✦ LIBER ✦

The use of ultra-dense array CGH analysis for the discovery of micro-copy number alterations and gene fusions in the cancer genome

✍ Scribed by Ewa Przybytkowski; Cristiano Ferrario; Mark Basik

Book ID: 115024452
Publisher: BioMed Central
Year: 2011
Tongue: English
Weight: 770 KB
Volume: 4
Category: Article
ISSN: 1755-8794
DOI: 10.1186/1755-8794-4-16

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Array rank order regression analysis for

Array rank order regression analysis for the detection of gene copy-number changes in human cancer

✍ Chun Cheng; Robert Kimmel; Paul Neiman; Lue Ping Zhao 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 259 KB

Overlay analysis of the oligonucleotide

Overlay analysis of the oligonucleotide array gene expression profiles and copy number abnormalities as determined by array comparative genomic hybridization in medulloblastomas

✍ Ken C. Lo; Michael R. Rossi; Tania Burkhardt; Scott L. Pomeroy; John K. Cowell 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 459 KB

## Abstract Combined analysis of gene expression array data and array‐based comparative genomic hybridization data have been used in a series of 26 pediatric brain tumors to define up‐ and downregulated genes that coincide with losses, gains, and amplifications involving specific chromosome regions

Clinicopathological features and global

Clinicopathological features and global genomic copy number alterations of pilomyxoid astrocytoma in the hypothalamus/optic pathway: comparative analysis with pilocytic astrocytoma using array-based comparative genomic hybridization

✍ Jeon, Yoon-Kyung; Cheon, Jung-Eun; Kim, Seung-Ki; Wang, Kyu-Chang; Cho, Byung-Ky 📂 Article 📅 2008 🏛 Nature Publishing Group 🌐 English ⚖ 552 KB

Tiling-resolution array-CGH reveals the

Tiling-resolution array-CGH reveals the pattern of DNA copy number alterations in acute lymphoblastic leukemia with 21q amplification: the result of telomere dysfunction and breakage/fusion/breakage cycles?

✍ Kuchinskaya, E; Nordgren, A; Heyman, M; Schoumans, J; Corcoran, M; Staaf, J; Bor 📂 Article 📅 2007 🏛 Nature Publishing Group 🌐 English ⚖ 140 KB

Genome-wide analysis of loss of heterozy

Genome-wide analysis of loss of heterozygosity and copy number amplification in uterine leiomyomas using the 100K single nucleotide polymorphism array

✍ Kellen L. Meadows; Danica M.K. Andrews; Zongli Xu; Gleta K. Carswell; Shannon K. 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 329 KB

Comprehensive analysis of loss of hetero

Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization

✍ Ken C. Lo; Dione Bailey; Tania Burkhardt; Paul Gardina; Yaron Turpaz; John K. Co 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 609 KB

## Abstract We have undertaken an extensive high‐resolution analysis of loss of heterozygosity (LOH) in 30 high grade gliomas using the Affymetrix 100K SNP mapping array. Only 70% of LOH events were accompanied by a copy number loss (CNA~loss~), and of the other 30%, the distal region of 17p prefer