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Control iPSC lines with clinically annotated genetic variants for versatile multi-lineage differentiation
Study
EGAS00001003684
-
UAMS Smoldering Myeloma Timeline Cohort
Study
EGAS00001003687
-
Infant Glioma Molecular Subtype
Study
EGAS00001003714
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Human adipose tissue immune cells
Study
EGAS00001003725
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From matrimonial practices to genetic diversity in Southeast Asian populations: the signature of the matrilineal puzzle
Study
EGAS00001003727
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DNA Methylation loss coupled with mitotic cell division promotes immune evasion of tumours with high mutation load
Study
EGAS00001003731
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A targeted gene panel that covers coding, noncoding, and short tandem repeat regions improves the diagnosis of patients with neurodegenerative diseases
Study
EGAS00001003737
-
Glioblastoma initiating cells are sensitive to histone demethylase inhibition due to epigenetic deregulation
Study
EGAS00001003750
-
Genetics and transcriptomes of pediatric B cell precursor leukemia with gain of chromosome 21
Study
EGAS00001003760
-
Extreme phenotypes define epigenetic and metabolic signatures in cardiovascular diseases.
Study
EGAS00001003780
-
Patient-Derived Lung Cancer Organoid
Study
EGAS00001003786
-
Methylation CYLD cutaneous syndrome
Study
EGAS00001003800
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UPF - Evolutionary Population Genetics lab Data Access Committee
Dac
EGAC00001000244
-
Whole-exome sequencing of Fanconi anemia-like inherited bone marrow failure syndrome
Study
EGAS00001003809
-
Epigenetic and metabolomic data from type 2 diabetes adolescents
Study
EGAS00001003816
-
Whole exome sequencing CYLD cutaneous syndrome
Study
EGAS00001003839
-
Targeted sequencing CYLD cutaneous syndrome
Study
EGAS00001003840
-
RNA sequencing CYLD cutaneous syndrome
Study
EGAS00001003841
-
English Longitudinal Study for Ageing (ELSA) Genetic Data Access
Dac
EGAC00001000270
-
Discovering genetic causes of optic atrophy syndromes through whole exome sequencing
Study
EGAS00001003850
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IDENTIFICATION AND TARGETED MANAGEMENT OF A PATIENT WITH A NEURODEGENERATIVE DISORDER CAUSED BY BIALLELIC MUTATIONS IN SLC5A6
Study
EGAS00001003861
-
Bioscientia Molecular Genetics DAC
Dac
EGAC00001000271
-
Systematic comparative analysis of single-nucleotide variants detection methods from single-cell RNA sequencing data
Study
EGAS00001003883
-
Sequencing data of multiple sarcoma samples for personalized medicine and endotype identification
Study
EGAS00001003981
-
Lindsey E. Jones et al. Patient-derived cells from recurrent tumors that model the evolution of IDH-mutant glioma. Neuro-Oncology Advances, 2020. We established robust, versatile, and well-characterized Patient Derived Cells (PDC) of an IDH1-mutant astrocytoma and an IDH1-mutant oligodendroglioma that represents defined evolutionary stages of chemotherapy-induced hypermutation. The PDCs retain tumor subtype defining features over time as well as classic hallmarks of cancer, including anchorage independent growth and cell immortality. The integrated phylogenies composed of PDCs,single-cell-derived PDCs, patient-derived xenografts, and corresponding spatiotemporal tumor tissue samples also provide new insight into the clonality, evolutionary pattern, and immense mutational load of hypermutated IDH mutant gliomas.
Study
EGAS00001003992
-
Mapping the breast cancer metastatic cascade onto circulating tumour DNA using genetic and epigenetic clonal tracking
Study
EGAS00001004014
-
Uncovering tumor intrinsic and extrinsic factors that regulate hepatocellular carcinoma growth using patient derived xenograft assays
Study
EGAS00001004020
-
Exome Sequencing of Spanish Patients with rare genetic diseases.
Study
EGAS00001004028
-
Human Pancreatic Islet RNAseq - Lund
Study
EGAS00001004042
-
GWAS data on human pancreatic islets from 191 donors - Lund
Study
EGAS00001004044
-
Phenotyping data on human pancreatic islets from 191 donors - Lund
Study
EGAS00001004056
-
Expression profiles and genetic makeup of metastases of a cancer of unknown primary.
Study
EGAS00001004059
-
Organoid cultures of early-onset colorectal cancers reveal distinct and rare genetic profiles
Study
EGAS00001004063
-
Evolutionary Origins of Recurrent Pancreatic Cancer
Study
EGAS00001004097
-
Comprehensive pharmacogenomic characterization of gastric cancer
Study
EGAS00001004106
-
Reference Exome Data for a Northern Brazilian population
Study
EGAS00001004112
-
CD8+ T-cell exhaustion induced by leukemic cells drives progression in Chronic Lymphocytic Leukemia
Study
EGAS00001004116
-
Genomic landscape of inflammatory breast cancer by whole-genome sequencing
Study
EGAS00001004117
-
Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis
Study
EGAS00001004145
-
Cancer immune control needs senescence induction by Stat1 dependent cell cycle regulator pathways in tumours
Study
EGAS00001004151
-
Native American gene flow into Polynesia predating Easter Island settlement
Study
EGAS00001004209
-
Association of DNA-methylation profiles with immune responses in breast cancer patients
Study
EGAS00001004211
-
single-stranded DNA study
Study
EGAS00001005093
-
Analysis of exonic somatic variants in light-chain amyloidosis (ALA) and ALA concomitant with multiple myeloma
Study
EGAS00001004214
-
Resequencing (MIPS) of candidate genes for Keratoconus (2020)
Study
EGAS00001004267
-
Genetic characterization of a Unique Neuroendocrine Transdifferentiation Prostate Circulating Tumor Cell - Derived eXplant (CDX) Model
Study
EGAS00001004272
-
RUNX1 mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
Study
EGAS00001004273
-
Whole genome sequencing of 76 tumor and normal samples from 11 SI-NET patients
Study
EGAS00001005096
-
Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma (arrays set)
Study
EGAS00001004314
-
Multiregion Whole-Exome Sequencing Uncovers the Genetic Evolution and Mutational Heterogeneity of Early-Stage Metastatic Melanoma.
Study
EGAS00001004320
-
Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurological disorders
Study
EGAS00001004326
-
METABRIC: Data from Batra et al (2021); DNA methylation landscapes of 1538 breast cancers reveal a replication-linked clock, epigenomic instability and cis-regulation
Study
EGAS00001004327
-
Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
-
MeDALL Epigenetics group
Dac
EGAC00001000578
-
Phylogenetic reconstruction of breast cancer
Study
EGAS00001004356
-
Sequencing of an adolescent patient with germline RET mutant alveolar rhabdomyosarcoma
Study
EGAS00001004359
-
Genetic diversity and continuity of the population of the UAE
Study
EGAS00001004362
-
Whole-genome sequencing of rare disease patients in a national healthcare system
Study
EGAS00001004364
-
Epigenetic analyses of methylation and nucleosome occupancy in cell-free DNA (cfNOMe)
Study
EGAS00001004370
-
Genomic study of an AT-AML
Study
EGAS00001004392
-
Search for genetic variants influencing gestational weight gain in type 1 diabetes patients by genome wide association method
Study
EGAS00001004408
-
Genome-wide associations of human gut microbiota variation and implications for causal inference analyses
Study
EGAS00001004420
-
Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
Study
EGAS00001004430
-
The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: Defining a Healthy Volunteer Cohort
Study
EGAS00001004434
-
DO NOT USE - Whole genome sequencing of SI-NETs from five patients
Study
EGAS00001004435
-
Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140
Study
EGAS00001004460
-
Collection of Genotypic and Ethnographic Information from Individuals of South African Ethnic Groups
Study
EGAS00001004472
-
Versatile workflow for cell-type resolved transcriptional and epigenetic profiles from cryopreserved human lung
Study
EGAS00001004477
-
Identifying the role of ID3 in DNA repair and maintenance of genome integrity
Study
EGAS00001004478
-
Targets of MEK inhibition in DIPG
Study
EGAS00001004495
-
An epigenetic single-cell atlas of IDH-mutant glioma reveals the role of ATRX in shaping tumor composition
Study
EGAS00001004523
-
Whole genome sequencing for novel neuromuscular disease gene discovery
Study
EGAS00001004535
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma
Study
EGAS00001004551
-
Whole Genome Sequencing of 317 individuals from the Pacific region
Study
EGAS00001004540
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma - RNA-seq
Study
EGAS00001004552
-
Profiling Genome-Wide DNA Methylation Patterns in Human Aortic and Mitral Valves
Study
EGAS00001004559
-
The Genetic Basis of Preeclampsia in an Andean Population Adapted to High Altitude
Study
EGAS00001004625
-
Measurable residual disease in elderly acute myeloid leukemia: results from the PETHEMA-FLUGAZA phase III clinical trial
Study
EGAS00001004574
-
A GWAS for cutaneous leishmaniasis in Brazil
Study
EGAS00001004596
-
The endometrial transcription landscape of MRKH syndrome
Study
EGAS00001004601
-
16 Year Life History and Genomic Evolution of an ER+ HER2- Breast Cancer
Study
EGAS00001004624
-
Genomewide detection of cytosine methylation by single molecule real-time sequencing
Study
EGAS00001004642
-
International consensus definition of DNA methylation subgroups in juvenile myelomonocytic leukemia
Study
EGAS00001004682
-
Mechanisms of active DNA demethylation in human monocytes
Study
EGAS00001004784
-
Chromosomal copy number heterogeneity predicts survival rates across cancers
Study
EGAS00001004702
-
Methylation analysis for plasma DNA of patients with organ transplantation
Study
EGAS00001004788
-
A novel orthotopic patient-derived xenograft model of radiation-induced glioma following medulloblastoma
Study
EGAS00001004709
-
STAT5 is a therapeutically targetable vulnerability in cutaneous T-cell lymphoma
Study
EGAS00001004719
-
Mutational Landscape and Tumor Burden Assessed by Cell-Free DNA in Diffuse Large B-Cell Lymphoma: a Population-based Study
Study
EGAS00001004733
-
Genetic ancestry contributes to somatic mutations in lung cancers from admixed Latin American populations
Study
EGAS00001004752
-
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
-
Epigenome-wide association study of asthma remission in whole blood and nasal epithelium
Study
EGAS00001004766
-
Rna-Seq Leiomyosarcoma subtypes
Study
EGAS00001004783
-
The genetic structure of Norway
Study
EGAS00001004826
-
AGECAN - Interespecies conservation of brain specific DNA methylation in aging and cancer
Study
EGAS00001004851
-
Genomic analysis of a hypermutated gliosarcoma
Study
EGAS00001004864
-
Targeted de-methylation of the FOXP3-TSDR
Study
EGAS00001004867
-
Genetic makeup of agnospheres
Study
EGAS00001004868
-
Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history
Study
EGAS00001005128
-
Targeted sequencing DDR genes in cancer stem cells
Study
EGAS00001004892