Short read fragment assembly of bacterial genomes

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Table 1.

The results of error correction on 454 GS20 reads

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Table 1.

Error correction using SA was applied to each set of reads after trimming ends of reads with phred scores averaging <20 over five bases. Reads were mapped to the original genome by querying a compressed suffix array as described in Lippert et al. (2005).

This Article

  1. Genome Res. 18: 324-330

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