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STimage: Robust and interpretable prediction of gene markers and cell types from spatial transcriptomics data
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EGAS50000001503
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EuCANCan: EUropean-CANadian Cancer network
Blog
eucancan
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Adjuvant nivolumab in resected esophageal or gastroesophageal junction cancer: exploratory biomarker analyses from CheckMate 577
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EGAS50000001663
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Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family
Study
EGAS00001000060
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Impact of mutational profiles on response of primary oestrogen receptor-positive breast cancers to oestrogen deprivation
Study
EGAS00001001940
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Inferring expressed genes by whole-genome sequencing of plasma DNA
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EGAS00001001754
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Inactivation of TGFβ receptors in stem cells drives cutaneous squamous cell carcinoma - 30 whole exomes
Study
EGAS00001001892
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Spatial genomic heterogeneity in multiple myeloma revealed by multi- region sequencing
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EGAS00001002111
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Chordoma_Sequencing_Project_Whole_Genome
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EGAS00001000409
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APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UG2G component)
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EGAS00001000545
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CD74-NRG1 fusions in lung adenocarcinoma
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EGAS00001000653
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Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
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EGAS00001000662
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Tracking the origins and drivers of subclonal metastatic expansion in prostate cancer
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EGAS00001000942
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Origins and functional consequence of somatic mitochondrial DNA mutations
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EGAS00001000968
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Frequent alterations in cytoskeleton remodeling genes in primary and metastatic Chinese lung adenocarcinomas
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EGAS00001000982
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Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients
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EGAS00001001257
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Trans-ethnic genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Study
EGAS00001001427
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Searching for variants associated with endometriosis
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EGAS00001001741
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A Genomic History of Aboriginal Australia
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EGAS00001001766
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Rare disruptive mutations in ciliary function genes contribute to testicular cancer susceptibility
Study
EGAS00001001789
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EATL-II STUDY
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EGAS00001001879
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Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
Study
EGAS00001001916
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Divergence between high metastatic tumor burden and low circulating tumor DNA concentration in metastasized breast cancer
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EGAS00001000625
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Transcriptional and functional profiling defines human small intestinal macrophage subsets
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EGAS00001002093
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Myelodysplastic cells in patients re-program mesenchymal stromal cells to establish a transplantable stem cell-niche disease unit.
Study
EGAS00001000716
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Resequencing_candidate_genes_for_male_spermatogenic_impairment
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EGAS00001002157
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Whole exome sequencing for gallbladder cancer in Xinhua Hospital Affiliated to Shanghai Jiao Tong University, School of Medicine
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EGAS00001000853
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Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
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EGAS00001002182
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miR-200-regulated CXCL12β promotes fibroblast heterogeneity and immunosuppression in ovarian cancers
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EGAS00001002184
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Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
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EGAS00001000941
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Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015
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EGAS00001001570
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The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
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EGAS00001001603
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Comparing nodal versus bony metastatic spread using tumour phylogenies
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EGAS00001001801
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Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies
Study
EGAS00001000274
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Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia
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EGAS00001000348
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Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Study
EGAS00001000443
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Reference epigenomes generated as part of the International Human Epigenomics Consortium (IHEC)
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EGAS00001000552
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Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis.
Study
EGAS00001000750
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Tracking the genomic evolution of esophageal adenocarcinoma through neoadjuvant chemotherapy
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EGAS00001001254
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RNA_seq_of_Toxoplasma_gondii_response_in_human_macrophages
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EGAS00001001708
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Novel mutational mechanisms and drivers in Pancreatic Neuroendocrine Tumours
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EGAS00001001732
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Exome Sequencing of Gastric Cancer
Study
EGAS00001000153
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Complete Genomics paired end sequencing; Ovarian cancer
Study
EGAS00001000158
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Exome_sequencing_of_blastic_plasmacytoid_dendritic_cell_neoplasms
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EGAS00001000171
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Association of Age at Diagnosis and Genetic Mutations in Patients with Neuroblastoma
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EGAS00001000213
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Exome-sequencing identifies new oncogenes and tumor suppressor genes recurrently altered in hepatocellular carcinoma
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EGAS00001000217
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Genome Landscape of High-Grade Serous Ovarian Cancer
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EGAS00001000397
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A Genomics-Based Classification of Human Lung Tumors
Study
EGAS00001000647
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High number of somatic mutations found in the healthy blood compartment of a 115-year-old woman reveals oligoclonal hematopoiesis
Study
EGAS00001000660
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Germline and somatic SMARCA4 mutations characterize small-cell carcinoma of the ovary, hypercalcemic type.
Study
EGAS00001000721