Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

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Figure 7.
Figure 7.

Copy number variations detected with SOLiD mate-paired reads in NA18507. (A) The size distribution of CNVs detected with SOLiD mate-paired reads. (B) Overlap of copy numbers computed from normalized SOLiD coverage and from Affymetrix array CGH (aCGH) (McCarroll and Altshuler 2007). Colors indicate CNV calls from aCGH. On the top of the figure are the numbers of SOLiD CNV calls that overlap with aCGH data at each copy number.

This Article

  1. Published in Advance June 22, 2009, doi: 10.1101/gr.091868.109 Genome Res. 19: 1527-1541

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