Genetic of Copy Number Variation: Copy Number Variation In Head and Neck Squamous Cell Carcinoma - Brossura

Hsu, Han Chu; Hsu, Fang-Rong

Brossura

ISBN 10: 3659354295 ISBN 13: 9783659354298

Casa editrice: LAP LAMBERT Academic Publishing, 2013

Riassunto

Copy number variation (CNV) is a variation of large fragment deletions, duplications, insertions and complex multi-loci polymorphism in genome. This variation may cause a change in gene numbers or chromosome abnormalities, and that may lead to disease, like schizophrenia and autism, and may even be related to the generation of tumor and tumor susceptibility. Cancer is the most prevalent diseases worldwide. Therefore, this thesis analyzes and discusses the correlation between the tumor and CNV. We have performed the disease-related CNV analysis using in Affymetrix Human SNP array 6.0, that have investigated blood samples and tumor samples of the head and neck squamous cell carcinoma (HNSCC) from Changhua Christian Hospital and Chang Gung Memorial Hospital in Taiwan respectively. Our aim is to understand HNSCC from a genetic and prognostic point of view and find a disease-specific performance in Taiwanese people.

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Informazioni sull'autore

She graduated from Master's Program of Biomedical Informatics, Feng Chia University, Taiwan. In her Master’s, she mainly focused on the relationships between human DNA and cancer. Currently, she is a RA at Institute of Information Science, Academia Sinica, Taipei, Taiwan, and analyzes ventricular hypertrophy related miRNA and messenger RNA.

Dettagli dell'edizione

• Editore: LAP LAMBERT Academic Publishing
• Data di pubblicazione: 2013
• Lingua: Inglese
• ISBN 10: 3659354295
• ISBN 13: 9783659354298
• Rilegatura: Copertina flessibile
• Numero di pagine: 72
• Contatto del produttore: non disponibile
• Persona responsabile: KreGa Onlinehandel GmbH; 4950000000000; info@krega-onlinehandel.de; ; Birkenweg 31; Brakel; 33034; Germania