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somatic copy number alterations (cnas)
How are CNAs Detected?
Various technologies are used to detect CNAs, including:
Comparative Genomic Hybridization (CGH)
: This technique compares the DNA of cancer cells to normal cells to identify gains and losses of DNA segments.
Next-Generation Sequencing (NGS)
: High-throughput sequencing can identify CNAs with high resolution and accuracy.
Single Nucleotide Polymorphism (SNP) Arrays
: These arrays can detect CNAs by analyzing variations in single nucleotide polymorphisms across the genome.
Frequently asked queries:
What are Somatic Copy Number Alterations (CNAs)?
How Do CNAs Contribute to Cancer?
How are CNAs Detected?
What are Some Examples of CNAs in Cancer?
What is the Clinical Significance of CNAs?
What are the Challenges in Studying CNAs?
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