Abstract

New DNA sequencing technologies can sequence up to one billion bases in a single day at low cost, putting large-scale sequencing within the reach of many scientists. Many researchers are forging ahead with projects to sequence a range of species using the new technologies. However, these new technologies produce read lengths as short as 35-40 nucleotides, posing challenges for genome assembly and annotation. Here we review the challenges and describe some of the bioinformatics systems that are being proposed to solve them. We specifically address issues arising from using these technologies in assembly projects, both de novo and for resequencing purposes, as well as efforts to improve genome annotation in the fragmented assemblies produced by short read lengths.

Keywords

BiologyComputational biologyDNA sequencingEvolutionary biologyGeneticsBioinformaticsGene

MeSH Terms

AnimalsComputational BiologyGenomeHumansSequence AnalysisDNA

Affiliated Institutions

Related Publications

Publication Info

Year
2008
Type
review
Volume
24
Issue
3
Pages
142-149
Citations
509
Access
Closed

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

509
OpenAlex
12
Influential
357
CrossRef

Cite This

Mihai Pop, Steven L. Salzberg (2008). Bioinformatics challenges of new sequencing technology. Trends in Genetics , 24 (3) , 142-149. https://doi.org/10.1016/j.tig.2007.12.006

Identifiers

DOI
10.1016/j.tig.2007.12.006
PMID
18262676
PMCID
PMC2680276

Data Quality

Data completeness: 86%