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Circumventing intratumoral heterogeneity to identify potential therapeutic targets in hepatocellular carcinoma. Details please contact lifuqiang@genomics and zhaoxin@genomics.cn.
Study
EGAS00001002207
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Comprehensive investigation of genome architecture of gastric adenocarcinoma with whole-genome sequencing in the Chinese population.
Study
EGAS00001002404
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Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
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Integrated genomic characterization of adrenocortical carcinoma
Study
EGAS00001000665
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Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas
Study
EGAS00001000643
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Prognostic relevance of microenvironmental factors CD163 and CD8 combined with EZH2 and chromosome 18 gain in a validation cohort of follicular lymphoma patients of the Lunenburg Lymphoma Biomarker Consortium
Study
EGAS00001002049
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Breast implant-associated anaplastic large cell lymphoma shallow whole genome sequencing for copy number analysis and Whole exome sequencing data.
Study
EGAS00001003962
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Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing - NGS targeted capture control cohort
Study
EGAS00001005325
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Engineering large chromosomal deletions by CRISPR-Cas9
Study
EGAS00001005134
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Aggressive genomic features in clinicallyindolent primary HHV8-negative effusion-based lymphoma
Study
EGAS00001002743
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Targeted sequencing data and shallow whole genome sequencing data of Follicular lymphoma.
Study
EGAS00001005755
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Paired data of primary and relapse central nervous system lymphoma and testicular lymphoma
Study
EGAS00001005833
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Tumor-specific expression of let-7i and miR-192 is associated with resistance to cisplatin-based chemoradiotherapy in patients with larynx and hypopharynx cancer
Study
EGAS00001004001
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POT1_splice_site_mutant_analysis
Study
EGAS00001000571
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Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma
Study
EGAS00001000884
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Study of pediatric hepatocellular carcinoma caused by bile salt export pump deficiency
Study
EGAS00001000749
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Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis.
Study
EGAS00001000750
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Genomic analysis of Smoothened inhibitor resistance in basal cell carcinoma
Study
EGAS00001000845
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Whole exome sequencing for gallbladder cancer in Xinhua Hospital Affiliated to Shanghai Jiao Tong University, School of Medicine
Study
EGAS00001000853
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Alternative splicing isoforms in patient-derived hepatocellular carcinoma cells
Study
EGAS00001002697
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Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies
Study
EGAS00001000274
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Therapeutic Targeting of Ependymoma as Informed by Oncogenic Enhancer Profiling
Study
EGAS00001002696
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Mutational patterns and regulatory networks in epigenetic subgroups of meningioma (H033)
Study
EGAS00001003481
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Genomic analysis of seminomas
Study
EGAS00001000943
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Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
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Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma
Study
EGAS00001001653
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Non-Mendalian inheritance of extrachromosal DNA elements can drive disease evolution in glioblastoma
Study
EGAS00001001878
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Pharmacogenomic landscape of patient-derived cells informs precision oncology therapy
Study
EGAS00001002515
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Spatiotemporal genomic architecture informs precision oncology in glioblsatoma
Study
EGAS00001001880
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Preferential infiltration of distinct Vγ9δ2 T cells into Glioblastoma multiforme
Study
EGAS00001002790
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A Protein Neddylation Inhibitor MLN4924 Suppresses Patient-Derived Glioblastoma Cells via Inhibition of ERK and AKT Signaling
Study
EGAS00001004018
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Mutation-specific non-canonical pathway of PTEN as a distinct therapeutic target for glioblastoma
Study
EGAS00001004753
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Genome-wide genetic and epigenetic dataset of pancreatic acinar cell carcinomas
Study
EGAS00001002533
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Whole exome sequencing of papillary thyroid carcinoma in the Chinese population
Study
EGAS00001001268
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463 newly diagnosed patients with Multiple Myeloma underwent whole exome sequencing of tumour and peripheral blood DNA.
Study
EGAS00001001147
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The Berlin (BLN) panel of glioblastoma cell lines: RNAseq of human gliomasphere cell lines and matched parental tumors
Study
EGAS00001001167
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Whole exome sequencing of cell-free DNA reveals temporo-spatial heterogeneity and identifies treatment-resistant clones in neuroblastoma
Study
EGAS00001002705
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Enhanced reduced representation bisulfite sequencing (eRRBS) on 45 multiple myeloma samples and 3 normal plasma cell
Study
EGAS00001004348
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Copy-number signatures and mutational processes in ovarian carcinoma
Study
EGAS00001002557
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Neuroblastoma relapse trio series from the AMC
Study
EGAS00001001183
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Human melanoma samples with and without resistance to BRAF inhibitor therapy
Study
EGAS00001000992
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Whole Genome sequencing of adult T-cell leukemia/lymphoma
Study
EGAS00001001210
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Anaplastic oligodendroglioma exome and RNA sequencing data
Study
EGAS00001001209
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These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
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Tracking the genomic evolution of esophageal adenocarcinoma through neoadjuvant chemotherapy
Study
EGAS00001001254
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Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis
Study
EGAS00001001258
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Integrated molecular analysis of adult T-cell leukemia/lymphoma
Study
EGAS00001001296
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Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients
Study
EGAS00001001257
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Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
Study
EGAS00001001916
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Telomerase activation by genomic rearrangements in high-risk neuroblastoma
Study
EGAS00001001308
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Reliable assessment of telomere maintenance mechanisms in neuroblastoma
Study
EGAS00001006510
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Genomic analysis of HPV positive versus HPV negative esophageal adenocarcinoma
Study
EGAS00001001340
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Independent development of lymphoid and histiocytic malignancies from a shared early precursor
Study
EGAS00001001353
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Genomes of Relapsing Neuroblastoma
Study
EGAS00001001387
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Carcinoma of the oral tongue (OTSCC) genomic landscape characterisation
Study
EGAS00001001329
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Genetic and epigenetic characterization of adenoid cystic carcinoma
Study
EGAS00001001457
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The role of the mammalian SWI/SNF chromatin remodeling complex in neuroendocrine prostate cancer
Study
EGAS00001004177
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Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418
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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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Genome-wide identification of distinct miRNA-mRNA target regulation pairs in Non-Hodgkin lymphomas: a report from the ICGC MMML-Seq consortium
Study
EGAS00001001394
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MINCR is a MYC-induced lncRNA able to modulate MYC’s transcriptional network in Burkitt lymphoma cells
Study
EGAS00001001199
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Whole-genome bisulfite sequencing analysis of low-grade astrocytomas in the ICGC PedBrain Tumor Project
Study
EGAS00001004019
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Genome-wide expression profiles to compare array-based, RNAseq and NanoString technologies in patients with resected pancreatic ductal carcinoma.
Study
EGAS00001002501
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Whole exome sequencing of an invasive diffuse intrinsic pontine glioma sampled from different sites
Study
EGAS00001002326
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Sequencing of paediatric High Grade Gliomas and DIPG
Study
EGAS00001002314
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Genomic profiling of paediatric high grade gliomas from the HERBY clinical trial
Study
EGAS00001002328
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The evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion
Study
EGAS00001002432
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Chromatin immunoprecipitation linked to next-generation whole genome sequencing (ChIP-Seq) for H3K36me3 in paediatric high grade glioma cell lines KKNS4 and SF188 with and without a G34V mutation in H3F3A
Study
EGAS00001001437
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Melanoma RNA Seq Data commitee
Dac
EGAC00001002928
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Genomic profiling of paediatric glioma cell lines
Study
EGAS00001003006
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Targets of MEK inhibition in DIPG
Study
EGAS00001004495
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Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
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A somatic reference standard for cancer genome sequencing with COLO829
Study
EGAS00001001385
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Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes
Study
EGAS00001001601
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MYO5B mutations in Pheochromocytoma/Paraganglioma promote cancer progression
Study
EGAS00001003991
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The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Study
EGAS00001001603
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Exome-sequencing of human B cell lymphoma cell lines
Study
EGAS00001001463
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Whole exome sequencing on primary retinoblastoma tissues and matching lymphocyte DNA.
Study
EGAS00001001690
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Copy number profiling of primary samples and cell lines of retinoblastoma
Study
EGAS00001001715
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Automated system for scoring hematoxylin and eosin-stained ovarian cancer sections by identifying single cells uncovered that stromal cell ratio is a significant predictor for overall survival and progression-free survival.
Study
EGAS00001001694
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Hodgkin's Lymphoma WGS Commitee
Dac
EGAC00001003015
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Transcriptional regulatory networks of tumor-associated macrophages that drive malignancy in mesenchymal glioblastoma
Study
EGAS00001002443
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Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis
Study
EGAS00001001723
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Searching for variants associated with endometriosis
Study
EGAS00001001741
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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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Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors
Study
EGAS00001001752
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Analysis of tumor periphery and center-specific mutations in renal cell carcinoma
Study
EGAS00001001784
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Mutational landscape of renal cell carcinoma with venous tumor thrombus
Study
EGAS00001001950
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Exome sequencing data from two myelosarcomas
Study
EGAS00001002562
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Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Study
EGAS00001001516
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A novel TP53-KPNA3 translocation defines a de novo treatment-resistant clone in osteosarcoma
Study
EGAS00001001805
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Clonal selection and double hit events involving tumor suppressor genes underlie relapse from total therapy
Study
EGAS00001001810
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Spatial genomic heterogeneity in multiple myeloma revealed by multi- region sequencing
Study
EGAS00001002111
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Subtype specific progression from DCIS to invasive breast cancer
Study
EGAS00001001866
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EATL-II STUDY
Study
EGAS00001001879
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Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma
Study
EGAS00001002811
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Whole-Genome Sequencing of Salivary Gland Adenoid Cystic Carcinoma
Study
EGAS00001002812
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Genomic profiling of esthesioneuroblastoma
Study
EGAS00001003225
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Cancer-Associated Mutations in Endometriosis without Cancer
Study
EGAS00001003576
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Multi-omics analysis of primary glioblastoma cell-lines shows recapitulation of pivotal molecular features of parental tumors
Study
EGAS00001001871