14982 results for "cancer studies using rna-seq"

in 21.55 milliseconds.

• Osteosarcoma whole genome rearrangement screen

  Genomic libraries (500 bps) will be generated from total genomic DNA derived from Osteosarcoma cancer patients and subjected to short paired end sequencing on the llumina platform. Paired reads will be mapped to build 37 of the human reference genome to facilitate the generation of genome wide copy number information, and the identification of novel rearranged cancer genes and gene fusions.

  Dataset EGAD00001000368

• Triple Negative Breast Cancer Whole Genome Validations

  We propose to definitively characterise the somatic genetics of Triple negative breast cancer through generation of comprehensive catalogues of somatic mutations in 500 cases by high coverage genome sequencing coupled with integrated transcriptomic and methylation analyses. This study will use a bespoke bait set to pulldown regions of interest found in whole genome sequencing to validate mutations found.

  Dataset EGAD00001000662

• Germline sequencing

  Detection of SNV/indels in the germline of pediatric cancer patients with a focus on CHEK2 germline variants. Included in this EGA upload are the parents of the children in EGA uplodad EGAD00001008763.

  Study EGAS00001006651

• MDACC-Yale-breast-cancer

  Dac EGAC00001000298

• DAC Barretos Cancer Hospital

  Dac EGAC00001001077

• Breast cancer sequencing data

  Dac EGAC00001003293

• SMC Breast Cancer DAC

  Dac EGAC00001002381

• National Cancer Center Singapore

  Dac EGAC00001001550

• Radboudumc Cancer Genomics DAC

  Dac EGAC00001001102

• Charbonneau Cancer Institute DAC

  Dac EGAC00001001165

• Charbonneau Cancer Institute DAC

  Dac EGAC00001001280

• Cancer Data Access Commitee

  Dac EGAC00001001436

• DAC Barretos Cancer Hospital

  Dac EGAC00001001592

• Spatial Characterization Breast Cancer

  Dac EGAC00001001673

• Gene expression and Cancer

  Dac EGAC00001001727

• Charbonneau Cancer Institute DAC

  Dac EGAC00001002096