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. 2016 May 10:17:208.
doi: 10.1186/s12859-016-1069-7.

SeqPurge: highly-sensitive adapter trimming for paired-end NGS data

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SeqPurge: highly-sensitive adapter trimming for paired-end NGS data

Marc Sturm et al. BMC Bioinformatics. .

Abstract

Background: Trimming of adapter sequences from short read data is a common preprocessing step during NGS data analysis. When performing paired-end sequencing, the overlap between forward and reverse read can be used to identify excess adapter sequences. This is exploited by several previously published adapter trimming tools. However, our evaluation on amplicon-based data shows that most of the current tools are not able to remove all adapter sequences and that adapter contamination may even lead to spurious variant calls.

Results: Here we present SeqPurge ( https://github.com/imgag/ngs-bits ), a highly-sensitive adapter trimmer that uses a probabilistic approach to detect the overlap between forward and reverse reads of Illumina sequencing data. SeqPurge can detect very short adapter sequences, even if only one base long. Compared to other adapter trimmers specifically designed for paired-end data, we found that SeqPurge achieves a higher sensitivity. The number of remaining adapter bases after trimming is reduced by up to 90 %, depending on the compared tool. In simulations with different error rates, we found that SeqPurge is also the most error-tolerant adapter trimmer in the comparison.

Conclusion: SeqPurge achieves a very high sensitivity and a high error-tolerance, combined with a specificity and runtime that are comparable to other state-of-the-art adapter trimmers. The very good adapter trimming performance, complemented with additional features such as quality-based trimming and basic quality control, makes SeqPurge an excellent choice for the pre-processing of paired-end NGS data.

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Figures

Fig. 1
Fig. 1
Read layout with adapter contamination (a) and insert match algorithm examples with different offsets (b). Inserts are colored grey, adapter remains are colored black. Reverse reads are displayed with reverse-complementary sequence to facilitate visual comparison of sequences

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