Unlabelled: Next-generation sequencing (NGS) technologies have raised a challenging de novo genome assembly problem that is further amplified in recently emerged single-cell sequencing projects. While various NGS assemblers can use information from several libraries of read-pairs, most of them were originally developed for a single library and do not fully benefit from multiple libraries. Moreover, most assemblers assume uniform read coverage, condition that does not hold for single-cell projects where utilization of read-pairs is even more challenging. We have developed an exSPAnder algorithm that accurately resolves repeats in the case of both single and multiple libraries of read-pairs in both standard and single-cell assembly projects.
Availability And Implementation: http://bioinf.spbau.ru/en/spades
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058921 | PMC |
http://dx.doi.org/10.1093/bioinformatics/btu266 | DOI Listing |
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