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Exome sequence of probands in Barrett's oesophagus families
Dataset
EGAD00001002181
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Dataset for white blood cell and cell-free DNA analyses for detection of residual disease in gastric cancew
Dataset
EGAD00001005750
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Lymphocyte LCM WGS (2020-02-20)
Dataset
EGAD00001005992
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Genome and transcriptome sequence data from a unknown - likely pancreatobiliary / intrahepatic cholangiocarcinoma in liver patient
Dataset
EGAD00001010989
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Whole exome sequencing (WES)
Dataset
EGAD00001011324
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RNA-seq of PBX1 knock-down or overexpressing cell lines
Dataset
EGAD00001011325
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Single-cell RNA and TCR sequencing of 37 PBMC pools of advanced HCC patients.
Dataset
EGAD00001011345
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Co-infection of fungi and bacteria in brain tissue from elderly persons and patients with Alzheimer's disease.
Dac
EGAC00001000797
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Wargo Group Data Access Committee for Neodjuvant Immune Checkpoint Blockade in High-Risk Resectable Melanoma
Dac
EGAC00001001008
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DAC - Molecular patterns of response and treatment failure after frontline venetoclax combinations in older patients with AML
Dac
EGAC00001001461
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DAC for study the impact of urbanization and diet on innate immune responses in healthy Tanzanians
Dac
EGAC00001001531
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T cell receptors of pathogenic CD4 T cells isolated by using distinct phenotypic markers in celiac disease
Dac
EGAC00001002292
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Patient-derived tumor organoids for personalized medicine in a rare case of hepatocellular carcinoma with neuroendocrine differentiation.
Dac
EGAC00001002458
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Evaluating the immune response in treatment-naive hospitalised patients with influenza and COVID-19 Data Access Committee
Dac
EGAC00001002503
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DAC Unravelling the contribution of HIF pathway and its therapeutic potential in human AML leukemia-initiating cells
Dac
EGAC00001002509
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Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants
Dac
EGAC00001002558
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EGAD00010000572
Dataset
EGAD00010000572
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RHD_NC_HC24_Cases
Dataset
EGAD00010000957
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Methylation_WB_RA
Dataset
EGAD00010002610
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Ultra-deep targeted sequencing for studying the accumulation of somatic mutations in cancer-free human skin
Study
EGAS00001004279
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Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia
Study
EGAS00001006878
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Quality of Whole Genome Sequencing from Blood versus Saliva Derived DNA in Cardiac Patients
Study
EGAS00001004115
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: Centromeric cohesion failure invokes a conserved choreography of chromosomal mis-segregations in pancreatic neuroendocrine tumours
Study
EGAS00001004239
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Candidate Gene Case Control Study of Human African Trypanosomiasis in the Democratic Republic of Congo
Study
EGAS00001004365
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Evolutionary trajectories and clonal migration underlying tumor progression and lymph node metastasis in resectable lung cancer
Study
EGAS00001005242