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 color-space 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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569514PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0137436PLOS

Publication Analysis

Top Keywords

novo assembly
8
satrap solid
4
solid assembler
4
assembler translation
4
translation program
4
program solid
4
solid dna
4
dna sequences
4
sequences typically
4
typically analyzed
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!