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POS-02.12: Analysis of genome-wide copy number changes in bladder cancers using array-based comparative genomic hybridization

✍ Scribed by S. Eguchi; Y. Yamamoto; Y. Chochi; T. Furuya; A. Oga; S. Kawauchi; S. Sakano; H. Matsuyama; K. Sasaki; N. Naito


Book ID
116948382
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
60 KB
Volume
70
Category
Article
ISSN
0090-4295

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Detection of exonic copy-number changes
✍ Yoann Saillour; Mireille CossΓ©e; France Leturcq; AurΓ©lie Vasson; Caroline Beugne πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 517 KB

Genomic copy-number variations (CNVs) involving large DNA segments are known to cause many genetic disorders. Depending on the changes, they are predicted to lead either to decreased or an increased gene expression. However, the ability to detect smaller exonic copy-number changes has not been explo