ADEPT, a dynamic next generation sequencing data error-detection program with trimming. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Feng, Shihai; Lo, Chien-Chi; Li, Po-E; Chain, Patrick
• Is Part Of: BMC bioinformatics. Volume 17:Issue 1(2016)
• Page Start: 1
• Page End: 7
• Publication Date: 2016-12
• Subjects: Next generation sequencing -- Illumina error prediction -- Local quality scores -- Position-specific quality; Bioinformatics -- Periodicals; Computational biology -- Periodicals; 570.285
• DOI: 10.1186/s12859-016-0967-z
• Languages: English
• ISSNs: 1471-2105

Abstract

Abstract Background Illumina is the most widely used next generation sequencing technology and produces millions of short reads that contain errors. These sequencing errors constitute a major problem in applications such asde novo genome assembly, metagenomics analysis and single nucleotide polymorphism discovery. Results In this study, we present ADEPT, a dynamic error detection method, based on the quality scores of each nucleotide and its neighboring nucleotides, together with their positions within the read and compares this to the position-specific quality score distribution of all bases within the sequencing run. This method greatly improves upon other available methods in terms of the true positive rate of error discovery without affecting the false positive rate, particularly within the middle of reads. Conclusions ADEPT is the only tool to date that dynamically assesses errors within reads by comparing position-specific and neighboring base quality scores with the distribution of quality scores for the dataset being analyzed. The result is a method that is less prone to position-dependent under-prediction, which is one of the most prominent issues in error prediction. The outcome is that ADEPT improves upon prior efforts in identifying true errors, primarily within the middle of reads, while reducing the false positive rate.