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Congenital_anosmia_1
Study
EGAS00001001124
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Genome-wide association analysis on five isolated populations - Erasmus Rucphen Family (ERF) Study
Study
EGAS00001001134
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HipSci___RNAseq___Rare_Monogenic Diabetese
Study
EGAS00001001137
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Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___single_cell_RNA_sequencing
Study
EGAS00001003519
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Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants
Study
EGAS00001003521
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Prediction of pigmentation phenotypes by SNP typing in a Northern German population
Study
EGAS00001001174
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Evolution of DNA repair defects during malignant progression of low-grade gliomas after temozolomide treatment.
Study
EGAS00001001179
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Genome_Diversity_in_Africa_Project___ancient_samples___standard_libraries
Study
EGAS00001001182
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Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison
Study
EGAS00001001191
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G&T-seq: parallel sequencing of the genomes and transcriptomes of single cells
Study
EGAS00001001204
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Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Study
EGAS00001001205
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Associations between APOE status and cognitive ability across the lifecourse
Study
EGAS00001001235
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The genomic landscape of childhood acute lymphoblastic leukaemia with intrachromosomal amplification of chromosome 21 (iAMP21-ALL)
Study
EGAS00001004998
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MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___Exome__Novaseq_
Study
EGAS00001003527
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Papuan Genomes: whole genome sequencing
Study
EGAS00001001247
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Prenatal lead exposure is associated with decreased cord blood DNA methylation of the glycoprotein VI gene involved in platelet activation and thrombus formation
Study
EGAS00001001575
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Cell-free DNA TAPS for early cancer detection
Study
EGAS00001004962
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UK10K NEURO UKSCZ
Study
EGAS00001000123
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DNA methylation and somatic mutations converge on cell cycle and define similar evolutionary histories in brain tumors
Study
EGAS00001001255
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Genetic heterogeneity and dynamics of transcriptional subtypes in matched primary and recurrent head and neck squamous cell carcinomas
Study
EGAS00001005005
-
Institut Curie Neuroblastoma Whole Genome Sequencing Diagnosis Relapse
Study
EGAS00001001184
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Primary prostate Hi-C
Study
EGAS00001005014
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Summary statistics of meta-analysis using two genome-wide association study of inflammatory bowel disease in Koreans.
Study
EGAS00001005026
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Transcriptomic and epigentic analysis of human peripheral blood NK cell subsets revealing role of Bcl11b in differentiation
Study
EGAS00001005025
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Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis
Study
EGAS00001001723