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DeAnnCNV: a tool for online detection and annotation of copy number variations from whole-exome sequencing data

Yuanwei Zhang1, Zhenhua Yu2, Rongjun Ban2

  • 1Molecular and Cell Genetics Laboratory, The CAS Key Laboratory of Innate Immunity and Chronic Disease, Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei 230027, China.

Nucleic Acids Research
|May 28, 2015
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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