BayesHammer: Bayesian clustering for error correction in single-cell sequencing

Error correction of sequenced reads remains a difficult task, especially in single-cell sequencing projects with extremely non-uniform coverage. While existing error correction tools designed for standard (multi-cell) sequencing data usually come up short in single-cell sequencing projects, algorith...

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Published inBMC genomics Vol. 14; no. Suppl 1; p. S7
Main Authors Nikolenko, Sergey I, Korobeynikov, Anton I, Alekseyev, Max A
Format Journal Article
LanguageEnglish
Published London BioMed Central 2013
Springer Nature B.V
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ISSN1471-2164
1471-2164
DOI10.1186/1471-2164-14-S1-S7

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Summary:Error correction of sequenced reads remains a difficult task, especially in single-cell sequencing projects with extremely non-uniform coverage. While existing error correction tools designed for standard (multi-cell) sequencing data usually come up short in single-cell sequencing projects, algorithms actually used for single-cell error correction have been so far very simplistic. We introduce several novel algorithms based on Hamming graphs and Bayesian subclustering in our new error correction tool B AYES H AMMER . While B AYES H AMMER was designed for single-cell sequencing, we demonstrate that it also improves on existing error correction tools for multi-cell sequencing data while working much faster on real-life datasets. We benchmark B AYES H AMMER on both k -mer counts and actual assembly results with the SPA DES genome assembler.
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ISSN:1471-2164
1471-2164
DOI:10.1186/1471-2164-14-S1-S7