SATRAP: SOLiD assembler translation program

3Citations
Citations of this article
9Readers
Mendeley users who have this article in their library.

Abstract

SOLiD DNA sequences are typically analyzed using a reference genome, while they are not recommended for de novo assembly of genomes or transcriptomes. This is mainly due to the difficulty in translating the SOLiD color-space data into normal base-space sequences. In fact, the nature of color-space is such that any misinterpreted color leads to a chain of further translation errors, producing totally wrong results. Here we describe SATRAP, a computer program designed to efficiently translate de novo assembled colorspace sequences into a base-space format. The program was tested and validated using simulated and real transcriptomic data; its modularity allows an easy integration into more complex pipelines, such as Oases for RNA-seq de novo assembly. SATRAP is available at http://satrap.cribi.unipd.it, either as a multi-step pipeline incorporating several tools for RNA-seq assembly or as an individual module for use with the Oases package.

Cite

CITATION STYLE

APA

Campagna, D., Gasparini, F., Franchi, N., Manni, L., Telatin, A., Vitulo, N., … Valle, G. (2015). SATRAP: SOLiD assembler translation program. PLoS ONE, 10(9). https://doi.org/10.1371/journal.pone.0137436

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