Abstract
DNA sequencing technology has been rapidly evolving, and produces a large number of short reads with a fast rising tendency. This has led to a resurgence of research in whole genome shotgun assembly algorithms. We start the assembly algorithm by clustering the short reads in a cloud computing framework, and the clustering process groups fragments according to their original consensus long-sequence similarity. We condense each group of reads to a chain of seeds, which is a kind of substring with reads aligned, and then build a graph accordingly. Finally, we analyze the graph to find Euler paths, and assemble the reads related in the paths into contigs, and then lay out contigs with mate-pair information for scaffolds. The result shows that our algorithm is efficient and feasible for a large set of reads such as in next-generation sequencing technology.
| Original language | English |
|---|---|
| Article number | 563 |
| Journal | BMC Medical Genomics |
| Volume | 8 |
| Issue number | 2 |
| DOIs | |
| State | Published - 29 May 2015 |
| Externally published | Yes |
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