Accurate and reliable high-throughput detection of copy number variation in the human genome

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Figure 5.
Figure 5.

The CNVfinder algorithm. (#) In case of a gap in genome coverage, two clones are considered as consecutive only if their closest extremities are separated by <1.3 Mb of sequence.

This Article

  1. Published in Advance November 22, 2006, doi: 10.1101/gr.5630906 Genome Res. 16: 1566-1574

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