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 1.
Figure 1.

Cumulative plot of sequence and clone coverage from uniquely placed fragments and uniquely placed mate pairs. The sequence coverage is derived from the fragment, 2 × 25 mate-paired, and 2 × 50 mate-paired libraries while the clone coverage is from only the mate-paired libraries (2 × 25 and 2 × 50).

This Article

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

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