-
Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour
Study
EGAS00001001836
-
Genomewide detection of cytosine methylation by single molecule real-time sequencing
Study
EGAS00001004642
-
Mutated H3 Histones Drive Human Pre-Leukemic Hematopoietic Stem Cell Expansion And Promote Leukemic Aggressiveness
Study
EGAS00001003288
-
Chromosome Y Philogeny in Sardinia
Study
EGAS00001000532
-
Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing
Study
EGAS00001001838
-
Tumor suppressor miR-133a modulates the prostate cancer epigenome by repressing BAZ2A
Study
EGAS00001000568
-
From matrimonial practices to genetic diversity in Southeast Asian populations: the signature of the matrilineal puzzle
Study
EGAS00001003727
-
Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis
Study
EGAS00001002642
-
DNA Methylation loss coupled with mitotic cell division promotes immune evasion of tumours with high mutation load
Study
EGAS00001003731
-
A system-wide approach to monitor responses to synergistic BRAF and EGFR inhibition in colorectal cancer cells
Study
EGAS00001002654
-
FinHer_Breast_Cancer_Study
Study
EGAS00001000648
-
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH1
Study
EGAS00001001854
-
Genetic subclone heterogeneity of tumor-initiating cells in human colorectal cancer
Study
EGAS00001001857
-
Whole transcriptome and exome sequencing of childhood ALL
Study
EGAS00001001858
-
Next-Generation Sequencing of AV Nodal Reentry Tachycardia patients
Study
EGAS00001002745
-
Glioblastoma initiating cells are sensitive to histone demethylase inhibition due to epigenetic deregulation
Study
EGAS00001003750
-
DIPG RNA and exome sequencing
Study
EGAS00001004749
-
Variation in the Glucose Transporter gene SLC2A2 is associated with glycaemic response to metformin
Study
EGAS00001001875
-
Growth Hormone (GH) -secreting Pituitary Adenoma
Study
EGAS00001003488
-
Kibbutzim Family study
Study
EGAS00001002782
-
The_contribution_of_POT1_variants_to_sporadic_melanoma_development
Study
EGAS00001001964
-
Second hit rare genetic variants in families with seemingly GBA gene associated Parkinson’s disease
Study
EGAS00001004777
-
Genetic control of the transcriptomic response of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans
Study
EGAS00001001895
-
Methylation analysis for plasma DNA of patients with organ transplantation
Study
EGAS00001004788
-
Knee_OA_Functional_Genomics
Study
EGAS00001001899
-
Familial psychosis associated with a missense mutation at MACF1 gene combined with the rare duplications DUP3p26.3 and DUP16p23.3, affecting the CNTN6 and CDH13 genes
Study
EGAS00001004791
-
Primary prostate Hi-C
Study
EGAS00001005014
-
Genomics analysis of mucinous tumours of the ovary and related neoplasms
Study
EGAS00001003545
-
Comprehensive Genomic and Transcriptomic Analysis of Rare Cancers for Guiding of Therapy (H021)
Study
EGAS00001004813
-
Summary statistics of meta-analysis using two genome-wide association study of inflammatory bowel disease in Koreans.
Study
EGAS00001005026
-
Genetics and transcriptomes of pediatric B cell precursor leukemia with gain of chromosome 21
Study
EGAS00001003760
-
BLUEPRINT ChIP-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000951
-
HipSci___Whole_Exome_sequencing___Battens
Study
EGAS00001001975
-
Mapping_genetic_variants_underlying_gene_regulation_in_inflammed_intestinal_cell_types_to_identify_novel_IBD_drug_targets
Study
EGAS00001003770
-
Physiological and genetic adaptations to diving in Sea Nomads
Study
EGAS00001002823
-
HipSci___Whole_Exome_sequencing___Macular_dystrophy
Study
EGAS00001001982
-
HipSci___Whole_Exome_sequencing___PID
Study
EGAS00001001983
-
HipSci HumanExome BeadChip analysis - Hereditary Spastic Paraplegia
Study
EGAS00001002006
-
HipSci HumanExome BeadChip analysis - Congenital Hyperinsulinia
Study
EGAS00001002010
-
HipSci HumanExome BeadChip analysis - Hypertrophic Cardiomyopathy
Study
EGAS00001002011
-
HipSci HumanExome BeadChip analysis - Battens disease
Study
EGAS00001002016
-
HipSci HumanHT 12 Expression BeadChip analysis - Alport syndrome
Study
EGAS00001002024
-
HipSci HumanHT 12 Expression BeadChip analysis - Hypertrophic Cardiomyopathy
Study
EGAS00001002026
-
HipSci HumanHT 12 Expression BeadChip analysis - Primary immune deficiency
Study
EGAS00001002027
-
HipSci HumanHT 12 Expression BeadChip analysis - Bleeding and Platelet disorders
Study
EGAS00001002028
-
HipSci HumanHT 12 Expression BeadChip analysis - Macular Dystrophy
Study
EGAS00001002029
-
HipSci HumanHT 12 Expression BeadChip analysis - Battens disease
Study
EGAS00001002031
-
Extreme phenotypes define epigenetic and metabolic signatures in cardiovascular diseases.
Study
EGAS00001003780
-
Characterization_of_genomic_landscape_of_Peripheral_T_cell_Lymphomas__not_otherwise_specified__PTCL_NOS_
Study
EGAS00001002057
-
Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma
Study
EGAS00001005054
-
Genetic makeup of agnospheres
Study
EGAS00001004868
-
Gene_Characterization_in_Carbohydrate_metabolic_alterations__neonatel_diabetes___congenital_hyperinsulinemic__in_early_childhood
Study
EGAS00001002074
-
Functional analysis of GATA2 synonymous mutations
Study
EGAS00001003817
-
Mutational analysis of an oligoprogressive sarcomatoid hepatocellular carcinoma treated with an immune checkpoint inhibitor.
Study
EGAS00001005064
-
RNA sequencing CYLD cutaneous syndrome
Study
EGAS00001003841
-
Same-day genomic and epigenomic diagnosis of brain tumors using realtime nanopore sequencing
Study
EGAS00001002213
-
Illumina Omni5 SNP chip genotyping of MacTel cases and unaffected controls for a genome-wide association study
Study
EGAS00001002249
-
Genetic_vulnerability_of_knockout_cancer_lines
Study
EGAS00001002253
-
Single_Cell_RNAseq_at_various_stages_of_HiPSCs_differentiating_toward_definitive_endoderm_and_endoderm_derived_lineages
Study
EGAS00001002278
-
Genetic landscape of inherited retinal dystrophies affected cases in Spain
Study
EGAS00001005104
-
Discovering genetic causes of optic atrophy syndromes through whole exome sequencing
Study
EGAS00001003850
-
Single cell phenotypic profiling of 27 DLBCL cases reveals marked inter- and intra-tumoral heterogeneity
Study
EGAS00001003860
-
Chronic myelomonocytic leukemia
Study
EGAS00001005107
-
Epigenomic profiling and transcriptomic profiling of LUAD patients tumor tissues and tumor adjacent tissues
Study
EGAS00001005132
-
Biological insights from the whole genome sequences of human embryonic stem cell lines
Study
EGAS00001002400
-
Comprehensive investigation of genome architecture of papillary thyroid cancer with whole-exon sequencing in the Chinese population.
Study
EGAS00001002402
-
Cell-free DNA TAPS for early cancer detection
Study
EGAS00001004962
-
Whole exome sequencing in patients with ALS and concomitant FTD lacking the C9orf72 repeat expansion
Study
EGAS00001002439
-
Comprehensive Molecular Analysis of Colon Cancer for the Identification and Validation of New Biomarkers
Study
EGAS00001002453
-
Genomic Profiling Reveals Spatial Intra-tumour Heterogeneity in Follicular Lymphoma
Study
EGAS00001002492
-
ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation.
Study
EGAS00001002507
-
Distinct genomic profile and specific targeted drug responses in adult cerebellar glioblastoma
Study
EGAS00001002517
-
Linking the epigenetic landscape in chronic lymphocytic leukemia to deregulated chromatin networks
Study
EGAS00001002518
-
Single-cell landscapes of primary glioblastomas and matched organoids and cell lines reveal variable retention of inter- and intra-tumor heterogeneity
Study
EGAS00001005227
-
The aim of this study was to identify underlying hub genes and dysregulated pathways associated with the development of HCC using bioinformatics analysis.
Study
EGAS00001002526
-
Integrative genomic analysis identifies multiple subtypes and therapeutic targets in acute erythroid leukemia
Study
EGAS00001002537
-
The genomic landscape of childhood acute lymphoblastic leukaemia with intrachromosomal amplification of chromosome 21 (iAMP21-ALL)
Study
EGAS00001004998
-
Single-cell RNA sequencing reveals cell-type specific eQTLs in peripheral blood mononuclear cells
Study
EGAS00001002560
-
Genetic history of the Comorian populations.
Study
EGAS00001002565
-
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001002602
-
Genetic heterogeneity and dynamics of transcriptional subtypes in matched primary and recurrent head and neck squamous cell carcinomas
Study
EGAS00001005005
-
Host genetic determinants of HIV infection
Study
EGAS00001005245
-
The Southern African Human Genome Programme
Study
EGAS00001002639
-
Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B
Study
EGAS00001005243
-
Transcriptomic and epigentic analysis of human peripheral blood NK cell subsets revealing role of Bcl11b in differentiation
Study
EGAS00001005025
-
Defining the metastasome in colorectal cancer: Implications for hypotheses on metastasis evolution and personalized therapy (HIPO-032)
Study
EGAS00001002717
-
Defective Homologous Recombination DNA Repair as Therapeutic Target in Advanced-Stage Chordoma (HIPO_021)
Study
EGAS00001002720
-
The_British_Autozygosity_Populations_BioResource
Study
EGAS00001002742
-
The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses
Study
EGAS00001002744
-
Genomic landscape of inflammatory breast cancer by whole-genome sequencing
Study
EGAS00001004117
-
Multiple migrations to the Philippines during the last 50,000 years
Study
EGAS00001005083
-
Whole genome sequencing of 76 tumor and normal samples from 11 SI-NET patients
Study
EGAS00001005096
-
Phylogenetic analysis of treatment-naive metastases using whole exome and genome sequencing data
Study
EGAS00001002777
-
Indonesian RNA-seq data
Study
EGAS00001003671
-
Evolutionary predictability of genetic versus non genetic resistance to anticancer drugs in melanoma
Study
EGAS00001005314
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Gastric_Organoids
Study
EGAS00001003151
-
DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Study
EGAS00001002797
-
Whole-exome sequencing of Fanconi anemia-like inherited bone marrow failure syndrome
Study
EGAS00001003809
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_adenocarcinoma
Study
EGAS00001003702
-
Whole-Genome Sequencing of Salivary Gland Adenoid Cystic Carcinoma
Study
EGAS00001002812