-
HipSci HumanExome BeadChip analysis-Rare_BBS
Study
EGAS00001001272
-
Induced Pluripotent Cells Derived from Differentiated Rod Photoreceptors Undergo Efficient Retinogenesis in Three-Dimensional Cultures
Study
EGAS00001001288
-
Epigenome and transcriptome profiling of chronic lymphocytic leukemia patients
Study
EGAS00001001821
-
Tumor-derived cell lines as pharmacogenomic models to predict therapeutic vulnerabilities in hepatocellular carcinoma
Study
EGAS00001003536
-
Targeting FGFR1 for treatment of soft-tissue sarcoma (H021)
Study
EGAS00001001844
-
UK10K_RARE_THYROID
Study
EGAS00001000131
-
Integrated Genomic Analysis of Chronic Lymphocytic Leukaemia
Study
EGAS00001001306
-
Phylogenetic evolution of metastatic melanoma.
Study
EGAS00001003582
-
Carcinoma of the oral tongue (OTSCC) genomic landscape characterisation
Study
EGAS00001001329
-
Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Study
EGAS00001001516
-
Genetic dysregulation of gene expression and splicing during a ten-year period of human aging in the PIVUS study
Study
EGAS00001003583
-
Somatic_Genetics_of_lesions_from_a_POT1_patient
Study
EGAS00001001343
-
Trans-ethnic genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Study
EGAS00001001427
-
GENETIC HISTORY OF ITALY
Study
EGAS00001001458
-
GoT2D: Genetics of Type 2 Diabetes, a study of the the genetic architecture of type 2 diabetes using low pass whole genome sequencing and high density SNP genotyping in 2,657 individuals.
Study
EGAS00001001459
-
TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism
Study
EGAS00001001501
-
Whole exome sequencing of germline DNA was performed and subsequent polymorphisms in genes known and putatively involved in the innate immune response to fungi were identified
Study
EGAS00001001542
-
PSCP_mutation_analysis_in_hESCs
Study
EGAS00001001561
-
The_genetic_evolution_of_precursor_lesions_in_pancreatic_cancer
Study
EGAS00001001573
-
The_Little_Princess_Knowledge_Bank_
Study
EGAS00001004237
-
Papuan_Genotyping
Study
EGAS00001001587
-
Integrated genomic characterization of IDH1 mutant Glioma malignant progression
Study
EGAS00001001588
-
Epigenetic dynamics of monocyte to macrophage differentiation
Study
EGAS00001001595
-
Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes
Study
EGAS00001001601
-
Genetic and expression landscape of Waldenstrom macroglobulinemia
Study
EGAS00001003603
-
Exome sequencing of patients with rare neurological disorders
Study
EGAS00001000159
-
Targeted sequencing of 12 genes in patients with HLH
Study
EGAS00001001605
-
Recapitulation of genetic predisposition to medulloblastoma in human neuroepithelial stem cells
Study
EGAS00001003620
-
HipSci___Whole_Exome_sequencing___HSP
Study
EGAS00001001979
-
Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing
Study
EGAS00001001838
-
Epigenetic profiling of human CD4+ memory T cells reveals their proliferative history and argues in favor of a progressive differentiation model driven by epigenetically controlled master regulators.
Study
EGAS00001001624
-
Oral mucosa organoids as a potential model for personalized therapies
Study
EGAS00001003628
-
HipSci_RNASEQ_Retinitis_Pigmentosa
Study
EGAS00001001996
-
HipSci_RNASEQ_Usher syndrome and congenital eye defects
Study
EGAS00001001997
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
-
HipSci HumanExome BeadChip analysis - Primary immune deficiency
Study
EGAS00001002012
-
BLUEPRINT DNA Methylation 450K data of mantle cell lymphoma
Study
EGAS00001001637
-
BLUEPRINT Epigenetic characterization of megakaryocytes and erythroblasts
Study
EGAS00001001641
-
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Cerebellar Ataxias
Study
EGAS00001002020
-
33 patients with Monoclonal Gammopathy of Undetermined Significance (MGUS) had whole exome sequencing performed. Cells were sorted by FACSAria using CD138, CD19 and CD56 to obtain a pure abnormal plasma cell population. Generated somatic variants were compared to a previous study of 463 multiple myeloma patients.
Study
EGAS00001001658
-
Investigating_the_genetics_of_immunity_against_Salmonella_in_humans
Study
EGAS00001001664
-
Genetic sequencing of MODY patients.
Study
EGAS00001001699
-
Histological Transformation and Progression in Follicular Lymphoma: a Clonal Evolution Study
Study
EGAS00001001709
-
ENU_NCI_H508_cetuximab_fixed_concentration_project
Study
EGAS00001001744
-
Whole-Genome Sequencing of a Healthy Aging Cohort.
Study
EGAS00001002306
-
ENU_NCI_H508_Cetuximab_SecondRound
Study
EGAS00001001745
-
Genome-wide search to find the genetic elements underlying visual contour perception
Study
EGAS00001003639
-
Latency and interval therapy affect the evolution in metastatic colorectal cancer
Study
EGAS00001003646
-
Tumor suppressor miR-133a modulates the prostate cancer epigenome by repressing BAZ2A
Study
EGAS00001000568
-
Genetic landscape of pediatric Adrenocortical Tumor
Study
EGAS00001000257
-
Whole genome sequencing of six ethnic groups from Burkina Faso, Cameroon, and Tanzania
Study
EGAS00001003648
-
multi-OMICs study of a pair of infant monozygotic twins with concordant B-cell ALL
Study
EGAS00001003651
-
RNA_Seq_in_Patients_with_Primordial_Dwarfism
Study
EGAS00001000283
-
Indonesian methylation data
Study
EGAS00001003653
-
UK10K OBESITY TWINSUK
Study
EGAS00001000306
-
Pilot study for Illumina TST170 NGS panel on cutaneous T cell lymphoma samples
Study
EGAS00001002567
-
Identifying genetic consequences of Epstein-Barr Virus transformation by comparing an individual’s genomic DNA with that of its lymphoblastoid cell line.
Study
EGAS00001000323
-
Native_American_Ancient_DNA_sequencing
Study
EGAS00001001802
-
UAMS Smoldering Myeloma Timeline Cohort
Study
EGAS00001003687
-
RRBS sequencing of 7 tumour regions and a normal sample from a single TRACERx patient.
Study
EGAS00001002484
-
Characterization of a human iPSC-derived endocrine pancreas model
Study
EGAS00001001803
-
Large-scale viral genome analysis identifies novel clinical associations between hepatitis B virus and chronically infected patients
Study
EGAS00001003689
-
Whole-exome sequencing of acute erythroid leukemia
Study
EGAS00001003696
-
Renal_habitat_WXS
Study
EGAS00001003703
-
The 3D evolution of glioma cell populations
Study
EGAS00001003710
-
Chromatin 3D interactions mediate genetic effects on gene expression (RNA-seq)
Dataset
EGAD00001004872
-
Whole exome sequencing of Finnish hereditary breast cancer families
Study
EGAS00001001835
-
Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour
Study
EGAS00001001836
-
Mutated H3 Histones Drive Human Pre-Leukemic Hematopoietic Stem Cell Expansion And Promote Leukemic Aggressiveness
Study
EGAS00001003288
-
Chromosome Y Philogeny in Sardinia
Study
EGAS00001000532
-
From matrimonial practices to genetic diversity in Southeast Asian populations: the signature of the matrilineal puzzle
Study
EGAS00001003727
-
DNA Methylation loss coupled with mitotic cell division promotes immune evasion of tumours with high mutation load
Study
EGAS00001003731
-
Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis
Study
EGAS00001002642
-
A system-wide approach to monitor responses to synergistic BRAF and EGFR inhibition in colorectal cancer cells
Study
EGAS00001002654
-
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH1
Study
EGAS00001001854
-
A targeted gene panel that covers coding, noncoding, and short tandem repeat regions improves the diagnosis of patients with neurodegenerative diseases
Study
EGAS00001003737
-
FinHer_Breast_Cancer_Study
Study
EGAS00001000648
-
Combination_therapies_for_personalized_cancer_medicine
Study
EGAS00001000655
-
Small variants in mtDNA Canary Islands - WES Illumina (ITER)
Study
EGAS00001005678
-
Whole_Genome_Sequencing_of_Human_Organoid_Lines
Study
EGAS00001003538
-
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
-
Variation in the Glucose Transporter gene SLC2A2 is associated with glycaemic response to metformin
Study
EGAS00001001875
-
Growth Hormone (GH) -secreting Pituitary Adenoma
Study
EGAS00001003488
-
Investigating genetic susceptibility to rheumatic heart disease in Oceania
Study
EGAS00001001881
-
Kibbutzim Family study
Study
EGAS00001002782
-
Genetic control of the transcriptomic response of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans
Study
EGAS00001001895
-
Knee_OA_Functional_Genomics
Study
EGAS00001001899
-
Genomics analysis of mucinous tumours of the ovary and related neoplasms
Study
EGAS00001003545
-
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
-
The_contribution_of_POT1_variants_to_sporadic_melanoma_development
Study
EGAS00001001964
-
HipSci___Whole_Exome_sequencing___Battens
Study
EGAS00001001975
-
HipSci___Whole_Exome_sequencing___BPD
Study
EGAS00001001976
-
Mapping_genetic_variants_underlying_gene_regulation_in_inflammed_intestinal_cell_types_to_identify_novel_IBD_drug_targets
Study
EGAS00001003770
-
HipSci___Whole_Exome_sequencing___Cardiomyopathy
Study
EGAS00001001980
-
Physiological and genetic adaptations to diving in Sea Nomads
Study
EGAS00001002823
-
HipSci___Whole_Exome_sequencing___Macular_dystrophy
Study
EGAS00001001982