5032 results for "*oma"

in 36.81 milliseconds.

• GIS-LUNGTCR1-2016_SNP-ARRAY_CONTROL

  This dataset contains 15 control SNP-array dataset from 15 EGFR mutant lung adenocarcinoma patients.

  Dataset EGAD00010001176

• Melanoma_SNP6

  Melanoma cell lines CNV by SNP6

  Dataset EGAD00010001216

• RMS_Infinium450K

  Infinium 450K in Rhabdomyosarcoma

  Dataset EGAD00010000897

• Copy number profiling of primary samples and cell lines of retinoblastoma

  Illumina SNP-arrays for matching retinoblastoma-blood pairs and retinoblastoma cell lines.

  Dataset EGAD00010000908

• Gencode_550K

  Lymphoma samples using HumanOmni

  Dataset EGAD00010000949

• Gencode_500K

  Lymphoma samples using 450k

  Dataset EGAD00010000948

• Gencode_15K

  Lymphoma samples using CytoSNP

  Dataset EGAD00010000947

• 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

• EGAD00010000688

  glioma normal samples using 250K

  Dataset EGAD00010000688

• dataset1

  BLUEPRINT DNA Methylation 450K data of mantle cell lymphoma

  Dataset EGAD00010001012

• Illumina_450K

  Primary renal cell carcinoma (RCC), RCC metastases and cell lines by Illumina 450K

  Dataset EGAD00010001001

• EGAD00010000756

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

  Dataset EGAD00010000756

• EGAD00010000754

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

  Dataset EGAD00010000754

• EGAD00010000752

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

  Dataset EGAD00010000752

• EGAD00010000750

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

  Dataset EGAD00010000750

• EGAD00010000758

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

  Dataset EGAD00010000758

• EGAD00010000562

  Medulloblastoma DNA methylation

  Dataset EGAD00010000562

• EGAD00010000552

  Neuroblastoma samples

  Dataset EGAD00010000552

• 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

• 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

• Single-cell multiomics reveals the interplay of clonal evolution and cellular plasticity in hepatoblastoma

  Dataset EGAD00001010049

• Biallelic HMBS Inactivation Defines a Homogenous Clinico-Molecular Subtype of Hepatocellular Carcinoma

  Dataset EGAD00001009745

• Pre-neoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma

  Dataset EGAD00001009669

• Medulloblastoma Illumina RNA-Seq

  Illumina RNA-sequencing of Medulloblastoma primary and relapse tumor.

  Dataset EGAD00001009425

• Medulloblastoma Illumina WGS

  Illumina whole genome sequencing of Medulloblastoma Blood, Primary tumor, and Relapse tumor

  Dataset EGAD00001009424

• Medulloblastoma PDX Primary tumor

  Dataset EGAD00001009484

• Medulloblastoma Cirlce-Seq

  Circle-Seq experiment.

  Dataset EGAD00001009483

• Oesophageal adenocarcinoma scRNAseq from LUD2015-005 study (NCT02735239, EudraCT 2015-005298-19)

  This dataset contains single-cell RNA-seq generated from the LUD2015-005 study (NCT02735239, EudraCT 2015-005298-19) and additional donors with Barrett's oesophagus using the 5' Single Cell Gene Expression assay from 10x Genomics. Samples were generated from oesophageal tumours, Barrett's oesophagus, and normal oesophagus and gastric tissues, with the aim of generating a reference atlas for cell types found in normal and disease-associated tissue states in the upper GI tract. This reference atlas was used as the basis for a deconvolution workflow to estimate the cell composition of bulk transcriptomes from these tissues, and to assess cell type-specific expression patterns of potential predictive biomarkers for immunochemotherapy regimens in this setting.

  Dataset EGAD00001009401

• sc-RNA-Seq soft tissue sarcoma tumoroid biobank

  Dataset EGAD00001009002

• RNA-Seq of primary pediatric kidney tumor controls for the soft tissue sarcoma tumoroid biobank

  Dataset EGAD00001008709

• RNA-Seq soft tissue sarcoma tumoroid biobank

  Dataset EGAD00001008467

• WGS soft tissue sarcoma tumoroid biobank

  Dataset EGAD00001008466

• The T cell receptor repertoire of tumor infiltrating T cells is predictive and prognostic for cancer survival

  Transcriptomic sequencing on pre-immunotherapy melanoma patients.

  Dataset EGAD00001007710

• Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma

  Dataset EGAD00001007762

• Single cell RNA-Seq of Clear Cell Sarcoma of the Kidney

  Dataset EGAD00001007498

• Immunotesting cohort with RNA-seq data of melanoma samples

  This dataset contains RNA-seq raw data in fastq format from 9 melanoma samples. The samples are formalin-fixed paraffin-embedded (FFPE) treated. For target enrichment SureSelect XT Human All Exon V6 was used. The libraries were sequenced in paired-end mode (2 x 50 nt) on a NovaSeq6000 S2 flow cell.

  Dataset EGAD00001006783

• Whole-genome sequencing of a thyroid carcinoma harboring a ETV6-NTRK3 fusion and a NTRK3 G623R mutation (HIPO-021)

  Dataset EGAD00001006243

• ChIP-Seq files for RMS.

  ChIP-Seq files accompanying the paper titled "Identification of Therapeutic Targets in Rhabdomyosarcoma Through Integrated Genomic, Epigenomic, and Proteomic Analyses".

  Dataset EGAD00001006398

• PromethION (and Illumina) WGS and MinION transcriptome for a patient with diffuse large B-cell lymphoma.

  Dataset EGAD00001006204