Literature DB >> 26139637

Error filtering, pair assembly and error correction for next-generation sequencing reads.

Robert C Edgar1, Henrik Flyvbjerg2.   

Abstract

MOTIVATION: Next-generation sequencing produces vast amounts of data with errors that are difficult to distinguish from true biological variation when coverage is low.
RESULTS: We demonstrate large reductions in error frequencies, especially for high-error-rate reads, by three independent means: (i) filtering reads according to their expected number of errors, (ii) assembling overlapping read pairs and (iii) for amplicon reads, by exploiting unique sequence abundances to perform error correction. We also show that most published paired read assemblers calculate incorrect posterior quality scores.
AVAILABILITY AND IMPLEMENTATION: These methods are implemented in the USEARCH package. Binaries are freely available at http://drive5.com/usearch. CONTACT: robert@drive5.com SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
© The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Mesh:

Year:  2015        PMID: 26139637     DOI: 10.1093/bioinformatics/btv401

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


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