Error-correcting properties of the SOLiD Exact Call Chemistry

BMC Bioinformatics

Research Article

Nick Goldman¹  Tim Massingham¹ 

[1] European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, UK;

关键词: Error Type;    Linear Code;    Parity Check;    Convolutional Code;    Parity Check Matrix;   

DOI  :  10.1186/1471-2105-13-145

 received in 2012-01-31, accepted in 2012-06-22,  发布年份 2012

来源: Springer

【 摘 要 】

BackgroundThe Exact Call Chemistry for the SOLiD Next-Generation Sequencing platform augments the two-base-encoding chemistry with an additional round of ligation, using an alternative set of probes, that allows some mistakes made when reading the first set of probes to be corrected. Additionally, the Exact Call Chemistry allows reads produced by the platform to be decoded directly into nucleotide sequence rather than its two-base ‘color’ encoding.ResultsWe apply the theory of linear codes to analyse the new chemistry, showing the types of sequencing mistakes it can correct and identifying those where the presence of an error can only be detected. For isolated mistakes that cannot be unambiguously corrected, we show that the type of substitution can be determined, and its location can be narrowed down to two or three positions, leading to a significant reduction in the the number of plausible alternative reads.ConclusionsThe Exact Call Chemistry increases the accuracy of the SOLiD platform, enabling many potential miscalls to be prevented. However, single miscalls in the color sequence can produce complex but localised patterns of error in the decoded nucleotide sequence. Analysis of similar codes shows that some exist that, if implemented in alternative chemistries, should have superior performance.

【 授权许可】

CC BY   
© Massingham and Goldman; licensee BioMed Central Ltd. 2012