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 6.
Figure 6.

The distribution of the 193 deletions identified in NA18507 with SOLiD by both the intra-read and inter-read approaches. (Inset) A 328-bp deletion detected using both the inter- and intra-read approaches. Four nonredundant molecules identify the deletion with the intra-read approach while 81 clones identify the deletion with the inter-read approach. This deletion has also been found in the Venter, Watson, and YH genomes.

This Article

  1. Genome Res. 19: 1527-1541

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