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Detection of Copy Number Alterations Using Single Cell Sequencing
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Analysis of sequence-based copy number variation detection tools for cancer studies

Sheida Nabavi1, Zhengqiu Cai, Peter J Tonellato

  • 1Center for Biomedical Informatics, Harvard Medical School.

AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science
|December 5, 2013
PubMed
Summary

No abstract available in PubMed .

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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.
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