4.6 Review

Bioinformatics challenges of new sequencing technology

Journal

TRENDS IN GENETICS
Volume 24, Issue 3, Pages 142-149

Publisher

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tig.2007.12.006

Keywords

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Funding

  1. NIGMS NIH HHS [R01 GM083873, R01 GM083873-05] Funding Source: Medline
  2. NLM NIH HHS [R01 LM006845-09, R01 LM006845-08, R01 LM006845] Funding Source: Medline
  3. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM083873] Funding Source: NIH RePORTER
  4. NATIONAL LIBRARY OF MEDICINE [R01LM006845] Funding Source: NIH RePORTER

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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.

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