-
SNP array files, IDAT files, from 34 members of a Family with a high prevalence of psychosis
Study
EGAS00001004592
-
Mutational Landscape and Tumor Burden Assessed by Cell-Free DNA in Diffuse Large B-Cell Lymphoma: a Population-based Study
Study
EGAS00001004733
-
The genetic structure of Norway
Study
EGAS00001004826
-
Young Boost Trial for Breast Cancer patients
Study
EGAS50000000797
-
Impact of Glycolysis Inhibition on the Epigenome of Synovial Fluid T Cells in Juvenile Idiopathic Arthritis
Study
EGAS50000000808
-
MethylBERT enables read-level DNA methylation pattern identification and tumour deconvolution using a Transformer-based model
Study
EGAS50000000806
-
HipSci_Illumina 450K Methylation analysis_Healthy volunteers
Study
EGAS00001000865
-
Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases
Study
EGAS00001007783
-
Canadian Prostate Cancer Genome Network
Study
EGAS00001000900
-
ATAC-Seq and CTCF ChIP-Seq on the OCIAML-2 cell line
Study
EGAS00001004741
-
Discordant_Monozygotic_Twins_ALS(Genetics)
Study
EGAS50000000908
-
WES samples of patients with anti-PD-1 resistant HNSCC from a non-randomized, open-label phase 1b clinical trial
Study
EGAS50000000729
-
Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Study
EGAS00001001461
-
A GWAS study with the AlpeDPD study cohort
Study
EGAS00001007855
-
Transcriptional and epigenetic profiling of bone marrow blood progenitors across age
Study
EGAS50000001623
-
First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes
Study
EGAS00001001004
-
Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family
Study
EGAS00001000060
-
A benchmark of DNA methylation deconvolution methods for tumoral fraction estimation using DecoNFlow
Study
EGAS50000001529
-
ATAC-seq, H3K27ac CUT&Tag, and UMI-4C in LCLs derived from constitutional MLH1 epimutation carriers and non-carrier relatives
Study
EGAS50000000499
-
Pediatric Papillary Thyroid Carcinoma Whole Exome Sequencing
Study
EGAS00001005187
-
HipSci HumanExome BeadChip analysis - monogenic diabetes
Study
EGAS00001001273
-
Comprehensive Deep Sequencing Atlas in HCC tumors
Study
EGAS00001007694
-
Nala GSI GSAv3 PGx Study
Study
EGAS00001007710
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_WES
Study
EGAS00001007745
-
HipSci_RNASEQ_Battens
Study
EGAS00001001987