation and somatic mutations converge on cell cycle and define similar evolutionary histories in brain tumors
Study
EGAS00001001255
-
Integrated genomic characterization of IDH1 mutant Glioma malignant progression
Study
EGAS00001001588
-
Genetics of non-syndromic idiopathic autism spectrum disorders in India
Study
EGAS00001006060
-
Genome wide variation in the Angolan Namib desert reveals unique Pre-Bantu ancestry
Study
EGAS00001007011
-
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Study
EGAS00001007045
-
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
-
Single cell multi-omic data of glioblastoma evolution under therapy
Study
EGAS00001004909
-
Detection of rare mutations, copy number variation, and DNA methylation in the same template DNA molecules
Study
EGAS00001006839
-
Transcriptome profiling of human plucked frontal and occipital hair follicles
Study
EGAS00001002832
-
Mutator phenotype and specific mutational signature explain an increased risk of hematological malignancies in patients with Xeroderma Pigmentosum
Study
EGAS00001004511
-
COVID19 Host Genetic Initiative
Study
EGAS00001005304
-
Spatial concordance of DNA methylation classification in diffuse glioma
Study
EGAS00001005434
-
Combination therapies to inhibit LCK tyrosine kinase and mTOR signaling in T-cell Acute Lymphoblastic Leukemia
Study
EGAS00001005945
-
Molecular programs of melanoma brain metastases (MBM)
Study
EGAS00001005976
-
Loss of Epigenetic Barrier is Required for Enhancer Hijacking-Mediated Oncogenic Transcription
Study
EGAS00001006140
-
Bulk-tissue RNA-sequencing paired nuclear and cytoplasmic fractions of anterior prefrontal cortex, cerebellar cortex and putamen tissues from post-mortem neuropathologically-confirmed control individuals.
Study
EGAS00001006380
-
HSP90 inhibitor resistant cell line
Study
EGAS00001006381
-
Genetic variants of the COL4A3, COL4A4, and COL4A5 genes contribute to thinned glomerular basement membrane lesions in sporadic IgA nephropathy patients
Study
EGAS00001006519
-
Gene copy number variation in pediatric mental illness in a general population
Study
EGAS00001006659
-
Erythroid/megakaryocytic differentiation confers BCL-XL dependency and venetoclax resistance in acute myeloid leukemia
Study
EGAS00001006819
-
BLUEPRINT Epigenetic characterization of megakaryocytes and erythroblasts
Study
EGAS00001001641
-
Identification of gene mutations and fusion genes in patients with Sézary Syndrome
Study
EGAS00001001706
-
Pre-neoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma
Study
EGAS00001006692
-
AfricanNeo aDNA Study
Study
EGAS00001007519
-
SMARCB1 loss activates patient-specific distal oncogenic enhancers in malignant rhabdoid tumors
Study
EGAS00001007590
-
Genetic Landscape of Esophageal Squamous Cell Carcinoma Defined by Exome Sequencing on Chinese Patient Cohort and Cell Lines
Study
EGAS00001000932
-
Multimodal Epigenetic Sequencing Analysis (MESA) of Cell-free DNA for Non-invasive Cancer Detection
Study
EGAS00001006462
-
The European MAPPYACTS trial: Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies
Study
EGAS00001005935
-
Nala GSI GSAv3 PGx Study
Study
EGAS00001007710
-
RNA-seq of Liver Cancer
Study
EGAS00001002879
-
Genomic_profiling_of_B_other_Adult_ALL_RNA
Study
EGAS00001003428
-
Genomic_profiling_of_B_other_Adult_ALL_WGS
Study
EGAS00001002474
-
Disease and phenotype relevant genetic variants identified from histone acetylomes in human hearts
Study
EGAS00001003586
-
Transcriptome Analysis Offers a Comprehensive Illustration of the Genetic Background of Pediatric Acute Myeloid Leukemia
Study
EGAS00001003701
-
Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria
Study
EGAS00001007036
-
RNAseq
Study
EGAS00001007165
-
Whole genome and whole exome sequencing of epilaptic patients
Study
EGAS00001002825
-
Chip_seq_oesophageal_adenocarcinoma_
Study
EGAS00001007180
-
Understanding_hematopoietic_stem_cell_mobilization_and_engraftment_
Study
EGAS00001004620
-
The genetic history of the southern Andes from present-day Mapuche ancestry
Study
EGAS00001007200
-
H3Africa AWIGEN Pilot MetaboChip
Dataset
EGAD00010001258
-
GLASS-NL DNA-Methylation
Study
EGAS00001007546
-
IMPRESS: Improved Methylation Profiling using Restriction Enzymes and smMIP Sequencing, Combined with New Biomarker Panel, Creating Multi-Cancer Detection Assay
Study
EGAS00001007559
-
Genetic Effects on the Skin Methylome in Healthy Older Twins
Study
EGAS00001007816
-
Identification of the cause of juvenile parkinsonism in a case_SYNJ1
Study
EGAS00001007686
-
Submission 208 - study_title 1
Study
EGAS50000000321
-
Pediatric Non-Down Syndrome Acute Megakaryoblastic Leukemia is Characterized by Distinct Genomic Subsets with Varying Outcomes
Study
EGAS00001002183