Reconstructing complex regions of genomes using long-read sequencing technology

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Figure 2.
Figure 2.

Concordant and discordant PacBio assemblies. (A) Alignment between PacBio (top) and Sanger (bottom) assemblies for CH17-227A2 using Miropeats (Parsons 1995) shows virtually no differences. Note the uniform sequence coverage between 200- and 300-fold. Mismatches/indels are indicated by vertical blue lines. (B) Alignment between PacBio and Sanger assemblies for clone CH17-41F14. A spike of increased sequence coverage across the internal repeat and the reduced complexity of the repeat compared with the Sanger assembly clearly define a collapse of a higher-order repeat from 20 to 12 kbp within the PacBio assembly. The uniformity of sequence coverage may be used as one indicator of potential misassembly.

This Article

  1. Genome Res. 24: 688-696

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