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Copy number variation (CNVs) of genomic sequences and their involvement in the development of endometriosis

✍ Scribed by Mafra, F.; Amaro, A.; Pelegrino, R.; Bianco, B.; Barbosa, C.; Christofolini, D.

Book ID
123461972
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
48 KB
Volume
100
Category
Article
ISSN
1556-5653

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## Abstract High‐resolution techniques for analysis of genome copy number (CN) enable the analysis of complex cancer somatic genetics. However, the analysis of these data is difficult, and failure to consider a number of issues in depth may result in false leads or unnecessary rejection of true pos