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A comprehensive assessment of somatic mutation detection in cancer using whole genome sequencing
Study
EGAS00001001539
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Super enhancers define regulatory subtypes and cell identity in neuroblastoma
Study
EGAS00001004551
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Whole genome sequencing of primary and metastatic Melanoma cases in an Australian cohort.
Study
EGAS00001001552
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PSCP_mutation_analysis_in_hESCs
Study
EGAS00001001561
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Mutational landscape of renal cell carcinoma with venous tumor thrombus
Study
EGAS00001001950
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Integrative multi-omic analyses of malignant pleural mesothelioma
Study
EGAS00001004812
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Integrated genomic characterization of IDH1 mutant Glioma malignant progression
Study
EGAS00001001588
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Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes
Study
EGAS00001001601
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A Phase II Trial of High Dose Interleukin-2 and Multi-site Stereotactic Ablative Radiotherapy for Patients with Metastatic Renal Cell Carcinoma
Study
EGAS00001003605
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Recapitulation of genetic predisposition to medulloblastoma in human neuroepithelial stem cells
Study
EGAS00001003620
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Whole-genome landscape of adult T-cell leukemia/lymphoma
Study
EGAS00001005237
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SCAT_osteosarcoma_sequencing
Study
EGAS00001000196
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RNASeq of PDX and CDX tumours treated with ADC
Study
EGAS00001004562
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BLUEPRINT DNA Methylation 450K data of mantle cell lymphoma
Study
EGAS00001001637
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Spatial and Temporal Homogeneity of Driver Mutations in Diffuse Intrinsic Pointine Glioma
Study
EGAS00001001654
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33 patients with Monoclonal Gammopathy of Undetermined Significance (MGUS) had whole exome sequencing performed. Cells were sorted by FACSAria using CD138, CD19 and CD56 to obtain a pure abnormal plasma cell population. Generated somatic variants were compared to a previous study of 463 multiple myeloma patients.
Study
EGAS00001001658
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Paired exome analysis in urothelial carcinoma
Study
EGAS00001001686
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Whole exome sequencing on primary retinoblastoma tissues and matching lymphocyte DNA.
Study
EGAS00001001690
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Identifying_Novel_Fusion_Genes_in_Myeloma
Study
EGAS00001000220
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Histological Transformation and Progression in Follicular Lymphoma: a Clonal Evolution Study
Study
EGAS00001001709
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Single-cell RNA sequencing on 5063 single T cells isolated from peripheral blood, tumour and adjacent normal tissues from six hepatocellular carcinoma patients.
Study
EGAS00001002072
-
UAMS Smoldering Myeloma Myeloma Sequencing
Study
EGAS00001003629
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Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing
Study
EGAS00001001736
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Evolutionary Genome Analysis of Transformation into Small Cell Carcinomas from Lung Adenocarcinomas
Study
EGAS00001001757
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HYPERMUTATION AND MALIGNANT PROGRESSION IN LOW-GRADE GLIOMA PATIENTS
Study
EGAS00001002368
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Genetic landscape of pediatric Adrenocortical Tumor
Study
EGAS00001000257
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ChIP Seq data of multiple myeloma and plasma cell leukaemia cell lines
Study
EGAS00001002414
-
Volasertib preclinical activity in high-risk hepatoblastoma
Study
EGAS00001004827
-
Pilot study for Illumina TST170 NGS panel on cutaneous T cell lymphoma samples
Study
EGAS00001002567
-
Analysis of tumor periphery and center-specific mutations in renal cell carcinoma
Study
EGAS00001001784
-
Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis
Study
EGAS00001001788
-
RRBS MDACC Lung PreCancer
Study
EGAS00001004610
-
Single cell RNA sequencing of lung adenocarcinoma.
Study
EGAS00001003681
-
Targeted_gene_fusion_sequencing__Fus_seq__in_mesothelioma
Study
EGAS00001000390
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A novel TP53-KPNA3 translocation defines a de novo treatment-resistant clone in osteosarcoma
Study
EGAS00001001805
-
Detecting and tracking circulating tumour DNA copy number profiles during first line chemotherapy in oesophagogastric adenocarcinoma
Study
EGAS00001003695
-
Characterization of patient-derived xenograft models of myxoid liposarcoma either sentitive or resistant to trabectedin
Study
EGAS00001003715
-
Whole exome sequencing for primary lung adenocarcinoma samples
Study
EGAS00001003680
-
Sporadic and endemic Burkitt lymphoma have frequent FOXO1 mutations but distinct hotspots in the AKT recognition motif
Study
EGAS00001003719
-
Cancer and germline exomes consisting of FASTQ paired-end reads from melanoma and lung cancer samples
Study
EGAS00001003723
-
Landscape of somatic mutations and clonal evolution in mantle cell lymphoma
Study
EGAS00001000510
-
DNA Methylation loss coupled with mitotic cell division promotes immune evasion of tumours with high mutation load
Study
EGAS00001003731
-
Tissue and plasma RNA from esophageal cancer and precursor lesions
Study
EGAS00001004939
-
Ultraviolet radiation drives mutations in a subset of mucosal melanomas
Study
EGAS00001004697
-
CASCADE metastatic melanoma study
Study
EGAS00001004950
-
Genomics_of_acral_lentiginous_melanoma
Study
EGAS00001003740
-
Targeted_sequencing_of_cylindroma_patients
Study
EGAS00001002708
-
whole-genome sequencing in 17 ESCC cases and whole-exome sequencing in 71 cases
Study
EGAS00001000709
-
CAF-S3 subset in human breast and ovarian cancers
Study
EGAS00001003344
-
Gene expression profile of mesothelial-derived carcinoma-associated fibroblasts
Study
EGAS00001003747