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Copy number analysis in EBV-positive nodal peripheral T cell lymphoma, unspecified

Kyusam Choi1, Hyunjeong Ju, Young Hyeh Ko

  • 1Samsung Biomedical Research Institute, Samsung Medical Center, Seoul, Korea.

Methods in Molecular Biology (Clifton, N.J.)
|February 16, 2013
PubMed

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Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...