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. Author manuscript; available in PMC: 2018 Jan 24.
Published in final edited form as: J Comput Biol. 2017 Apr 18;24(11):1071–1080. doi: 10.1089/cmb.2017.0013

FIG. 3.

FIG. 3

Comparison of the N50, U50, NG50, UG50, and UG50% for different bacterial and viral datasets using four different assemblers. Contigs for the bacteria dataset were retrievedfrom Magoc et al. (2013), whereas all other contigs were generated in-house. All datasets were sequenced by using the Illumina MiSeq.