-
HGG panel sequencing
Study
EGAS50000000221
-
Cerebrospinal fluid cfDNA sequencing for classification of central nervous system glioma
Study
EGAS50000000060
-
Cancer Genomics, ICR, summary data
Dac
EGAC50000000050
-
PARK7/DJ-1 deficiency modulates microglial activation in response to LPS-induced inflammation
Study
EGAS50000000202
-
Whole Exome Sequencing of Multiple Myeloma Patients
Study
EGAS50000000394
-
cfDNA Methylomes for HCC Detection and Postoperative Monitoring
Study
EGAS50000000450
-
Whole-genome variant calling of individuals from the study of allergic diseases in the Canary Islands
Study
EGAS50000000299
-
Identification of germline variants in Medullary thyroid carcinoma (MTC) by whole- exome sequencing
Study
EGAS50000000061
-
Brazilian Thyroid WES
Dataset
EGAD50000000086
-
Single cell chromatin accessibility allows analysis of the transposable element landscape, revealing shared features of immune tissue-residency
Study
EGAS50000000350
-
WGS
Dataset
EGAD50000000594
-
RNA-seq
Dataset
EGAD50000000595
-
ATAC sequencing of Treg cell subsets
Study
EGAS50000000457
-
Plasma mutation profile of precursor lesions and colorectal cancer using the Oncomine Colon cfDNA Assay
Dataset
EGAD50000000679
-
ISA Nutrition 2015
Dataset
EGAD00010002678
-
cytogenetically visibile inversions
Dataset
EGAD50000000635
-
Whole-exome sequencing of acute myeloid leukemias with aberrations of chromosome 7
Study
EGAS50000000429
-
Full AfricanNeo ModernDNA Study
Study
EGAS50000000006
-
Mid-pass Whole-genome Sequencing in a Malagasy Cohort Uncovers Body Composition Associations
Study
EGAS50000000496
-
The landscape of Usher syndrome-associated transcript isoforms in the human neural retina
Study
EGAS50000000504
-
Center of Medical Genetics Ghent - lab BMN
Dac
EGAC50000000351
-
Genetic investigation of 12q-amplified osteosarcomas
Dataset
EGAD50000000707
-
Genetic investigation of 12q-amplified osteosarcomas
Dac
EGAC50000000340
-
Lactate metabolism in cancer stem cell fate regulation
Study
EGAS50000000063
-
Contribution of specific cell types to the development of Barrett’s esophagus and carcinoma via germline genetic risk
Dac
EGAC50000000235