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Detecting PKD1 variants in Polycystic Kidney Disease patients by single-molecule long-read sequencing
Study
EGAS00001002106
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RNA-sequencing of six Pilocytic astrocytoma tumors
Study
EGAS00001002149
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Multisample genomic analysis of solid childhood cancers using high resolution SNP-arrays, Whole Exome Sequencing and Targeted Deep Sequencing.
Study
EGAS00001002662
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Family-based GWAS for CRSwNP
Study
EGAS00001002665
-
Genetics of Microcephalic Osteodysplatics Primordial Dwarfism
Study
EGAS00001000064
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Samples from the Greek island of Crete, MANOLIS cohort
Study
EGAS00001000067
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Whole genome bisulfite sequencing of hepatitis B virus-associated hepatocellular carcinoma tumor and non-cancerous samples
Study
EGAS00001002230
-
An Unusual Genomic Variant of Pancreatic Ductal Adenocarcinoma with an Indolent Clinical Course
Study
EGAS00001002192
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UK10K NEURO FSZNK
Study
EGAS00001000119
-
UK10K_RARE_NEUROMUSCULAR
Study
EGAS00001000101
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Genome-wide DNA methylation profiles by MeDIP-seq of cord blood cells and cord blood mononuclear cells obtained from twins conceived through in vitro fertilization and naturally conceived controls
Study
EGAS00001002248
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This study explored and validated the clinical application of targeted NGS of circulating tumor DNA in identifying tumor-specific mutations and uncovering clinical actionable targets in a variety of solid tumors in large patient cohorts.
Study
EGAS00001002251
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UK10K NEURO ASD SKUSE
Study
EGAS00001000114
-
Whole exome sequencing of cell-free DNA reveals temporo-spatial heterogeneity and identifies treatment-resistant clones in neuroblastoma
Study
EGAS00001002705
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UK10K NEURO IMGSAC
Study
EGAS00001000120
-
UK10K_NEURO_MUIR
Study
EGAS00001000122
-
The_life_history_of_colorectal_cancer_metastases_study_WGS_X10
Study
EGAS00001000864
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We performed whole-exome sequencing and whole epigenome sequencing (RRBS) of samples collected from different time points during radiotherapy from thirty-four ESCC patients. We compared the genetic and epigenetic features of the different time biopsy samples to reveal the changes in ESCC received radiotherapy.
Study
EGAS00001002719
-
Triple_Negative_Breast_Cancer_Whole_Genomes
Study
EGAS00001000092
-
Genetic_Overlap_between_Metabolic_and_Psychiatric_disease
Study
EGAS00001002723
-
Evolutionary analysis of pancreatic cancer and coexistent precursor lesions using whole exome sequencing data
Study
EGAS00001002778
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__pancreas
Study
EGAS00001002726
-
UK10K RARE COLOBOMA
Study
EGAS00001000127
-
UK10K_RARE_FIND
Study
EGAS00001000128
-
Himalayan_population_genetic_study
Study
EGAS00001002731
-
X chromosomal genetic variants are associated with childhood obesity
Study
EGAS00001002738
-
UK10K_OBESITY_SCOOP
Study
EGAS00001000124
-
Somatic_mutation_and_clonal_evolution_in_premalignant_lung_disease___WGS
Study
EGAS00001002747
-
BAMSE (Swedish abbreviation for Children, Allergy, Milieu, Stockholm, Epidemiology)
Study
EGAS00001002746
-
UK10K_RARE_CILIOPATHIES
Study
EGAS00001000126
-
UK10K_RARE_SIR
Study
EGAS00001000130
-
Whole-Genome Sequencing of a Healthy Aging Cohort.
Study
EGAS00001002306
-
Whole_exome_sequencing_of_rare_autoimmune_related_phenotypes
Study
EGAS00001000228
-
A_study_of_the_genetic_basis_of_evation_by_Acute_Myeloid_Leukaemia_of_Graft_vs_Leukaemia_effects_after_allogeneic_bone_marrow_transplantation
Study
EGAS00001000145
-
Sequencing of paediatric High Grade Gliomas and DIPG
Study
EGAS00001002314
-
Investigation_of_mutational_signatures_associated_with_DNMT3A_deficiency_
Study
EGAS00001002329
-
Colorectal adenomas and carcinomas NKI-AvL TGO series Gut2009
Study
EGAS00001002758
-
Comprehensive genetic analysis of uveal melanoma heterogeneity during metastatic progression
Study
EGAS00001002761
-
Insular Celtic population structure and genomic footprints of migration
Study
EGAS00001002769
-
whole genome sequence data of multifocal hepatocellular carcinoma
Study
EGAS00001002338
-
Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome
Study
EGAS00001002344
-
Botswana 15 autosomal unlinked microsatellites
Study
EGAS00001002380
-
Cell fate mapping of human glioblastoma reveals an invariant stem cell hierarchy pre- and post-treatment
Study
EGAS00001002424
-
The demographic history and mutational load of African hunter-gatherers and farmers
Study
EGAS00001002457
-
Sex-biased patterns shaped the genetic history of Roma
Study
EGAS00001004207
-
Sampling of multi-centric lower grade glioma influences management and provides insight into gliomagenesis
Study
EGAS00001002495
-
Local In Time Statistics for processual research
Study
EGAS00001002520
-
Genome-wide genetic and epigenetic dataset of pancreatic acinar cell carcinomas
Study
EGAS00001002533
-
A biobank of patient-derived pediatric brain tumor models
Study
EGAS00001002536
-
Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma
Study
EGAS00001002811