Assembling millions of short DNA sequences using SSAKE

367Citations
Citations of this article
532Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Summary: Novel DNA sequencing technologies with the potential for up to three orders magnitude more sequence throughput than conventional Sanger sequencing are emerging. The instrument now available from Solexa Ltd, produces millions of short DNA sequences of 25 nt each. Due to ubiquitous repeats in large genomes and the inability of short sequences to uniquely and unambiguously characterize them, the short read length limits applicability for de novo sequencing. However, given the sequencing depth and the throughput of this instrument, stringent assembly of highly identical sequences can be achieved. We describe SSAKE, a tool for aggressively assembling millions of short nucleotide sequences by progressively searching through a prefix tree for the longest possible overlap between any two sequences. SSAKE is designed to help leverage the information from short sequence reads by stringently assembling them into contiguous sequences that can be used to characterize novel sequencing targets. © 2007 Oxford University Press.

Cite

CITATION STYLE

APA

Warren, R. L., Sutton, G. G., Jones, S. J. M., & Holt, R. A. (2007). Assembling millions of short DNA sequences using SSAKE. Bioinformatics, 23(4), 500–501. https://doi.org/10.1093/bioinformatics/btl629

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free