-
Genetic landscape of pediatric Low Grade Gliomas & Glioneuronal tumors
Study
EGAS00001000255
-
Native_American_Ancient_DNA_sequencing
Study
EGAS00001001802
-
Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region mutation and known pathogenic mutation in SPG11
Study
EGAS00001001849
-
Whole_genome_sequencing_of_Italian_genetic_isolates__Friuli_Venezia_Giulia
Study
EGAS00001000252
-
Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies
Study
EGAS00001000274
-
Recent genetic history of Denmark
Study
EGAS00001001868
-
Identification_of_low_frequency_variants_associated_with_ulcerative_colitis_using_whole_genome_sequencing
Study
EGAS00001000329
-
Genetic landscape of pediatric Medulloblastoma
Study
EGAS00001000347
-
Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia
Study
EGAS00001000348
-
Balanced_Brain_Tumour_Whole_Genome_Sequencing
Study
EGAS00001000360
-
Identification_of_rare_variants_associated_with_cardiovascular_traits_in_Cilento_isolates
Study
EGAS00001000620
-
A sequence-based genetic dissection of human immune cell types and implications for immune-related disease.
Study
EGAS00001000574
-
Novel regional age-associated DNA methylation changes within human common disease-associated loci
Study
EGAS00001001910
-
Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
-
Identification_of_the_underlying_causal_variant_in_a_multi_generational_family_with_autosomal_dominant_common_variable_immunodeficiency
Study
EGAS00001000269
-
HG Transcriptome sequencing in the INTERVAL cohort
Study
EGAS00001003346
-
Breast_Cancer_FRT_RNA_seq
Study
EGAS00001000420
-
HipSci_RNASEQ_Spastic_paraplegia
Study
EGAS00001001991
-
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Study
EGAS00001000443
-
Genetic_factors_underlying_premature_MI_in_Greek_families_without_vessel_disease
Study
EGAS00001000478
-
Whole_Genome_sequencing_of_individuals_from_Val_Borbera__Italy
Study
EGAS00001000458
-
An_exome_sequencing_study_of_the_HIV_elite_long_term_non_progressors_and_rapid_progressors__CASCADE_cohorts_
Study
EGAS00001000522
-
Detecting PKD1 variants in Polycystic Kidney Disease patients by single-molecule long-read sequencing
Study
EGAS00001002106
-
Assessing the impact of low frequency coding variants on disease risk using the Exomechip
Study
EGAS00001000584
-
The molecular landscape of colorectal cancer (17 cases)
Study
EGAS00001002174