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Determination of the molecular nature of the Vel blood group by exome sequencing
Study
EGAS00001000069
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Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Study
EGAS00001001461
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Genomic landscape of human diversity across Madagascar
Study
EGAS00001002549
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Epigenomic profiling and transcriptomic profiling of LUAD patients tumor tissues and tumor adjacent tissues
Study
EGAS00001005132
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Genetic landscape of pediatric Medulloblastoma
Study
EGAS00001000347
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Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Study
EGAS00001001516
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Inhibiton of the GABPB1L-containing GABP tetramer is sufficient to reverse replicative immortality in TERT promoter mutant glioblastoma cells.
Study
EGAS00001002582
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Genetic and epigenetic characterization of adenoid cystic carcinoma
Study
EGAS00001001457
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Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations
Study
EGAS00001003027
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Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015
Study
EGAS00001001570
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Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Study
EGAS00001002599
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HipSci - Human Induced Pluripotent Stem Cells Initiative
Study
EGAS00001001465
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DNA methylomes of monozygotic twins clinically discordant for multiple sclerosis
Study
EGAS00001003147
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GILD_ExomeSeq_PTNHL
Study
EGAS00001001613
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MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
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Multisample genomic analysis of solid childhood cancers using high resolution SNP-arrays, Whole Exome Sequencing and Targeted Deep Sequencing.
Study
EGAS00001002662
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Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population
Study
EGAS00001002641
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Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma
Study
EGAS00001001665
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Liver biopsy derived induced pluripotent stem cells provide an unlimited supply for the generation of patient-specific hepatocyte-like cells
Study
EGAS00001002676
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Whole-exome sequencing of breast cancer metastasis and corresponding blood samples
Study
EGAS00001001695
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Genetic sequencing of MODY patients.
Study
EGAS00001001699
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Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
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We performed whole-exome sequencing and whole epigenome sequencing (RRBS) of samples collected from different time points during radiotherapy from thirty-four ESCC patients. We compared the genetic and epigenetic features of the different time biopsy samples to reveal the changes in ESCC received radiotherapy.
Study
EGAS00001002719
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Inherited genetic predisposition to childhood acute lymphoblastic leukemia investigated using a genome wide association study.
Study
EGAS00001002809
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PAGE: Prenatal Assessment of Genomes and Exomes
Study
EGAS00001001713