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Chromatin 3D interactions mediate genetic effects on gene expression
Study
EGAS00001003485
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The Genetic History of Greenlandic-European contact
Study
EGAS00001004933
-
Whole-exome sequencing of hepatocellular carcinoma biopsies (proteogenomic study)
Study
EGAS00001005073
-
Chronic myelomonocytic leukemia
Study
EGAS00001005107
-
A Phase II Trial of High Dose Interleukin-2 and Multi-site Stereotactic Ablative Radiotherapy for Patients with Metastatic Renal Cell Carcinoma
Study
EGAS00001003605
-
Whole Exome Sequencing of High grade T1 non-muscle invasive bladder cancer
Study
EGAS00001004603
-
RRBS MDACC Lung PreCancer
Study
EGAS00001004610
-
RNA-sequençing of 21 inflammatory hepatocellular adenomas
Study
EGAS00001003685
-
CAR_T_cell_Study
Study
EGAS00001004718
-
High intensity sequencing of plasma cfDNA and WBC gDNA
Study
EGAS00001003755
-
Genetic_vulnerability_of_knockout_cancer_lines
Study
EGAS00001002253
-
Transcriptome sequencing of myelodysplasia
Study
EGAS00001002346
-
Transcriptomic analysis of TFEB overexpression in LT-HSC, ST-HSC and MEP
Study
EGAS00001004969
-
The genomic landscape of childhood acute lymphoblastic leukaemia with intrachromosomal amplification of chromosome 21 (iAMP21-ALL)
Study
EGAS00001004998
-
Targeted sequencing of paired tumour/blood of 78 Ta stage bladder cancer patients
Study
EGAS00001005766
-
Transcriptome sequencing of hepatocellular carcinoma biopsies (proteogenomic study)
Study
EGAS00001005074
-
Whole genome sequencing of 76 tumor and normal samples from 11 SI-NET patients
Study
EGAS00001005096
-
Phylogenetic reconstruction of breast cancer
Study
EGAS00001004356
-
Lothian Birth Cohort 1921 whole genome sequencing study
Study
EGAS00001003818
-
Whole genome sequencing of adult glioblastoma nuclei
Study
EGAS00001005256
-
Single-cell transcriptome sequencing of regulatory and conventional T cells in breast cancer patients and healthy individuals.
Study
EGAS00001002933
-
Lymphoctye_colony_WGS
Study
EGAS00001002948
-
Multiple esclerosis and mixed microbial infections
Study
EGAS00001002957
-
Genomic landscape of signals of positive natural selection in North Eurasia
Study
EGAS00001003955
-
Next Generation Children project - WGS study of patients in NICU and PICU and their families
Study
EGAS00001003002
-
Exome Sequencing of Spanish Patients with rare genetic diseases.
Study
EGAS00001004028
-
Intellance-2: omics data on recurrent glioblastoma patients participating in the Intellance-2 clinical trial, prior to treatment.
Study
EGAS00001005437
-
Bone marrow derived stromal cells from Myelodysplastic Syndromes
Study
EGAS00001005051
-
FAM50A_Disruption_in_TOV21G_Cells___RNAseq
Study
EGAS00001004156
-
Lothian Birth Cohort 1936 whole genome sequencing study
Study
EGAS00001003819
-
Single_cell_resolution_of_human_CNV_body_map
Study
EGAS00001003162
-
Sequencing of cancer autopsies and ctDNA
Study
EGAS00001005109
-
RNA-seq on neuroblastoma PDX model COG-N-519 treated with control miR-1283 and test miR-99b-5p mimics
Study
EGAS00001005581
-
Analysis of exonic somatic variants in light-chain amyloidosis (ALA) and ALA concomitant with multiple myeloma
Study
EGAS00001004214