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Small intestinal plasma cells transcriptome profiles
Study
EGAS00001003345
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Use_of_Deep_Sequencing_to_Dectect_Clonal_Mutations_In_Sun_Exposed_Skin_Epidermis_PART2
Study
EGAS00001000603
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PAGE: Prenatal Assessment of Genomes and Exomes
Study
EGAS00001001713
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HSC_population_dynamics___LEUK4_samples
Study
EGAS00001004247
-
Spatial and temporal genomic evolution in glioblastoma
Study
EGAS00001001033
-
Deciphering Intratumoral Molecular Heterogeneity in Clear Cell Renal Cell Carcinoma with a Radiogenomics Platform
Study
EGAS00001003846
-
Meisal temporal lobe epilepsy sequencing study
Study
EGAS00001003922
-
Mapping_regulatory_variation_in_sensory_neurons_using_IPS_lines_from_the_HIPSCI_project
Study
EGAS00001001149
-
A personalised medicine approach for ponatinib-resistant chronic myeloid leukaemia
Study
EGAS00001001150
-
Sequencing data of multiple sarcoma samples for personalized medicine and endotype identification
Study
EGAS00001003981
-
Reconstruction of complex rearrangement patterns causing the initiation of clear cell renal cell carcinoma.
Study
EGAS00001004015
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Inter and intra - tumor heterogeneity in Colorectal Cancer
Study
EGAS00001002150
-
Identification of point mutations, expression perturbations, and gene fusions in T-cell acute lymphoblastic leukemia by RNA-seq
Study
EGAS00001000536
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Targeted_sequencing_of_blood_DNA_from_Human_twins_
Study
EGAS00001002210
-
Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations
Study
EGAS00001003040
-
Molecular profiling of longitudinally observed small colorectal polyps: a cohort study
Study
EGAS00001003284
-
Genome Wide Association Study:GR@ACE Stage I
Study
EGAS00001003424
-
Evolution of GBM through therapy
Study
EGAS00001003546
-
Exome-sequencing of two UFM individuals and their Fragile X family members.
Study
EGAS00001001737
-
ENU_CCK_81_cetuximab_pilot_project
Study
EGAS00001001743
-
Native_American_Ancient_DNA_sequencing
Study
EGAS00001001802
-
Population whole-genome bisulfite sequencing across two tissues highlights environment as principal source of human methylome variation
Study
EGAS00001001569
-
CONSERTING: integrating copy number analysis with structural variation detection
Study
EGAS00001001202
-
Integrative single-cell and cell-free plasma RNA transcriptomics elucidates placental cellular dynamics
Study
EGAS00001002449
-
LifeLines-DEEP population multi-omix cohort from the noth of the Netherlands.
Study
EGAS00001001704