-
Autozygosity_pilot___Pakistani_from_Birmingham
Study
EGAS00001000511
-
Autozygosity_pilot___British_Pakistani_from_Birmingham_2
Study
EGAS00001000567
-
Low_coverage_whole_genome_sequencing_of_samples_from_the__Cretan_Greek_isolate_collection_HELIC_MANOLIS
Study
EGAS00001000392
-
HipSci-Whole Exome sequencing-healthy volunteers
Study
EGAS00001000592
-
HipSci-RNAseq-healthy volunteers
Study
EGAS00001000593
-
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Kazakhs (DNA samples from the Scientific Center of Obstetrics, Gynecology and Perinatology, Almaty, Kazakhstan; Gulnara Svyatova, Principal Investigator
Study
EGAS00001000417
-
Harnessing_transposons_for_drug_resistance_gene_discovery_in_cancer
Study
EGAS00001000468
-
Molecular Signature of Saudi Thyroid Cancer Using whole exome sequencing
Study
EGAS00001000680
-
Autozygosity_pilot_Born_in_Bradford
Study
EGAS00001000462
-
Bone_Cancer___Rare_Types_Whole_Genome
Study
EGAS00001000501
-
Genetic_factors_underlying_premature_MI_in_Greek_families_without_vessel_disease
Study
EGAS00001000478
-
Identification_of_rare_variants_associated_with_cardiovascular_traits_in_Cilento_isolates
Study
EGAS00001000620
-
Sequencing_probands_and_families_with_severe_insulin_resistance_syndromes
Study
EGAS00001000488
-
miRNA_expression_in_response_to_LPS_stimulus_in_macrophages
Study
EGAS00001000691
-
BRAF_and_MEK_resistant_cell_line_clones
Study
EGAS00001000172
-
CPC-GENE Prostate Cancer Heterogeneity Study
Study
EGAS00001000549
-
Assessing the impact of low frequency coding variants on disease risk using the Exomechip
Study
EGAS00001000584
-
Osteosarcoma_RNAseq
Study
EGAS00001000615
-
Combination_therapies_for_personalized_cancer_medicine
Study
EGAS00001000655
-
Exploration of CNV’s and SNV’s in cancers with well-known genetic rearrangements: Identification of additional genetic changes in rearrangements-driven cancer
Study
EGAS00001000673
-
Epigenetic Intratumor Heterogeneity and Clonal Evolution in Aggressive Prostate Cancer
Study
EGAS00001000682
-
Association studies using the Metabochip array - Samples analysed by the WTCCC (1958 British Birth Cohort (58BC), Hypertension cohort (HT), Type 2 Diabetes Cohort (T2D) and Coronary Artery Disease (CAD) cohort)
Study
EGAS00000000115
-
Lung_Cancer_Whole_Genomes
Study
EGAS00001000148
-
Paroxysmal neurological disorders
Study
EGAS00001000048
-
Samples from the Greek island of Crete, MANOLIS cohort
Study
EGAS00001000067