15028 results for "cancer studies using rna-seq"

in 17.97 milliseconds.

• SNP_dataset_1

  Tissue samples using Illumina HumanOmniExpress-FFPE-12 v1.0 BeadChip

  Dataset EGAD00010001179

• SNP Array CB1003

  SNP Array from CB1003 using Cytoscan HD, Thermo Fisher Scientific

  Dataset EGAD00010002225

• T cell receptors of pathogenic CD4 T cells isolated by using distinct phenotypic markers in celiac disease

  Study EGAS00001005582

• Mitochondrial variants in CPCGene samples

  VCF files containing mitochondrial variant calls using MToolbox

  Dataset EGAD00001003361

• ICGC PanCancer Analysis of Whole Genomes

  The Pancancer Analysis of Whole Genomes (PCAWG) study is an international collaboration to identify common patterns of mutation in more than 2,800 cancer whole genomes from the International Cancer Genome Consortium. Building upon previous work which examined cancer coding regions (Cancer Genome Atlas Research Network, The Cancer Genome Atlas Pan-Cancer analysis project, Nat. Genet. 2013 45:1113), this project is exploring the nature and consequences of somatic and germline variations in both coding and non-coding regions, with specific emphasis on cis-regulatory sites, non-coding RNAs, and large-scale structural alterations.

  Study EGAS00001001692

• The landscape of cancer genes and mutational processes in breast cancer

  The landscape of cancer genes and mutational processes in breast cancer

  Dataset EGAD00001000133

• EGAD00010000462

  SJLGG Case samples using Gene Expression Array

  Dataset EGAD00010000462

• TGCT_Phase1_Controls

  UK TGCT control samples using the Infinium 1.2M array

  Dataset EGAD00010001243

• TGCT_OncoArray_Cases

  UK TGCT case samples using theInfinium OncoArray-500K BeadChip

  Dataset EGAD00010001247

• TGCT_OncoArray_Controls

  UK TGCT controls samples using theInfinium OncoArray-500K BeadChip

  Dataset EGAD00010001246