4055 results for "*oma"

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• Single-cell Omics Glioma Team Data Access Committee

  Dac EGAC00001002256

• Retinoblastoma Data Access Committee - Institut Curie

  Dac EGAC00001002275

• Berlin Neuroblastoma Dataset DAC

  Dac EGAC00001002310

• Lund Melanoma DAC

  Dac EGAC00001002322

• Lymphoma Group

  Dac EGAC00001002336

• Medulloblastoma cfDNA Data Access Commitee

  Dac EGAC00001002368

• DAC Committee for the "PIK3CA mutation in a case of CTNNB1 mutant sinonasal glomangiopericytoma" study

  Dac EGAC00001002371

• Cancer Clinical Research Trust DAC for the 23 WES samples of melanoma subtypes

  Dac EGAC00001002402

• Berlin Neuroblastoma Dataset DAC

  Dac EGAC00001002409

• Patient-derived tumor organoids for personalized medicine in a rare case of hepatocellular carcinoma with neuroendocrine differentiation.

  Dac EGAC00001002458

• DAC for intraphepatic cholangiocarcinoma

  Dac EGAC00001002521

• Berlin Neuroblastoma Patient Genomics Data Access Committee DAC

  Dac EGAC00001002532

• The genomic landscape of early-stage ovarian high grade serous carcinoma Data Access Commitee

  Dac EGAC00001002547

• Sarcoma biology and genomics data access commitee

  Dac EGAC00001002609

• Sarcoma biology and genomics data access committee

  Dac EGAC00001002610

• UEA Genetics of Cholesteatoma DAC

  Dac EGAC00001002612

• Melanoma Institute Australia Data Access Committee

  Dac EGAC00001002614

• Chondrosarcoma DAC

  Dac EGAC00001002632

• Pheochromocytoma and paraganglioma single nuclei RNA-seq

  Dac EGAC00001002657

• Chordoma tissue methylation data

  Dac EGAC00001002759

• Melanoma Study Commitee

  Dac EGAC00001002788

• DAC Sysbio Melanoma

  Dac EGAC00001002793

• Lymphoma Biology and Survival / Applied Tumor Genomics / University of Helsinki

  Dac EGAC00001002849

• Somatic mutations predict an aggressive phenotype in meningioma but do not drive grade progression

  Dac EGAC00001002858

• Tracking the evolution of esophageal squamous cell carcinoma under dynamic immune selection by multi-omics sequencing

  Dac EGAC00001002881

• Data Access Committee for Pediatric Medulloblastoma

  Dac EGAC00001002896

• Follicular lymphoma at diagnosis, treated in first line with immunochemotherapy Data Acces Comitee

  Dac EGAC00001002912

• Iberian Roma Data Access Commitee

  Dac EGAC00001002958

• HCV lymphoma exome sequencing Data Access Commitee

  Dac EGAC00001002999

• Multiple myeloma long-term survivor data access commitee

  Dac EGAC00001003078

• DAC Myeloma Genomic Lab

  Dac EGAC00001003079

• Melanoma Institute Australia Data Access Committee

  Dac EGAC00001003081

• LOGGIC-OE0497_ped_glioma-DAC

  Dac EGAC00001003147

• Multiple myeloma follow-up Data Access Commitee

  Dac EGAC00001003155

• EGAD00000000051

  Sequencing data from matching Renal Carcinoma samples

  Dataset EGAD00000000051

• EGAD00000000052

  Sequencing data from natching Pancreatic Carcinoma samples

  Dataset EGAD00000000052

• EGAD00000000114

  Whole transcriptome sequence data from 18 ovarian clear-cell carcinoma samples and one TOV21G ovarian clear-cell carcinoma cell line

  Dataset EGAD00000000114

• EGAD00000000119

  Genotypes from cell lines derived from breast carcinoma tissue

  Dataset EGAD00000000119

• EGAD00010000574

  Pleuropulmonary blastoma samples using 250K

  Dataset EGAD00010000574

• EGAD00010000584

  WTCCC2 Glaucoma samples using Illumina 670k array

  Dataset EGAD00010000584

• EGAD00010000608

  SNP6 data for seminoma samples

  Dataset EGAD00010000608

• EGAD00010000688

  glioma normal samples using 250K

  Dataset EGAD00010000688

• EGAD00010000672

  Purified plasma cells from bone marrow of Multiple myeloma patient

  Dataset EGAD00010000672

• EGAD00010000682

  glioma samples tumor using 250K

  Dataset EGAD00010000682

• EGAD00010000684

  glioma normal samples using cytoscan

  Dataset EGAD00010000684

• EGAD00010000686

  glioma samples tumor using cytoscan

  Dataset EGAD00010000686

• EGAD00010000750

  German glioma control germline genotypes using Illumina HumanExome-12v1_A array

  Dataset EGAD00010000750

• EGAD00010000752

  German glioma case germline genotypes using Illumina HumanExome-12v1_A array

  Dataset EGAD00010000752

• EGAD00010000754

  UK glioma case germline genotypes using Illumina HumanExome-12v1_A array

  Dataset EGAD00010000754

• EGAD00010000756

  French glioma control germline genotypes using Illumina HumanExome-12v1_A array

  Dataset EGAD00010000756

• EGAD00010000758

  French glioma case germline genotypes using Illumina HumanExome-12v1_A array

  Dataset EGAD00010000758

• Genetic and epigenetic characterization of adenoid cystic carcinoma

  Whole genome sequences of ACC primagrafts, Histone modification maps and transcription factor binding maps for ACC primagrafts and primary tumors. Processed ChIP-seq data is available on GEO under accession number GSE76465.

  Dataset EGAD00001001662

• Genomic analysis of HPV-positive versus HPV-negative oesophageal adenocarcinoma

  Whole exome sequencing was performed to explore the mutational landscape and potential molecular signature of HPV-positive versus HPV-negative OAC. Four hr-HPV-positive and 8 HPV-negative treatment-naive fresh-frozen OAC tissue specimens and matched normal tissue were analysed to identify somatic genomic mutations

  Dataset EGAD00001001660

• TERT rearrangements are frequent in neuroblastoma and identify aggressive tumors

  Whole genome sequencing detected structural rearrangements of TERT in 17/75 high stage neuroblastoma with 5 cases resulting from chromothripsis. Rearrangements were associated with increased TERT expression and targeted immediate up- and down-stream regions of TERT, placing in 7 cases a super-enhancer close to the breakpoints. TERT rearrangements (23%), ATRX deletions (11%) and MYCN amplifications (37%) identify three almost non-overlapping groups of high stage neuroblastoma, each associated with very poor prognosis. This submission contains all newly sequenced samples only.study_refcenter AMC

  Dataset EGAD00001001635

• EGAD00010000051

  Cell line derived from microdissected primary pancreatic ductal adenocarcinoma tissues

  Dataset EGAD00010000051

• EGAD00010000377

  DNA methylation analysis of 6 primary lymphoma samples

  Dataset EGAD00010000377

• EGAD00010000395

  Myeloma case sample genotype using Affymetrix SNP6.0

  Dataset EGAD00010000395

• EGAD00010000429

  DNA methylation analysis of 4 primary lymphoma samples

  Dataset EGAD00010000429

• EGAD00010000452

  Chondrosarcoma case sample genotype using Affymetrix SNP6.0

  Dataset EGAD00010000452

• EGAD00010000468

  Uveal melanoma matched Tumour and blood samples

  Dataset EGAD00010000468

• EGAD00010000488

  Chondroblastoma case sample genotype using Affymetrix SNP6.0

  Dataset EGAD00010000488

• EGAD00010000552

  Neuroblastoma samples

  Dataset EGAD00010000552

• EGAD00010000562

  Medulloblastoma DNA methylation

  Dataset EGAD00010000562

• Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

  Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

  Dataset EGAD00001000001

• Osteosarcoma Sequencing

  Osteosarcoma Sequencing

  Dataset EGAD00001000007

• Familial Melanoma Sequencing

  Familial Melanoma Sequencing

  Dataset EGAD00001000016

• ICGC Germany PedBrain Medulloblastoma Pilot_2_LM

  ICGC Germany PedBrain Medulloblastoma Pilot_2_LM

  Dataset EGAD00001000027

• Pancreatic adenocarcinoma QCMG 20110901

  Pancreatic adenocarcinoma QCMG 20110901

  Dataset EGAD00001000049

• Acral melanoma study whole genomes

  Acral melanoma study whole genomes

  Dataset EGAD00001000060

• Acral melanoma study whole exomes

  Acral melanoma study whole exomes

  Dataset EGAD00001000061

• Kaposi sarcoma exome

  Kaposi sarcoma exome

  Dataset EGAD00001000071

• Integrative Oncogenomics of Multiple Myeloma

  Integrative Oncogenomics of Multiple Myeloma

  Dataset EGAD00001000074

• Splenic Marginal Zone Lymphoma with villous lymphocytes exome sequencing

  Splenic Marginal Zone Lymphoma with villous lymphocytes exome sequencing

  Dataset EGAD00001000081

• Glioma cell lines rearrangement screen

  Glioma cell lines rearrangement screen

  Dataset EGAD00001000090

• Pancreatic adenocarcinoma QCMG 20120201

  Pancreatic adenocarcinoma QCMG 20120201

  Dataset EGAD00001000096

• Meningioma Exome

  Meningioma Exome

  Dataset EGAD00001000099

• SCAT osteosarcoma sequencing

  SCAT osteosarcoma sequencing

  Dataset EGAD00001000107

• Identifying Novel Fusion Genes in Myeloma

  Identifying Novel Fusion Genes in Myeloma

  Dataset EGAD00001000112

• Osteosarcoma Exome Sequencing

  Osteosarcoma Exome Sequencing

  Dataset EGAD00001000118

• Chordoma Exome Sequencing

  Chordoma Exome Sequencing

  Dataset EGAD00001000119

• DATA_SET_ICGC_PedBrainTumor_Medulloblastoma

  DATA_SET_ICGC_PedBrainTumor_Medulloblastoma

  Dataset EGAD00001000122

• Chondrosarcoma Exome

  Chondrosarcoma Exome

  Dataset EGAD00001000125

• Burden of Disease in Sarcoma

  Burden of Disease in Sarcoma

  Dataset EGAD00001000127

• Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

  Sequence reads for pediatric GBM samples for manuscript: Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

  Dataset EGAD00001000134

• DATA FILES FOR NBL

  Neuroblastoma whole genome sequencing

  Dataset EGAD00001000135

• Tumor sample of a serious ovarian carcinoma

  Tumor sample of a serious ovarian carcinoma

  Dataset EGAD00001000139

• Blood sample of serious ovarian carcinoma patient

  Blood sample of serious ovarian carcinoma patient

  Dataset EGAD00001000140

• Osteosarcoma Whole Genome

  Osteosarcoma Whole Genome

  Dataset EGAD00001000147

• Subgroup-specific structural variation across 1,000 medulloblastoma genomes

  Subgroup-specific structural variation across 1,000 medulloblastoma genomes

  Dataset EGAD00001000158

• Whole Genome Sequencing accompanying Genetic landscape of pediatric Rhabdomyosarcoma

  Whole Genome Sequencing accompanying Genetic landscape of pediatric Rhabdomyosarcoma.

  Dataset EGAD00001000164

• Identification of SPEN as a novel cancer gene and FGFR2 as a potential therapeutic target in adenoid cystic carcinoma

  Identification of SPEN as a novel cancer gene and FGFR2 as a potential therapeutic target in adenoid cystic carcinoma

  Dataset EGAD00001000175

• UK10K_RARE_COLOBOMA REL-2012-01-13

  UK10K_RARE_COLOBOMA REL-2012-01-13

  Dataset EGAD00001000179

• UK10K_RARE_COLOBOMA REL-2012-02-22

  UK10K_RARE_COLOBOMA REL-2012-02-22

  Dataset EGAD00001000185

• Neuroblastoma samples

  Neuroblastoma samples

  Dataset EGAD00001000196

• Neuroblastoma samples (Analyses_vcf files)

  Neuroblastoma samples (Analyses_vcf files)

  Dataset EGAD00001000202

• UK10K_RARE_COLOBOMA REL-2012-07-05

  UK10K_RARE_COLOBOMA REL-2012-07-05

  Dataset EGAD00001000206

• A common single nucleotide variant in T is strongly associated with chordoma

  Chordoma is a rare malignant bone tumor that expresses the transcription factor T. We conducted an association study of 40 patients with chordoma and 358 ancestry-matched, unaffected individuals with replication in an independent cohort. Whole-exome and Sanger sequencing of T exons reveals a strong risk association ( allelic odds ratio (OR) = 4.9, P = 3.3x10-11, CI= 2.9-8.1) with the common (minor allelic frequency >5%) non-synonymous SNP rs2305089 in chordoma, which is exceptional in cancer genetics.

  Dataset EGAD00001000226

• Melanoma-TIL Study Exomes

  Melanoma-TIL Study Exomes

  Dataset EGAD00001000243

• Integrative Oncogenomics of multiple myeloma

  Integrative Oncogenomics of multiple myeloma

  Dataset EGAD00001000246

• Integrative Oncogenomics of multiple myeloma

  Integrative Oncogenomics of multiple myeloma

  Dataset EGAD00001000247