Fragment assembly with short reads.

TitleFragment assembly with short reads.
Publication TypeJournal Article
Year of Publication2004
AuthorsChaisson M, Pevzner P, Tang H
JournalBioinformatics
Volume20
Issue13
Pagination2067-74
Date Published2004 Sep 1
ISSN1367-4803
KeywordsAlgorithms, Base Sequence, Contig Mapping, Feasibility Studies, Gene Expression Profiling, Molecular Sequence Data, Sequence Alignment, Sequence Analysis, DNA
Abstract

MOTIVATION: Current DNA sequencing technology produces reads of about 500-750 bp, with typical coverage under 10x. New sequencing technologies are emerging that produce shorter reads (length 80-200 bp) but allow one to generate significantly higher coverage (30x and higher) at low cost. Modern assembly programs and error correction routines have been tuned to work well with current read technology but were not designed for assembly of short reads.

RESULTS: We analyze the limitations of assembling reads generated by these new technologies and present a routine for base-calling in reads prior to their assembly. We demonstrate that while it is feasible to assemble such short reads, the resulting contigs will require significant (if not prohibitive) finishing efforts.

AVAILABILITY: Available from the web at http://www.cse.ucsd.edu/groups/bioinformatics/software.html

DOI10.1093/bioinformatics/bth205
PubMed URLhttp://www.ncbi.nlm.nih.gov/pubmed/15059830?dopt=Abstract
Alternate JournalBioinformatics
PubMed ID15059830