A novel approach for determining cancer genomic breakpoints in the presence of normal DNA.
CDKN2A (encodes p16(INK4A) and p14(ARF)) deletion, which results in both Rb and p53 inactivation, is the most common chromosomal anomaly in human cancers. To precisely map the deletion breakpoints is important to understanding the molecular mechanism of genomic rearrangement and may also be useful f...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2007-04-01
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Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC1847701?pdf=render |