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Data Analysis Software detects genomic aberrations.

2013-04-29 14:30:21| Industrial Newsroom - All News for Today

Providing analysis of structural variation from CGH array, SNP array, and NGS platforms, Nexus Copy Number v7 supports small sequence variations, such as point mutations, InDels, and inversions. Sequence variations can be interpreted alongside copy number changes for integrated view of genomic aberrations. This feature allows identification of mutations overlapping copy number aberrations or homozygous regions in addition to identification of novel disease causing mutations. This story is related to the following:Data Analysis Software |

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