-
HipSci___Whole_Exome_sequencing___Ataxia
Study
EGAS00001001978
-
HipSci HumanExome BeadChip analysis - Usher syndrome and congenital eye defects
Study
EGAS00001002008
-
HipSci HumanExome BeadChip analysis - Alport Syndrome
Study
EGAS00001002009
-
UK10K COHORT ALSPAC
Study
EGAS00001000090
-
Reference Exome Data for a Northern Brazilian population
Study
EGAS00001004112
-
Spatiotemporal evolution and inter-patient heterogeneity in primary and recurrent/metastatic head and neck squamous cell carcinoma
Study
EGAS00001007464
-
Exome_Sequencing__to_Identify_Causes_of_Leukaemia_Predisposing_Congenital_Neutropenias
Study
EGAS00001000100
-
UK10K_RARE_HYPERCHOL
Study
EGAS00001000129
-
HipSci HumanExome BeadChip analysis - Bleeding and Platelet disorders
Study
EGAS00001002013
-
Hypothalamic transcriptome in Prader-Willi syndrome
Study
EGAS00001002901
-
HipSci HumanExome BeadChip analysis - Retinitis Pigmentosa
Study
EGAS00001002015
-
An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney disease
Study
EGAS00001001003
-
Genetic_factors_underlying_premature_coronary_heart_disease_in_patients_with_normal_coronary_arteries
Study
EGAS00001000133
-
Native American gene flow into Polynesia predating Easter Island settlement
Study
EGAS00001004209
-
Pediatric Low-Grade Glioma RNA and Targeted Sequencing
Study
EGAS00001004242
-
Matched_Pair_Cancer_Cell_line_Whole_Genomes
Study
EGAS00001000160
-
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Spastic Paraplegia
Study
EGAS00001002021
-
Spatial_transcriptome_analysis_of_Paediatric_Thymus
Study
EGAS00001004281
-
HipSci HumanHT 12 Expression BeadChip analysis - Kabuki syndrome
Study
EGAS00001002022
-
Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
-
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells_RNA
Study
EGAS00001000367
-
HipSci HumanHT 12 Expression BeadChip analysis - Congenital Hyperinsulinia
Study
EGAS00001002025
-
Genomic Epidemiology of Complex Diseases in Population-based Brazilian Cohorts
Study
EGAS00001001245
-
Genome-Wide Association Study of aspirin-induced PUD in a UK cohort
Study
EGAS00001002052
-
Rna-Seq Leiomyosarcoma subtypes
Study
EGAS00001004783
-
Papuan Genomes: whole genome sequencing
Study
EGAS00001001247
-
Engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus
Study
EGAS00001001252
-
Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients
Study
EGAS00001001257
-
Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
Study
EGAS00001002102
-
Sequencing_probands_and_families_with_severe_insulin_resistance_syndromes
Study
EGAS00001000488
-
Detecting PKD1 variants in Polycystic Kidney Disease patients by single-molecule long-read sequencing
Study
EGAS00001002106
-
HipSci RNA sequencing for embryonic stem cell control lines
Study
EGAS00001001727
-
HipSci___Whole_Exome_sequencing___Usher syndrome and congenital eye defects
Study
EGAS00001001985
-
The Genetic Landscape of BCL2 Break Negative Follicular Lymphoma
Study
EGAS00001002164
-
Tracing the origins of relapse in AML to stem cells
Study
EGAS00001002225
-
HipSci Illumina 450K Methylation analysis - monogenic diabetes
Study
EGAS00001001275
-
Pediatric Non-Down Syndrome Acute Megakaryoblastic Leukemia is Characterized by Distinct Genomic Subsets with Varying Outcomes
Study
EGAS00001002183
-
HipSci HumanHT 12v4 Expression BeadChip analysis-Rare_BBS
Study
EGAS00001001276
-
Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS).
Study
EGAS00001002193
-
MeDALL epigenetics study
Study
EGAS00001002169
-
Scalable whole-genome single-cell library preparation without pre-amplification
Study
EGAS00001002170
-
Novel Epigenetic Markers for Toxicity after Intraoperative and Conventional Radiotherapy for Breast Cancer
Study
EGAS00001001279
-
Pediatric HGG WES and RNA-Seq
Study
EGAS00001005687
-
Aging and genome-wide patterns of DNA methylation in an African rainforest hunter-gathering population
Study
EGAS00001002226
-
Regions of common inter-individual DNA methylation differences in human monocytes.
Study
EGAS00001002265
-
Genetic_Heterogeneity_of_the_familial_gastric_neuroendocrine_tumors
Study
EGAS00001002273
-
Determination_of_cell_specific_regulatory_enhancers_in_hematopoetic_models
Study
EGAS00001000586
-
Sequencing of paediatric High Grade Gliomas and DIPG
Study
EGAS00001002314
-
Divergence between high metastatic tumor burden and low circulating tumor DNA concentration in metastasized breast cancer
Study
EGAS00001000625
-
Genome of the Netherlands
Study
EGAS00001000644