7297 results for "canc*"

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• Genetic mechanisms of resistance to chemotherapy in breast cancer

  Resistance towards chemotherapy is one of the main causes of treatment failure and deathamong breast cancer patients.The main objective of this project is toidentify genetic mechanisms causing some breast cancer patients not torespond to a particluar type of chemotherapy (epirubicin) while otherpatients respond very well to the same treatment. In the project wewill perform genome / exome sequencing of a selection of breast cancerpatients (n=30). These patients are drawn from a cohort where allpatients have recieved treatment with epirubicin monotherapy before surgical removal of alocally advanced breast tumour, and where all patients have beensubjected to objective evaluation of the response to thetherapy. Subsequent to sequencing, we will analyse the data andcompare with the clinical data for each patient (object response totherapy). The main aim being to identify mutations that are associatedwith resistance to epirubicin. Identification of mutations with strongpredictive value, may have a direct impact on cancer treatment sinceit opens the possibility for genetic testing of a tumour, and desicionon which drug is likely to work best, prior to treatment start.

  Dataset EGAD00001000264

• Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR01

  Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR01

  Dataset EGAD00001000272

• Breast Cancer Exome Sequencing

  Breast Cancer Exome Sequencing

  Dataset EGAD00001000110

• Mutational landscapes of primary triple negative breast cancers - Exomes

  Mutational landscapes of primary triple negative breast cancers - Exomes

  Dataset EGAD00001000113

• Mutational landscapes of primary triple negative breast cancers - WGS

  Mutational landscapes of primary triple negative breast cancers - WGS

  Dataset EGAD00001000115

• Breast Cancer Whole Genome Sequencing

  Breast Cancer Whole Genome Sequencing

  Dataset EGAD00001000121

• HER2 positive Breast Cancer

  HER2 positive Breast Cancer

  Dataset EGAD00001000126

• Breast Cancer Matched Pair Cell Line Whole Genomes

  Breast Cancer Matched Pair Cell Line Whole Genomes

  Dataset EGAD00001000130

• Mutational landscapes of primary triple negative breast cancers - RNA seq

  Mutational landscapes of primary triple negative breast cancers - RNA seq

  Dataset EGAD00001000132

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

  The landscape of cancer genes and mutational processes in breast cancer

  Dataset EGAD00001000133

• Mutational processes moulding the genomes of 21 breast cancers

  The expression data for this study can be found here: http://www.ebi.ac.uk/arrayexpress/experiments/E-MTAB-1088/and its SNP6 data can be found here:http://www.ebi.ac.uk/arrayexpress/experiments/E-MTAB-1087/

  Dataset EGAD00001000138

• Triple Negative Breast Cancer Whole Genomes

  Triple Negative Breast Cancer Whole Genomes

  Dataset EGAD00001000141

• Lung Cancer Whole Genomes

  Lung Cancer Whole Genomes

  Dataset EGAD00001000144

• Matched Pair Cancer Cell line Whole Genomes

  Matched Pair Cancer Cell line Whole Genomes

  Dataset EGAD00001000145

• A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome

  A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome

  Dataset EGAD00001000149

• Massive genomic rearrangement acquired in a single catastrophic event during cancer development

  Massive genomic rearrangement acquired in a single catastrophic event during cancer development

  Dataset EGAD00001000002

• CLL cancer Sample Sequencing

  CLL cancer Sample Sequencing

  Dataset EGAD00001000004

• Various Cancer Fusion Gene Sequencing

  Various Cancer Fusion Gene Sequencing

  Dataset EGAD00001000005

• CLL Cancer Whole Genome Sequencing

  CLL Cancer Whole Genome Sequencing

  Dataset EGAD00001000013

• Renal Cancer Exome Sequencing

  Agilent whole exome hybridisation capture will be performed on genomic DNA derived from 25 renal cancers and matched normal DNA from the same patients. Three lanes of Illumina GA sequencing will be performed on the resulting 50 exome libraries and mapped to build 37 of the human reference genome to facilitate the identification of novel cancer genes.

  Dataset EGAD00001000014

• Human Colorectal Cancer Exome Sequencing

  Human Colorectal Cancer Exome Sequencing

  Dataset EGAD00001000031

• "Single nucleotide variant detection in multiple foci of three prostate cancer tumors"

  "Single nucleotide variant detection in multiple foci of three prostate cancer tumors"

  Dataset EGAD00001000035

• "Copy number variant detection in multiple foci of three prostate cancer tumors"

  "Copy number variant detection in multiple foci of three prostate cancer tumors"

  Dataset EGAD00001000036

• Somatic mutation of SF3B1 in myelodysplasia with ring sideroblasts and other cancers

  Somatic mutation of SF3B1 in myelodysplasia with ring sideroblasts and other cancers

  Dataset EGAD00001000045

• Gastric Cancer Exome Sequencing

  Gastric Cancer Exome Sequencing

  Dataset EGAD00001000046