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Security Overview
Documentation
about/security
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Upcycling and merging data to challenge the dogma and identify new therapeutic targets for Glioblastoma
Blog
upcycling-and-merging-data-to-challenge-glioblastoma
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Evolution and clinical impact of genetic epistasis within EGFR-mutant lung cancers
Study
EGAS00001002604
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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
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Baseline RNAseq analysis of POETIC Good/Poor Responders to aromatase inhibitors based on change in Ki67
Study
EGAS00001007302
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Transposable elements are co-opted as oncogenic regulatory elements by lineage-specific transcription factors in prostate cancer
Study
EGAS00001007188
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Epigenetic reprogramming shapes monocytes and heterologous T cell derived cytokine responses in BCG vaccination
Study
EGAS00001007498
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Homologous recombination DNA repair deficiency and activity of PARP inhibition in primary triple negative breast cancer
Study
EGAS00001004190
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Next Generation Sequencing Characterization of Hematopoietic Stem and Progenitors Cells in Human Systemic Lupus Eryhtematosus
Study
EGAS00001003679
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Oncolytic virotherapy mediated anti-tumor response in primary cutaneous B-cell lymphoma: a single-cell perspective
Study
EGAS00001004904
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Second hit rare genetic variants in families with seemingly GBA gene associated Parkinson’s disease
Study
EGAS00001004777
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Study of Melanoma Risk in Australia and the United Kingdom
Study
phs000519
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The UCSD / O'Connor "TSP" (Twin/Sibling/Pedigree) Resource in Hypertension
Study
phs002230
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Proteogenomic Characterization Unveils Biomarkers Associated With Chemoresistance in Muscle Invasive Bladder Cancer
Study
phs004049
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Single-Gene vs. Panel Sequencing in Advanced HR+/HER2− Breast Cancer
Study
EGAS00001008200
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CDK4/6 inhibition in advanced chordoma: final results of the NCT PMO-1601
Study
EGAS00001007985
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University of Miami Udall Center of Excellence Identification of Rare Variants in PD through Whole Exome Sequencing
Study
phs000908
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Zostavax vaccination-induced changes in the T cell receptor repertoire to varicella zoster virus
Study
phs001082
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Mitochondrial Abnormalities in Schizophrenia and Bipolar Disorder
Study
phs002395
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Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders
Study
phs001876
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National Eye Institute (NEI) Genetic Epidemiology of Age-Related Macular Degeneration in the Old Order Amish
Study
phs001361
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Rare Disease Susceptibility Alleles in Children with Crohn Disease
Study
phs000926
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Novel Strategies to Eliminate Resistance to B-cell Receptor Inhibitor Therapy in Lymphoid Malignancies
Study
phs003042
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Genome Sequencing Reveals That RAD50 Hypomorphism Results in Enhanced Sensitivity to Checkpoint Kinase Inhibition Combined with Chemotherapy
Study
phs000706
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Transcriptome sequencing across a prostate cancer cohort identifies PCAT-1, an unannotated lincRNA implicated in disease progression
Study
phs000443
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Rare Mendelian Disease in Old Order Amish and Mennonite Patients
Study
phs000623
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L1-Seq and Genome-Wide SNP Genotyping in a Multiethnic Asian Population
Study
phs000732
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A Phase III Randomized Study of Nivolumab Plus Ipilimumab Versus Nivolumab in Stage IV Squamous Cell Lung Cancer
Study
phs003412
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Integrative Somatic and Germline Computational Biology to Redefine Clinical Actionability in Solid Tumors
Study
phs003141
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Somatic Mutations in 3,929 HPV-Positive Exfoliated Cervical Cell Samples
Study
phs003691
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Nivolumab plus chemotherapy or ipilimumab in gastroesophageal cancer: CheckMate 649 biomarker analyses
Study
EGAS50000000747
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Identifying genetic variants that alter TCR usage in the peripheral repertoire
Study
EGAS00001008189
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Identification and characterization of molecular markers in aging and neuronal disorders
Study
JGAS000230