Basecalling with LifeTrace

Article Properties
  • Language
    English
  • DOI (url)
  • Publication Date
    2001/05/01
  • Journal
  • Indian UGC (Journal)
  • Refrences
    12
  • Citations
    10
  • Dirk Walther
  • Gábor Bartha
  • Macdonald Morris
Abstract
Cite
Walther, Dirk, et al. “Basecalling With LifeTrace”. Genome Research, vol. 11, no. 5, 2001, pp. 875-88, https://doi.org/10.1101/gr.177901.
Walther, D., Bartha, G., & Morris, M. (2001). Basecalling with LifeTrace. Genome Research, 11(5), 875-888. https://doi.org/10.1101/gr.177901
Walther D, Bartha G, Morris M. Basecalling with LifeTrace. Genome Research. 2001;11(5):875-88.
Journal Categories
Science
Biology (General)
Science
Biology (General)
Genetics
Technology
Chemical technology
Biotechnology
Description

Can a new algorithm improve the accuracy of DNA sequencing? This paper presents LifeTrace, a novel basecalling algorithm designed to convert raw chromatogram data into nucleotide sequences, addressing challenges in electrophoresis sequencing. LifeTrace emphasizes local chromatogram information to better handle variable peak spacing. LifeTrace was tested against Phred, a widely used basecalling software, using MegaBACE capillary sequencing machines. LifeTrace significantly reduced substitution and insertion/deletion errors, generating more aligned bases in dye-primer and dye-terminator chromatograms. It introduces a new gap-quality score for deletion error detection. LifeTrace offers high-quality basecalls and reliable quality scores, proving effective for MegaBACE capillary sequencing. Its performance improvements translate to more accurate SNP detection and improved genome analysis. The new benchmark protocol offers better discernment in basecaller performance, furthering research into genomics and biotechnology.

Genome Research, known for its focus on genomic technologies, provides the perfect platform for this research. This paper’s detailed description of LifeTrace directly addresses improving basecalling accuracy, aligning with the journal's dedication to innovations in genome analysis and sequencing technology. The emphasis on benchmark testing and SNP detection enhances the study’s significance for genomic research.

Refrences
Citations
Citations Analysis
The first research to cite this article was titled Selecting for Functional Alternative Splices in ESTs and was published in 2002. The most recent citation comes from a 2009 study titled Selecting for Functional Alternative Splices in ESTs . This article reached its peak citation in 2008 , with 3 citations.It has been cited in 7 different journals, 14% of which are open access. Among related journals, the Genome Research cited this research the most, with 3 citations. The chart below illustrates the annual citation trends for this article.
Citations used this article by year