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Whole Exome sequencing of Gingivo-buccal Cancer : ICGC-India Project_Batch04
Study
EGAS00001002852
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Exome and RNA sequencing data from 32 ocular and extraocular sebaceous carcinomas
Study
EGAS00001002869
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Association of Age at Diagnosis and Genetic Mutations in Patients with Neuroblastoma
Study
EGAS00001000213
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Exome-sequencing identifies new oncogenes and tumor suppressor genes recurrently altered in hepatocellular carcinoma
Study
EGAS00001000217
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Targeted sequencing of head and neck squamous cell carcinomas
Study
EGAS00001002979
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Spatial Transcriptomics on prostate cancer heterogeneity
Study
EGAS00001003001
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Genome Landscape of High-Grade Serous Ovarian Cancer
Study
EGAS00001000397
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CTCF/cohesin-binding sites are frequently mutated in cancer
Study
EGAS00001003010
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Heritable pulmonary arterial hypertension in a large Iberian family
Study
EGAS00001003123
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A Genomics-Based Classification of Human Lung Tumors
Study
EGAS00001000647
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Understanding human fetal pancreas development using subpopulation sorting and RNA sequencing
Study
EGAS00001003127
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Whole Exome Sequencing of 60 tumor/normal matched liver Cancers (HCC)
Study
EGAS00001003063
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FBSeq: RNA sequencing of human fetal brain.
Study
EGAS00001003214
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A spatiotemporal organ-wide gene expression and cell atlas of the developing human heart
Study
EGAS00001003996
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MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__Exome_
Study
EGAS00001003313
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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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Single-cell RNA-seq of immune cells sorted from human melanoma tumors
Study
EGAS00001003363
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Germline and somatic SMARCA4 mutations characterize small-cell carcinoma of the ovary, hypercalcemic type.
Study
EGAS00001000721
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Whole-exome ultra-high throughput sequencing in brain samples of suicide victims who had suffered from major depressive disorder and control subjects who had died from other causes.
Study
EGAS00001003081
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Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma
Study
EGAS00001000884
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65 prostate cancer cases WGS and transcriptome sequencing project
Study
EGAS00001000888
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SeqControl: Process Control for DNA Sequencing
Study
EGAS00001000899
-
Genetic_profiling_of_mucosal_melanoma
Study
EGAS00001001115
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DIME study: Safety, dose-response and efficacy of treatment with Anaerobutyricum soehgenii on glucose metabolism in human subjects with metabolic syndrome
Study
EGAS00001003498
-
Feasibility and safety of a multi-cancer blood test for screening and intervention
Study
EGAS00001004372
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CTCF-dependent enhancer hijacking by the EVI1 oncogene in leukemia
Study
EGAS00001004808
-
Comparison of 3 protocols for deriving pancreatic progenitors from hPSC with RNA-seq and ATAC-seq
Study
EGAS00001003513
-
Chemotherapy induces canalization of cell state in childhood B-cell precursor acute lymphoblastic leukemia
Study
EGAS00001004407
-
Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets
Study
EGAS00001001002
-
Whole-genome plasma sequencing reveals focal amplifications as a driving force in metastatic prostate cancer
Study
EGAS00001001018
-
Neuroblastoma relapse trio series from the AMC
Study
EGAS00001001183
-
Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma
Study
EGAS00001001190
-
Comparative analysis of somatic variant calling on matched FF and FFPE WGS samples
Study
EGAS00001004456
-
Whole exome sequencing of long-term, never relapse exceptional responders of trastuzumab-treated HER2+ metastatic breast cancer
Study
EGAS00001004486
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___Exome__Novaseq_
Study
EGAS00001003527
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma - RNA-seq
Study
EGAS00001004552
-
Preeclampsia InterPregGen Consortium: Large-scale GWAS meta-analysis of maternal preclampsia cases and controls from Europe and Central Asia. Plus extension of earlier European fetal preeclampsia GWAS meta-analysis (see EGAS00001001048) by adding Central Asian fetal preeclampsia cases and controls. Datasets provided under this study are GWAS meta-analysis summary statistics and individual level GWAS genotype data. Related InterPregGen Consortium data are also provided under studies EGAS00001000416 and EGAS00001000417 (whole genome sequence data for 100 unrelated Uzbeks and 100 unrelated Kazakhs) and EGAS00001001048 (European fetal preeclampsia GWAS summary statistics and genotype data
Study
EGAS00001001266
-
Recurrent adeno-associated virus 2-related insertional mutagenesis in human hepatocellular carcinomas
Study
EGAS00001001284
-
Chromosomal copy number heterogeneity predicts survival rates across cancers
Study
EGAS00001004702
-
Barcoding reveals complex clonal dynamics of de novo transformed human mammary cells
Study
EGAS00001001310
-
MGMT genomic rearrangements contribute to chemotherapy resistance in gliomas
Study
EGAS00001004544
-
A comprehensive assessment of somatic mutation detection in cancer using whole genome sequencing
Study
EGAS00001001539
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma
Study
EGAS00001004551
-
Integrated genomic characterization of IDH1 mutant Glioma malignant progression
Study
EGAS00001001588
-
Spatial and Temporal Homogeneity of Driver Mutations in Diffuse Intrinsic Pointine Glioma
Study
EGAS00001001654