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 2.
Figure 2.

Uniquely placed mate pairs provide a more comprehensive sampling of the human genome than the unique placement of each of the tags independently. The coverage is separated by mate-paired data treated as single tags before pairing (mate pairs, unpaired; blue) and mate-paired data treated as mate pairs (mate pairs, paired; pink).

This Article

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

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