single-pass sequencing read accuracy improver
DescriptionSprai is a tool to correct sequencing errors in single-pass reads for de novo assembly. It is originally designed for correcting sequencing errors in single-molecule DNA sequencing reads, especially in Continuous Long Reads (CLRs) generated by PacBio RS sequencers. The goal of Sprai is not maximizing the accuracy of error-corrected reads. Instead, Sprai aims at maximizing the continuity (i.e., N50 contig length) of assembled contigs after error correction.
900 other people were interested in this package here. The newest known version of this software is 0.9.9.23+dfsg-2 (Information last updated about 20 hours ago.)
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