-
An Unusual Genomic Variant of Pancreatic Ductal Adenocarcinoma with an Indolent Clinical Course
Study
EGAS00001002192
-
Whole-Genome Sequencing of a Healthy Aging Cohort.
Study
EGAS00001002306
-
Understanding_population_genetics_and_patterns_of_genome_wide_heterozygosity_in_a_sample_of_the_Croatian_isolated_populations__ESGIDalmatians_
Study
EGAS00001000336
-
Sampling of multi-centric lower grade glioma influences management and provides insight into gliomagenesis
Study
EGAS00001002495
-
PanCuRx Translational Research Initiative
Study
EGAS00001002543
-
Cryptic Relatedness in the Singapore Living Biobank Project
Study
EGAS00001002619
-
Genome-wide analysis of genetic risk factors for rheumatic heart disease in Aboriginal Australians provides support for pathogenic molecular mimicry
Study
EGAS00001002678
-
Genomic analysis Nasopharyngeal cancer through whole exome sequencing and whole genomic sequencing.
Study
EGAS00001002788
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_WGS
Study
EGAS00001002857
-
The PEMDAC phase 2 study of pembrolizumab and entinostat in patients with metastatic uveal melanoma
Study
EGAS00001005478
-
A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers.
Study
EGAS00001002975
-
Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma.
Study
EGAS00001000399
-
Integrated Genomic, Epigenetic, and Expression Analyses of Ovarian Cancer Cell Lines
Study
EGAS00001002998
-
Indonesian Genome Diversity Project
Study
EGAS00001003054
-
The evolutionary landscape of colorectal tumorigenesis
Study
EGAS00001003066
-
Duplexseq_of_the_interstrand_crosslinks_WGS
Study
EGAS00001006545
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003138
-
High Altitude Pulmonary Hypertension
Study
EGAS00001003171
-
Population_dynamics_in_abnormal_haematopoiesis
Study
EGAS00001003181
-
Whole genome shotgun sequencing and somatic mutations data in Hepatocellular carcinoma
Study
EGAS00001002578
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
Pancreatic cancer organoids recapitulate disease and allow personalized drug screening
Study
EGAS00001003369
-
Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history
Study
EGAS00001005128
-
STREP GENE: Genetics and Severe Streptococcal Infections
Study
EGAS00001003421
-
Whole genome sequencing with linked reads of pediatric glioblastoma samples
Study
EGAS00001003432
-
Mutational patterns and regulatory networks in epigenetic subgroups of meningioma (H033)
Study
EGAS00001003481
-
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD43291_Novaseq__WG_
Study
EGAS00001003502
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___WG__Novaseq_
Study
EGAS00001003524
-
MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___Exome__Novaseq_
Study
EGAS00001003526
-
A_study_of_the_molecular_pathogenesis_of_Splenic_Marginal_Zone_and_Diffuse_Large_B_Cell_Lymphoma
Study
EGAS00001000335
-
South Asia Rheumatic Heart Disease Genetics Network
Study
EGAS00001003565
-
Pediatric Whole Genome Sequencing Diagnostic Utility
Study
EGAS00001001623
-
Indonesian methylation data
Study
EGAS00001003653
-
Control iPSC lines with clinically annotated genetic variants for versatile multi-lineage differentiation
Study
EGAS00001003684
-
The 3D evolution of glioma cell populations
Study
EGAS00001003710
-
An integrative model of pathway convergence in genetically heterogeneous blast crisis chronic myeloid leukemia (CML)
Study
EGAS00001001751
-
Genomic, transcriptomic and epigenomic profiling of GCTB
Study
EGAS00001003730
-
A targeted gene panel that covers coding, noncoding, and short tandem repeat regions improves the diagnosis of patients with neurodegenerative diseases
Study
EGAS00001003737
-
Genetic landscape of pediatric ependymoma
Study
EGAS00001000254
-
Patient-Derived Lung Cancer Organoid
Study
EGAS00001003786
-
Sequencing of an organoid biobank for childhood kidney cancers that captures disease and tissue heterogeneity.
Study
EGAS00001003853
-
Genomic and epigenomic characterization of juvenile myelomonocytic leukemia (JMML)
Study
EGAS00001002511
-
A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma
Study
EGAS00001003974
-
Organoid cultures of early-onset colorectal cancers reveal distinct and rare genetic profiles
Study
EGAS00001004063
-
Evolutionary Origins of Recurrent Pancreatic Cancer
Study
EGAS00001004097
-
CD8+ T-cell exhaustion induced by leukemic cells drives progression in Chronic Lymphocytic Leukemia
Study
EGAS00001004116
-
Canadian Prostate Cancer Genome Network
Study
EGAS00001000900
-
Targets of MEK inhibition in DIPG
Study
EGAS00001004495
-
SNP array files, IDAT files, from 34 members of a Family with a high prevalence of psychosis
Study
EGAS00001004592
-
Mutational Landscape and Tumor Burden Assessed by Cell-Free DNA in Diffuse Large B-Cell Lymphoma: a Population-based Study
Study
EGAS00001004733
-
The genetic structure of Norway
Study
EGAS00001004826
-
HipSci_Illumina 450K Methylation analysis_Healthy volunteers
Study
EGAS00001000865
-
Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases
Study
EGAS00001007783
-
Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Study
EGAS00001001461
-
Whole exome sequencing of Parkinson's disease patients from the United Kingdom
Study
EGAS00001002156
-
A GWAS study with the AlpeDPD study cohort
Study
EGAS00001007855
-
First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes
Study
EGAS00001001004
-
Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family
Study
EGAS00001000060
-
Pediatric Papillary Thyroid Carcinoma Whole Exome Sequencing
Study
EGAS00001005187
-
HipSci HumanExome BeadChip analysis - monogenic diabetes
Study
EGAS00001001273
-
Comprehensive Deep Sequencing Atlas in HCC tumors
Study
EGAS00001007694
-
Nala GSI GSAv3 PGx Study
Study
EGAS00001007710
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_WES
Study
EGAS00001007745
-
HipSci_RNASEQ_Battens
Study
EGAS00001001987
-
HipSci_RNASEQ_Ataxia
Study
EGAS00001001992
-
T2D-GENES: Exome sequencing
Study
EGAS00001001460
-
HipSci_RNASEQ_BPD
Study
EGAS00001001993
-
HipSci_RNASEQ_Hypertrophic_Cardiomyopathy
Study
EGAS00001001994
-
TRACERx 100: metastatic samples
Study
EGAS00001002415
-
HipSci___Whole_Exome_sequencing___Cardiomyopathy
Study
EGAS00001001980
-
HipSci_RNASEQ_Congenital_hyperinsulinia
Study
EGAS00001001988
-
HipSci_RNASEQ_Macular_Dystrophy
Study
EGAS00001001995
-
Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
-
Double mutant DNMT3A AML: a unique subtype
Study
EGAS00001007966
-
HipSci HumanExome BeadChip analysis - Kabuki syndrome
Study
EGAS00001002007
-
Whole-exome sequencing of breast cancer metastasis and corresponding blood samples
Study
EGAS00001001695
-
HipSci HumanExome BeadChip analysis - Macular Dystrophy
Study
EGAS00001002014
-
WES analysis of a mixed cohort of pituitary tumors
Study
EGAS00001001714
-
mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Study
EGAS00001005202
-
Targeted sequencing of follicular lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001005238
-
The_Little_Princess_Knowledge_Bank_RNAseq
Study
EGAS00001005244
-
Reconstructing the dispersals and adaptive history of Bantu-speaking populations in Africa and North America
Study
EGAS00001002078
-
Epigenetic age deceleration reflects fitness improvements following a six-month endurance exercise intervention
Study
EGAS00001008221
-
RNA-sequencing data from 195 B-cell precursor acute lymphoblastic leukemias and mate pair whole genome sequencing data from 15 B-cell precursor acute lymphoblastic leukemias
Study
EGAS00001001795
-
Molecular subtypes of pancreatic neuroendocrine tumors mutated in MEN1/DAXX/ ATRX explain biological variability
Study
EGAS00001008272
-
IDENTIFICATION AND TARGETED MANAGEMENT OF A PATIENT WITH A NEURODEGENERATIVE DISORDER CAUSED BY BIALLELIC MUTATIONS IN SLC5A6
Study
EGAS00001003861
-
Genetics_of_gene_expression_in_human_macrophage_response_to_Salmonella
Study
EGAS00001002236
-
Investigating genetic susceptibility to rheumatic heart disease in Oceania
Study
EGAS00001001881
-
Sequencing of pancreatic cancer primary tumors and metastases
Study
EGAS00001002186
-
Resolving_the_Genetic_Architecture_of_Aseptic_Loosening_After_Total_Hip_Replacement
Study
EGAS00001001883
-
The molecular landscape of colorectal cancer reveals genetic mutations.
Study
EGAS00001001893
-
Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma
Study
EGAS00001005328
-
HER2_positive_Breast_Cancer_
Study
EGAS00001000042
-
SmMIP-tools:a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data
Study
EGAS00001005359
-
Whole exome sequencing (bam files) of 55 samples of myxofibrosarcoma and 44 matched pairs
Study
EGAS00001005442
-
Pancreatic islets PISA RNA-seq samples
Study
EGAS00001005535
-
PCGP Ph-like ALL
Study
EGAS00001000654
-
HipSci_RNASEQ_PID
Study
EGAS00001001990
-
whole genome sequence data of multifocal hepatocellular carcinoma
Study
EGAS00001002338
-
HipSci___Whole_Exome_sequencing___Alport
Study
EGAS00001001974