Abstract

BackgroundA major obstacle in single-cell sequencing is sample contamination with foreign DNA. To guarantee clean genome assemblies and to prevent the introduction of contamination into public databases, considerable quality control efforts are put into post-sequencing analysis. Contamination screening generally relies on reference-based methods such as database alignment or marker gene search, which limits the set of detectable contaminants to organisms with closely related reference species. As genomic coverage in the tree of life is highly fragmented, there is an urgent need for a reference-free methodology for contaminant identification in sequence data.ResultsWe present acdc, a tool specifically developed to aid the quality control process of genomic sequence data. By combining supervised and unsupervised methods, it reliably detects both known and de novo contaminants. First, 16S rRNA gene prediction and the inclusion of ultrafast exact alignment techniques allow sequence classification using existing knowledge from databases. Second, reference-free inspection is enabled by the use of state-of-the-art machine learning techniques that include fast, non-linear dimensionality reduction of oligonucleotide signatures and subsequent clustering algorithms that automatically estimate the number of clusters. The latter also enables the removal of any contaminant, yielding a clean sample. Furthermore, given the data complexity and the ill-posedness of clustering, acdc employs bootstrapping techniques to provide statistically profound confidence values. Tested on a large number of samples from diverse sequencing projects, our software is able to quickly and accurately identify contamination. Results are displayed in an interactive user interface. Acdc can be run from the web as well as a dedicated command line application, which allows easy integration into large sequencing project analysis workflows.ConclusionsAcdc can reliably detect contamination in single-cell genome data. In addition to database-driven detection, it complements existing tools by its unsupervised techniques, which allow for the detection of de novo contaminants. Our contribution has the potential to drastically reduce the amount of resources put into these processes, particularly in the context of limited availability of reference species. As single-cell genome data continues to grow rapidly, acdc adds to the toolkit of crucial quality assurance tools.Electronic supplementary materialThe online version of this article (doi:10.1186/s12859-016-1397-7) contains supplementary material, which is available to authorized users.

Highlights

  • A major obstacle in single-cell sequencing is sample contamination with foreign DNA

  • We present a novel software tool called acdc (Automated Contamination Detection and Confidence estimation for single-cell genome data), which seamlessly integrates reference-based with reference-free methods

  • Besides using k-mers as a characteristic genomic signature, we looked into using coverage, too

Read more

Summary

Introduction

A major obstacle in single-cell sequencing is sample contamination with foreign DNA. Contamination screening generally relies on referencebased methods such as database alignment or marker gene search, which limits the set of detectable contaminants to organisms with closely related reference species. Single-cell sequencing (SCS) is one of the most powerful methods in genome discovery and analysis. A primary challenge in single-cell sequence data is the potential presence of contamination and the detection thereof [7]. Foreign DNA which does not belong to the target genome of a given single cell, might be introduced into a sample in different ways. Sources of contamination can include unclean lysis or whole genome amplification reagents, in addition to sample introduced non-target DNA [8, 9]

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call