11769 results for "cancer rna-seq"

in 32.49 milliseconds.

• The NOWAC blood-breast cancer commitee data access agreement

  Dac EGAC00001000684

• Ludwig Data Access Committee for the Study of Oesophageal Cancer

  Dac EGAC00001000978

• Children's Cancer Therapy Development Institute Data Access Commitee

  Dac EGAC00001001160

• Latency and interval therapy affect the evolution in metastatic colorectal cancer.

  Dac EGAC00001001198

• Zero Childhood Cancer

  Dac EGAC00001001683

• Whole Exome Sequencing of Mixed Histology Lung Cancer at MDACC

  Dac EGAC00001002034

• Peter MacCallum Cancer Centre Research Data Access Committee

  Dac EGAC00001002510

• Garvan/St Vincent’s Prostate Cancer Tissue and Data Access Committee

  Dac EGAC00001002769

• Hoag Family Cancer Institute Carcinoid Multiomic Study Data Access Committee

  Dac EGAC00001003084

• TCR sequencing of TIL in breast cancer data access committee

  Dac EGAC00001003173

• EGAD00010000554

  SNP 6.0 arrays of small cell lung cancer

  Dataset EGAD00010000554

• EGAD00010000556

  SNP 6.0 arrays of small cell lung cancer

  Dataset EGAD00010000556

• OvCan2

  Digital images of ovarian cancer metastases

  Dataset EGAD00010001099

• Human Throid Cancer and CDK4/6 inhibition Data Access Commitee

  Dac EGAC00001003446

• Netherlands Cancer Institute (NKI) - Wilbert Zwart Group

  Dac EGAC00001003257

• Unraveling the genetics of transformed splenic marginal zone lymphoma

  Study EGAS00001006389

• Mechanisms of duodenal adenoma development in familial polyposis syndromes

  Study EGAS00001006561

• Resident memory CD8 T cell in human lung cancer

  Study EGAS00001004707

• Single cell RNAseq of PBMC from bladder cancer patients

  Study EGAS00001004458

• Genomic Analysis of a Metastatic Fusion-negative Embryonal Rhabdomyosarcoma

  Study EGAS00001006946

• University of Melbourne Centre for Cancer Research (UMCCR) Data Access Committee

  Dac EGAC00001003567

• INTEGRATIVE MOLECULAR ANALYSIS OF SKIN TUMORS FROM CYLD CUTANEOUS SYNDROME PATIENTS

  CYLD cutaneous syndrome (CCS) is a rare autosomal dominant disorder characterized by germline CYLD mutations and by multiple benign skin tumors dependent on NF-kB pathway. We assembled a large cohort of CCS rare skin tumors that was profiled with whole exome or genome sequencing, RNA sequencing and methylation arrays to better understand genetic mechanisms of CCS tumorogenesis.

  Dataset EGAD50000000362

• Ischemia Reperfusion Responses in Human Lung Transplants at the Single Cell Resolution

  Ischemia reperfusion is an unavoidable step of organ transplantation. Development of therapeutics for lung injury during transplantation has proved challenging; understanding lung injury from human data at the single cell resolution is required to accelerate the development of therapeutics. Donor lung biopsies from six human lung transplant cases were collected at the end of cold preservation and 2-hour reperfusion and underwent single cell RNA sequencing.

  Dataset EGAD50000000704

• Single-cell Transcriptome Analysis of Plasma Cells Across the Disease Spectrum of Multiple Myeloma

  This dataset includes FastQ files of single-cell RNA sequencing data of 5' GEX and VDJ libraries from CD138+ plasma cells enriched from 72 bone marrow aspirates from patients diagnosed with a monoclonal gammopathy from the multiple myeloma spectrum, including MGUS (n=13), SMM (n = 22), NDMM (n = 17), RRMM (n = 15) and PCL (n = 2); and 3 controls.

  Dataset EGAD50000001179

• Transcriptome profiling of head and neck squamous cell carcinomas with paired patient-derived xenografts

  This dataset includes transcriptome profiling of 88 head and neck primary patient tumor samples and 45 paired patient-derived xenograft samples that successfully engrafted in mice. NGS was performed using the Illumina TruSeq stranded total RNA sample preparation kit on the Illumina NovaSeq X Plus platform at the Princess Margaret Genomics Centre. This dataset consists of paired-end fastq files.

  Dataset EGAD50000000995