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Targeted sequencing of paired tumour/blood of 78 Ta stage bladder cancer patients
Study
EGAS00001005766
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Transcriptome sequencing of hepatocellular carcinoma biopsies (proteogenomic study)
Study
EGAS00001005074
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Whole genome sequencing of 76 tumor and normal samples from 11 SI-NET patients
Study
EGAS00001005096
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Phylogenetic reconstruction of breast cancer
Study
EGAS00001004356
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Lothian Birth Cohort 1921 whole genome sequencing study
Study
EGAS00001003818
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Whole genome sequencing of adult glioblastoma nuclei
Study
EGAS00001005256
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Single-cell transcriptome sequencing of regulatory and conventional T cells in breast cancer patients and healthy individuals.
Study
EGAS00001002933
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Lymphoctye_colony_WGS
Study
EGAS00001002948
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Multiple esclerosis and mixed microbial infections
Study
EGAS00001002957
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Genomic landscape of signals of positive natural selection in North Eurasia
Study
EGAS00001003955
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Next Generation Children project - WGS study of patients in NICU and PICU and their families
Study
EGAS00001003002
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Exome Sequencing of Spanish Patients with rare genetic diseases.
Study
EGAS00001004028
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Intellance-2: omics data on recurrent glioblastoma patients participating in the Intellance-2 clinical trial, prior to treatment.
Study
EGAS00001005437
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Bone marrow derived stromal cells from Myelodysplastic Syndromes
Study
EGAS00001005051
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FAM50A_Disruption_in_TOV21G_Cells___RNAseq
Study
EGAS00001004156
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Lothian Birth Cohort 1936 whole genome sequencing study
Study
EGAS00001003819
-
Single_cell_resolution_of_human_CNV_body_map
Study
EGAS00001003162
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Sequencing of cancer autopsies and ctDNA
Study
EGAS00001005109
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RNA-seq on neuroblastoma PDX model COG-N-519 treated with control miR-1283 and test miR-99b-5p mimics
Study
EGAS00001005581
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Analysis of exonic somatic variants in light-chain amyloidosis (ALA) and ALA concomitant with multiple myeloma
Study
EGAS00001004214